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August 21-23, 2014 Santa Clara, California 
a SENS Research Foundation Conference 
Program Guide
2 
Dear Colleagues, 
a SENS Research Foundation Conference 
August 21-23, 2014 
Hyatt Regency Hotel 
Santa Clara, California 
It is our pleasure to welcome you to the 2014 Rejuvenation Biotechnology Conference. 
The continuing growth of research into the underlying causes of the diseases of aging 
brings with it the opportunity to build a Rejuvenation Biotechnology industry, an 
industry which builds on the strengths of regenerative medicine. Together over the next 
three days, we believe we can help create this new industry and inspire each other – as 
clinicians, researchers, patient advocates, regulators, venture capitalists, investors and 
industry leaders – to work together to make this happen. 
This conference has been designed to offer something for everyone: from the 
inspirational words of our scientific, business, and venture capital speakers to the latest 
research on diseases, such as Alzheimer’s Disease, cancer, cardiovascular disease, and 
diabetes. An entire track of sessions will cover the regulatory, financial, and economic 
issues involved in building a Rejuvenation Biotechnology industry. We have also 
scheduled plenty of time for networking with each other during our meal breaks, Poster 
sessions and our evening entertainment. 
We would like to thank each of your for attending the Rejuvenation Biotechnology 
Conference and bringing your expertise to our gathering. You have the vision, the 
knowledge, the wherewithal and the experience to come together to pave the way 
into the future. Throughout this conference, we ask you to stay engaged, deepen your 
understanding of the field, build communities of interest and create collaborations that 
will help shape the future of the industry. 
Thank you for choosing this conference. Enjoy your time here, and once again welcome to 
the Rejuvenation Biotechnology Conference. 
Mike Kope 
CEO, SENS Research Foundation 
Aubrey de Grey 
CSO, SENS Research Foundation
TO PARKING STRUCTURE 
Welcome Letter. 2 
Conference Schedule . 4 
Speaker Biographies. 14 
Sponsors . 26 
Poster Abstracts . 33 
NAPA I NAPA II NAPA III 
SONOMA 
MENDOCINO 
SANTA CLARA 
CONVENTION 
CENTER 
TUSCA 
COURTYARD 
TUSCA RESTAURANT 
POOL ELEVATOR 
CABANAS 
WHIRLPOOL 
SWIMMING POOL 
@ THE MARKET 
TERRA COURTYARD 
Networking Meals, Posters and 
Exhibits in Ballrooms EFGH 
EVOLUTION 
CAFE AND BAR 
FRONT 
DESK 
ELEVATORS 
CONCIERGE 
UP TO BALLROOM 
HOTEL ENTRANCE 
GIFT SHOP 
ATM 
REGENCY CLUB® 
MAGNOLIA 
NETWORK 
MEETING 
CENTER 
RESTROOMS 
TRUYA SUSHI 
LOUNGE 
RESTROOMS 
RESTROOMS 
Keynotes, Plenary & Concurrent Panels, 
and Performances in Ballrooms ABCD 
Registration in LOBBY WEST 
Ballrooms 
LOBBY 
WEST 
A 
B 
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Table of Contents
Conference Schedule 
Registration (until 5:00 pm) - [LOBBY WEST] 
Networking Breakfast - [Ballrooms EFGH] 
Opening Remarks - Michael Kope, CEO , SENS Research Foundation - [Ballrooms ABCD] 
Keynote: George Church, Professor of Genetics, Harvard Medical School, Professor of Health 
Sciences and Technology, Harvard and MIT: New Epigenome Analysis and Engineering 
Technologies for Reversal of Aging - [Ballrooms ABCD] 
Molecular and Cellular Damage as the Cause of the Diseases of Aging Panel - [Ballrooms ABCD] 
This panel will discuss the idea that the diseases of aging may stem from molecular and cellular 
damage that accrues with age. Topics of discussion will include the types of damage that may 
be involved, examples of how this applies to one or more diseases, and thoughts on how basic 
research and industry could use this concept to drive therapeutic target identification and drug 
treatment/development. 
• Richard Barker, Director, Center for the Advancement of Sustainable Medical Innovation: 
(Moderator) 
• Aubrey de Grey, Co-Founder and Chief Science Officer, SENS Research Foundation 
• Caleb Finch, ARCO/Kieschnick Professor of Gerontology and Biological Science and University 
Professor, USC Davis School of Gerontology 
• Jeff Karp, Associate Professor, Harvard Medical School, Co-Director of the Center for 
Regenerative Therapeutics, Brigham and Women’s Hospital 
• Stephen Minger, Chief Scientist, Cellular Sciences, GE Healthcare Life Sciences, UK 
Networking Lunch & Exhibits - [Ballrooms EFGH] 
8:00 am 
8:00 am 
9:00 am 
9:30 am 
10:30 am 
12:00 pm 
Day 1: Thursday, August 21, 2014 
4
[Ballroom A] [Ballroom D] [Ballrooms BC] 
Alzheimer’s Disease Session 1 
This session will highlight two types of 
cellular and molecular damage currently 
being researched as therapeutic targets for 
Alzheimer’s Disease. Speakers will discuss 
how tau tangles and cell loss are believed 
to lead to Alzheimer’s Disease, current 
ideas on how to remove or repair tau 
tangles, and how cell replacement can be 
used to treat Alzheimer’s. 
• Jean Hébert, Professor, Departments of 
Neuroscience and Genetics, Albert Einstein 
College of Medicine: A Twist of Fate - 
Reprogramming Neural Precursor Cells 
to Generate New Neocortical Neurons 
• Einar Sigurdsson, Associate Professor, 
Department of Neuroscience & 
Physiology, New York University: Tau 
Immunotherapy and Imaging 
• Claude Wischik, Professor of Old Age 
Psychiatry, University of Aberdeen, 
Executive Chairman, TauRX Therapeutics, 
Ltd.: Status of the First Phase 3 Clinical 
Trials Targeting the Tauopathy of 
Alzheimer’s Disease: Origins, Rationale 
and Design Considerations 
Cardiovascular Disease Session 1 
Building upon the idea discussed by the 
morning panel of using damage repair 
therapeutics to treat the diseases of aging, 
this session will consider cellular and 
molecular damage that can be targeted 
for cardiovascular disease therapy. 
Presentations will explain how cellular or 
molecular damage may lead to cardiovas-cular 
disease and how this damage may 
be removed or repaired. 
• Guillermo Garcia Cardena, Associate 
Professor of Pathology, Harvard Medical 
School, Director of the Laboratory for 
Systems Biology, Center for Excellence in 
Vascular Biology, Brigham and Women’s 
Hospital: Mechanical Forces, Vascular 
Inflammation and Atherosclerosis 
• W. Gray Jerome, Associate Professor and 
Director, Graduate Program in Cellular 
and Molecular Pathology, Vanderbilt 
University Medical Center: Chewing 
the Fat: Cholesterol, Autophagy and 
Lysosome Dysfunction 
• Michael Sherratt, Lecturer, Center 
for Regenerative Medicine, 
University of Manchester: Causes 
and Consequences of Age-Related 
Extracellular Matrix Remodelling 
Toward a New Investment 
Paradigm Panel 
This panel will discuss the challenges in 
bringing new and especially preventative 
therapies to treat the diseases of aging 
from the research lab to the market. 
The panel will offer and discuss new 
investment paradigms that could drive 
drug and therapeutic development. 
• David Brindley, Research Fellow, 
University of Oxford/Center for the 
Advancement of Sustainable Medical 
Innovation: (Moderator) 
• Neil Littman, Business Development 
Officer, California Institute for 
Regenerative Medicine 
• James O’Neill, Partner and 
Chief Operating Officer, Mithril 
Capital Management 
• Bernard Siegel, Executive Director, 
Genetics Policy Institute 
• Michael West, CEO, BioTime, Inc. 
1:00 pm CONCURRENT SESSIONS. PLEASE CHOOSE ONE: 
Conference Schedule 
5
Conference Schedule 
Day 1: Thursday, August 21, 2014 
Alzheimer’s Disease Session 2 
A third type of damage being targeted for 
Alzheimer’s therapeutics, A-beta aggregates, 
will be discussed during this session. Speak-ers 
will address how A-beta aggregates are 
believed to lead to Alzheimer’s Disease and 
current ideas on how to prevent or remove 
them. This session will also discuss how 
changing the way researchers, regulators, 
and pharmaceutical companies view the 
disease will change Alzheimer’s Disease 
drug development. Particular attention will 
be paid to the Accelerate Cure/Treatments 
for Alzheimer’s Disease (ACT-AD) proposal 
and recent guidance from the FDA. 
• Ashley Bush, Head of the Oxidation 
Disorders Laboratory, Mental Health 
Research Institute, University of 
Melbourne, Director of the Laboratory 
for Oxidation Biology Genetics and 
Aging Unit, Massachusetts General 
Hospital, Associate Professor, 
Department of Psychiatry, Harvard 
Medical School: Iron in Aging and 
Neurodegenerative Disease 
• Rachelle Doody, Professor of Neurology, 
Director, Alzheimer’s Disease and Memory 
Disorders Center, Baylor College of 
Medicine: Approaches to Brain Aging 
and Alzheimer’s Disease: What are We 
Learning from Clinical Trials? 
• Eric Siemers, Medical Director, 
Alzheimer’s Disease Team, Eli Lilly: 
New Paradigms in Alzheimer’s 
Disease Drug Development 
Cardiovascular Disease Session 2 
In this session, examples of current 
pharmaceutical advances in cardiovascular 
disease therapeutics will be presented. 
The talks will describe how these 
therapeutics remove or repair molecular 
and cellular damage and, in doing so, 
delay or prevent cardiovascular disease. 
• Gabor Forgacs, Professor, Biophysics 
Laboratory, Department of Physics 
& Astronomy, University of Missouri- 
Columbia, Founder, Organovo: The Role 
of Bioprinting in Rejuvenation 
• Linda Marban, CEO, Capricor 
Therapeutics: Raising Capricor: 
Building a Biotech Company 
from Bench to Bedside 
• James Yoo, Professor, Associate Director 
and Chief Scientific Officer, Wake Forest 
Institute for Regenerative Medicine: 
Tissue Engineering Solutions for 
Cardiovascular Tissue Pathologies 
The Economic Impact of an Aging 
Population on the Healthcare 
System Panel 
This panel will discuss the impending 
economic crisis the healthcare system 
will soon face caring for the ever-growing 
elderly population and possible solutions 
to this crisis, such as an outcomes-based 
healthcare model. 
• David Brindley, Research Fellow, 
University of Oxford/Center for the 
Advancement of Sustainable Medical 
Innovation: (Moderator) 
• Catalina Hoffman, Founder, Catalina 
Hoffmann Holding Group 
• Peter Nakada, Managing Director of Risk 
Markets, Risk Management Solutions, Inc. 
2:30 pm CONCURRENT SESSIONS. PLEASE CHOOSE ONE: 
[Ballroom A] [Ballroom D] [Ballrooms BC] 
6
Performance by Comedian Hal Sparks - [Ballrooms ABCD] 
Currently starring in the Disney XD show, LAB RATS, actor/comedian Hal Sparks began his 
professional career while still a teenager in Chicago. As a member of the famed Second City 
Troupe, his quick wit and affable personality quickly gained him recognition and acclaim 
and he was named the “Funniest Teenager In Chicago” by the Chicago Sun Times. Sparks 
went on to host the Emmy Award- winning “Talk Soup” on E! Entertainment Television, 
winning rave reviews from fans and critics alike. He starred for five seasons on Showtime’s 
hit series “Queer As Folk” and appeared in the films “Extract,” “Spiderman 2” and “Dude, 
Where’s My Car?.” Sparks recently starred in his own one hour Showtime comedy special, 
“Charmageddon,” which is now a best-selling DVD. He is a star commentator on VH1’s popular 
“I Love the 80’s” series and can be heard every Wednesday on the nationally syndicated 
“Stephanie Miller Radio Show.” Hal is also a pop culture expert and regularly appears on such 
shows as “Joy Behar” and CNN’s “Your Money.” His numerous other television appearances 
include “The Tonight Show,” “Larry King Live,” “Charlie Rose,” “Good Morning America,” “The 
View,” “Jimmy Kimmel” and MTV. In addition to a busy acting and stand-up career, he is an 
accomplished musician. Hal and his band, Zero 1, recently released their debut album. 
8:00 pm 
Afternoon Break & Exhibits - [Ballrooms EFGH] 
Advancing Regenerative Therapies in Alzheimer’s and Cardiovascular Disease Panel - [Ballrooms ABCD] 
This panel will bring together speakers from sessions throughout the day to consider the promise 
of a damage repair strategy to develop therapeutics for the diseases of aging. Discussion will 
include a summary of the accomplishments of the Alzheimer’s community in suggesting an 
innovative drug development strategy as well as debate about how such a strategy could 
apply to cardiovascular therapies. In particular, the panel will consider the impact applying 
a strategy similar to the ACT-AD proposal would have on cardiovascular disease therapeutic 
development, investment in cardiovascular drug development, and the healthcare system. 
• Aubrey de Grey, CSO, SENS Research Foundation: (Moderator) 
• Rachelle Doody, Professor of Neurology, Director, Alzheimer’s Disease and Memory Disorders 
Center, Baylor College of Medicine 
• Neil Littman, Business Development Officer, California Institute for Regenerative Medicine (CIRM) 
• Linda Marban, CEO, Capricor Therapeutics 
• Eric Siemers, Medical Director, Alzheimer’s Disease Team, Eli Lilly 
Poster Session/ Buffet Dinner & Exhibits - [Ballrooms EFGH] 
4:00 pm 
4:30 pm 
6:00 pm 
Conference Schedule 
7
Conference Schedule 
Registration (until 5:00 pm) - [LOBBY WEST] 
Networking Breakfast & Exhibits - [Ballrooms EFGH] 
Opening Remarks by Edward James Olmos, Actor - [Ballrooms ABCD] 
Keynote: Jim O’Neill, Partner and Chief Operating Officer, Mithril Capital Management: 
Fight Aging with a Durable Business - [Ballrooms ABCD] 
Toward a New Research Paradigm Panel - [Ballrooms ABCD] 
This panel will explore new ways to approach research to tackle the diseases of aging. In particular, 
consideration will be given to the effects a damage repair paradigm would have on developing 
new strategies to identify and study therapeutic targets, fostering more collaboration between 
researchers studying different diseases, and changing the way translational research and drug 
development are approached. 
• Richard Barker, Director, Center for the Advancement of Sustainable Medical Innovation: 
(Moderator) 
• Julie Allickson, Director, Translational Research, Wake Forest Institute for Regenerative Medicine 
• Judith Campisi, Professor, Buck Institute for Research on Aging 
• Howard Foyt, Vice President, Clinical Development and Chief Medical Officer, Viacyte, Inc 
• Daniel Kraft, Faculty Chair for Medicine, Singularity University 
Networking Lunch & Exhibits - [Ballrooms EFGH] 
8:00 am 
8:00 am 
9:00 am 
9:30 am 
10:30 am 
12:00 pm 
Day 2: Friday, August 22, 2014 
8
Cancer Session 
This session will highlight current break-throughs 
in cancer research. Additionally, 
the impact the I-SPY TRIAL 2 (Investigation 
of Serial studies to Predict Your Therapeutic 
Response with Imaging and Molecular 
Analysis 2) program has had on drug 
development, particularly Alzheimer’s 
drugs, will be discussed. 
• Judith Campisi, Professor, Buck Institute 
for Research on Aging: Cancer and 
Aging: Rival Demons? 
• Laura Esserman, Professor, Departments 
of Surgery and Radiology, and Affiliate 
Faculty, Institute for Health Policy 
Studies and Director, Carol Franc Buck 
Breast Care Center; Co-Leader, Breast 
Oncology Program, UCSF Helen Diller 
Family Comprehensive Cancer Center, 
University of California, San Francisco: 
Accelerating Knowledge Turns: The 
I-SPY Model and Drug Development 
• Claudia Gravekamp, Associate Professor, 
Albert Einstein College of Medicine: 
Curing Cancer in the Elderly Through 
Novel Strategies 
Parkinson’s Disease Session 
This session will feature the latest in 
Parkinson’s Disease research. A causal 
relationship between molecular and/ 
or cellular damage and Parkinson’s 
Disease will be explored. The speakers 
will also consider how this research 
could lead to preventative or damage 
repair treatment of the disease. 
• Julie Andersen, Professor, Buck Institute 
for Research on Aging: Senescence and 
the Aging Brain 
• Jeanne Loring, Professor, Scripps 
Research Institute: Negotiating the 
Mine Field in the Quest for a Parkinson’s 
Disease Cell Therapy 
• Dale Schenk, CEO, Prothena 
Corporation: Challenges and Hopes in 
Preventing and Developing Meaningful 
Therapeutic Strategies for Alzheimer’s 
and Parkinson’s Diseases 
Risk-Benefit Analysis in Therapies for 
the Diseases and Disabilities of Aging 
Today, the translation of healthcare 
innovations into patient outcomes is 
an inherently multi-stakeholder effort. 
Consequently, there is a major need to 
maintain rigor and independence in the 
regulation of healthcare innovations, 
while improving regulatory transparency 
and opportunities for multi-stakeholder 
input to accommodate fundamental 
changes in the life-science ecosystem and 
global healthcare demands. A key strategy 
in this endeavor is the development and 
utilization of novel risk-benefit appraisal 
methodologies, leveraging advances 
in patient reported outcomes (PROMS), 
stratified medicines – including ‘big data’ 
and risk management methodologies 
utilized presently in other industries. 
• David Brindley, Research Fellow, 
University of Oxford/Center for the 
Advancement of Sustainable Medical 
Innovation: (Moderator) 
• Richard Barker, Director, Center for 
the Advancement of Sustainable 
Medical Innovation 
• Chris Hornsby, Head of Model 
Development, Life Risks, Risk 
Management Solutions, Inc. 
• Brock Reeve, Executive Director, Harvard 
Stem Cell Institute 
1:00 pm CONCURRENT SESSIONS. PLEASE CHOOSE ONE: 
[Ballroom A] [Ballroom D] [Ballrooms BC] 
2:30 pm Afternoon Break & Exhibits - [Ballrooms EFGH] 
Conference Schedule 
9
Conference Schedule 
Day 2: Friday, August 22, 2014 
Performance by Comedian Dan Nainan - [Ballrooms ABCD] 
Dan Nainan got his start by taking a comedy class to get over the nervousness of speaking 
on stage in his job as a demo engineer with Intel Corporation. After leaving Intel to pursue 
comedy, he has toured with Russell Peters and other notable comedians. Dan has appeared 
on network television including “Last Comic Standing” as well as in feature films, on radio 
and in an Apple commercial. He just completed a comedy tour of India. 
8:00 pm 
Advancing Regenerative Therapies in Cancer and Parkinson’s Disease Panel - [Ballrooms ABCD] 
This panel will bring together speakers from throughout the day to summarize the impact of 
the I-SPY TRIAL 2 program on drug trial design for Alzheimer’s therapeutics and speculate on 
the applicability of trial designs similar to the one proposed for Alzheimer’s Disease to the 
development of therapeutics for other diseases of aging, such as Parkinson’s Disease and cancer. 
• Aubrey de Grey, CSO, SENS Research Foundation: (Moderator) 
• Rachelle Doody, Professor of Neurology, Director, Alzheimer’s Disease and Memory Disorders 
Center, Baylor College of Medicine 
• Laura Esserman, Professor, Departments of Surgery and Radiology, and Affiliate Faculty, 
Institute for Health Policy Studies and Director, Carol Franc Buck Breast Care Center; Co-Leader, 
Breast Oncology Program, UCSF Helen Diller Family Comprehensive Cancer Center, University 
of California, San Francisco 
• Jeanne Loring, Professor, Scripps Research Institute 
• Brock Reeve, Executive Director, Harvard Stem Cell Institute 
• Dale Schenk, CEO, Prothena Corporation 
Networking Dinner/ Poster Session & Exhibits - [Ballrooms EFGH] 
3:30 pm 
5:30 pm 
Concert by Cecilia Noël 
Originally from Lima, Perú, Cecilia’s career began at the age of eight with a starring role in a 
Peruvian television show. As a teenager, Cecilia’s mother sent her to Argentina and Germany 
to take voice, violin, and piano lessons. Encouraged by the legendary Stan Getz to move to the 
US, Cecilia relocated to New York City and briefly performed as a dancer with Jo Jo’s Dance 
Factory and Menudo. Cecilia moved to Los Angeles in 1989 and in the early 1990s formed 
Cecilia Noël and The Wild Clams. The group received quick attention for their explosive live 
shows and were consequently booked at the House of Blues and the Playboy Jazz Festival. 
Critics have long called her the “Latin Tina Turner.” “Salsoul”, the genre Cecilia created to 
describe her sound, combines elements of salsa, soul, jazz, funk, and Afro-cuban. Cecilia also 
performs and records with husband and former Men At Work frontman Colin Hay. 
10
Networking Breakfast & Exhibits - [Ballrooms EFGH] 
Conference Schedule 
Keynote: Peter Diamandis, Co-founder and Vice Chairman, Human Longevity, Inc, Founder and 
CEO, X PRIZE Foundation: Creating a Culture of Innovation and Breakthroughs - [Ballrooms ABCD] 
Applying a Damage Repair Paradigm to Developing Therapies for the Diseases of Aging 
Panel - [Ballrooms ABCD] 
Building upon the discussion of a damage repair paradigm from days 1 and 2, this panel will weigh 
the benefits of application of a damage repair paradigm to drug development to combat the 
diseases of aging. Discussion will include the feasibility of applying such a strategy, the advantages 
and disadvantages such a model would confer, and an analysis of the regulatory changes that 
would be required to make such a paradigm possible. 
