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LegoChem Bioscience, Inc.A Leading Chemistry-Based Venture Company COMPANY OVERVIEW
Contents Company Overview Business Approach Project Overview Summary
Mission Statement ABOUT ABOUT          BUSINESS          PROJECT          SUMMARY LegoChem Biosciences ( “LCB”) is committed to the discovery and development of novel small-molecule drugs employing faster and more efficient ways by combining LegoChemistry and early ADME/T screening platform technologies.
Corporate Overview Established in May 2006  (Daeduk Science Town, Daejeon, Korea ) Raised 10.3 billion Korean wons (≈ 10 million US$) since its inception Has built sustainable pipelines in the therapeutic areas of antibiotics, anticoagulants, and oncology The frontrunner, 2nd generation oxazolidinone antibiotics against MRSA is now in regulatory preclinical studies CRO: MPI in USA Novel FXa Inhibitor (anticoagulants) is in regulatory preclinical studies jointly with Green Cross, and is licensed out at the candidate stage to Green Cross in June 2009  Experienced  and seasoned executive and scientific management  team  Preparing IPO to KOSDAQ ABOUT ABOUT          BUSINESS          PROJECT          SUMMARY
Management Team ABOUT ABOUT          BUSINESS          PROJECT          SUMMARY  Yong Zu Kim, Ph.D Tae Kyo Park, Ph.D Sung Ho Woo, Ph.D Sejin Park Young Lag Cho, Ph.D Ho Young Song, Ph.D HyangSuk Lee Chemistry  Sr. Director Project Leader at LGLS  18 journal, 5 patent publications Ph.D. / Chemistry, Yonsei U. CFO / VP GM, R&D Management, 20 yrs at LGLS Co-Founder of LCB, BS/Economy, Korea Univ CEO & President Director of New Drug R&D , 23 yrs at LGLS Co-Founder of LCB, Ph.D. /Chemistry, KAIST Head of Biology / VP Project  Leader, 5 yrs at LGLS Co-Founder of LCB, Ph.D. / Microbio, Ohio state  CTO &  Sr. VP Project  Leader, 10 yrs at LGLS Co-Founder of LCB, Ph.D. /Chemistry, MIT Chemistry Director Principal Research at LGLS, Ph.D. / Seoul Nation U. 8 journal, 2 patent publications Biology Director Research Scientist, 11 yrs at LGLS, 4 journal, 10 patent pub. MS /Biochem, Yonsei U.
Business Strategy and Model BUSINESS ABOUT          BUSINESS          PROJECT          SUMMARY Model 1 : Independent R&D Internal research & development up to phase 2a License-out at early ~ mid stage (i.e. Oxazolidinone antibiotics, FXa Inhibitor) Model 2 : Collaborative R&D Joint research with strong biology platform up to phase IIa License-out at early ~ mid stage (i.e. Anticancer : HSP90, Mitochondriotropic) Model 3 : Sponsored R&D Sponsored R&D cost from partner up to candidate stage License-out to partner at candidate stage and developed  & commercialized by partner (i.e. FVIIa Inhibitor) RISK CORE COMPETENCY Biology Based Med Chem Based
BUSINESS ABOUT          BUSINESS          PROJECT          SUMMARY Proprietary Drug Development (chemistry –driven challenge) Strategic Alliances ,[object Object]
◆Early stage L/OCore Technology ,[object Object]
LegoChemistry
Screening
Early ADMETDrug development through collaborative research (Biology-driven challenge) ,[object Object]
◆Early~mid stage L/OBusiness Research Service ,[object Object]
◆ Early ADME/T serviceGate Decision System Business Model
Preclinical Candidate Confirmation Pre-Candidate Confirmation Phase I Candidate Confirmation BUSINESS ABOUT          BUSINESS          PROJECT          SUMMARY Establish 3 level gate systems for preclinical candidates, and define the evaluation criteria based on experience and know-how, to pre-validate and apply failing factors during the post preclinical development phase Lead 3rd Gate 2nd Gate 1st Gate Efficacy Focus ,[object Object]
Selectivity
Metabolic stability
CYP inhibition  (DDI)

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Legochem Company ppt

  • 1. LegoChem Bioscience, Inc.A Leading Chemistry-Based Venture Company COMPANY OVERVIEW
  • 2. Contents Company Overview Business Approach Project Overview Summary
  • 3. Mission Statement ABOUT ABOUT BUSINESS PROJECT SUMMARY LegoChem Biosciences ( “LCB”) is committed to the discovery and development of novel small-molecule drugs employing faster and more efficient ways by combining LegoChemistry and early ADME/T screening platform technologies.
