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Published byDuane McKenzie Modified over 7 years ago
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Darren Cunningham CEO dcunningham@inflectionbio.com
Presentation by Darren Cunningham CEO
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Overview 1 in 3 will get cancer – many will not survive ***
Our mission develop groundbreaking new treatments for those suffering with cancer
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Business Model Value Inflection: 10-15 YEAR DEVELOPMENT LEAD
DISC TARGET HITS LEAD PRE-CLIN IND PHASE 1 PHASE 2 PHASE 3 APP LAUNCH LEAD PRE-CLINICAL IND PACKAGE EARLY CLINICAL LICENSE IN PARTNER/ EXIT/IPO Value Inflection: 4 – 5 YEAR DEVELOPMENT
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Phase I Value Creation Potential
Phase I Oncology Exits $100m - >$300m
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Collaboration with CNIO - June 2013
Spanish National Cancer Research Centre
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Secure Partner after Phase I
Pipeline – Targeted Therapeutics TARGET RESEARCH PRE-CLIN IND PHASE I NSCLC Secure Partner after Phase I IBL-300s (PIM/PI3K/mTOR) OTHER K-RAS TUMOURS B-CELL LYMPHOMAS IBL-202 (PIM/PI3K) MULTIPLE MYELOMA B-CELL LYMPHOMAS IBL-100s (Pan-PIM) HAEM MALIGNANCIES Secure Partner at IND Comprising first-in-class agents protected by composition of matter patents
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PIM Kinase a driver of resistance in AKT/PI3K
PIM expression dramatically elevated by PI3K/AKT pathway inhibition PIM mediates feedback loop driving acquired resistance to a number of treatment modalities. Underpins rationale for co-targeting PI3K and PIM; huge clinical opportunity
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Lung cancer leading cause of cancer death (1.6m ww)
IBL-300s – Targeting Molecular Subsets in NSCLC(Stage IV) Lung cancer leading cause of cancer death (1.6m ww) - NSCLC ~80% = $10bn market by 2020 De novo PI3k activation Mutant K-Ras EGFR TKI Resistant Squamous cc – PIK3CA/ PTEN mutations ~30% PIM and PI3K inhibitors act synergistically in vitro and in vivo PIM mediates PI3K/AKT resistance NSCLC - K-Ras mutated in 15-30% Downstream activation include PI3K/AKT/mTOR PIM inhibition shuts down growth in mutant K-Ras NSCLC cell lines NSCLC - EGFR mutations in ~10% de novo Cancer recurs (~12mo) with ~10% due to PI3K activation PIM elevated in EGFR TKI resistant lines Role for PI3K and PIM co-targeting in NSCLC Rationale for IBL-300s
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Research Collaboration Network
Network spanning US, EU, Australia NSCLC, pancreatic, ovarian, multiple myeloma, DLBCL, MCL, CLL, neuroblastoma, breast cancer, mechanistic
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ONCOLOGY ADVISORY PANEL
Leadership MANAGEMENT ONCOLOGY ADVISORY PANEL Darren Cunningham CEO 15 year record in licensing, M&A, IP, fundraising, IR Amarin, Elan, PWC B. Comm, M. Acc, FCA Dr. Michael O’Neill Director R&D 22 year drug discovery and development Eli Lilly, Almirall, Merck BA Psychology, PhD Dr. Martin Page 30+ years experience in oncology R&D Previous VP, Global Head of Oncology Res. J&J Roles with OSI Pharma, Oxford Glycosciences, and Glaxo-Wellcome Prof. Josep Tabernero Director, Vall d’Hebron Institute of Oncology Led clinical development of PI3K pathway inhibitors ESMO Executive Board Prof. Funda Meric-Bernstam Professor of Surgical Oncology; and Chair Department of Investigational Cancer Therapeutics, M. D. Anderson Cancer Center
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Corporate profile Incorporated 2012
Headquartered in Dublin, with base in London 2 full time employees Internship program, 3 in 2015 PhD in TCD via Innovation Partnership 6 board members; panel of international scientific advisors 6 CROs (UK, France, China, India) >10 research collaborations (US, Ireland, UK, Germany, Sweden, Australia) ~€2.2m raised to date (EI, VC and privates)
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Thank you Darren Cunningham
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