• Richard Barker, Director, Center for the Advancement of Sustainable Medical Innovation: 
(Moderator) 
• Julie Allickson, Director, Translational Research, Wake Forest Institute for Regenerative Medicine 
• Stephen Minger, Chief Scientist, Cellular Sciences, GE Healthcare Life Sciences, UK 
• Evan Snyder, Director, Center for Stem Cell and Regenerative Medicine, Director, Stem Cell Research 
Center and Core Facility, Sanford-Burnham Medical Research Institute 
Networking Lunch & Exhibits - [Ballrooms EFGH] 
8:00 am 
9:00 am 
10:00 am 
11:30 am 
Day 3: Saturday, August 23, 2014 
11
Conference Schedule 
Day 3: Saturday, August 23, 2014 
Musculoskeletal Disease Session 
This session will highlight current muscu-loskeletal 
disease research. Presenters will 
discuss how molecular or cellular damage 
is believed to lead to their musculoskeletal 
disease of interest and how their research 
may contribute to delaying or preventing 
the disease. 
• Christy Carter, Assistant Professor, 
Department of Aging and Geriatric 
Research, Institute on Aging, University of 
Florida: What is Sarcopenia? Definitions, 
Diagnosis and Developing Interventions 
• Young Jang, Assistant Professor, 
Georgia Institute of Technology: The 
Rejuvenation of Aged Skeletal Muscle 
by Systematic Factors 
Diabetes Session 
Breakthroughs in diabetes research will be 
presented in this session. The molecular 
and cellular causes of diabetes will be 
considered and strategies to remove, repair, 
or replace such damage will be discussed. 
• Camillo Ricordi, Stacy Joy Goodman 
Professor of Surgery, Distinguished Professor 
of Medicine, Director, Diabetes Research 
Institute and Cell Transplant Program, 
University of Miami: Cellular Therapies 
and Regenerative Medicine Strategies 
for Treatment of Diabetes 
• David Schaffer, Professor, University of 
California, Berkeley, Director, Berkeley 
Stem Cell Center: Molecular Elucidation 
and Engineering of Stem Cell Therapies 
for the Nervous System 
Regulating a Damage Repair 
Approach to Cure the Diseases of 
Aging Panel 
Escalating societal healthcare needs have 
driven an unprecedented era of biomedical 
innovation. However, the development of 
candidate technologies without consider-ation 
of a robust regulatory strategy is likely 
to contribute to stymied patient access and 
commercial viability. Therefore, this session 
will consider worldwide efforts to rapidly 
and proportionally develop international 
regulatory processes to accommodate 
increasingly heterogeneous and unfamiliar 
healthcare technologies and their swift 
translation from lab to bedside. 
• David Brindley, Research Fellow, 
University of Oxford/Center for the 
Advancement of Sustainable Medical 
Innovation: (Moderator) 
• Bob Clay, Chief Regulatory Officer, 
Kinapse & Manging Director, Highbury 
Regulatory Science 
• Andrew Martello, Managing Director, 
Spoonful of Sugar 
• Evan Snyder, Director, Center for 
Stem Cell and Regenerative Medicine, 
Director, Stem Cell Research Center 
and Core Facility, Sanford-Burnham 
Medical Research Institute 
12:30 pm CONCURRENT SESSIONS. PLEASE CHOOSE ONE: 
[Ballroom A] [Ballroom D] [Ballrooms BC] 
12
Break 
Advancing Regenerative Therapies in Musculoskeletal Disease and Diabetes Panel - [Ballrooms ABCD] 
This panel will bring together speakers from the morning sessions to consider the possibility of 
applying a drug trial design similar to the ones emerging from the Alzheimer’s Disease and cancer 
communities. The feasibility of applying such a model will be considered with the biology of the 
disease, regulatory concerns, and pharmaceutical needs in mind. 
• Aubrey de Grey, CSO, SENS Research Foundation: (Moderator) 
• Christy Carter, Assistant Professor, Department of Aging and Geriatric Research, Institute on 
Aging, University of Florida 
• Andrew Martello, Managing Director, Spoonful of Sugar 
• Camillo Ricordi, Stacy Joy Goodman Professor of Surgery, Distinguished Professor of Medicine, 
Director, Diabetes Research Institute and Cell Transplant Program, University of Miami 
• Young Jang, Assistant Professor, Georgia Institute of Technology 
Building a Rejuvenation Biotechnology Industry - [Ballrooms ABCD] 
This panel will synthesize the discussions from all of the conference sessions and panels. A cross-section 
of academics, pharmaceutical reps, policy makers, and other presenters will revisit the 
merits of a damage repair paradigm to address the diseases of aging considered at this conference. 
Panelists will consider the changes that would be required to lay the groundwork for a new industry 
perspective focused on addressing damage indications for the diseases of aging either through 
preventing or repairing such damage. 
• Michael Kope, CEO, SENS Research Foundation: (Moderator) 
• George Church, Professor of Genetics, Harvard Medical School, Professor of Health Sciences 
and Technology, Harvard and MIT 
• Dana Goldman, Leonard D. Schaeffer Chair and Director of the Schaeffer Center for Health Policy 
and Economics, University of Southern California 
• Stephen Minger, Chief Scientist, Cellular Sciences, GE Healthcare Life Sciences, UK 
• Brock Reeve, Executive Director, Harvard Stem Cell Institute 
Conference Concludes 
1:30 pm 
2:00 pm 
3:00 pm 
4:30 pm 
Conference Schedule 
13
Julie Allickson 
Dr. Allickson focuses 
on the translation of 
regenerative 
medicine products 
including cell 
therapy, tissue 
engineering, 
biomaterials and 
devices. This process 
begins at Proof-of- 
Concept where early discussions with 
regulators and clinicians are critical in 
moving the technology from the bench to 
the bedside. 
Prior to joining the institute, she was an 
Executive Officer of the company and Vice 
President of Laboratory Operations and 
R & D at Cryo-Cell International, Inc., an 
AABB accredited Cord Blood Bank. Prior to 
this position, she worked for the Univer-sity 
Of Miami School Of Medicine, Diabe-tes 
Research Institute as the Laboratory 
Director of the cGMP Hematopoietic Cell 
Processing Facility. She was responsible 
for the design and implementation of the 
State Licensed Clinical Flow Cytometry 
Laboratory. 
Dr . Allickson was the lead in Regulatory 
Affairs for the processing laboratory of Islet 
and Hematopoietic Cell products which 
included oversight of all Investigational 
New Drugs (IND) and external regulations. 
Prior to this, she worked for the American 
Red Cross managing the Hematopoietic 
Cell Processing and Platelet Serology 
Laboratory and serving as a member of the 
National Stem Cell Task Force. 
She has a Doctorate in Health Sciences and 
a Master’s Degree in Medical Laboratory 
Sciences. She is one of the founding mem-bers 
of the International Society of Cellular 
Therapy and a member of the American 
Association of Blood Banks (AABB) for 25 
years. She is currently Chair of the AABB 
Standards Committee for Cell Therapy 
Product Services. Dr. Allickson is also on 
the Technical Advisory Board for Tissue 
Engineered Products under ICCBBA and the 
ISCT Commercialization Committee. 
Julie Andersen 
As a renowned 
expert on Parkin-son’s 
disease, Dr. 
Andersen is 
pursuing a wide 
array of leads 
toward treatments 
for this complex 
neurodegenerative 
disorder. She has 
identified several early risk signals for 
Parkinson’s, an age-related illness that 
causes a progressive decline in movement 
and muscle control. The symptoms can 
include shaking hands and difficulty with 
walking. 
Amongst the early risk signals identified 
by Dr. Andersen are elevated levels of iron 
and declining amounts of a protective 
antioxidant called glutathione. Recently, 
the Andersen lab has also discovered 
valuable clues by examining the roles 
of enzymes and other proteins involved 
in nerve cell degeneration. Normally, 
proteins carry out the routine work inside 
cells. But some enzymes can promote the 
symptoms of Parkinson’s disease. Blocking 
those enzymes might slow down the 
disease. Other therapies might result from 
the opposite tactic: reinforcing the work 
of different enzymes that guard against 
Parkinson’s disease. These enzymes seem 
to prevent damage to genes that protect 
the nervous system. 
The Andersen lab is also involved in identi-fying 
potential biomarkers for Parkinson’s 
that may allow early interventional therapy. 
Dr. Andersen earned a doctorate in 
Neuromolecular Biology at the University 
of California, Los Angeles (UCLA). She 
completed a postdoctoral fellowship at 
Harvard Medical School and Massachusetts 
General Hospital before going to the 
University of Southern California as an 
assistant then an associate professor at the 
Andrus Gerontology Center. She joined the 
Buck Institute in 2000. 
Richard Barker 
Richard is a strategic 
advisor, speaker and 
author on health-care 
and life 
sciences. He is 
Director of the 
Centre for the 
Advancement of 
Sustainable Medical 
Innovation, a major 
European initiative aimed at transforming 
the R&D and regulatory processes in life 
sciences to bring advances more rapidly 
and affordably to patients. 
He is also chairman of the South London 
Academic Health Science Network, accel-erating 
innovation in this region of the 
NHS, and Chairman of Stem Cells for Safer 
Medicines, a public-private partnership 
developing stem cell technology for 
predicting the safety profile of new medi-cines. 
He is a board member of Celgene, a 
major US-based bio-therapeutics company 
and of iCo Therapeutics, a Canadian 
bioscience company. 
His 25-year business career in healthcare 
has spanned biopharmaceuticals, diag-nostics 
and medical informatics – both in 
the USA and Europe. Most recently he was 
Director General of the Association of the 
British Pharmaceutical Industry, member 
of the Executive Committee of EFPIA (the 
European industry association) and Council 
member of IFPMA (the international 
equivalent). 
As a co-founder of Life Sciences UK, 
member of the NHS Stakeholder Forum, 
vice-chair of the UK Clinical Trials Collab-oration 
and in many other roles, he has 
advised successive UK governments on 
healthcare issues, especially those relating 
to developing, valuing and using new 
healthcare technologies. 
His past leadership roles include head of 
McKinsey’s European healthcare practice, 
General Manager of Healthcare Solutions 
for IBM and Chief Executive of Chiron 
Diagnostics. He was also Chairman and 
Chief Executive of Molecular Staging, a US 
bioscience company, now part of Qiagen. 
Speaker Biographies 
14
David Brindley 
David is an interna-tional 
thought-leader 
in the 
translation of 
life-science 
innovations into 
commercially viable 
products and 
services. His 
expertise spans the 
‘Valley of Death,’ encompassing regulation, 
engineering and finance. Currently David’s 
professional activities include: research into 
the optimization of risk: benefit appraisal 
techniques for healthcare innovations, 
leading the CASMI Translational Stem Cell 
Consortium and providing timely and 
pragmatic advice to a range of stakeholders 
in healthcare translation, notably the 
venture capital community. 
Examples of David’s work can be found in 
a range of high impact journals including 
Nature, Nature Biotechnology, Nature Medi-cine 
and Cell Stem Cell. David also produces 
a popular blog, Cell Therapy Industry 2027, 
with the Centre for the Commercialisation 
of Regenerative Medicine. David is an 
active Fellow of the Royal Institution of 
Great Britain and the Royal Society for the 
Advancement of Arts and Manufacturing. 
David has successfully passed the Charted 
Analyst in Alternative Investments (CAIA) 
Level 1 examination. 
David completed his undergraduate studies 
in Biochemical Engineering at University 
College London (with First Class Honors) and 
his Masters, investigating the commercial-ization 
of regenerative therapies, jointly at 
the Harvard Stem Cell Institute and Harvard 
Business School. Currently he is pursuing a 
DPhil (PhD) in Musculoskeletal Sciences at 
the University of Oxford. 
Ashley Bush 
Ashley I. Bush (MB 
BS, DPM, FRANZCP, 
PhD, FTSE) heads 
the Oxidation 
Biology Unit at the 
Florey Institute of 
Neuroscience & 
Mental Health, is 
Professor of 
Neuroscience and 
Pathology at The University of Melbourne, 
NHMRC Australia Fellow, co-director of 
Speaker Biographies 
biomarker development for the Australian 
Imaging Biomarker Lifestyle Study (AIBL), 
Chief Scientific Officer of the Cooperative 
Research Center for Mental Health, and has 
staff appointments in Psychiatry and Radiol-ogy 
at the Massachusetts General Hospital. 
He has received numerous awards includ-ing 
the Potamkin Prize and the Beeson 
Award. Professor Bush has authored over 
300 publications, with >21,000 citations 
(the most highly-cited Australian neurosci-entist 
of the last 10 years), 23 patents and 
founded 4 biotechnology companies. His 
lab discovered the interaction of beta-am-yloid 
with transitional metals as a major 
factor in Alzheimer’s disease pathology, as 
well as the roles of APP and tau in neuronal 
iron homeostasis. 
Judith Campisi 
Judith Campisi 
received a PhD in 
Biochemistry from 
the State University 
of New York at Stony 
Brook, and post-doctoral 
training in 
cell cycle regulation 
and cancer at the 
Dana-Farber Cancer 
Institute and Harvard Medical School. As an 
Assistant Professor at the Boston University 
Medical School, she began to focus her 
laboratory on role of cellular senescence in 
suppressing the development cancer, but 
soon became convinced that senescent cells 
also contributed to aging. She left Boston 
University as an Associate Professor to 
accept a Senior Scientist position at the 
Lawrence Berkeley National Laboratory in 
1991. In 2002, she established a laboratory 
at the Buck Institute for Age Research, 
where she is a Professor. 
At both institutions, Campisi established 
a broad program to understand various 
aspects of aging, with an emphasis on the 
interface between cancer and aging. Her lab-oratory 
made several pioneering discoveries 
in these areas. Her research continues to 
challenge and alter existing 
In recognition of the quality of her research 
and leadership, Campisi received numerous 
awards, including two MERIT awards from 
the US National Institute on Aging, awards 
from the AlliedSignal Corporation, Geron-tological 
Society of America and American 
Federation for Aging Research, and the 
Longevity prize from the IPSEN Foundation. 
She serves on numerous national and 
international editorial and advisory boards. 
Guillermo García-Cardeña 
Guillermo Garcia 
Cardena is an 
Associate Professor 
of Pathology at 
Harvard Medical 
School, and the 
Director of the 
Laboratory for 
Systems Biology at 
the Center for 
Excellence in Vascular Biology, Brigham and 
Women’s Hospital, Boston. He received his 
Ph.D. degree from Yale University, working 
with William C. Sessa on the molecular 
regulation of nitric oxide production in 
vascular endothelium. His postdoctoral 
research with Michael A. Gimbrone Jr. at 
Harvard Medical School was on studies of 
endothelial cell gene expression, hemody-namics, 
and atherogenesis. 
Christy Carter 
Dr. Carter received 
her PhD in Experi-mental 
and Biologi-cal 
Psychology from 
the University of 
North Carolina at 
Chapel Hill and her 
post-doctoral 
training at The Wake 
Forest University 
School of Medicine in Winston-Salem, 
North Carolina. 
Globally , Dr. Carter’s current research inter-ests 
lie in preserving physical function and 
healthspan during aging; and in particular 
focuses on the use of a preclinical rodent 
model of aging to test a variety of late-life 
interventions designed to mitigate sarco-penia. 
Furthermore, she has demonstrated 
that the application of standardized physical 
performance measures to a variety of animal 
models of aging may help to define simi-larities 
between species in the underlying 
mechanisms of sarcopenia, the age-related 
decline in performance, disability, and 
longevity. Indeed the assessment of behav-ioral 
outcomes is essential for measuring the 
efficacy of any late-life intervention in the 
context of mitigating declining performance 
and improving healthspan. She has extended 
15
this area of research to other special aging 
populations such as the frail and obese, and 
has developed combinatorial therapies, 
using these compounds in conjunction with 
behavioral modification such as exercise. 
George Church 
George Church is 
Professor of Genetics 
at Harvard Medical 
School and Director 
of PersonalGenomes. 
org, which provides 
the world’s only 
open-access 
information on 
human Genomic, 
Environmental & Trait data (GET). His 1984 
Harvard PhD included the first methods for 
direct genome sequencing, molecular 
multiplexing & barcoding. These led to the 
first genome sequence (pathogen, Helico-bacter 
pylori) in 1994. His innovations have 
contributed to nearly all “next generation” 
genome sequencing methods and compa-nies 
(CGI, Life, Illumina, nanopore). This plus 
chip-based DNA synthesis and stem cell 
engineering resulted in founding additional 
application-based companies spanning 
fields of medical diagnostics (Knome, 
Alacris, AbVitro, Pathogenica ) and synthetic 
biology / therapeutics ( Joule, Gen9, Editas, 
Egenesis, enEvolv, WarpDrive). 
He has also pioneered new privacy, bio-safety 
, environmental & biosecurity policies. 
He is director of NIH Center for Excellence 
in Genomic Science. His honors include 
election to NAS & NAE & Franklin Bower 
Laureate for Achievement in Science. He has 
coauthored 330 papers, 60 patents & one 
book (Regenesis). 
Bob Clay 
Bob Clay recently 
established his own 
regulatory consul-tancy 
practice 
through Highbury 
Regulatory Science, 
prior to this he was 
a VP Global 
Regulatory Affairs 
at AstraZeneca with 
responsibility for oncology, infection and 
personalised healthcare. Bob is Chief 
Regulatory Officer at Kinapse and a 
member of the board of TOPRA. He is a 
member of the Expert Scientific Advisory 
Committee for Medicines for Malaria Venture 
(MMV) and several working groups at CPTR 
(Critical Path for TB Regimens). He has an 
interest in the impact of regulation on the 
development of innovative medicines and 
healthcare policy matters. 
Bob is a regulatory strategist with more than 
30 years’ experience in drug development, 
leading the global regulatory approval of 
products across a range of therapy areas 
including metabolic diseases, neuroscience, 
cancer and infection. Bob graduated in 
Pharmacy from the University of Bath and 
subsequently completed an MSc in BioPhar-macy, 
from the University of London, and an 
MBA, from the Open University. Following 
completion of his professional training in 
hospital pharmacy he joined the pharma-ceutical 
industry as a formulation scientist 
at the UK laboratories of Rhone-Poulenc. 
Later, he joined the UK Licensing Authority 
as a pharmaceutical assessor and has held 
regulatory affairs leadership roles with 
several pharmaceutical companies including 
Wellcome, Zambon, Pfizer and AstraZeneca. 
Aubrey de Grey 
Dr. de Grey is the 
biomedical geron-tologist 
who 
researched the idea 
for and founded 
SENS Research 
Foundation. He 
received his BA in 
Computer Science 
and Ph.D. in Biology 
from the University of Cambridge in 1985 
and 2000, respectively. Dr. de Grey is 
Editor-in-Chief of Rejuvenation Research, is a 
Fellow of both the Gerontological Society of 
America and the American Aging Association, 
and sits on the editorial and scientific 
advisory boards of numerous journals and 
organizations. He is the Chief Science Officer 
of the SENS Research Foundation. 
Peter Diamandis 
Dr. Peter H. Diamandis 
is an international 
pioneer in the fields of 
innovation, incentive 
competitions and 
commercial space. 
In the field of 
Innovation, Diamandis 
is Chairman and CEO 
of the X PRIZE Foundation, best known for its 
$10 million Ansari X PRIZE for private 
spaceflight. Today the X PRIZE leads the world 
in designing and operating large-scale global 
competitions to solve market failures. 
Diamandis is also the Co-Founder and 
Vice-Chairman of Human Longevity Inc. (HLI), 
a genomics and cell therapy-based diag-nostic 
and therapeutic company focused on 
extending the healthy human lifespan. He is 
also the Co-Founder and Executive Chairman 
of Singularity University, a graduate-level 
Silicon Valley institution that studies expo-nentially 
growing technologies, their ability 
to transform industries and solve humanity’s 
grand challenges. 
In the field of commercial space, Diamandis 
is Co-Founder/Co-Chairman of Planetary 
Resources, a company designing spacecraft 
to enable the detection and mining of 
asteroid for precious materials. 
Diamandis is the New York Times Bestselling 
author of Abundance – The Future Is Better 
Than You Think. Abundance was #1 on 
Amazon and #2 on New York Times. He was 
also named one of “The World’s 50 Greatest 
Leaders” – by Fortune Magazine. 
He earned an undergraduate degree in 
Molecular Genetics and a graduate degree in 
Aerospace Engineering from the Massachu-setts 
Institute of Technology, and received his 
M.D. from Harvard Medical School. 
Diamandis’ mission is to open the space 
frontier for humanity. His personal motto is: 
“The best way to predict the future is to create 
it yourself.” 
Rachelle Doody 
Dr. Doody is the Effie 
Marie Cain Chair in 
Alzheimer’s Disease 
Research and 
Professor of 
Neurology at Baylor 
College of Medicine, 
where she directs 
the Alzheimer’s 
Disease and Memory 
Disorders Center (ADMDC). She received a B.A. 
from Rice University, a M.D. from Baylor 
College of Medicine, and completed intern-ship 
and residency training at the Royal 
Victoria Hospital and Montreal Neurologic 
Institute in Montreal, and at Baylor College of 
Speaker Biographies 
16
Medicine and has a Ph.D. in Cognitive 
Anthropology from Rice University where she 
studied the brain and language. 