  • 4. Corporate Overview Established in May 2006 (Daeduk Science Town, Daejeon, Korea ) Raised 10.3 billion Korean wons (≈ 10 million US$) since its inception Has built sustainable pipelines in the therapeutic areas of antibiotics, anticoagulants, and oncology The frontrunner, 2nd generation oxazolidinone antibiotics against MRSA is now in regulatory preclinical studies CRO: MPI in USA Novel FXa Inhibitor (anticoagulants) is in regulatory preclinical studies jointly with Green Cross, and is licensed out at the candidate stage to Green Cross in June 2009 Experienced and seasoned executive and scientific management team Preparing IPO to KOSDAQ ABOUT ABOUT BUSINESS PROJECT SUMMARY
  • 5. Management Team ABOUT ABOUT BUSINESS PROJECT SUMMARY Yong Zu Kim, Ph.D Tae Kyo Park, Ph.D Sung Ho Woo, Ph.D Sejin Park Young Lag Cho, Ph.D Ho Young Song, Ph.D HyangSuk Lee Chemistry Sr. Director Project Leader at LGLS 18 journal, 5 patent publications Ph.D. / Chemistry, Yonsei U. CFO / VP GM, R&D Management, 20 yrs at LGLS Co-Founder of LCB, BS/Economy, Korea Univ CEO & President Director of New Drug R&D , 23 yrs at LGLS Co-Founder of LCB, Ph.D. /Chemistry, KAIST Head of Biology / VP Project Leader, 5 yrs at LGLS Co-Founder of LCB, Ph.D. / Microbio, Ohio state CTO & Sr. VP Project Leader, 10 yrs at LGLS Co-Founder of LCB, Ph.D. /Chemistry, MIT Chemistry Director Principal Research at LGLS, Ph.D. / Seoul Nation U. 8 journal, 2 patent publications Biology Director Research Scientist, 11 yrs at LGLS, 4 journal, 10 patent pub. MS /Biochem, Yonsei U.
  • 6. Business Strategy and Model BUSINESS ABOUT BUSINESS PROJECT SUMMARY Model 1 : Independent R&D Internal research & development up to phase 2a License-out at early ~ mid stage (i.e. Oxazolidinone antibiotics, FXa Inhibitor) Model 2 : Collaborative R&D Joint research with strong biology platform up to phase IIa License-out at early ~ mid stage (i.e. Anticancer : HSP90, Mitochondriotropic) Model 3 : Sponsored R&D Sponsored R&D cost from partner up to candidate stage License-out to partner at candidate stage and developed & commercialized by partner (i.e. FVIIa Inhibitor) RISK CORE COMPETENCY Biology Based Med Chem Based
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  • 8.
  • 11.
  • 12.
  • 13. ◆ Early ADME/T serviceGate Decision System Business Model
  • 14.
  • 20.
  • 23.