She has published over 170 original research 
articles, most dealing with the diagnosis, 
progression, or treatment of Alzheimer’s 
Disease. She has received multiple research 
grants, including a Zenith Award from 
the National Alzheimer’s Association, and 
designed and conducted numerous clinical 
trials of Alzheimer’s Disease therapies. She 
participates in National and International 
collaborative efforts, review boards, and 
advisory boards including Steering 
Committees for the NIH AD Cooperative 
Study and AD Neuroimaging Initiatives, and 
the Steering Committee for the Texas AD 
Research and Care Consortium. 
Current research interests include studies to 
understand and model the progression of 
Alzheimer’s Disease, studies of clinical het-erogeneity, 
and research and development 
of new medications to treat Alzheimer’s 
Disease. She works with many biopharma-ceutical 
and large pharma collaborators in 
the assessment and experimental testing of 
a diverse group of potential AD therapies. 
She has served on the Texas Council on 
Alzheimer’s Disease and Related Disorders, 
and the Board of Directors for the Houston 
and Southeast Texas Chapter of the Alzhei-mer’s 
Association. 
Laura Esserman 
Dr. Esserman is a 
surgeon and breast 
cancer oncology 
specialist, and is the 
Director of the Carol 
Franc Buck Breast 
Care Center at the 
University of 
California, San 
Francisco (UCSF). In 
1996, she started the Center of Excellence for 
Breast Cancer Care at UCSF to integrate 
clinical care and research, automate tools for 
the capture of patient and clinical data, and 
develop systems to tailor care to biology, 
patient preference, and performance. 
Dr. Esserman is nationally and internationally 
known as a leader in the field of breast 
cancer and has published over 200 articles. 
She served as a member of a taskforce for 
President Obama’s Council of Advisors on 
Science and Technology (PCAST) Working 
Speaker Biographies 
Group on Advancing Innovation in Drug 
Development and Evaluation. The group was 
tasked with making recommendations to 
the federal government about how to best 
support science-based innovation in the 
process of drug development and regulatory 
evaluation. 
She is the Principle Investigator of the I-SPY 
TRIAL program, a multi-site neoadjuvant 
clinical trial (which includes phase 2 and 
3 trials) that has evolved into a model for 
translational research and innovation in 
clinical trial design. Dr. Esserman has recently 
launched a University of California-wide 
breast cancer initiative called the Athena 
Breast Health Network, a program designed 
to follow 150,000 women from screening 
through treatment and outcomes, incorpo-rating 
the latest in molecular testing and 
web-based tools into the course of care. 
Athena is in the final stages of launching a 
statewide demonstration project and phase 
1/2 trial of personalized screening. 
Caleb Finch 
Caleb Finch Ph.D. is 
ARCO Professor of 
Gerontology and 
Biological Sciences 
at the University of 
Southern California, 
with adjunct 
appointments in the 
Department of 
Anthropology, 
Molecular Biology, Neurobiology, Psychol-ogy, 
Physiology, and Neurology. Major 
research interest is the neurobiology of 
aging and human evolution. Finch received 
his undergraduate degree from Yale in 1961 
(Biophysics) and Ph.D. from Rockefeller 
University in 1969 (Biology). 
His life work is the fundamental biology of 
human aging, started in grad school and 
continued since 1972 at USC. Discoveries 
include a new form of neurotoxicity of 
amyloid peptides relevant to Alzheimer 
disease and the role of shared inflammatory 
pathways in normal and pathological aging 
process. Fifteen of his mentored students 
hold senior positions in universities or 
pharmaceutical corporations. 
Finch has received most of the major awards 
in biomedical gerontology, including the 
Robert W. Kleemeier Award (1985), the 
Sandoz Premier Prize (1995), and the Irving 
Wright Award (1999). He was founding 
Director of the NIA-funded USC Alzheimer 
Disease Research Center (1984), and 
continues as coDirector and coPI. He also 
co-founded Acumen Pharmaceuticals, 
which develops therapeutics for Alzheimer 
disease. He has written four books, most 
recently, The Biology of Human Longevity: 
Inflammation and Nutrition in the Evolution 
of Lifespans (Academic Press, 2007). Recent 
interests include the paleopathology of 
human aging and emerging environmental 
factors in aging, particularly air pollution 
components from fossil fuels. 
Gabor Forgacs 
Dr. Gabor Forgacs is 
a theoretical 
physicist turned 
bioengineer turned 
innovator and 
entrepreneur. He is 
the George H. 
Vineyard Professor of 
Biological Physics at 
the University of 
Missouri-Columbia, the Executive and 
Scientific Director of the Shipley Center for 
Innovation at Clarkson University and 
scientific founder of Organovo, Inc. and 
Modern Meadow, Inc. 
He was trained as a theoretical physicist 
at the Roland Eotvos University, Budapest, 
Hungary and the Landau Institute of 
Theoretical Physics, Moscow, USSR. He 
also has a degree in biology. His research 
interests span from topics in theoretical 
physics to physical mechanisms in early 
embryonic development. 
He is the co-author of the celebrated 
text in the field, “Biological Physics of 
the Developing Embryo” (Cambridge 
University Press, 2005) that discusses the 
fundamental morphogenetic mechanisms 
evident in early development. These 
mechanisms are being applied to building 
living structures of prescribed shape and 
functionality using bioprinting, a novel tis-sue 
engineering technology he pioneered. 
He is the author of over 160 peer-reviewed 
scientific articles and 5 books. 
He has been recognized by numerous 
awards and citations. In particular, he 
was named as one of the “100 most 
innovative people in business in 2010” by 
FastCompany. 
17
Howard Foyt 
Howard Foyt, M.D., 
Ph.D. FACP, Vice 
President, Clinical 
Development and 
Chief Medical Officer 
at ViaCyte, Inc., has 
over 18 years of 
clinical development 
experience in 
pharmaceutical and 
biotechnology environments. Dr. Foyt’s 
background as an endocrinologist and his 
multiple NDA and IND applications 
position him as ViaCyte’s strategic leader 
for clinical and regulatory operations. Prior 
to ViaCyte, Dr. Foyt served as Senior Vice 
President and Chief Medical Officer at 
Cebix, Inc., a company focused on treat-ments 
for complications of type 1 diabetes. 
Before Cebix, he was Vice President, 
Clinical Development at Metabasis 
Therapeutics, Inc. Dr. Foyt’s pharmaceutical 
experience includes senior positions at 
Pfizer Global Research & Development and 
Parke-Davis Pharmaceutical Research. 
As a clinician, Dr. Foyt was Assistant 
Professor and Medical Director of 
the University Diabetes Center at the 
University of Texas Medical Branch. He 
earned his medical degree from Baylor 
College of Medicine where he also earned 
a Ph.D. in Cell Biology. Dr. Foyt completed 
his residency in internal medicine at 
Baylor and an endocrinology fellowship 
at the National Institute of Diabetes and 
Digestive and Kidney Diseases, National 
Institutes of Health. 
Dana Goldman 
Dana Goldman is a 
Professor and the 
Leonard D. Schaeffer 
Chair in Health 
Policy at the 
University of 
Southern California. 
He is also the 
inaugural director of 
the Schaeffer Center 
for Health Policy and Economics, one of the 
nation’s premier health policy research 
institutions. Dr. Goldman is the author of 
over 150 articles and book chapters, 
including publications in the most presti-gious 
medical, economic, health policy, and 
statistics journals. He is a health policy 
advisor to the Congressional Budget Office, 
Covered California (California’s insurance 
exchange), and the Fred Hutchinson Cancer 
Institute. He serves on several editorial 
boards including Health Affairs and the 
American Journal of Managed Care, and is 
the founding editor of the Forum for Health 
Economics and Policy. Dr. Goldman’s work 
has been featured in the New York Times, 
Wall Street Journal, Washington Post, 
Business Week, U.S. News and World Report, 
The Economist, NBC Nightly News, CNN, 
National Public Radio, and other media. In 
2009, he was elected to the National 
Academy of Science’s Institute of Medicine 
in recognition of his professional achieve-ment. 
He was the first recipient of the 
MetLife Foundation’s Silver Scholar Award, 
honoring his research on aging; the Eugene 
Garfield Economic Impact Prize, recogniz-ing 
outstanding research demonstrating 
how medical research impacts the econ-omy; 
the National Institute for Health Care 
Management Research Foundation award 
for excellence in health policy; and the 
Alice S. Hersh New Investigator Award 
recognizing contributions of a young 
scholar to health services research. He is 
also a founder and managing director of 
Precision Health Economics, a consulting 
firm to the health care industry. Dr. Gold-man 
received his B.A. summa cum laude 
from Cornell University and a Ph.D. in 
Economics from Stanford University. 
Claudia Gravekamp 
Claudia Gravekamp, 
PhD, is an Associate 
Professor in the 
Department of 
Microbiology and 
Immunology of the 
Albert Einstein 
College of Medicine 
in New York, and a 
member of the 
Albert Einstein Cancer Center. She received 
her PhD in 1988 in the field of Tumor 
Immunology at the Erasmus University in 
Rotterdam, The Netherlands. From 1987 
to1993, she served as head of the Labora-tory 
for Leptospirosis at the Royal Tropical 
Institute in Amsterdam, The Netherlands. In 
1993, she started as a Research Fellow in 
Medicine at the Channing Laboratory of the 
Brigham and Women’s Hospital, Harvard 
Medical School, and soon became an 
Instructor in Medicine until 1998. There, she 
developed vaccines against Group B 
Streptococcus and gained expertise in the 
design and development of gene-driven 
vaccines. From 1998 to 2006, she was an 
Associate Member in the Institute for Drug 
Development of the Cancer Therapy and 
Research Center and an Assistant Professor 
at the University of Texas Health Science 
Center, in San Antonio, where she began to 
develop a program aimed at genetic 
vaccines for breast cancer. From 2006-2008, 
she was a Scientist at the California Pacific 
Medical Center Research Institute in San 
Francisco, continuing to develop novel 
immunotherapeutic approaches to cancer 
using attenuated Listeria monocytogenes as 
a platform to deliver anti-cancer agents 
selectively to the tumor microenvironment 
at young and old age. She has been funded 
by grants from the NIH, other grant agencies 
and private industry since 1999, published 
55 scientific articles, is a member of the 
Editorial Board of Mechanisms of Ageing 
and Development, and is ad-hoc reviewer 
for various scientific journals. 
Catalina Hoffman 
Catalina Hoffman is 
a leader in the 
elderly sector for her 
trajectory as 
entrepreneur, 
business woman 
and Hoffmann 
Method’s creator. 
She graduated with 
a PDD from the IESE 
Business School of Navarra University. She 
has studied Occupational Therapy and is a 
specialist in cognitive stimulation. The 
Hoffmann Method offers an innovative 
system of care and personalized attention 
which takes into account the physical, 
cognitive, psychological and social areas. It 
has achieved improvements in the health 
and quality of life of many people. It 
includes a network of partners in the social, 
health, scientific and technological sphere. 
She is a member of the Board of Spain Start-up’s 
Governing Council. She was named 
President of SECOT in June 2013. She is 
an associate and mentor of the European 
Professional Women’s Network. From 
this network, she is godmother of Mapel 
Project of Ayuda en Acción (NOG), aimed to 
craftswoman entrepreneurs in Ecuador. 
She also received national and international 
recognitions including The Harvard 
Business School Expansion Award for the 
Speaker Biographies 
18
Entrepreneurship. She was added to The 
Top 100 Women Leaders in Spain 2012. 
Plataforma Editorial published her first 
book “Emprender soñando”. The Prince of 
Girona Foundation granted her the Award 
of Business Woman 2013. The Association of 
Young Entrepreneur of Madrid named her 
the Young Entrepreneur of Madrid 2014. 
In 2013, she created the Catalina Hoffmann 
Holding Group, a group of companies 
specialized in different areas of science, 
health, health care, new technologies, 
consulting, innovation and development 
of new products and services. It includes 
Vitalia, Hoffman Elderly,Hoffmann Health- 
Care Innovation and Catalina Hoffmann 
Foundation. 
Chris Hornsby 
Chris’ academic 
background is in 
applied mathemat-ics 
and epidemiol-ogy, 
his doctoral 
research at Univer-sity 
College London 
was focused on 
probabilistic models 
of the multistage 
development of cancer. Chris joined the 
LifeRisks group at RMS in 2008 working 
initially as lead developer of the RMS 
Longevity Risk Model and subsequently 
more broadly on insurance capital reserv-ing 
and risk transfer applications in respect 
of both life catastrophe and longevity. 
Chris has played a key role, through the 
provision of expert risk analysis, in the early 
development of capital markets based 
solutions for hedging longevity risk. 
Jean Hébert 
Jean Hébert Jean 
Hébert completed 
his PhD at the 
University of 
California, San 
Francisco, under the 
mentorship of Gail 
Martin where he 
studied cell-signaling 
factors that regulate 
some of the early steps in mammalian 
development. For these studies, he used 
embryonic stem cells and mouse genetics. 
As a postdoctoral fellow in Susan McCon-nell’s 
lab at Stanford University, he then 
focused his attention on how the neocortex, 
Speaker Biographies 
the part of our brains that we use for our 
highest cognitive and perceptual functions, 
develops. Continuing along these interests, 
he currently heads his own research lab at 
the Albert Einstein College of Medicine 
where his group has primarily undertaken 
two lines of investigation. 
The first is understanding how a simple 
sheet of neuroepithelial cells early in 
embryogenesis develops into the adult 
neocortex, seat of our consciousness. 
Conditional genetic approaches in the 
mouse, whereby candidate genes that 
regulate neocortex formation are deleted 
or overexpressed specifically in neural 
precursor cells, comprise the central method 
driving these studies. 
The second line of investigation aims to 
establish ways of regenerating the principle 
neurons of the adult cerebral cortex when 
these neurons are lost due to trauma or 
degeneration, including degeneration due 
to aging. Since endogenous precursors do 
not replace cortical neurons when they are 
lost, two strategies are being developed: 
manipulating these precursors with molec-ular 
genetic techniques to start generating 
neurons and transplanting engineered 
precursors that are programmed to disperse 
in the cortex and differentiate into cortical 
projection neurons. 
Young Jang 
Young Jang received 
his Ph.D. in Biomedi-cal 
Sciences (Cell 
Biology) from 
University of Texas in 
2008, and completed 
his postdoctoral 
training from 
Barshop Institute for 
Longevity and Aging 
Studies and the laboratory of Amy Wagers 
at Harvard University and Harvard Stem 
Cell Institute. In 2014, he was appointed as 
an Assistant Professor in the School of 
Applied Physiology and a faculty member 
in the Parker H. Petit Institute for Bioengi-neering 
and Bioscience at Georgia Institute 
of Technology. 
The primary research focus of the Jang 
laboratory is to understand the molec-ular 
and biochemical mechanisms of 
age-related muscle loss and function. The 
Jang laboratory applies bioengineering 
approaches and stem cell-based therapies 
to study skeletal muscle dysfunction 
during aging and in age-associated muscle 
diseases. The laboratory develops and 
applies novel tools using a combination of 
animal and stem cell models. 
W. Gray Jerome 
Dr. Jerome is 
Associate Professor 
of Pathology, 
Microbiology and 
Immunology and 
Associate Professor 
of Cancer Biology at 
Vanderbilt Univer-sity. 
He is also 
Co-Director of the 
Cell Imaging Shared Resource at Vanderbilt. 
Jay is a Past-president of the Microscopy 
Society of America, the Co-Editor of a 
textbook on confocal microscopy, and an 
Editor for the journal Microscopy and 
Microanalysis. 
Jay’s research focuses on intracellular lipid 
metabolism and how disruption of normal 
lipid metabolism contributes to disease. His 
most recent studies investigate how lipids, 
particularly cholesterol, affects lysosome 
function and how alterations in lysosome 
function feedback to influence lipid 
metabolism. Lysosomes are key homeo-static 
organelles and lysosome dysfunction 
is associated with a number of diseases 
that become more prevalent with age. Dr. 
Jerome has shown that cholesterol overload 
inhibits lysosome function and disrupts cell 
homeostasis, particularly in inflammatory 
cells which can easily become overloaded 
with cholesterol. His group has also shown 
that lysosomal cholesterol-engorgement 
shifts other aspects of cellular lipid balance 
in ways that can push cells further into the 
disease state. 
Jeffrey Karp 
Jeff Karp is an 
Associate Professor 
at Brigham and 
Women’s Hospital, 
Harvard Medical 
School, and is 
Principal Faculty at 
the Harvard Stem 
Cell Institute and 
affiliate faculty at MIT 
through the Harvard-MIT Division of Health 
Sciences and Technology. His research uses 
19
materials and biology to solve medical 
problems with emphasis on nanoscale/ 
microscale materials and bio-inspiration. He 
has published more than 100 peer-reviewed 
papers and book chapters and has given over 
130 national and international invited lectures 
and has 50 issued or pending patents. Several 
technologies that he has invented are 
currently being translated into medical 
products to improve the quality of life of 
suffering patients. 
In 2011 the Boston Business Journal recog-nized 
Dr. Karp as a Champion in Healthcare 
Innovation and in 2013 the Institute for 
Chemical Engineers (IChemE) awarded one 
of his technologies the Most Innovative 
Product of the Year. MIT’s Technology 
Review Magazine (TR35) also recognized 
Dr. Karp as being one of the top innovators 
in the world under the age of 35. He has 
received the Society for Biomaterials Young 
Investigator Award and his work has been 
selected as one of Popular Mechanic’s 
“Top 20 New Biotech Breakthroughs that 
Will Change Medicine”. Dr. Karp was also 
elected in 2013 to the American Institute 
for Medical and Biological Engineering’s 
College of Fellows and as a Kavli Fellow. 
Dr. Karp is also an acclaimed mentor. He 
was selected as the Outstanding Faculty 
Undergraduate Mentor among all Faculty 
at MIT and received the HST McMahon 
Mentoring award for being the top mentor 
among all faculty who mentor Harvard- 
MIT students. 
Michael Kope 
Michael Kope is 
President, Chief 
Executive Officer, 
and Co-founder of 
the SENS Research 
Foundation. Mr. 
Kope received his 
J.D. from the 
University of 
Michigan in 1990. 
He has served as the University of 
Michigan’s Intellectual Property Counsel; 
as Director of Corporate Development for 
Aviron, and for MedImmune, Inc.; and as 
CEO and officer of a number of start-ups in 
the biotechnology space. He specializes in 
business development and consulting, 
and is widely experienced with biotech-nology 
organizations. 
Mike has negotiated a broad range of 
business acquisition and partnership 
agreements, designed strategies for 
technology protection and promotion in 
many fields of research, and facilitated a 
number of successful startups. 
Daniel Kraft 
Daniel Kraft is a 
Stanford and 
Harvard trained 
physician-scientist, 
inventor, entrepre-neur 
and innovator. 
Dr. Kraft has over 20 
years of experience 
in clinical practice, 
biomedical research 
and healthcare innovation. Daniel chairs 
the Medicine track for Singularity Univer-sity 
and is Founding Executive Director for 
FutureMed (now called Exponential 
Medicine), a program which explores 
convergent, exponentially developing 
technologies and their potential in 
biomedicine and healthcare. 
Following undergraduate degrees at 
Brown University and medical school at 
Stanford, Dr. Kraft was board certified in 
the Harvard combined Internal Medicine 
and Pediatrics residency program at the 
Massachusetts General Hospital and 
Boston Children’s Hospital. He went on 
to complete Stanford fellowships in 
hematology/oncology & bone marrow 
transplantation, and to conduct extensive 
research in stem cell biology and 
regenerative medicine. He has multiple 
scientific publications (including in the 
journals Nature and Science) and medical 
device, immunology and stem cell related 
patents through faculty positions with 
Stanford University School of Medicine 
and as clinical faculty for the pediatric 
bone marrow transplantation service at 
University of California San Francisco. 
Dr. Kraft recently founded Bioniq Health, 
focused on enabling connected, data 
driven, and integrated personalized 
medicine. He is also the inventor of the 
MarrowMiner, an FDA approved device 
for the minimally invasive harvest of 
bone marrow, and founded RegenMed 
Systems, a company developing tech-nologies 
to enable adult stem cell based 
regenerative therapies. 
Neil Littman 
Neil Littman is the 
Business Develop-ment 
Officer at the 
California Institute 
for Regenerative 
Medicine. Mr. 
Littman is responsi-ble 
for facilitating 
opportunities for 
outside investment 
in stem cell research in California by 
biopharma companies, investors, and 
disease foundations. 
Prior to joining CIRM in 2012, Mr. Littman 
was a Senior Associate in the Merchant 
Banking Group at Burrill & Company, a 
diversified global financial services firm 
focused on the life sciences industry based 
in San Francisco. While at Burrill & Company, 
Mr. Littman’s responsibilities included both 
strategic advisory and capital raises for 
biopharma companies throughout the U.S. 
and internationally. 
Mr. Littman’s strategic advisory experience 
includes buy-side and sell-side M&A, as well 
as in-licensing and out-licensing of both 
development stage and commercial prod-ucts. 
Prior to joining Burrill & Company in 
2009, Mr. Littman worked in the Healthcare 
Investment Banking group at Thomas Weisel 
Partners where he focused on strategic 
advisory and public and private financings. 
Prior to Thomas Weisel Partners, Mr. Littman 
worked in the Healthcare Investment 
Banking group at Deutsche Bank Securities. 
Mr. Littman received a Master of Science 
in Biotechnology with a concentration in 
Biotechnology Enterprise from The Johns 
Hopkins University, and a Bachelor of Arts in 
Molecular, Cellular and Development Biology 
from the University of Colorado Boulder. 
Jeanne Loring 
Jeanne Loring, Ph.D., 
is a Professor and 
the founding 
Director of the 
Center for Regenera-tive 
Medicine at The 
Scripps Research 
Institute in La Jolla. 
Her research team 
focuses on large-scale 
analysis of genomics and epigenetics 
of human pluripotent stem cells (hPSCs) and 
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20
their derivatives, in order to ensure the 
quality and safety of these cells for clinical 
use. The team’s translational projects include 
development of cell therapies for Parkin-son’s 
disease, multiple sclerosis, and 
Alzheimer disease, and epigenetic modeling 
of autism. The team is also producing an 
ethnically diverse library of iPSC (induced 
pluripotent stem cell) lines for use in 
pharmaceutical screening. In addition, her 
lab is developing a “zoo” of induced 
pluripotent stem cells from endangered 
species to aid in their conservation. 
Dr. Loring is committed to educating both 
scientists and the public. She has trained 
more than 400 scientists over the last 10 
years in intensive laboratory courses in 
human ES and iPSC biology, and is author 
of a comprehensive laboratory manual on 
human pluripotent stem cells (“Human 
Stem Cell Manual: a Laboratory Guide, in 
second edition, 2012). She is frequently 
quoted in major newspapers, and gives 
numerous public lectures and interviews 
to inform the public about biological and 
societal issues associated with stem cell 
research, including the ethics of stem 
cell generation and clinical use, the legal 
implications of stem cell patents, and 
public education about the dangers of 
unregulated stem cell treatments (“stem 
cell tourism”). Dr. Loring serves on both 
bioethics and scientific advisory boards. 
Linda Marban 
Linda Marban is 
currently CEO, 
President and 
Director of Caprico 
Therapeutics. She 
combines her 
background in 
research with her 
business experience 
to lead Capricor and 
create a path to commercialization for its 
novel stem-cell cardiac therapies. Dr. 
Marban was the lead negotiator in procur-ing 
the license agreements that are the 
foundation of Capricor’s intellectual 
property portfolio. Under her direction as 
Chief Executive Officer, Capricor secured 
approximately $27.0 million in nondilutive 
grants and a loan award which funds 
Capricor’s R&D programs and clinical trials 
involving its CAP-1002 product. Dr. Marban’s 
deep knowledge of the cardiac space in 
particular, allows her to provide unique 
Speaker Biographies 
direction for the company’s development 
and growth. From 2003 to 2009, Dr. Marban 
was with Excigen, Inc., a biotechnology 
start-up company, where she was responsi-ble 
for business development, operations, 
pre-clinical research, and supervising the 
development of gene therapy products in a 
joint development agreement with Gen-zyme 
Corp. While at Excigen, she also 
negotiated a joint development and 
sublicense agreement with Medtronic Corp. 
utilizing Excigen’s technology and super-vised 
the building of a lab in which the work 
was to be performed. 
Dr . Marban began her career in academic 
science at the Cleveland Clinic Foundation 
working on the biophysical properties of 
cardiac muscle. She moved to a postdoc-toral 
fellowship at Johns Hopkins University 
and advanced to the rank of Research 
Assistant Professor in the Department of 
Pediatrics, continuing her work on the 
mechanism of contractile dysfunction in 
heart failure. Dr. Marban earned a Ph.D. 
from Case Western Reserve University in 
cardiac physiology. 
Andrew Martello 
Andrew Martello is 
co-founder & CEO of 
Spoonful of Sugar 
(SoS). He leads an 
expert team 
developing 
academically-led 
adherence consul-tancy 
and evi-dence- 
based 
adherence solutions to global healthcare 
providers and the pharmaceutical industry. 
SoS is a University College London spinout 
company that applies the learnings of a 
15-year research program in behavioral 
medicine, specifically, how patients engage 
with long-term illnesses and treatment. 
Over the past five years, Andrew has 
been directly involved in the planning 
and implementation of multi-country 
adherence and patient support programs 
utilizing the latest research into illness and 
medicines-related behavior. As part of this 
work, Andrew has led the development of 
proprietary software designed to diagnose 
and treat both perceptual and practical 
barriers to optimal adherence at an 
individual patient level. 
Passionate about the role of digital 
technology in changing health behaviors, 
Andrew’s main interest is the role of 
personalized medicine, from both a clinical 
and psychological perspective and its real 
world application. 
Prior to founding SoS, Andrew spent over 
ten years working for and consulting with 
the pharmaceutical industry, predominantly 
in HIV medicine. 
Much of his work in this field focused on 
the development of strategies supporting a 
greater understanding of the patient’s per-spective 
throughout the drug development 
and product lifestyle pathway. This included 
the development of novel formulations and 
devices, packaging and support services to 
optimize the use of medicines. 
This work not only focused on the devel-oped 
world but also included innovative 
strategies to widen access to medicines 
throughout the developing world. 
Andrew’s previous assignments have been 
with GlaxoSmithKline, Abbott Laboratories, 
Novartis and Sandoz Biopharmaceuticals. 
Stephen Minger 
Dr. Stephen Minger 
received his PhD in 
Pathology (Neuro-sciences) 
in 1992 
from the Albert 
Einstein College of 
Medicine in New 
York City. After 
post-doctoral work 
in central nervous 
system gene therapy, neural transplantation 
and neural stem cell biology, he was 
appointed a Lecturer in Biomolecular 
Sciences at King’s College London in 1998. 
He was appointed a Senior Lecturer in Stem 
Cell Biology in 2005 and was the Director of 
the Stem Cell Biology Laboratory from 2002 
until joining GE Healthcare in 2009. 
Over the past 20 years, Stephen’s research 
group has been at the forefront of human 
stem cell research. In 2002, they were 
awarded one of the first two licenses 
granted by the UK Human Fertilisation and 
Embryology Authority for the derivation 
of human embryonic stem (hES) cells and 
his group was the first to deposit a hES cell 
line into the UK Stem Cell Bank. Stephen’s 
21
was also one of the first two groups in the 
UK to be granted a research license by 
the HFEA in 2008 to pursue Somatic Cell 
Nuclear Transfer (SCNT) to generate “hybrid 
human embryos” for fundamental research 
into genetic forms of neurodegenerative 
conditions. He was activity involved with 
the UK Department of Health and in the 
consultation that led to the passage of 
the Human Embryo Bill of 2009 and the 
inclusion of new forms of animal-human 
embryos within primary legislation. 
In the summer of 2013, Stephen was 
appointed Chief Scientist for Cellular 
Sciences, GE Healthcare Life Sciences, and 
is now responsible for long-term global 
research strategy for technology develop-ment 
in cell therapy, regenerative medicine, 
cellular technologies, in vivo diagnostic 
imaging and molecular pathology/person-alized 
medicine. 
Peter Nakada 
Peter Nakada leads 
the RMS Capital 
Markets and 
LifeRisks groups. 
After joining the 
company in 2005, 
he formed the RMS 
Capital Markets 
group to provide an 
infrastructure for 
capital markets participants to understand 
catastrophe risk. He focuses on taking the 
company’s catastrophe risk expertise into 
adjacent markets and leads the RMS 
LifeRisks team to provide excess mortality 
and longevity risk analytics to life insurers 
and capital markets investors. 
Nakada began his career in financial services 
as a general account fixed income portfolio 
manager for Prudential Insurance Company. 
Prior to joining RMS, Nakada was a partner 
at Oliver, Wyman & Company, where he 
specialized in advising banks and insurers 
on aspects of risk, capital, and shareholder 
value. In 2000, Nakada co-founded ERisk, 
a spinoff from Oliver, Wyman & Company, 
which provides software-as-a-service for 
enterprise risk management and economic 
capital quantification. 
Nakada has co-authored many articles on 
topics related to risk, capital, and share-holder 
value, as well as the securitization of 
catastrophic risk. His articles include “Risk, 
Capital & Value Measurement in Financial 
Institutions – Part I: The Debtholder’s 
Perspective (1998),”P&C RAROC: A Catalyst 
for Improved Capital Management in 
the Property and Casualty Insurance 
Industry” (1999), “Understanding Longevity 
Risk: Insights from Structural Cause-of-Im-provement 
Models” (2012) and “Quantifying 
the Mortality-Longevity Offset”(2013). 
Nakada holds a bachelor’s degree in 
engineering sciences from Harvard College 
and a master’s degree in engineering 
management from Stanford University. He 
earned the Chartered Financial Analyst® 
designation in 1990. 
Edward James Olmos 
Edward James 
Olmos (Axford) has 
achieved extraordi-nary 
success as an 
actor, producer and 
humanitarian. The 
Tony, Emmy and 
Academy Award® 
Nominated actor, is 
probably best 
known to young audiences for his work on 
television series “Battlestar Galatica” as 
Admiral William Adama. Although the 
series kept the actor busy during its run 
from 2003 through 2009, it didn’t stop him 
from directing the HBO movie “Walkout” 
in 2007, for which he earned a DGA 
Nomination in the Outstanding Directorial 
Achievement in Movies for Television 
category. 
Olmos earned two Golden Globe and 
Emmy Award nominations, resulting in 
a win from each. In 1988, he received an 
Academy Award® nomination for Best Actor 
for his starring role in Stand and Deliver 
and won the Golden Globe for his portrayal 
of Jaime Escalante in Stand and Deliver. 
Olmos’ career in entertainment spans over 
30 years. In that time he created a signa-ture 
style and aesthetic that he applies to 
every artist endeavor. His dedication to his 
craft has brought him worldwide attention. 
Olmos went on to appear in the films 
Wolfen, Blade Runner, and the Ballad of 
Gregorio Cortez before starring in his 
biggest role to date, that of Lieutenant 
Martin Castillo in the iconic 80’s television 
series “Miami Vice”. 
He directed and starred in his first motion 
picture, American Me, in 1992. 
Olmos’ passion for the arts grows every 
year, but he never forgets to give back to 
the communities that support him with 
their dedication. 
He is an international advocate, spokesman, 
and humanitarian working with organi-zations 
such as Thank You Ocean, Project 
Hope Foundation, Children’s Hospital of 
Los Angeles, The Boy’s and Girl’s Club of 
America, The River Keepers, Dr. Andros’ 
Diabetic Foot Global Conference and he 
speaks up to 150 times a year in schools, 
universities, and corporations. 
Jim O’Neill 
Jim O’Neill is partner 
and chief operating 
officer at Mithril, a 
growth fund for 
transformative and 
durable technology 
companies in fields 
such as cyber-security; 
next 
generation finance; 
medical robotics; rail integration; enter-prise 
cloud services; 3D seismic technol-ogy; 
and data integration, visualization, 
and analysis. Mithril invests with convic-tion 
and helps teams successfully navigate 
high-growth periods. 
Before helping to launch Mithril, Jim was 
a managing director of Clarium, a global 
macro investment fund. He also ran the Thiel 
Foundation and co-founded the 20 Under 
20 Thiel Fellowship and Breakout Labs. 
Previously, as the principal associate 
deputy secretary of health and human 
services, Jim helped manage an agency 
whose 67,000 employees regulate more 
than 25% of the U.S. economy. His main 
areas of policy and program responsibility 
included the Food and Drug Administra-tion, 
the National Institutes of Health, the 
Centers for Disease Control and Prevention, 
security, intelligence, preparedness, and 
health diplomacy. He also made invest-ments 
in drug, vaccine, and diagnostic 
research on the steering committee of 
the $200 million Biomedical Advanced 
Research and Development Authority. 
Speaker Biographies 
22
Brock Reeve 
Brock Reeve is 
Executive Director 
of the Harvard Stem 
Cell Institute. In 
partnership with the 
Faculty Directors, he 
has overall responsi-bility 
for the 
operations and 
strategy of the 
Institute whose mission is to use stem cells, 
both as tools and as therapies, to under-stand 
and treat the root causes of leading 
degenerative diseases. 
HSCI is comprised of the schools of Harvard 
University and all its affiliated hospitals and 
research institutions. Under the leadership 
of the Executive Committee, HSCI invests in 
scientific research and its faculty has grown 
to include over 300 Principal and Affiliated 
members. The Institute is engaged with 
several leading pharmaceutical companies 
and foundations in joint research projects 
and its faculty have founded several stem 
cell-related startup companies and serve on 
leading Scientific Advisory Boards. 
Brock came to this role from the commercial 
sector with extensive experience in both 
management consulting and operations for 
technology-based companies, with a focus 
on life sciences. Brock received a BA and 
MPhil from Yale University and an MBA from 
Harvard Business School. 
Camillo Ricordi 
Camillo Ricordi is 
Professor and 
Director of the 
Diabetes Research 
Institute (DRI; www. 
diabetesresearch. 
org ) and the Cell 
Transplant Program 
at the University of 
Miami. 
Dr. Ricordi and collaborators developed 
the method for large scale production of 
human pancreatic islets, and he led the 
team that performed the first series of 
successful clinical islet allotransplants to 
reverse diabetes. The procedure is now 
used by laboratories performing clinical 
islet transplants worldwide. Ricordi was 
president of the Cell Transplant Society, 
on the NIH-NIAID Expert Panel on clinical 
Speaker Biographies 
approaches for tolerance induction, on 
the FDA Biologic Response Modifiers 
Advisory Committee and on the NIH-NIDDK 
Strategic Planning Committee. 
Ricordi is currently serving as Chairperson 
of the NIH funded Clinical Islet Transplanta-tion 
(CIT) Consortium, which standardized 
cell manufacturing protocols in North 
America and Europe and just completed 
the first multicenter FDA Phase III trial for 
what could become the first biologically 
active cell product approved in the US by 
the FDA. 
Ricordi has received numerous honors and 
awards and was also Knighted by the Presi-dent 
of the Republic of Italy. He is currently 
serving on the editorial boards of CellR4 
(Editor-in-Chief; www.cellr4.org) and Cell 
Transplantation (Co-Editor-in-Chief ). In 
2013 he was appointed President of the 
Ri.MED Foundation by the Italian Prime 
Minister (http://www.fondazionerimed.eu), 
one of the largest European investments in 
Biomedical Research, Biotechnologies and 
Regenerative Medicine. Ricordi also serves 
as President of The Cure Alliance (www. 
thecurealliance.org) and Chairman of the 
Diabetes Research Institute Federation 
(www.diabetesresearch.org). He has 
authored over 700 scientific publications 
and 19 awarded patents. 
David Schaffer 
David Schaffer is a 
Professor of 
Chemical and 
Biomolecular 
Engineering, 
Bioengineering, and 
Neuroscience at 
University of 
California, Berkeley, 
where he also 
serves as the Director of the Berkeley Stem 
Cell Center. He graduated from Stanford 
University with a B.S. degree in Chemical 
Engineering in 1993. Afterward, he 
attended Massachusetts Institute of 
Technology and earned his Ph.D. also in 
Chemical Engineering in 1998. Finally, he 
did a postdoctoral fellowship in the 
laboratory of Fred Gage at the Salk Institute 
for Biological Studies in La Jolla, CA before 
moving to UC Berkeley in 1999. 
At Berkeley, Dr. Schaffer applies 
engineering principles to enhance stem 
cell and gene therapy approaches for 
neuroregeneration, work that includes 
novel approaches for molecular engineer-ing 
and evolution of new viral vectors as 
well as new technologies to investigate 
and control stem cell fate decisions. 
David Schaffer has received an NSF 
CAREER Award, Office of Naval Research 
Young Investigator Award, Whitaker 
Foundation Young Investigator Award, and 
was named a Technology Review Top 100 
Innovator. He was also awarded the Bio-medical 
Engineering Society Rita Shaffer 
Young Investigator Award in 2000, the 
American Chemical Society BIOT Division 
Young Investigator Award in 2006, and 
was inducted into the College of Fellows 
of the American Institute of Medical and 
Biological Engineering in 2010. 
Dale Schenk 
Dr. Dale Schenk, 
Chief Executive 
Officer of Prothena, 
plc, was previously 
Chief Scientific 
Officer and Execu-tive 
Vice President at 
Elan Pharmaceuti-cals 
where he 
provided the 
leadership and scientific direction for Elan¹s 
research and development programs. Prior 
to joining Elan, Dr. Schenk was a founding 
scientist of Athena Neurosciences, which 
was acquired by Elan Pharmaceuticals. 
Dr . Schenk has pioneered the immuno-therapeutic 
approaches for the treatment 
of amyloidosis, as exemplified for Alzhei-mer 
¹s disease, Parkinson’s disease and light 
chain (AL) Amyloidosis. Dr. Schenk¹s work 
in this area, as well as in early detection, 
testing and other pathways to these 
diseases, has led specifically to the most 
advanced potential treatment approach 
for Alzheimer¹s disease. Clinical trials are 
also currently underway for AL amyloi-dosis 
and Parkinon’s disease that utilize 
immunotherapy. 
Dr . Schenk earned his BA and PhD in 
Pharmacology and Physiology from the 
University of California, San Diego. 
23
Michael Sherratt 
Following a PhD 
and postdoctoral 
positions with 
Professor Cay Kielty 
at the University of 
Manchester, 
Michael was 
awarded an AgeUK 
Fellowship and 
Senior Fellowship. 
He is currently a Lecturer in Molecular 
Biochemistry at the University of Manches-ter 
and director of the BioAFM (atomic 
force microscopy) Facility at the same 
institution. For the past four years he has 
served as treasurer of the British Society for 
Research on Ageing and his main research 
interests are in the effects of ageing on 
tissue extracellular matrix structure and 
mechanical function. 
Using biochemical, ultra-structural, bioin-formatic 
and micro-mechanical approaches, 
Michael’s work suggests that: i) elastic 
fibre associated proteins (which are highly 
enriched in Cys, Trp and Tyr amino acid 
residues) may be differentially susceptible 
to UV-radiation and oxidation in ageing 
tissues and ii) the effects of ageing on tissue 
mechanical properties are localized in large 
arteries such as the aorta. 
In collaboration with colleagues in the 
Manchester X-ray Imaging Facility he is now 
developing new imaging methodologies 
to characterize the effects of intra-luminal 
pressure on the 3D structure of young and 
aged arteries. 
Bernard Siegel 
Bernard Siegel, J.D., 
is the founder and 
Executive Director 
of Genetics Policy 
Institute (GPI), a 
nonprofit organiza-tion 
with offices in 
Palm Beach, Florida; 
Silicon Valley, 
California and 
Washington, D.C. He founded and co-chairs 
the annual World Stem Cell Summit, 
founded and serves editor-in-chief of the 
peer-reviewed World Stem Cell Report and 
is the editor of the 360 Stem Cell & Regener-ative 
Medicine weekly newsletter. He 
founded and is the spokesperson for the 
Stem Cell Action Coalition, a 100+ member 
international alliance of nonprofits and 
research institutions leading the global 
“Pro-Cures Movement.” 
In 2002, he filed the first court case relating 
to reproductive cloning and is widely 
credited for debunking the claim of the 
group claiming that they cloned the first 
baby. He also played a pivotal leadership 
role in galvanizing a global movement that 
successfully lobbied the United Nations to 
reject a treaty that called for a prohibition 
of nuclear transfer, or therapeutic cloning. 
As a recognized policy expert on stem cell 
research, regenerative medicine and cloning, 
he works with leading scientists and patient 
advocates, raising public awareness and 
educating lawmakers, the media and public 
on stem cells and regenerative medicine. He 
is a frequent panelist and keynote speaker 
on the subject of stem cells, public policy 
and patient advocacy. 
Eric Siemers 
Eric Siemers, M.D. is 
the Senior Medical 
Director of the 
Alzheimer’s Disease 
Global Develop-ment 
Team at Eli 
Lilly and Company. 
He earned his MD 
with highest 
distinction from the 
Indiana University School of Medicine in 
1982. After an internship in the Department 
of Internal Medicine at the Indiana Univer-sity 
School of Medicine, he completed his 
residency in the Department of Neurology 
in 1986. Prior to joining Lilly, he founded 
and headed the Indiana University Move-ment 
Disorder Clinic; his previous research 
included investigations of Parkinson’s 
disease and Huntington’s disease, and he 
established one of the first centers for 
surgical PD treatments in the US. 
Dr . Siemers currently directs late stage 
clinical research efforts at Lilly concerning 
investigational treatments for Alzheimer’s 
disease, and is more broadly involved 
with other neurological indications such 
as Parkinson’s disease. Major research 
interests include the use of biomarkers 
in investigational drug research and the 
development of trial designs that broadly 
characterize the effects of investigational 
drugs on chronic diseases. 
Dr . Siemers is a founding member and 
current Chair of the Alzheimer’s Association 
Research Roundtable. He is a member of 
the Steering Committee for the Alzheimer’s 
Disease Neuroimaging Initiative (ADNI). He 
served as the chair of the Industry Scientific 
Advisory Board for ADNI in 2007. Dr. Siemers 
is a current member of the New York 
Academy of Sciences Alzheimer’s Disease 
Leadership Counsel. He participated as a 
member of the NIA working group that 
proposed criteria for preclinical Alzheimer’s 
disease in 2011. He is a past member of the 
Board of Directors of the American Society 
of Experimental Neurotherapeutics. 