  • 30. PK (t1/2, Vd, CL, AUC)
  • 32. BA(rat) > 20%Gate Decision System
  • 33. Platform Technology: LegoChemistry BUSINESS ABOUT BUSINESS PROJECT SUMMARY “New Lego block” molded into existing best chemical structures New Pieces of Lego Block Way of Implementation AREA Disease area with experience Validated (existing) target METHOD Fragment-based approach Multi-component reactions Replacement of existing subgroup Previously unknown Known but not well-explored LCB has more than 20 drug-like unique scaffolds Derived from same Lego Block Successful cases FXa inhibitor (LCB02-0133) Antibiotics (LCB01-0371) C A B Time to candidate : 12 ~ 18 months
  • 34.
  • 37. Over 5 years
  • 38. 5,800 : 1
  • 39. Average 5 years
  • 40. 500 : 1 (or less)
  • 41. Less than 3 yearsR&D Productivity (Candidate for discovery) ☞ Merck Standard The synthesis of core competencies
  • 42. BUSINESS ABOUT BUSINESS PROJECT SUMMARY More than 5 clinical pipelines for new drug by 2012 (Benchmarking: Gilead Science) Initiate pipeline (’06 ~’08) Grow pipeline (’09 ~’11) Sustain pipeline (’12 ~ ) 2 Preclinical candidates, 1 License-out 1 Co-Research contract 3 Clinical pipeline 2 License-out 1 preclinical study/year 5 Clinical pipeline 3 License-out 1 clinical study / year Output Collaboration network Global network Global licensing-out Independent research and development company Manage the process from discovery to development Core Competencies Mid-term Business Plan
  • 43. Research Projects PROJECT ABOUT BUSINESS PROJECT SUMMARY Project Selection Guideline Management’s Previous Experience antibiotics, anticoagulants, anticancer Attractiveness to big pharm unmet medical needs Portfolio Balance (risk management) best-in-class vs. first-in-class Projects Antibiotics Oxazolidinone antibiotics , MDR-TB Gram(-) antibiotics Anticoagulants FXa inhibitor (Partnered with Green Cross) FVIIa inhibitor (Partnered with Hanmi) FXIa inhibitor Anti-cancer HSP 90 (Partnered with BoramPharma) Mitochondriotropic Others DDR2 / HIF-1(Wondonin) / CD-99
  • 44. Project Roadmap PROJECT ABOUT BUSINESS PROJECT SUMMARY (by Green Cross)
  • 45. Discovery Projects: Summary PROJECT ABOUT BUSINESS PROJECT SUMMARY
  • 46. Scope of IP landscape ABOUT BUSINESS PROJECT SUMMARY SUMMARY FXa inhibitors FVIIa inhibitors Anticancer Patent to be published + Antibiotics
  • 47. Summary of LCB ABOUT BUSINESS PROJECT SUMMARY SUMMARY Experienced and skilled researchers Hands on experience on driving project from early lead discovery to FDA approval Established experience and network for licensing-out, collaboration, and negotiation with multi-national pharmaceutical companies Excellence of Core Technology Unique distinction of LegoChemistry scaffold approach Ability to generate consistent project pipeline ( >20 novel Scaffold, 25,000 compounds focused library) Systematic research plan via Gate Decision System Established guidelines for key stage decision to distinguish between ‘good’ and ‘bad’ drugs Implementing ‘fast track’ new drug discovery Passion for new drug development New drug discovery is the only way to survive! “Establishing a new drug pipeline is dependent on securing drug-like leads, and LCB has the necessary technology, system and passion to deliver it.”
  • 48. Contact LegoChem Biosciences, Inc. Daejeon Bio Venture Town, 461-8 Jeonmin-dong, Yuseong-gu, Daejeon, 305-811, South Korea http://www.legochembio.com/ CONTACT: Sung-Ho Woo, Ph.D. Biology Director & Senior VP [Tel] +82-42-861-0688 [Fax] +82-42-861-0689 E-mail: sungwoo@legochembio.com Request for more materials ONE PAGE: Brief outline of a project in a one page PDF file PROJECT PPT: Detailed version of a project description and a 5 MIN VIDEO presentation COMPANY DOC: Comprehensive overview of company’s business plan and project description in written format.