Einar M. Sigurdsson 
Einar M. Sigurdsson, 
Ph.D. is a tenured 
Associate Professor 
of Neuroscience and 
Physiology, and 
Psychiatry at New 
York University 
School of Medicine. 
A native of Iceland, 
he received a 
master’s degree in Pharmacy from the 
University of Iceland, and a Ph.D. in Pharma-cology 
from Loyola University Chicago 
Medical Center. He subsequently obtained 
postdoctoral training at New York University 
School of Medicine. 
His current research focuses on pathogen-esis, 
therapy and diagnosis for age-related 
protein conformational disorders, in 
particular Alzheimer’s disease. 
His honors include a Zenith Fellows Award 
and the Margaret M. Cahn Research Award 
from the Alzheimer´s Association, and the 
Irma T. Hirschl Career Scientist Award. He is 
presently serving as a standing member on 
an NIH study section. 
Dr. Sigurdsson and his collaborators pio-neered 
the use of modified Aβ derivatives 
as potential immunotherapy for Alzheimer’s 
disease. Furthermore, they showed for the 
first time that active and passive immuniza-tion 
as well as chelators delayed the onset 
of prion disease in mice, with follow up 
immunization studies leading to prevention 
of clinical symptoms in mice. 
On the diagnostic front, Dr. Sigurdsson 
and colleagues published the initial report 
on detection of amyloid plaques in living 
Speaker Biographies 
24
mouse brains by magnetic resonance imag-ing. 
Lately, he has pioneered the approach 
to harness the immune system to target 
pathological tau protein in Alzheimer’s 
disease and other tauopathies. 
Evan Y. Snyder 
Dr. Snyder earned 
his M.D. and his Ph.D. 
in neuroscience 
from the University 
of Pennsylvania in 
1980. He completed 
residencies in 
pediatrics and 
neurology at 
Children’s Hospi-tal- 
Boston, Harvard Medical School and 
postdoctoral research at Harvard Medical 
School. In 1992, Dr. Snyder was appointed an 
instructor in neurology at Harvard Medical 
School and was promoted to assistant 
professor in 1996. 
He is regarded as one of the fathers of 
the stem cell field, having identified over 
2 decades ago that cells that came to be 
called stem cells were a source of neural 
plasticity. He was the first to demonstrate 
that non-hematopoietic stem cells could 
mediate cell and gene replacement, home 
to injury, and perform protective, trophic, 
pro-regenerative, and anti-inflammatory 
actions. He was the first to isolate human 
neural stem cells. 
In 2003, after 23 years at Harvard, Dr. Snyder 
was recruited to Sanford Burnham Medical 
Research Institute as professor and director 
of the Stem Cells and Regeneration program. 
Michael D. West 
Michael D. West, 
Ph.D. became Chief 
Executive Officer of 
Biotime during 
October 2007, and 
has served on the 
Board of Directors 
since 2002. Prior to 
becoming Chief 
Executive Officer, Dr. 
West served as Chief Executive Officer, 
President, and Chief Scientific Officer of 
Advanced Cell Technology, Inc., a company 
engaged in developing human stem cell 
technology for use in regenerative medicine. 
Speaker Biographies 
Dr . West also founded Geron Corporation 
of Menlo Park, California, and from 1990 to 
1998 he was a Director and Vice-President, 
where he initiated and managed programs 
in telomerase diagnostics, oligonucle-otide- 
based telomerase inhibition as 
anti-tumor therapy, and the cloning and 
use of telomerase in telomerase-mediated 
therapy wherein telomerase is utilized to 
immortalize human cells. From 1995 to 1998 
he organized and managed the research 
between Geron and its academic collabora-tors 
James Thomson and John Gearhart that 
led to the first isolation of human embryonic 
stem and human embryonic germ cells. 
Dr . West received a B.S. Degree from 
Rensselaer Polytechnic Institute in 1976, 
an M.S. Degree in Biology from Andrews 
University in 1982, and a Ph.D. from Baylor 
College of Medicine in 1989 concentrating 
on the biology of cellular aging. 
Claude Wischik 
Claude Wischik is 
Professor of Old Age 
Psychiatry at the 
University of 
Aberdeen and 
Executive Chairman 
of TauRx Therapeu-tics. 
He studied 
medicine in 
Australia, then PhD 
and post-doctoral research at the MRC 
Laboratory of Cambridge, UK. He also 
completed psychiatric training in 
Cambridge. 
During his PhD he discovered that the 
neurofibrillary tangle is composed of the 
microtubule associated protein Tau. He also 
discovered that they could be dissolved 
by diaminophenothiazines. He established 
a team which developed in vitro and in 
vivo systems to establish plausibility of 
developing Tau Aggregation Inhibitor (TAI) 
therapy for AD. 
He cofounded TauRx Therapeutics to 
develop diagnostics and therapeutics for 
AD based on the TAI approach. In the first 
ever TAI phase 2 trial, TauRx demonstrated 
the feasibility of arresting disease progres-sion 
over 12 months. TauRx is currently 
conducting a global phase 3 trial of its lead 
compound in approximately 1,500 subjects 
in 22 countries. 
James Yoo 
Dr. Yoo is a surgeon 
and researcher. He is 
currently a Professor, 
Associate Director 
and Chief Scientific 
Officer at the Wake 
Forest Institute for 
Regenerative 
Medicine. Dr. Yoo’s 
research efforts 
have been directed toward the clinical 
translation of tissue engineering techno­logies 
and cell-based therapies. Dr. Yoo’s 
background in cell biology and medicine 
has facilitated the transfer of several 
cell-based technologies from the bench-top 
to the bedside. 
A few notable examples of successful clinical 
translation include the bladder, urethra, 
vagina and muscle cell therapy for incon-tinence. 
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internationally. 
25
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Save the Date 
SENS7 Conference 
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Queens’ College 
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SENS 2014 Conference Program Guide

  • 1. August 21-23, 2014 Santa Clara, California a SENS Research Foundation Conference Program Guide
  • 2. 2 Dear Colleagues, a SENS Research Foundation Conference August 21-23, 2014 Hyatt Regency Hotel Santa Clara, California It is our pleasure to welcome you to the 2014 Rejuvenation Biotechnology Conference. The continuing growth of research into the underlying causes of the diseases of aging brings with it the opportunity to build a Rejuvenation Biotechnology industry, an industry which builds on the strengths of regenerative medicine. Together over the next three days, we believe we can help create this new industry and inspire each other – as clinicians, researchers, patient advocates, regulators, venture capitalists, investors and industry leaders – to work together to make this happen. This conference has been designed to offer something for everyone: from the inspirational words of our scientific, business, and venture capital speakers to the latest research on diseases, such as Alzheimer’s Disease, cancer, cardiovascular disease, and diabetes. An entire track of sessions will cover the regulatory, financial, and economic issues involved in building a Rejuvenation Biotechnology industry. We have also scheduled plenty of time for networking with each other during our meal breaks, Poster sessions and our evening entertainment. We would like to thank each of your for attending the Rejuvenation Biotechnology Conference and bringing your expertise to our gathering. You have the vision, the knowledge, the wherewithal and the experience to come together to pave the way into the future. Throughout this conference, we ask you to stay engaged, deepen your understanding of the field, build communities of interest and create collaborations that will help shape the future of the industry. Thank you for choosing this conference. Enjoy your time here, and once again welcome to the Rejuvenation Biotechnology Conference. Mike Kope CEO, SENS Research Foundation Aubrey de Grey CSO, SENS Research Foundation
  • 3. TO PARKING STRUCTURE Welcome Letter. 2 Conference Schedule . 4 Speaker Biographies. 14 Sponsors . 26 Poster Abstracts . 33 NAPA I NAPA II NAPA III SONOMA MENDOCINO SANTA CLARA CONVENTION CENTER TUSCA COURTYARD TUSCA RESTAURANT POOL ELEVATOR CABANAS WHIRLPOOL SWIMMING POOL @ THE MARKET TERRA COURTYARD Networking Meals, Posters and Exhibits in Ballrooms EFGH EVOLUTION CAFE AND BAR FRONT DESK ELEVATORS CONCIERGE UP TO BALLROOM HOTEL ENTRANCE GIFT SHOP ATM REGENCY CLUB® MAGNOLIA NETWORK MEETING CENTER RESTROOMS TRUYA SUSHI LOUNGE RESTROOMS RESTROOMS Keynotes, Plenary & Concurrent Panels, and Performances in Ballrooms ABCD Registration in LOBBY WEST Ballrooms LOBBY WEST A B C D H G F E 3 Table of Contents
  • 4. Conference Schedule Registration (until 5:00 pm) - [LOBBY WEST] Networking Breakfast - [Ballrooms EFGH] Opening Remarks - Michael Kope, CEO , SENS Research Foundation - [Ballrooms ABCD] Keynote: George Church, Professor of Genetics, Harvard Medical School, Professor of Health Sciences and Technology, Harvard and MIT: New Epigenome Analysis and Engineering Technologies for Reversal of Aging - [Ballrooms ABCD] Molecular and Cellular Damage as the Cause of the Diseases of Aging Panel - [Ballrooms ABCD] This panel will discuss the idea that the diseases of aging may stem from molecular and cellular damage that accrues with age. Topics of discussion will include the types of damage that may be involved, examples of how this applies to one or more diseases, and thoughts on how basic research and industry could use this concept to drive therapeutic target identification and drug treatment/development. • Richard Barker, Director, Center for the Advancement of Sustainable Medical Innovation: (Moderator) • Aubrey de Grey, Co-Founder and Chief Science Officer, SENS Research Foundation • Caleb Finch, ARCO/Kieschnick Professor of Gerontology and Biological Science and University Professor, USC Davis School of Gerontology • Jeff Karp, Associate Professor, Harvard Medical School, Co-Director of the Center for Regenerative Therapeutics, Brigham and Women’s Hospital • Stephen Minger, Chief Scientist, Cellular Sciences, GE Healthcare Life Sciences, UK Networking Lunch & Exhibits - [Ballrooms EFGH] 8:00 am 8:00 am 9:00 am 9:30 am 10:30 am 12:00 pm Day 1: Thursday, August 21, 2014 4
  • 5. [Ballroom A] [Ballroom D] [Ballrooms BC] Alzheimer’s Disease Session 1 This session will highlight two types of cellular and molecular damage currently being researched as therapeutic targets for Alzheimer’s Disease. Speakers will discuss how tau tangles and cell loss are believed to lead to Alzheimer’s Disease, current ideas on how to remove or repair tau tangles, and how cell replacement can be used to treat Alzheimer’s. • Jean Hébert, Professor, Departments of Neuroscience and Genetics, Albert Einstein College of Medicine: A Twist of Fate - Reprogramming Neural Precursor Cells to Generate New Neocortical Neurons • Einar Sigurdsson, Associate Professor, Department of Neuroscience & Physiology, New York University: Tau Immunotherapy and Imaging • Claude Wischik, Professor of Old Age Psychiatry, University of Aberdeen, Executive Chairman, TauRX Therapeutics, Ltd.: Status of the First Phase 3 Clinical Trials Targeting the Tauopathy of Alzheimer’s Disease: Origins, Rationale and Design Considerations Cardiovascular Disease Session 1 Building upon the idea discussed by the morning panel of using damage repair therapeutics to treat the diseases of aging, this session will consider cellular and molecular damage that can be targeted for cardiovascular disease therapy. Presentations will explain how cellular or molecular damage may lead to cardiovas-cular disease and how this damage may be removed or repaired. • Guillermo Garcia Cardena, Associate Professor of Pathology, Harvard Medical School, Director of the Laboratory for Systems Biology, Center for Excellence in Vascular Biology, Brigham and Women’s Hospital: Mechanical Forces, Vascular Inflammation and Atherosclerosis • W. Gray Jerome, Associate Professor and Director, Graduate Program in Cellular and Molecular Pathology, Vanderbilt University Medical Center: Chewing the Fat: Cholesterol, Autophagy and Lysosome Dysfunction • Michael Sherratt, Lecturer, Center for Regenerative Medicine, University of Manchester: Causes and Consequences of Age-Related Extracellular Matrix Remodelling Toward a New Investment Paradigm Panel This panel will discuss the challenges in bringing new and especially preventative therapies to treat the diseases of aging from the research lab to the market. The panel will offer and discuss new investment paradigms that could drive drug and therapeutic development. • David Brindley, Research Fellow, University of Oxford/Center for the Advancement of Sustainable Medical Innovation: (Moderator) • Neil Littman, Business Development Officer, California Institute for Regenerative Medicine • James O’Neill, Partner and Chief Operating Officer, Mithril Capital Management • Bernard Siegel, Executive Director, Genetics Policy Institute • Michael West, CEO, BioTime, Inc. 1:00 pm CONCURRENT SESSIONS. PLEASE CHOOSE ONE: Conference Schedule 5
  • 6. Conference Schedule Day 1: Thursday, August 21, 2014 Alzheimer’s Disease Session 2 A third type of damage being targeted for Alzheimer’s therapeutics, A-beta aggregates, will be discussed during this session. Speak-ers will address how A-beta aggregates are believed to lead to Alzheimer’s Disease and current ideas on how to prevent or remove them. This session will also discuss how changing the way researchers, regulators, and pharmaceutical companies view the disease will change Alzheimer’s Disease drug development. Particular attention will be paid to the Accelerate Cure/Treatments for Alzheimer’s Disease (ACT-AD) proposal and recent guidance from the FDA. • Ashley Bush, Head of the Oxidation Disorders Laboratory, Mental Health Research Institute, University of Melbourne, Director of the Laboratory for Oxidation Biology Genetics and Aging Unit, Massachusetts General Hospital, Associate Professor, Department of Psychiatry, Harvard Medical School: Iron in Aging and Neurodegenerative Disease • Rachelle Doody, Professor of Neurology, Director, Alzheimer’s Disease and Memory Disorders Center, Baylor College of Medicine: Approaches to Brain Aging and Alzheimer’s Disease: What are We Learning from Clinical Trials? • Eric Siemers, Medical Director, Alzheimer’s Disease Team, Eli Lilly: New Paradigms in Alzheimer’s Disease Drug Development Cardiovascular Disease Session 2 In this session, examples of current pharmaceutical advances in cardiovascular disease therapeutics will be presented. The talks will describe how these therapeutics remove or repair molecular and cellular damage and, in doing so, delay or prevent cardiovascular disease. • Gabor Forgacs, Professor, Biophysics Laboratory, Department of Physics & Astronomy, University of Missouri- Columbia, Founder, Organovo: The Role of Bioprinting in Rejuvenation • Linda Marban, CEO, Capricor Therapeutics: Raising Capricor: Building a Biotech Company from Bench to Bedside • James Yoo, Professor, Associate Director and Chief Scientific Officer, Wake Forest Institute for Regenerative Medicine: Tissue Engineering Solutions for Cardiovascular Tissue Pathologies The Economic Impact of an Aging Population on the Healthcare System Panel This panel will discuss the impending economic crisis the healthcare system will soon face caring for the ever-growing elderly population and possible solutions to this crisis, such as an outcomes-based healthcare model. • David Brindley, Research Fellow, University of Oxford/Center for the Advancement of Sustainable Medical Innovation: (Moderator) • Catalina Hoffman, Founder, Catalina Hoffmann Holding Group • Peter Nakada, Managing Director of Risk Markets, Risk Management Solutions, Inc. 2:30 pm CONCURRENT SESSIONS. PLEASE CHOOSE ONE: [Ballroom A] [Ballroom D] [Ballrooms BC] 6
  • 7. Performance by Comedian Hal Sparks - [Ballrooms ABCD] Currently starring in the Disney XD show, LAB RATS, actor/comedian Hal Sparks began his professional career while still a teenager in Chicago. As a member of the famed Second City Troupe, his quick wit and affable personality quickly gained him recognition and acclaim and he was named the “Funniest Teenager In Chicago” by the Chicago Sun Times. Sparks went on to host the Emmy Award- winning “Talk Soup” on E! Entertainment Television, winning rave reviews from fans and critics alike. He starred for five seasons on Showtime’s hit series “Queer As Folk” and appeared in the films “Extract,” “Spiderman 2” and “Dude, Where’s My Car?.” Sparks recently starred in his own one hour Showtime comedy special, “Charmageddon,” which is now a best-selling DVD. He is a star commentator on VH1’s popular “I Love the 80’s” series and can be heard every Wednesday on the nationally syndicated “Stephanie Miller Radio Show.” Hal is also a pop culture expert and regularly appears on such shows as “Joy Behar” and CNN’s “Your Money.” His numerous other television appearances include “The Tonight Show,” “Larry King Live,” “Charlie Rose,” “Good Morning America,” “The View,” “Jimmy Kimmel” and MTV. In addition to a busy acting and stand-up career, he is an accomplished musician. Hal and his band, Zero 1, recently released their debut album. 8:00 pm Afternoon Break & Exhibits - [Ballrooms EFGH] Advancing Regenerative Therapies in Alzheimer’s and Cardiovascular Disease Panel - [Ballrooms ABCD] This panel will bring together speakers from sessions throughout the day to consider the promise of a damage repair strategy to develop therapeutics for the diseases of aging. Discussion will include a summary of the accomplishments of the Alzheimer’s community in suggesting an innovative drug development strategy as well as debate about how such a strategy could apply to cardiovascular therapies. In particular, the panel will consider the impact applying a strategy similar to the ACT-AD proposal would have on cardiovascular disease therapeutic development, investment in cardiovascular drug development, and the healthcare system. • Aubrey de Grey, CSO, SENS Research Foundation: (Moderator) • Rachelle Doody, Professor of Neurology, Director, Alzheimer’s Disease and Memory Disorders Center, Baylor College of Medicine • Neil Littman, Business Development Officer, California Institute for Regenerative Medicine (CIRM) • Linda Marban, CEO, Capricor Therapeutics • Eric Siemers, Medical Director, Alzheimer’s Disease Team, Eli Lilly Poster Session/ Buffet Dinner & Exhibits - [Ballrooms EFGH] 4:00 pm 4:30 pm 6:00 pm Conference Schedule 7
  • 8. Conference Schedule Registration (until 5:00 pm) - [LOBBY WEST] Networking Breakfast & Exhibits - [Ballrooms EFGH] Opening Remarks by Edward James Olmos, Actor - [Ballrooms ABCD] Keynote: Jim O’Neill, Partner and Chief Operating Officer, Mithril Capital Management: Fight Aging with a Durable Business - [Ballrooms ABCD] Toward a New Research Paradigm Panel - [Ballrooms ABCD] This panel will explore new ways to approach research to tackle the diseases of aging. In particular, consideration will be given to the effects a damage repair paradigm would have on developing new strategies to identify and study therapeutic targets, fostering more collaboration between researchers studying different diseases, and changing the way translational research and drug development are approached. • Richard Barker, Director, Center for the Advancement of Sustainable Medical Innovation: (Moderator) • Julie Allickson, Director, Translational Research, Wake Forest Institute for Regenerative Medicine • Judith Campisi, Professor, Buck Institute for Research on Aging • Howard Foyt, Vice President, Clinical Development and Chief Medical Officer, Viacyte, Inc • Daniel Kraft, Faculty Chair for Medicine, Singularity University Networking Lunch & Exhibits - [Ballrooms EFGH] 8:00 am 8:00 am 9:00 am 9:30 am 10:30 am 12:00 pm Day 2: Friday, August 22, 2014 8
  • 9. Cancer Session This session will highlight current break-throughs in cancer research. Additionally, the impact the I-SPY TRIAL 2 (Investigation of Serial studies to Predict Your Therapeutic Response with Imaging and Molecular Analysis 2) program has had on drug development, particularly Alzheimer’s drugs, will be discussed. • Judith Campisi, Professor, Buck Institute for Research on Aging: Cancer and Aging: Rival Demons? • Laura Esserman, Professor, Departments of Surgery and Radiology, and Affiliate Faculty, Institute for Health Policy Studies and Director, Carol Franc Buck Breast Care Center; Co-Leader, Breast Oncology Program, UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco: Accelerating Knowledge Turns: The I-SPY Model and Drug Development • Claudia Gravekamp, Associate Professor, Albert Einstein College of Medicine: Curing Cancer in the Elderly Through Novel Strategies Parkinson’s Disease Session This session will feature the latest in Parkinson’s Disease research. A causal relationship between molecular and/ or cellular damage and Parkinson’s Disease will be explored. The speakers will also consider how this research could lead to preventative or damage repair treatment of the disease. • Julie Andersen, Professor, Buck Institute for Research on Aging: Senescence and the Aging Brain • Jeanne Loring, Professor, Scripps Research Institute: Negotiating the Mine Field in the Quest for a Parkinson’s Disease Cell Therapy • Dale Schenk, CEO, Prothena Corporation: Challenges and Hopes in Preventing and Developing Meaningful Therapeutic Strategies for Alzheimer’s and Parkinson’s Diseases Risk-Benefit Analysis in Therapies for the Diseases and Disabilities of Aging Today, the translation of healthcare innovations into patient outcomes is an inherently multi-stakeholder effort. Consequently, there is a major need to maintain rigor and independence in the regulation of healthcare innovations, while improving regulatory transparency and opportunities for multi-stakeholder input to accommodate fundamental changes in the life-science ecosystem and global healthcare demands. A key strategy in this endeavor is the development and utilization of novel risk-benefit appraisal methodologies, leveraging advances in patient reported outcomes (PROMS), stratified medicines – including ‘big data’ and risk management methodologies utilized presently in other industries. • David Brindley, Research Fellow, University of Oxford/Center for the Advancement of Sustainable Medical Innovation: (Moderator) • Richard Barker, Director, Center for the Advancement of Sustainable Medical Innovation • Chris Hornsby, Head of Model Development, Life Risks, Risk Management Solutions, Inc. • Brock Reeve, Executive Director, Harvard Stem Cell Institute 1:00 pm CONCURRENT SESSIONS. PLEASE CHOOSE ONE: [Ballroom A] [Ballroom D] [Ballrooms BC] 2:30 pm Afternoon Break & Exhibits - [Ballrooms EFGH] Conference Schedule 9
  • 10. Conference Schedule Day 2: Friday, August 22, 2014 Performance by Comedian Dan Nainan - [Ballrooms ABCD] Dan Nainan got his start by taking a comedy class to get over the nervousness of speaking on stage in his job as a demo engineer with Intel Corporation. After leaving Intel to pursue comedy, he has toured with Russell Peters and other notable comedians. Dan has appeared on network television including “Last Comic Standing” as well as in feature films, on radio and in an Apple commercial. He just completed a comedy tour of India. 8:00 pm Advancing Regenerative Therapies in Cancer and Parkinson’s Disease Panel - [Ballrooms ABCD] This panel will bring together speakers from throughout the day to summarize the impact of the I-SPY TRIAL 2 program on drug trial design for Alzheimer’s therapeutics and speculate on the applicability of trial designs similar to the one proposed for Alzheimer’s Disease to the development of therapeutics for other diseases of aging, such as Parkinson’s Disease and cancer. • Aubrey de Grey, CSO, SENS Research Foundation: (Moderator) • Rachelle Doody, Professor of Neurology, Director, Alzheimer’s Disease and Memory Disorders Center, Baylor College of Medicine • Laura Esserman, Professor, Departments of Surgery and Radiology, and Affiliate Faculty, Institute for Health Policy Studies and Director, Carol Franc Buck Breast Care Center; Co-Leader, Breast Oncology Program, UCSF Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco • Jeanne Loring, Professor, Scripps Research Institute • Brock Reeve, Executive Director, Harvard Stem Cell Institute • Dale Schenk, CEO, Prothena Corporation Networking Dinner/ Poster Session & Exhibits - [Ballrooms EFGH] 3:30 pm 5:30 pm Concert by Cecilia Noël Originally from Lima, Perú, Cecilia’s career began at the age of eight with a starring role in a Peruvian television show. As a teenager, Cecilia’s mother sent her to Argentina and Germany to take voice, violin, and piano lessons. Encouraged by the legendary Stan Getz to move to the US, Cecilia relocated to New York City and briefly performed as a dancer with Jo Jo’s Dance Factory and Menudo. Cecilia moved to Los Angeles in 1989 and in the early 1990s formed Cecilia Noël and The Wild Clams. The group received quick attention for their explosive live shows and were consequently booked at the House of Blues and the Playboy Jazz Festival. Critics have long called her the “Latin Tina Turner.” “Salsoul”, the genre Cecilia created to describe her sound, combines elements of salsa, soul, jazz, funk, and Afro-cuban. Cecilia also performs and records with husband and former Men At Work frontman Colin Hay. 10
  • 11. Networking Breakfast & Exhibits - [Ballrooms EFGH] Conference Schedule Keynote: Peter Diamandis, Co-founder and Vice Chairman, Human Longevity, Inc, Founder and CEO, X PRIZE Foundation: Creating a Culture of Innovation and Breakthroughs - [Ballrooms ABCD] Applying a Damage Repair Paradigm to Developing Therapies for the Diseases of Aging Panel - [Ballrooms ABCD] Building upon the discussion of a damage repair paradigm from days 1 and 2, this panel will weigh the benefits of application of a damage repair paradigm to drug development to combat the diseases of aging. Discussion will include the feasibility of applying such a strategy, the advantages and disadvantages such a model would confer, and an analysis of the regulatory changes that would be required to make such a paradigm possible. • Richard Barker, Director, Center for the Advancement of Sustainable Medical Innovation: (Moderator) • Julie Allickson, Director, Translational Research, Wake Forest Institute for Regenerative Medicine • Stephen Minger, Chief Scientist, Cellular Sciences, GE Healthcare Life Sciences, UK • Evan Snyder, Director, Center for Stem Cell and Regenerative Medicine, Director, Stem Cell Research Center and Core Facility, Sanford-Burnham Medical Research Institute Networking Lunch & Exhibits - [Ballrooms EFGH] 8:00 am 9:00 am 10:00 am 11:30 am Day 3: Saturday, August 23, 2014 11
  • 12. Conference Schedule Day 3: Saturday, August 23, 2014 Musculoskeletal Disease Session This session will highlight current muscu-loskeletal disease research. Presenters will discuss how molecular or cellular damage is believed to lead to their musculoskeletal disease of interest and how their research may contribute to delaying or preventing the disease. • Christy Carter, Assistant Professor, Department of Aging and Geriatric Research, Institute on Aging, University of Florida: What is Sarcopenia? Definitions, Diagnosis and Developing Interventions • Young Jang, Assistant Professor, Georgia Institute of Technology: The Rejuvenation of Aged Skeletal Muscle by Systematic Factors Diabetes Session Breakthroughs in diabetes research will be presented in this session. The molecular and cellular causes of diabetes will be considered and strategies to remove, repair, or replace such damage will be discussed. • Camillo Ricordi, Stacy Joy Goodman Professor of Surgery, Distinguished Professor of Medicine, Director, Diabetes Research Institute and Cell Transplant Program, University of Miami: Cellular Therapies and Regenerative Medicine Strategies for Treatment of Diabetes • David Schaffer, Professor, University of California, Berkeley, Director, Berkeley Stem Cell Center: Molecular Elucidation and Engineering of Stem Cell Therapies for the Nervous System Regulating a Damage Repair Approach to Cure the Diseases of Aging Panel Escalating societal healthcare needs have driven an unprecedented era of biomedical innovation. However, the development of candidate technologies without consider-ation of a robust regulatory strategy is likely to contribute to stymied patient access and commercial viability. Therefore, this session will consider worldwide efforts to rapidly and proportionally develop international regulatory processes to accommodate increasingly heterogeneous and unfamiliar healthcare technologies and their swift translation from lab to bedside. • David Brindley, Research Fellow, University of Oxford/Center for the Advancement of Sustainable Medical Innovation: (Moderator) • Bob Clay, Chief Regulatory Officer, Kinapse & Manging Director, Highbury Regulatory Science • Andrew Martello, Managing Director, Spoonful of Sugar • Evan Snyder, Director, Center for Stem Cell and Regenerative Medicine, Director, Stem Cell Research Center and Core Facility, Sanford-Burnham Medical Research Institute 12:30 pm CONCURRENT SESSIONS. PLEASE CHOOSE ONE: [Ballroom A] [Ballroom D] [Ballrooms BC] 12
  • 13. Break Advancing Regenerative Therapies in Musculoskeletal Disease and Diabetes Panel - [Ballrooms ABCD] This panel will bring together speakers from the morning sessions to consider the possibility of applying a drug trial design similar to the ones emerging from the Alzheimer’s Disease and cancer communities. The feasibility of applying such a model will be considered with the biology of the disease, regulatory concerns, and pharmaceutical needs in mind. • Aubrey de Grey, CSO, SENS Research Foundation: (Moderator) • Christy Carter, Assistant Professor, Department of Aging and Geriatric Research, Institute on Aging, University of Florida • Andrew Martello, Managing Director, Spoonful of Sugar • Camillo Ricordi, Stacy Joy Goodman Professor of Surgery, Distinguished Professor of Medicine, Director, Diabetes Research Institute and Cell Transplant Program, University of Miami • Young Jang, Assistant Professor, Georgia Institute of Technology Building a Rejuvenation Biotechnology Industry - [Ballrooms ABCD] This panel will synthesize the discussions from all of the conference sessions and panels. A cross-section of academics, pharmaceutical reps, policy makers, and other presenters will revisit the merits of a damage repair paradigm to address the diseases of aging considered at this conference. Panelists will consider the changes that would be required to lay the groundwork for a new industry perspective focused on addressing damage indications for the diseases of aging either through preventing or repairing such damage. • Michael Kope, CEO, SENS Research Foundation: (Moderator) • George Church, Professor of Genetics, Harvard Medical School, Professor of Health Sciences and Technology, Harvard and MIT • Dana Goldman, Leonard D. Schaeffer Chair and Director of the Schaeffer Center for Health Policy and Economics, University of Southern California • Stephen Minger, Chief Scientist, Cellular Sciences, GE Healthcare Life Sciences, UK • Brock Reeve, Executive Director, Harvard Stem Cell Institute Conference Concludes 1:30 pm 2:00 pm 3:00 pm 4:30 pm Conference Schedule 13
  • 14. Julie Allickson Dr. Allickson focuses on the translation of regenerative medicine products including cell therapy, tissue engineering, biomaterials and devices. This process begins at Proof-of- Concept where early discussions with regulators and clinicians are critical in moving the technology from the bench to the bedside. Prior to joining the institute, she was an Executive Officer of the company and Vice President of Laboratory Operations and R & D at Cryo-Cell International, Inc., an AABB accredited Cord Blood Bank. Prior to this position, she worked for the Univer-sity Of Miami School Of Medicine, Diabe-tes Research Institute as the Laboratory Director of the cGMP Hematopoietic Cell Processing Facility. She was responsible for the design and implementation of the State Licensed Clinical Flow Cytometry Laboratory. Dr . Allickson was the lead in Regulatory Affairs for the processing laboratory of Islet and Hematopoietic Cell products which included oversight of all Investigational New Drugs (IND) and external regulations. Prior to this, she worked for the American Red Cross managing the Hematopoietic Cell Processing and Platelet Serology Laboratory and serving as a member of the National Stem Cell Task Force. She has a Doctorate in Health Sciences and a Master’s Degree in Medical Laboratory Sciences. She is one of the founding mem-bers of the International Society of Cellular Therapy and a member of the American Association of Blood Banks (AABB) for 25 years. She is currently Chair of the AABB Standards Committee for Cell Therapy Product Services. Dr. Allickson is also on the Technical Advisory Board for Tissue Engineered Products under ICCBBA and the ISCT Commercialization Committee. Julie Andersen As a renowned expert on Parkin-son’s disease, Dr. Andersen is pursuing a wide array of leads toward treatments for this complex neurodegenerative disorder. She has identified several early risk signals for Parkinson’s, an age-related illness that causes a progressive decline in movement and muscle control. The symptoms can include shaking hands and difficulty with walking. Amongst the early risk signals identified by Dr. Andersen are elevated levels of iron and declining amounts of a protective antioxidant called glutathione. Recently, the Andersen lab has also discovered valuable clues by examining the roles of enzymes and other proteins involved in nerve cell degeneration. Normally, proteins carry out the routine work inside cells. But some enzymes can promote the symptoms of Parkinson’s disease. Blocking those enzymes might slow down the disease. Other therapies might result from the opposite tactic: reinforcing the work of different enzymes that guard against Parkinson’s disease. These enzymes seem to prevent damage to genes that protect the nervous system. The Andersen lab is also involved in identi-fying potential biomarkers for Parkinson’s that may allow early interventional therapy. Dr. Andersen earned a doctorate in Neuromolecular Biology at the University of California, Los Angeles (UCLA). She completed a postdoctoral fellowship at Harvard Medical School and Massachusetts General Hospital before going to the University of Southern California as an assistant then an associate professor at the Andrus Gerontology Center. She joined the Buck Institute in 2000. Richard Barker Richard is a strategic advisor, speaker and author on health-care and life sciences. He is Director of the Centre for the Advancement of Sustainable Medical Innovation, a major European initiative aimed at transforming the R&D and regulatory processes in life sciences to bring advances more rapidly and affordably to patients. He is also chairman of the South London Academic Health Science Network, accel-erating innovation in this region of the NHS, and Chairman of Stem Cells for Safer Medicines, a public-private partnership developing stem cell technology for predicting the safety profile of new medi-cines. He is a board member of Celgene, a major US-based bio-therapeutics company and of iCo Therapeutics, a Canadian bioscience company. His 25-year business career in healthcare has spanned biopharmaceuticals, diag-nostics and medical informatics – both in the USA and Europe. Most recently he was Director General of the Association of the British Pharmaceutical Industry, member of the Executive Committee of EFPIA (the European industry association) and Council member of IFPMA (the international equivalent). As a co-founder of Life Sciences UK, member of the NHS Stakeholder Forum, vice-chair of the UK Clinical Trials Collab-oration and in many other roles, he has advised successive UK governments on healthcare issues, especially those relating to developing, valuing and using new healthcare technologies. His past leadership roles include head of McKinsey’s European healthcare practice, General Manager of Healthcare Solutions for IBM and Chief Executive of Chiron Diagnostics. He was also Chairman and Chief Executive of Molecular Staging, a US bioscience company, now part of Qiagen. Speaker Biographies 14
  • 15. David Brindley David is an interna-tional thought-leader in the translation of life-science innovations into commercially viable products and services. His expertise spans the ‘Valley of Death,’ encompassing regulation, engineering and finance. Currently David’s professional activities include: research into the optimization of risk: benefit appraisal techniques for healthcare innovations, leading the CASMI Translational Stem Cell Consortium and providing timely and pragmatic advice to a range of stakeholders in healthcare translation, notably the venture capital community. Examples of David’s work can be found in a range of high impact journals including Nature, Nature Biotechnology, Nature Medi-cine and Cell Stem Cell. David also produces a popular blog, Cell Therapy Industry 2027, with the Centre for the Commercialisation of Regenerative Medicine. David is an active Fellow of the Royal Institution of Great Britain and the Royal Society for the Advancement of Arts and Manufacturing. David has successfully passed the Charted Analyst in Alternative Investments (CAIA) Level 1 examination. David completed his undergraduate studies in Biochemical Engineering at University College London (with First Class Honors) and his Masters, investigating the commercial-ization of regenerative therapies, jointly at the Harvard Stem Cell Institute and Harvard Business School. Currently he is pursuing a DPhil (PhD) in Musculoskeletal Sciences at the University of Oxford. Ashley Bush Ashley I. Bush (MB BS, DPM, FRANZCP, PhD, FTSE) heads the Oxidation Biology Unit at the Florey Institute of Neuroscience & Mental Health, is Professor of Neuroscience and Pathology at The University of Melbourne, NHMRC Australia Fellow, co-director of Speaker Biographies biomarker development for the Australian Imaging Biomarker Lifestyle Study (AIBL), Chief Scientific Officer of the Cooperative Research Center for Mental Health, and has staff appointments in Psychiatry and Radiol-ogy at the Massachusetts General Hospital. He has received numerous awards includ-ing the Potamkin Prize and the Beeson Award. Professor Bush has authored over 300 publications, with >21,000 citations (the most highly-cited Australian neurosci-entist of the last 10 years), 23 patents and founded 4 biotechnology companies. His lab discovered the interaction of beta-am-yloid with transitional metals as a major factor in Alzheimer’s disease pathology, as well as the roles of APP and tau in neuronal iron homeostasis. Judith Campisi Judith Campisi received a PhD in Biochemistry from the State University of New York at Stony Brook, and post-doctoral training in cell cycle regulation and cancer at the Dana-Farber Cancer Institute and Harvard Medical School. As an Assistant Professor at the Boston University Medical School, she began to focus her laboratory on role of cellular senescence in suppressing the development cancer, but soon became convinced that senescent cells also contributed to aging. She left Boston University as an Associate Professor to accept a Senior Scientist position at the Lawrence Berkeley National Laboratory in 1991. In 2002, she established a laboratory at the Buck Institute for Age Research, where she is a Professor. At both institutions, Campisi established a broad program to understand various aspects of aging, with an emphasis on the interface between cancer and aging. Her lab-oratory made several pioneering discoveries in these areas. Her research continues to challenge and alter existing In recognition of the quality of her research and leadership, Campisi received numerous awards, including two MERIT awards from the US National Institute on Aging, awards from the AlliedSignal Corporation, Geron-tological Society of America and American Federation for Aging Research, and the Longevity prize from the IPSEN Foundation. She serves on numerous national and international editorial and advisory boards. Guillermo García-Cardeña Guillermo Garcia Cardena is an Associate Professor of Pathology at Harvard Medical School, and the Director of the Laboratory for Systems Biology at the Center for Excellence in Vascular Biology, Brigham and Women’s Hospital, Boston. He received his Ph.D. degree from Yale University, working with William C. Sessa on the molecular regulation of nitric oxide production in vascular endothelium. His postdoctoral research with Michael A. Gimbrone Jr. at Harvard Medical School was on studies of endothelial cell gene expression, hemody-namics, and atherogenesis. Christy Carter Dr. Carter received her PhD in Experi-mental and Biologi-cal Psychology from the University of North Carolina at Chapel Hill and her post-doctoral training at The Wake Forest University School of Medicine in Winston-Salem, North Carolina. Globally , Dr. Carter’s current research inter-ests lie in preserving physical function and healthspan during aging; and in particular focuses on the use of a preclinical rodent model of aging to test a variety of late-life interventions designed to mitigate sarco-penia. Furthermore, she has demonstrated that the application of standardized physical performance measures to a variety of animal models of aging may help to define simi-larities between species in the underlying mechanisms of sarcopenia, the age-related decline in performance, disability, and longevity. Indeed the assessment of behav-ioral outcomes is essential for measuring the efficacy of any late-life intervention in the context of mitigating declining performance and improving healthspan. She has extended 15
  • 16. this area of research to other special aging populations such as the frail and obese, and has developed combinatorial therapies, using these compounds in conjunction with behavioral modification such as exercise. George Church George Church is Professor of Genetics at Harvard Medical School and Director of PersonalGenomes. org, which provides the world’s only open-access information on human Genomic, Environmental & Trait data (GET). His 1984 Harvard PhD included the first methods for direct genome sequencing, molecular multiplexing & barcoding. These led to the first genome sequence (pathogen, Helico-bacter pylori) in 1994. His innovations have contributed to nearly all “next generation” genome sequencing methods and compa-nies (CGI, Life, Illumina, nanopore). This plus chip-based DNA synthesis and stem cell engineering resulted in founding additional application-based companies spanning fields of medical diagnostics (Knome, Alacris, AbVitro, Pathogenica ) and synthetic biology / therapeutics ( Joule, Gen9, Editas, Egenesis, enEvolv, WarpDrive). He has also pioneered new privacy, bio-safety , environmental & biosecurity policies. He is director of NIH Center for Excellence in Genomic Science. His honors include election to NAS & NAE & Franklin Bower Laureate for Achievement in Science. He has coauthored 330 papers, 60 patents & one book (Regenesis). Bob Clay Bob Clay recently established his own regulatory consul-tancy practice through Highbury Regulatory Science, prior to this he was a VP Global Regulatory Affairs at AstraZeneca with responsibility for oncology, infection and personalised healthcare. Bob is Chief Regulatory Officer at Kinapse and a member of the board of TOPRA. He is a member of the Expert Scientific Advisory Committee for Medicines for Malaria Venture (MMV) and several working groups at CPTR (Critical Path for TB Regimens). He has an interest in the impact of regulation on the development of innovative medicines and healthcare policy matters. Bob is a regulatory strategist with more than 30 years’ experience in drug development, leading the global regulatory approval of products across a range of therapy areas including metabolic diseases, neuroscience, cancer and infection. Bob graduated in Pharmacy from the University of Bath and subsequently completed an MSc in BioPhar-macy, from the University of London, and an MBA, from the Open University. Following completion of his professional training in hospital pharmacy he joined the pharma-ceutical industry as a formulation scientist at the UK laboratories of Rhone-Poulenc. Later, he joined the UK Licensing Authority as a pharmaceutical assessor and has held regulatory affairs leadership roles with several pharmaceutical companies including Wellcome, Zambon, Pfizer and AstraZeneca. Aubrey de Grey Dr. de Grey is the biomedical geron-tologist who researched the idea for and founded SENS Research Foundation. He received his BA in Computer Science and Ph.D. in Biology from the University of Cambridge in 1985 and 2000, respectively. Dr. de Grey is Editor-in-Chief of Rejuvenation Research, is a Fellow of both the Gerontological Society of America and the American Aging Association, and sits on the editorial and scientific advisory boards of numerous journals and organizations. He is the Chief Science Officer of the SENS Research Foundation. Peter Diamandis Dr. Peter H. Diamandis is an international pioneer in the fields of innovation, incentive competitions and commercial space. In the field of Innovation, Diamandis is Chairman and CEO of the X PRIZE Foundation, best known for its $10 million Ansari X PRIZE for private spaceflight. Today the X PRIZE leads the world in designing and operating large-scale global competitions to solve market failures. Diamandis is also the Co-Founder and Vice-Chairman of Human Longevity Inc. (HLI), a genomics and cell therapy-based diag-nostic and therapeutic company focused on extending the healthy human lifespan. He is also the Co-Founder and Executive Chairman of Singularity University, a graduate-level Silicon Valley institution that studies expo-nentially growing technologies, their ability to transform industries and solve humanity’s grand challenges. In the field of commercial space, Diamandis is Co-Founder/Co-Chairman of Planetary Resources, a company designing spacecraft to enable the detection and mining of asteroid for precious materials. Diamandis is the New York Times Bestselling author of Abundance – The Future Is Better Than You Think. Abundance was #1 on Amazon and #2 on New York Times. He was also named one of “The World’s 50 Greatest Leaders” – by Fortune Magazine. He earned an undergraduate degree in Molecular Genetics and a graduate degree in Aerospace Engineering from the Massachu-setts Institute of Technology, and received his M.D. from Harvard Medical School. Diamandis’ mission is to open the space frontier for humanity. His personal motto is: “The best way to predict the future is to create it yourself.” Rachelle Doody Dr. Doody is the Effie Marie Cain Chair in Alzheimer’s Disease Research and Professor of Neurology at Baylor College of Medicine, where she directs the Alzheimer’s Disease and Memory Disorders Center (ADMDC). She received a B.A. from Rice University, a M.D. from Baylor College of Medicine, and completed intern-ship and residency training at the Royal Victoria Hospital and Montreal Neurologic Institute in Montreal, and at Baylor College of Speaker Biographies 16
  • 17. Medicine and has a Ph.D. in Cognitive Anthropology from Rice University where she studied the brain and language. She has published over 170 original research articles, most dealing with the diagnosis, progression, or treatment of Alzheimer’s Disease. She has received multiple research grants, including a Zenith Award from the National Alzheimer’s Association, and designed and conducted numerous clinical trials of Alzheimer’s Disease therapies. She participates in National and International collaborative efforts, review boards, and advisory boards including Steering Committees for the NIH AD Cooperative Study and AD Neuroimaging Initiatives, and the Steering Committee for the Texas AD Research and Care Consortium. Current research interests include studies to understand and model the progression of Alzheimer’s Disease, studies of clinical het-erogeneity, and research and development of new medications to treat Alzheimer’s Disease. She works with many biopharma-ceutical and large pharma collaborators in the assessment and experimental testing of a diverse group of potential AD therapies. She has served on the Texas Council on Alzheimer’s Disease and Related Disorders, and the Board of Directors for the Houston and Southeast Texas Chapter of the Alzhei-mer’s Association. Laura Esserman Dr. Esserman is a surgeon and breast cancer oncology specialist, and is the Director of the Carol Franc Buck Breast Care Center at the University of California, San Francisco (UCSF). In 1996, she started the Center of Excellence for Breast Cancer Care at UCSF to integrate clinical care and research, automate tools for the capture of patient and clinical data, and develop systems to tailor care to biology, patient preference, and performance. Dr. Esserman is nationally and internationally known as a leader in the field of breast cancer and has published over 200 articles. She served as a member of a taskforce for President Obama’s Council of Advisors on Science and Technology (PCAST) Working Speaker Biographies Group on Advancing Innovation in Drug Development and Evaluation. The group was tasked with making recommendations to the federal government about how to best support science-based innovation in the process of drug development and regulatory evaluation. She is the Principle Investigator of the I-SPY TRIAL program, a multi-site neoadjuvant clinical trial (which includes phase 2 and 3 trials) that has evolved into a model for translational research and innovation in clinical trial design. Dr. Esserman has recently launched a University of California-wide breast cancer initiative called the Athena Breast Health Network, a program designed to follow 150,000 women from screening through treatment and outcomes, incorpo-rating the latest in molecular testing and web-based tools into the course of care. Athena is in the final stages of launching a statewide demonstration project and phase 1/2 trial of personalized screening. Caleb Finch Caleb Finch Ph.D. is ARCO Professor of Gerontology and Biological Sciences at the University of Southern California, with adjunct appointments in the Department of Anthropology, Molecular Biology, Neurobiology, Psychol-ogy, Physiology, and Neurology. Major research interest is the neurobiology of aging and human evolution. Finch received his undergraduate degree from Yale in 1961 (Biophysics) and Ph.D. from Rockefeller University in 1969 (Biology). His life work is the fundamental biology of human aging, started in grad school and continued since 1972 at USC. Discoveries include a new form of neurotoxicity of amyloid peptides relevant to Alzheimer disease and the role of shared inflammatory pathways in normal and pathological aging process. Fifteen of his mentored students hold senior positions in universities or pharmaceutical corporations. Finch has received most of the major awards in biomedical gerontology, including the Robert W. Kleemeier Award (1985), the Sandoz Premier Prize (1995), and the Irving Wright Award (1999). He was founding Director of the NIA-funded USC Alzheimer Disease Research Center (1984), and continues as coDirector and coPI. He also co-founded Acumen Pharmaceuticals, which develops therapeutics for Alzheimer disease. He has written four books, most recently, The Biology of Human Longevity: Inflammation and Nutrition in the Evolution of Lifespans (Academic Press, 2007). Recent interests include the paleopathology of human aging and emerging environmental factors in aging, particularly air pollution components from fossil fuels. Gabor Forgacs Dr. Gabor Forgacs is a theoretical physicist turned bioengineer turned innovator and entrepreneur. He is the George H. Vineyard Professor of Biological Physics at the University of Missouri-Columbia, the Executive and Scientific Director of the Shipley Center for Innovation at Clarkson University and scientific founder of Organovo, Inc. and Modern Meadow, Inc. He was trained as a theoretical physicist at the Roland Eotvos University, Budapest, Hungary and the Landau Institute of Theoretical Physics, Moscow, USSR. He also has a degree in biology. His research interests span from topics in theoretical physics to physical mechanisms in early embryonic development. He is the co-author of the celebrated text in the field, “Biological Physics of the Developing Embryo” (Cambridge University Press, 2005) that discusses the fundamental morphogenetic mechanisms evident in early development. These mechanisms are being applied to building living structures of prescribed shape and functionality using bioprinting, a novel tis-sue engineering technology he pioneered. He is the author of over 160 peer-reviewed scientific articles and 5 books. He has been recognized by numerous awards and citations. In particular, he was named as one of the “100 most innovative people in business in 2010” by FastCompany. 17
  • 18. Howard Foyt Howard Foyt, M.D., Ph.D. FACP, Vice President, Clinical Development and Chief Medical Officer at ViaCyte, Inc., has over 18 years of clinical development experience in pharmaceutical and biotechnology environments. Dr. Foyt’s background as an endocrinologist and his multiple NDA and IND applications position him as ViaCyte’s strategic leader for clinical and regulatory operations. Prior to ViaCyte, Dr. Foyt served as Senior Vice President and Chief Medical Officer at Cebix, Inc., a company focused on treat-ments for complications of type 1 diabetes. Before Cebix, he was Vice President, Clinical Development at Metabasis Therapeutics, Inc. Dr. Foyt’s pharmaceutical experience includes senior positions at Pfizer Global Research & Development and Parke-Davis Pharmaceutical Research. As a clinician, Dr. Foyt was Assistant Professor and Medical Director of the University Diabetes Center at the University of Texas Medical Branch. He earned his medical degree from Baylor College of Medicine where he also earned a Ph.D. in Cell Biology. Dr. Foyt completed his residency in internal medicine at Baylor and an endocrinology fellowship at the National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health. Dana Goldman Dana Goldman is a Professor and the Leonard D. Schaeffer Chair in Health Policy at the University of Southern California. He is also the inaugural director of the Schaeffer Center for Health Policy and Economics, one of the nation’s premier health policy research institutions. Dr. Goldman is the author of over 150 articles and book chapters, including publications in the most presti-gious medical, economic, health policy, and statistics journals. He is a health policy advisor to the Congressional Budget Office, Covered California (California’s insurance exchange), and the Fred Hutchinson Cancer Institute. He serves on several editorial boards including Health Affairs and the American Journal of Managed Care, and is the founding editor of the Forum for Health Economics and Policy. Dr. Goldman’s work has been featured in the New York Times, Wall Street Journal, Washington Post, Business Week, U.S. News and World Report, The Economist, NBC Nightly News, CNN, National Public Radio, and other media. In 2009, he was elected to the National Academy of Science’s Institute of Medicine in recognition of his professional achieve-ment. He was the first recipient of the MetLife Foundation’s Silver Scholar Award, honoring his research on aging; the Eugene Garfield Economic Impact Prize, recogniz-ing outstanding research demonstrating how medical research impacts the econ-omy; the National Institute for Health Care Management Research Foundation award for excellence in health policy; and the Alice S. Hersh New Investigator Award recognizing contributions of a young scholar to health services research. He is also a founder and managing director of Precision Health Economics, a consulting firm to the health care industry. Dr. Gold-man received his B.A. summa cum laude from Cornell University and a Ph.D. in Economics from Stanford University. Claudia Gravekamp Claudia Gravekamp, PhD, is an Associate Professor in the Department of Microbiology and Immunology of the Albert Einstein College of Medicine in New York, and a member of the Albert Einstein Cancer Center. She received her PhD in 1988 in the field of Tumor Immunology at the Erasmus University in Rotterdam, The Netherlands. From 1987 to1993, she served as head of the Labora-tory for Leptospirosis at the Royal Tropical Institute in Amsterdam, The Netherlands. In 1993, she started as a Research Fellow in Medicine at the Channing Laboratory of the Brigham and Women’s Hospital, Harvard Medical School, and soon became an Instructor in Medicine until 1998. There, she developed vaccines against Group B Streptococcus and gained expertise in the design and development of gene-driven vaccines. From 1998 to 2006, she was an Associate Member in the Institute for Drug Development of the Cancer Therapy and Research Center and an Assistant Professor at the University of Texas Health Science Center, in San Antonio, where she began to develop a program aimed at genetic vaccines for breast cancer. From 2006-2008, she was a Scientist at the California Pacific Medical Center Research Institute in San Francisco, continuing to develop novel immunotherapeutic approaches to cancer using attenuated Listeria monocytogenes as a platform to deliver anti-cancer agents selectively to the tumor microenvironment at young and old age. She has been funded by grants from the NIH, other grant agencies and private industry since 1999, published 55 scientific articles, is a member of the Editorial Board of Mechanisms of Ageing and Development, and is ad-hoc reviewer for various scientific journals. Catalina Hoffman Catalina Hoffman is a leader in the elderly sector for her trajectory as entrepreneur, business woman and Hoffmann Method’s creator. She graduated with a PDD from the IESE Business School of Navarra University. She has studied Occupational Therapy and is a specialist in cognitive stimulation. The Hoffmann Method offers an innovative system of care and personalized attention which takes into account the physical, cognitive, psychological and social areas. It has achieved improvements in the health and quality of life of many people. It includes a network of partners in the social, health, scientific and technological sphere. She is a member of the Board of Spain Start-up’s Governing Council. She was named President of SECOT in June 2013. She is an associate and mentor of the European Professional Women’s Network. From this network, she is godmother of Mapel Project of Ayuda en Acción (NOG), aimed to craftswoman entrepreneurs in Ecuador. She also received national and international recognitions including The Harvard Business School Expansion Award for the Speaker Biographies 18
  • 19. Entrepreneurship. She was added to The Top 100 Women Leaders in Spain 2012. Plataforma Editorial published her first book “Emprender soñando”. The Prince of Girona Foundation granted her the Award of Business Woman 2013. The Association of Young Entrepreneur of Madrid named her the Young Entrepreneur of Madrid 2014. In 2013, she created the Catalina Hoffmann Holding Group, a group of companies specialized in different areas of science, health, health care, new technologies, consulting, innovation and development of new products and services. It includes Vitalia, Hoffman Elderly,Hoffmann Health- Care Innovation and Catalina Hoffmann Foundation. Chris Hornsby Chris’ academic background is in applied mathemat-ics and epidemiol-ogy, his doctoral research at Univer-sity College London was focused on probabilistic models of the multistage development of cancer. Chris joined the LifeRisks group at RMS in 2008 working initially as lead developer of the RMS Longevity Risk Model and subsequently more broadly on insurance capital reserv-ing and risk transfer applications in respect of both life catastrophe and longevity. Chris has played a key role, through the provision of expert risk analysis, in the early development of capital markets based solutions for hedging longevity risk. Jean Hébert Jean Hébert Jean Hébert completed his PhD at the University of California, San Francisco, under the mentorship of Gail Martin where he studied cell-signaling factors that regulate some of the early steps in mammalian development. For these studies, he used embryonic stem cells and mouse genetics. As a postdoctoral fellow in Susan McCon-nell’s lab at Stanford University, he then focused his attention on how the neocortex, Speaker Biographies the part of our brains that we use for our highest cognitive and perceptual functions, develops. Continuing along these interests, he currently heads his own research lab at the Albert Einstein College of Medicine where his group has primarily undertaken two lines of investigation. The first is understanding how a simple sheet of neuroepithelial cells early in embryogenesis develops into the adult neocortex, seat of our consciousness. Conditional genetic approaches in the mouse, whereby candidate genes that regulate neocortex formation are deleted or overexpressed specifically in neural precursor cells, comprise the central method driving these studies. The second line of investigation aims to establish ways of regenerating the principle neurons of the adult cerebral cortex when these neurons are lost due to trauma or degeneration, including degeneration due to aging. Since endogenous precursors do not replace cortical neurons when they are lost, two strategies are being developed: manipulating these precursors with molec-ular genetic techniques to start generating neurons and transplanting engineered precursors that are programmed to disperse in the cortex and differentiate into cortical projection neurons. Young Jang Young Jang received his Ph.D. in Biomedi-cal Sciences (Cell Biology) from University of Texas in 2008, and completed his postdoctoral training from Barshop Institute for Longevity and Aging Studies and the laboratory of Amy Wagers at Harvard University and Harvard Stem Cell Institute. In 2014, he was appointed as an Assistant Professor in the School of Applied Physiology and a faculty member in the Parker H. Petit Institute for Bioengi-neering and Bioscience at Georgia Institute of Technology. The primary research focus of the Jang laboratory is to understand the molec-ular and biochemical mechanisms of age-related muscle loss and function. The Jang laboratory applies bioengineering approaches and stem cell-based therapies to study skeletal muscle dysfunction during aging and in age-associated muscle diseases. The laboratory develops and applies novel tools using a combination of animal and stem cell models. W. Gray Jerome Dr. Jerome is Associate Professor of Pathology, Microbiology and Immunology and Associate Professor of Cancer Biology at Vanderbilt Univer-sity. He is also Co-Director of the Cell Imaging Shared Resource at Vanderbilt. Jay is a Past-president of the Microscopy Society of America, the Co-Editor of a textbook on confocal microscopy, and an Editor for the journal Microscopy and Microanalysis. Jay’s research focuses on intracellular lipid metabolism and how disruption of normal lipid metabolism contributes to disease. His most recent studies investigate how lipids, particularly cholesterol, affects lysosome function and how alterations in lysosome function feedback to influence lipid metabolism. Lysosomes are key homeo-static organelles and lysosome dysfunction is associated with a number of diseases that become more prevalent with age. Dr. Jerome has shown that cholesterol overload inhibits lysosome function and disrupts cell homeostasis, particularly in inflammatory cells which can easily become overloaded with cholesterol. His group has also shown that lysosomal cholesterol-engorgement shifts other aspects of cellular lipid balance in ways that can push cells further into the disease state. Jeffrey Karp Jeff Karp is an Associate Professor at Brigham and Women’s Hospital, Harvard Medical School, and is Principal Faculty at the Harvard Stem Cell Institute and affiliate faculty at MIT through the Harvard-MIT Division of Health Sciences and Technology. His research uses 19
  • 20. materials and biology to solve medical problems with emphasis on nanoscale/ microscale materials and bio-inspiration. He has published more than 100 peer-reviewed papers and book chapters and has given over 130 national and international invited lectures and has 50 issued or pending patents. Several technologies that he has invented are currently being translated into medical products to improve the quality of life of suffering patients. In 2011 the Boston Business Journal recog-nized Dr. Karp as a Champion in Healthcare Innovation and in 2013 the Institute for Chemical Engineers (IChemE) awarded one of his technologies the Most Innovative Product of the Year. MIT’s Technology Review Magazine (TR35) also recognized Dr. Karp as being one of the top innovators in the world under the age of 35. He has received the Society for Biomaterials Young Investigator Award and his work has been selected as one of Popular Mechanic’s “Top 20 New Biotech Breakthroughs that Will Change Medicine”. Dr. Karp was also elected in 2013 to the American Institute for Medical and Biological Engineering’s College of Fellows and as a Kavli Fellow. Dr. Karp is also an acclaimed mentor. He was selected as the Outstanding Faculty Undergraduate Mentor among all Faculty at MIT and received the HST McMahon Mentoring award for being the top mentor among all faculty who mentor Harvard- MIT students. Michael Kope Michael Kope is President, Chief Executive Officer, and Co-founder of the SENS Research Foundation. Mr. Kope received his J.D. from the University of Michigan in 1990. He has served as the University of Michigan’s Intellectual Property Counsel; as Director of Corporate Development for Aviron, and for MedImmune, Inc.; and as CEO and officer of a number of start-ups in the biotechnology space. He specializes in business development and consulting, and is widely experienced with biotech-nology organizations. Mike has negotiated a broad range of business acquisition and partnership agreements, designed strategies for technology protection and promotion in many fields of research, and facilitated a number of successful startups. Daniel Kraft Daniel Kraft is a Stanford and Harvard trained physician-scientist, inventor, entrepre-neur and innovator. Dr. Kraft has over 20 years of experience in clinical practice, biomedical research and healthcare innovation. Daniel chairs the Medicine track for Singularity Univer-sity and is Founding Executive Director for FutureMed (now called Exponential Medicine), a program which explores convergent, exponentially developing technologies and their potential in biomedicine and healthcare. Following undergraduate degrees at Brown University and medical school at Stanford, Dr. Kraft was board certified in the Harvard combined Internal Medicine and Pediatrics residency program at the Massachusetts General Hospital and Boston Children’s Hospital. He went on to complete Stanford fellowships in hematology/oncology & bone marrow transplantation, and to conduct extensive research in stem cell biology and regenerative medicine. He has multiple scientific publications (including in the journals Nature and Science) and medical device, immunology and stem cell related patents through faculty positions with Stanford University School of Medicine and as clinical faculty for the pediatric bone marrow transplantation service at University of California San Francisco. Dr. Kraft recently founded Bioniq Health, focused on enabling connected, data driven, and integrated personalized medicine. He is also the inventor of the MarrowMiner, an FDA approved device for the minimally invasive harvest of bone marrow, and founded RegenMed Systems, a company developing tech-nologies to enable adult stem cell based regenerative therapies. Neil Littman Neil Littman is the Business Develop-ment Officer at the California Institute for Regenerative Medicine. Mr. Littman is responsi-ble for facilitating opportunities for outside investment in stem cell research in California by biopharma companies, investors, and disease foundations. Prior to joining CIRM in 2012, Mr. Littman was a Senior Associate in the Merchant Banking Group at Burrill & Company, a diversified global financial services firm focused on the life sciences industry based in San Francisco. While at Burrill & Company, Mr. Littman’s responsibilities included both strategic advisory and capital raises for biopharma companies throughout the U.S. and internationally. Mr. Littman’s strategic advisory experience includes buy-side and sell-side M&A, as well as in-licensing and out-licensing of both development stage and commercial prod-ucts. Prior to joining Burrill & Company in 2009, Mr. Littman worked in the Healthcare Investment Banking group at Thomas Weisel Partners where he focused on strategic advisory and public and private financings. Prior to Thomas Weisel Partners, Mr. Littman worked in the Healthcare Investment Banking group at Deutsche Bank Securities. Mr. Littman received a Master of Science in Biotechnology with a concentration in Biotechnology Enterprise from The Johns Hopkins University, and a Bachelor of Arts in Molecular, Cellular and Development Biology from the University of Colorado Boulder. Jeanne Loring Jeanne Loring, Ph.D., is a Professor and the founding Director of the Center for Regenera-tive Medicine at The Scripps Research Institute in La Jolla. Her research team focuses on large-scale analysis of genomics and epigenetics of human pluripotent stem cells (hPSCs) and Speaker Biographies 20
  • 21. their derivatives, in order to ensure the quality and safety of these cells for clinical use. The team’s translational projects include development of cell therapies for Parkin-son’s disease, multiple sclerosis, and Alzheimer disease, and epigenetic modeling of autism. The team is also producing an ethnically diverse library of iPSC (induced pluripotent stem cell) lines for use in pharmaceutical screening. In addition, her lab is developing a “zoo” of induced pluripotent stem cells from endangered species to aid in their conservation. Dr. Loring is committed to educating both scientists and the public. She has trained more than 400 scientists over the last 10 years in intensive laboratory courses in human ES and iPSC biology, and is author of a comprehensive laboratory manual on human pluripotent stem cells (“Human Stem Cell Manual: a Laboratory Guide, in second edition, 2012). She is frequently quoted in major newspapers, and gives numerous public lectures and interviews to inform the public about biological and societal issues associated with stem cell research, including the ethics of stem cell generation and clinical use, the legal implications of stem cell patents, and public education about the dangers of unregulated stem cell treatments (“stem cell tourism”). Dr. Loring serves on both bioethics and scientific advisory boards. Linda Marban Linda Marban is currently CEO, President and Director of Caprico Therapeutics. She combines her background in research with her business experience to lead Capricor and create a path to commercialization for its novel stem-cell cardiac therapies. Dr. Marban was the lead negotiator in procur-ing the license agreements that are the foundation of Capricor’s intellectual property portfolio. Under her direction as Chief Executive Officer, Capricor secured approximately $27.0 million in nondilutive grants and a loan award which funds Capricor’s R&D programs and clinical trials involving its CAP-1002 product. Dr. Marban’s deep knowledge of the cardiac space in particular, allows her to provide unique Speaker Biographies direction for the company’s development and growth. From 2003 to 2009, Dr. Marban was with Excigen, Inc., a biotechnology start-up company, where she was responsi-ble for business development, operations, pre-clinical research, and supervising the development of gene therapy products in a joint development agreement with Gen-zyme Corp. While at Excigen, she also negotiated a joint development and sublicense agreement with Medtronic Corp. utilizing Excigen’s technology and super-vised the building of a lab in which the work was to be performed. Dr . Marban began her career in academic science at the Cleveland Clinic Foundation working on the biophysical properties of cardiac muscle. She moved to a postdoc-toral fellowship at Johns Hopkins University and advanced to the rank of Research Assistant Professor in the Department of Pediatrics, continuing her work on the mechanism of contractile dysfunction in heart failure. Dr. Marban earned a Ph.D. from Case Western Reserve University in cardiac physiology. Andrew Martello Andrew Martello is co-founder & CEO of Spoonful of Sugar (SoS). He leads an expert team developing academically-led adherence consul-tancy and evi-dence- based adherence solutions to global healthcare providers and the pharmaceutical industry. SoS is a University College London spinout company that applies the learnings of a 15-year research program in behavioral medicine, specifically, how patients engage with long-term illnesses and treatment. Over the past five years, Andrew has been directly involved in the planning and implementation of multi-country adherence and patient support programs utilizing the latest research into illness and medicines-related behavior. As part of this work, Andrew has led the development of proprietary software designed to diagnose and treat both perceptual and practical barriers to optimal adherence at an individual patient level. Passionate about the role of digital technology in changing health behaviors, Andrew’s main interest is the role of personalized medicine, from both a clinical and psychological perspective and its real world application. Prior to founding SoS, Andrew spent over ten years working for and consulting with the pharmaceutical industry, predominantly in HIV medicine. Much of his work in this field focused on the development of strategies supporting a greater understanding of the patient’s per-spective throughout the drug development and product lifestyle pathway. This included the development of novel formulations and devices, packaging and support services to optimize the use of medicines. This work not only focused on the devel-oped world but also included innovative strategies to widen access to medicines throughout the developing world. Andrew’s previous assignments have been with GlaxoSmithKline, Abbott Laboratories, Novartis and Sandoz Biopharmaceuticals. Stephen Minger Dr. Stephen Minger received his PhD in Pathology (Neuro-sciences) in 1992 from the Albert Einstein College of Medicine in New York City. After post-doctoral work in central nervous system gene therapy, neural transplantation and neural stem cell biology, he was appointed a Lecturer in Biomolecular Sciences at King’s College London in 1998. He was appointed a Senior Lecturer in Stem Cell Biology in 2005 and was the Director of the Stem Cell Biology Laboratory from 2002 until joining GE Healthcare in 2009. Over the past 20 years, Stephen’s research group has been at the forefront of human stem cell research. In 2002, they were awarded one of the first two licenses granted by the UK Human Fertilisation and Embryology Authority for the derivation of human embryonic stem (hES) cells and his group was the first to deposit a hES cell line into the UK Stem Cell Bank. Stephen’s 21
  • 22. was also one of the first two groups in the UK to be granted a research license by the HFEA in 2008 to pursue Somatic Cell Nuclear Transfer (SCNT) to generate “hybrid human embryos” for fundamental research into genetic forms of neurodegenerative conditions. He was activity involved with the UK Department of Health and in the consultation that led to the passage of the Human Embryo Bill of 2009 and the inclusion of new forms of animal-human embryos within primary legislation. In the summer of 2013, Stephen was appointed Chief Scientist for Cellular Sciences, GE Healthcare Life Sciences, and is now responsible for long-term global research strategy for technology develop-ment in cell therapy, regenerative medicine, cellular technologies, in vivo diagnostic imaging and molecular pathology/person-alized medicine. Peter Nakada Peter Nakada leads the RMS Capital Markets and LifeRisks groups. After joining the company in 2005, he formed the RMS Capital Markets group to provide an infrastructure for capital markets participants to understand catastrophe risk. He focuses on taking the company’s catastrophe risk expertise into adjacent markets and leads the RMS LifeRisks team to provide excess mortality and longevity risk analytics to life insurers and capital markets investors. Nakada began his career in financial services as a general account fixed income portfolio manager for Prudential Insurance Company. Prior to joining RMS, Nakada was a partner at Oliver, Wyman & Company, where he specialized in advising banks and insurers on aspects of risk, capital, and shareholder value. In 2000, Nakada co-founded ERisk, a spinoff from Oliver, Wyman & Company, which provides software-as-a-service for enterprise risk management and economic capital quantification. Nakada has co-authored many articles on topics related to risk, capital, and share-holder value, as well as the securitization of catastrophic risk. His articles include “Risk, Capital & Value Measurement in Financial Institutions – Part I: The Debtholder’s Perspective (1998),”P&C RAROC: A Catalyst for Improved Capital Management in the Property and Casualty Insurance Industry” (1999), “Understanding Longevity Risk: Insights from Structural Cause-of-Im-provement Models” (2012) and “Quantifying the Mortality-Longevity Offset”(2013). Nakada holds a bachelor’s degree in engineering sciences from Harvard College and a master’s degree in engineering management from Stanford University. He earned the Chartered Financial Analyst® designation in 1990. Edward James Olmos Edward James Olmos (Axford) has achieved extraordi-nary success as an actor, producer and humanitarian. The Tony, Emmy and Academy Award® Nominated actor, is probably best known to young audiences for his work on television series “Battlestar Galatica” as Admiral William Adama. Although the series kept the actor busy during its run from 2003 through 2009, it didn’t stop him from directing the HBO movie “Walkout” in 2007, for which he earned a DGA Nomination in the Outstanding Directorial Achievement in Movies for Television category. Olmos earned two Golden Globe and Emmy Award nominations, resulting in a win from each. In 1988, he received an Academy Award® nomination for Best Actor for his starring role in Stand and Deliver and won the Golden Globe for his portrayal of Jaime Escalante in Stand and Deliver. Olmos’ career in entertainment spans over 30 years. In that time he created a signa-ture style and aesthetic that he applies to every artist endeavor. His dedication to his craft has brought him worldwide attention. Olmos went on to appear in the films Wolfen, Blade Runner, and the Ballad of Gregorio Cortez before starring in his biggest role to date, that of Lieutenant Martin Castillo in the iconic 80’s television series “Miami Vice”. He directed and starred in his first motion picture, American Me, in 1992. Olmos’ passion for the arts grows every year, but he never forgets to give back to the communities that support him with their dedication. He is an international advocate, spokesman, and humanitarian working with organi-zations such as Thank You Ocean, Project Hope Foundation, Children’s Hospital of Los Angeles, The Boy’s and Girl’s Club of America, The River Keepers, Dr. Andros’ Diabetic Foot Global Conference and he speaks up to 150 times a year in schools, universities, and corporations. Jim O’Neill Jim O’Neill is partner and chief operating officer at Mithril, a growth fund for transformative and durable technology companies in fields such as cyber-security; next generation finance; medical robotics; rail integration; enter-prise cloud services; 3D seismic technol-ogy; and data integration, visualization, and analysis. Mithril invests with convic-tion and helps teams successfully navigate high-growth periods. Before helping to launch Mithril, Jim was a managing director of Clarium, a global macro investment fund. He also ran the Thiel Foundation and co-founded the 20 Under 20 Thiel Fellowship and Breakout Labs. Previously, as the principal associate deputy secretary of health and human services, Jim helped manage an agency whose 67,000 employees regulate more than 25% of the U.S. economy. His main areas of policy and program responsibility included the Food and Drug Administra-tion, the National Institutes of Health, the Centers for Disease Control and Prevention, security, intelligence, preparedness, and health diplomacy. He also made invest-ments in drug, vaccine, and diagnostic research on the steering committee of the $200 million Biomedical Advanced Research and Development Authority. Speaker Biographies 22
  • 23. Brock Reeve Brock Reeve is Executive Director of the Harvard Stem Cell Institute. In partnership with the Faculty Directors, he has overall responsi-bility for the operations and strategy of the Institute whose mission is to use stem cells, both as tools and as therapies, to under-stand and treat the root causes of leading degenerative diseases. HSCI is comprised of the schools of Harvard University and all its affiliated hospitals and research institutions. Under the leadership of the Executive Committee, HSCI invests in scientific research and its faculty has grown to include over 300 Principal and Affiliated members. The Institute is engaged with several leading pharmaceutical companies and foundations in joint research projects and its faculty have founded several stem cell-related startup companies and serve on leading Scientific Advisory Boards. Brock came to this role from the commercial sector with extensive experience in both management consulting and operations for technology-based companies, with a focus on life sciences. Brock received a BA and MPhil from Yale University and an MBA from Harvard Business School. Camillo Ricordi Camillo Ricordi is Professor and Director of the Diabetes Research Institute (DRI; www. diabetesresearch. org ) and the Cell Transplant Program at the University of Miami. Dr. Ricordi and collaborators developed the method for large scale production of human pancreatic islets, and he led the team that performed the first series of successful clinical islet allotransplants to reverse diabetes. The procedure is now used by laboratories performing clinical islet transplants worldwide. Ricordi was president of the Cell Transplant Society, on the NIH-NIAID Expert Panel on clinical Speaker Biographies approaches for tolerance induction, on the FDA Biologic Response Modifiers Advisory Committee and on the NIH-NIDDK Strategic Planning Committee. Ricordi is currently serving as Chairperson of the NIH funded Clinical Islet Transplanta-tion (CIT) Consortium, which standardized cell manufacturing protocols in North America and Europe and just completed the first multicenter FDA Phase III trial for what could become the first biologically active cell product approved in the US by the FDA. Ricordi has received numerous honors and awards and was also Knighted by the Presi-dent of the Republic of Italy. He is currently serving on the editorial boards of CellR4 (Editor-in-Chief; www.cellr4.org) and Cell Transplantation (Co-Editor-in-Chief ). In 2013 he was appointed President of the Ri.MED Foundation by the Italian Prime Minister (http://www.fondazionerimed.eu), one of the largest European investments in Biomedical Research, Biotechnologies and Regenerative Medicine. Ricordi also serves as President of The Cure Alliance (www. thecurealliance.org) and Chairman of the Diabetes Research Institute Federation (www.diabetesresearch.org). He has authored over 700 scientific publications and 19 awarded patents. David Schaffer David Schaffer is a Professor of Chemical and Biomolecular Engineering, Bioengineering, and Neuroscience at University of California, Berkeley, where he also serves as the Director of the Berkeley Stem Cell Center. He graduated from Stanford University with a B.S. degree in Chemical Engineering in 1993. Afterward, he attended Massachusetts Institute of Technology and earned his Ph.D. also in Chemical Engineering in 1998. Finally, he did a postdoctoral fellowship in the laboratory of Fred Gage at the Salk Institute for Biological Studies in La Jolla, CA before moving to UC Berkeley in 1999. At Berkeley, Dr. Schaffer applies engineering principles to enhance stem cell and gene therapy approaches for neuroregeneration, work that includes novel approaches for molecular engineer-ing and evolution of new viral vectors as well as new technologies to investigate and control stem cell fate decisions. David Schaffer has received an NSF CAREER Award, Office of Naval Research Young Investigator Award, Whitaker Foundation Young Investigator Award, and was named a Technology Review Top 100 Innovator. He was also awarded the Bio-medical Engineering Society Rita Shaffer Young Investigator Award in 2000, the American Chemical Society BIOT Division Young Investigator Award in 2006, and was inducted into the College of Fellows of the American Institute of Medical and Biological Engineering in 2010. Dale Schenk Dr. Dale Schenk, Chief Executive Officer of Prothena, plc, was previously Chief Scientific Officer and Execu-tive Vice President at Elan Pharmaceuti-cals where he provided the leadership and scientific direction for Elan¹s research and development programs. Prior to joining Elan, Dr. Schenk was a founding scientist of Athena Neurosciences, which was acquired by Elan Pharmaceuticals. Dr . Schenk has pioneered the immuno-therapeutic approaches for the treatment of amyloidosis, as exemplified for Alzhei-mer ¹s disease, Parkinson’s disease and light chain (AL) Amyloidosis. Dr. Schenk¹s work in this area, as well as in early detection, testing and other pathways to these diseases, has led specifically to the most advanced potential treatment approach for Alzheimer¹s disease. Clinical trials are also currently underway for AL amyloi-dosis and Parkinon’s disease that utilize immunotherapy. Dr . Schenk earned his BA and PhD in Pharmacology and Physiology from the University of California, San Diego. 23
  • 24. Michael Sherratt Following a PhD and postdoctoral positions with Professor Cay Kielty at the University of Manchester, Michael was awarded an AgeUK Fellowship and Senior Fellowship. He is currently a Lecturer in Molecular Biochemistry at the University of Manches-ter and director of the BioAFM (atomic force microscopy) Facility at the same institution. For the past four years he has served as treasurer of the British Society for Research on Ageing and his main research interests are in the effects of ageing on tissue extracellular matrix structure and mechanical function. Using biochemical, ultra-structural, bioin-formatic and micro-mechanical approaches, Michael’s work suggests that: i) elastic fibre associated proteins (which are highly enriched in Cys, Trp and Tyr amino acid residues) may be differentially susceptible to UV-radiation and oxidation in ageing tissues and ii) the effects of ageing on tissue mechanical properties are localized in large arteries such as the aorta. In collaboration with colleagues in the Manchester X-ray Imaging Facility he is now developing new imaging methodologies to characterize the effects of intra-luminal pressure on the 3D structure of young and aged arteries. Bernard Siegel Bernard Siegel, J.D., is the founder and Executive Director of Genetics Policy Institute (GPI), a nonprofit organiza-tion with offices in Palm Beach, Florida; Silicon Valley, California and Washington, D.C. He founded and co-chairs the annual World Stem Cell Summit, founded and serves editor-in-chief of the peer-reviewed World Stem Cell Report and is the editor of the 360 Stem Cell & Regener-ative Medicine weekly newsletter. He founded and is the spokesperson for the Stem Cell Action Coalition, a 100+ member international alliance of nonprofits and research institutions leading the global “Pro-Cures Movement.” In 2002, he filed the first court case relating to reproductive cloning and is widely credited for debunking the claim of the group claiming that they cloned the first baby. He also played a pivotal leadership role in galvanizing a global movement that successfully lobbied the United Nations to reject a treaty that called for a prohibition of nuclear transfer, or therapeutic cloning. As a recognized policy expert on stem cell research, regenerative medicine and cloning, he works with leading scientists and patient advocates, raising public awareness and educating lawmakers, the media and public on stem cells and regenerative medicine. He is a frequent panelist and keynote speaker on the subject of stem cells, public policy and patient advocacy. Eric Siemers Eric Siemers, M.D. is the Senior Medical Director of the Alzheimer’s Disease Global Develop-ment Team at Eli Lilly and Company. He earned his MD with highest distinction from the Indiana University School of Medicine in 1982. After an internship in the Department of Internal Medicine at the Indiana Univer-sity School of Medicine, he completed his residency in the Department of Neurology in 1986. Prior to joining Lilly, he founded and headed the Indiana University Move-ment Disorder Clinic; his previous research included investigations of Parkinson’s disease and Huntington’s disease, and he established one of the first centers for surgical PD treatments in the US. Dr . Siemers currently directs late stage clinical research efforts at Lilly concerning investigational treatments for Alzheimer’s disease, and is more broadly involved with other neurological indications such as Parkinson’s disease. Major research interests include the use of biomarkers in investigational drug research and the development of trial designs that broadly characterize the effects of investigational drugs on chronic diseases. Dr . Siemers is a founding member and current Chair of the Alzheimer’s Association Research Roundtable. He is a member of the Steering Committee for the Alzheimer’s Disease Neuroimaging Initiative (ADNI). He served as the chair of the Industry Scientific Advisory Board for ADNI in 2007. Dr. Siemers is a current member of the New York Academy of Sciences Alzheimer’s Disease Leadership Counsel. He participated as a member of the NIA working group that proposed criteria for preclinical Alzheimer’s disease in 2011. He is a past member of the Board of Directors of the American Society of Experimental Neurotherapeutics. Einar M. Sigurdsson Einar M. Sigurdsson, Ph.D. is a tenured Associate Professor of Neuroscience and Physiology, and Psychiatry at New York University School of Medicine. A native of Iceland, he received a master’s degree in Pharmacy from the University of Iceland, and a Ph.D. in Pharma-cology from Loyola University Chicago Medical Center. He subsequently obtained postdoctoral training at New York University School of Medicine. His current research focuses on pathogen-esis, therapy and diagnosis for age-related protein conformational disorders, in particular Alzheimer’s disease. His honors include a Zenith Fellows Award and the Margaret M. Cahn Research Award from the Alzheimer´s Association, and the Irma T. Hirschl Career Scientist Award. He is presently serving as a standing member on an NIH study section. Dr. Sigurdsson and his collaborators pio-neered the use of modified Aβ derivatives as potential immunotherapy for Alzheimer’s disease. Furthermore, they showed for the first time that active and passive immuniza-tion as well as chelators delayed the onset of prion disease in mice, with follow up immunization studies leading to prevention of clinical symptoms in mice. On the diagnostic front, Dr. Sigurdsson and colleagues published the initial report on detection of amyloid plaques in living Speaker Biographies 24
  • 25. mouse brains by magnetic resonance imag-ing. Lately, he has pioneered the approach to harness the immune system to target pathological tau protein in Alzheimer’s disease and other tauopathies. Evan Y. Snyder Dr. Snyder earned his M.D. and his Ph.D. in neuroscience from the University of Pennsylvania in 1980. He completed residencies in pediatrics and neurology at Children’s Hospi-tal- Boston, Harvard Medical School and postdoctoral research at Harvard Medical School. In 1992, Dr. Snyder was appointed an instructor in neurology at Harvard Medical School and was promoted to assistant professor in 1996. He is regarded as one of the fathers of the stem cell field, having identified over 2 decades ago that cells that came to be called stem cells were a source of neural plasticity. He was the first to demonstrate that non-hematopoietic stem cells could mediate cell and gene replacement, home to injury, and perform protective, trophic, pro-regenerative, and anti-inflammatory actions. He was the first to isolate human neural stem cells. In 2003, after 23 years at Harvard, Dr. Snyder was recruited to Sanford Burnham Medical Research Institute as professor and director of the Stem Cells and Regeneration program. Michael D. West Michael D. West, Ph.D. became Chief Executive Officer of Biotime during October 2007, and has served on the Board of Directors since 2002. Prior to becoming Chief Executive Officer, Dr. West served as Chief Executive Officer, President, and Chief Scientific Officer of Advanced Cell Technology, Inc., a company engaged in developing human stem cell technology for use in regenerative medicine. Speaker Biographies Dr . West also founded Geron Corporation of Menlo Park, California, and from 1990 to 1998 he was a Director and Vice-President, where he initiated and managed programs in telomerase diagnostics, oligonucle-otide- based telomerase inhibition as anti-tumor therapy, and the cloning and use of telomerase in telomerase-mediated therapy wherein telomerase is utilized to immortalize human cells. From 1995 to 1998 he organized and managed the research between Geron and its academic collabora-tors James Thomson and John Gearhart that led to the first isolation of human embryonic stem and human embryonic germ cells. Dr . West received a B.S. Degree from Rensselaer Polytechnic Institute in 1976, an M.S. Degree in Biology from Andrews University in 1982, and a Ph.D. from Baylor College of Medicine in 1989 concentrating on the biology of cellular aging. Claude Wischik Claude Wischik is Professor of Old Age Psychiatry at the University of Aberdeen and Executive Chairman of TauRx Therapeu-tics. He studied medicine in Australia, then PhD and post-doctoral research at the MRC Laboratory of Cambridge, UK. He also completed psychiatric training in Cambridge. During his PhD he discovered that the neurofibrillary tangle is composed of the microtubule associated protein Tau. He also discovered that they could be dissolved by diaminophenothiazines. He established a team which developed in vitro and in vivo systems to establish plausibility of developing Tau Aggregation Inhibitor (TAI) therapy for AD. He cofounded TauRx Therapeutics to develop diagnostics and therapeutics for AD based on the TAI approach. In the first ever TAI phase 2 trial, TauRx demonstrated the feasibility of arresting disease progres-sion over 12 months. TauRx is currently conducting a global phase 3 trial of its lead compound in approximately 1,500 subjects in 22 countries. James Yoo Dr. Yoo is a surgeon and researcher. He is currently a Professor, Associate Director and Chief Scientific Officer at the Wake Forest Institute for Regenerative Medicine. Dr. Yoo’s research efforts have been directed toward the clinical translation of tissue engineering techno­logies and cell-based therapies. Dr. Yoo’s background in cell biology and medicine has facilitated the transfer of several cell-based technologies from the bench-top to the bedside. A few notable examples of successful clinical translation include the bladder, urethra, vagina and muscle cell therapy for incon-tinence. Other technologies that are being developed for translation include therapies for renal, liver and cardiovascular patholo-gies, skin bioprinting and skin expander for the treatment of burn patients. Dr. Yoo has served in many institutional, national and international committees and advisory boards. He has successfully organized and directed many scientific meetings and symposia, and managed numerous multi-institutional and interna-tional collaborative research projects and programs. He has actively contributed to the scientific community through publica-tion, meeting presentations and lectures internationally. 25
  • 26. Sierra Sciences shares the SENS Research Foundation’s mission of extending the human lifespan and pursuing healthy longevity. Cure Aging or Die Trying Mountain View, CA www.SierraSci.com Congratulations SRF, on your innagural U.S. Conference!
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  • 32. Save the Date SENS7 Conference September 3 to 7, 2015 Queens’ College Cambridge, England