Vivoryon Therapeutics N.v. · EURONEXT:VVY

Vivoryon Therapeutics — Probiodrug — FY2014 Earnings Presentation

22 slides from Vivoryon Therapeutics's earnings presentation, Mar 31, 2015

  1. Slide 1: The 2014 financial year: Full year results

    The 2014 financial year Full year results Halle (Saale), 31 March 2015 Konrad Glund Hendrik Liebers Inge Lues CEO CFO CDO 1

  2. Slide 2: Important notice and disclaimer

    Important notice and disclaimer This Presentation has been prepared and issued by Probiodrug AG (the “Company”) and has not been independently verified by any third party. No representation or warranty is given as to the achievement or reasonableness of, and no reliance should be placed on, any proj

  3. Slide 3: Content

    Content 1. Corporate introduction 2. Results 2014 3. Outlook 4. Q & A 3

  4. Slide 4: Investment highlights

    Investment highlights  Alzheimer’s Disease (“AD”) is a devastating neurological disease affecting Alzheimer’s Disease: major over 35 million people world-wide* 1 burden, no cure  No cure or long-term beneficial treatment available  No new drugs approved since 2007**  Developing a differentiated

  5. Slide 5: Strategy & business model

    Strategy & business model Focus key capabilities Pre-clinical Phase 1 Phase 2 Phase 3 Market Clinical proof of concept Potential starting point for partnering discussions Strategic objectives  Continue to develop PQ912 through Phase 2a clinical trials and beyond  Advance development of PBD-C06 and

  6. Slide 6: Management team

    Management team Management team Biography Konrad Glund,  Co-founder of Probiodrug, CEO since 2006 PhD, CEO  Led development of DP 4 inhibitors, transactions with Merck, Novartis, OSI and Ferring Co-founder  COO & VP business development OSI (Prosidion) in 2004-2006 Chairman of the  > 10 deals at

  7. Slide 7: Alzheimer's Disease: growing burden, no cure

    Alzheimer's Disease: growing burden, no cure Worldwide patient population will triple in Alzheimer's Disease introduction* the next 30 years**  Leading cause of dementia, ultimately CAGR leading to death +3% 115  Large burden on families 35  Growing cost for society  Available treatments margina

  8. Slide 8: Original Abeta approach

    Original Abeta approach Probiodrug targets toxic structures in Alzheimer's Disease Considerations  Most new drug Most new drugs have focused on Abeta formation or Abeta/plaque clearance treatments have targeted Abeta or plaques  Therapies have focused on: 1. Reduction of Abeta formation 2. Clearan

  9. Slide 9: Probiodrug's differentiated approach

    Probiodrug’s differentiated approach Probiodrug targets toxic structures in Alzheimer's Disease Considerations  Probiodrug and others Most new drugs have focused on Abeta formation or Abeta/plaque clearance have progressed insights on Abeta and its role in AD  Abeta has a physiological function 

  10. Slide 10: Focused proprietary pipeline

    Focused proprietary pipeline Pre- Product Phase 1 Phase 2 clinical PQ912  Small molecule QC inhibitor First patient enrolled March 2015 PBD-C06  pGlu-Abeta specific monoclonal antibody PQ1565  Small molecule QC inhibitor Clinical proof of concept 10

  11. Slide 11: Content

    Content 1. Corporate introduction 2. Results 2014 3. Outlook 4. Q & A 11

  12. Slide 12: Highlights

    Highlights 2014  Successful initial public offering (IPO) on Euronext Amsterdam raising EUR 23,2 million  Cash and cash equivalents of EUR 20,9 million as of 31 December 2014  Net loss of EUR 11.4 million compared with EUR 9.8 million in 2013, in line with expectations  Lead product for treating

  13. Slide 13: Key financial figures

    Key financial figures 2014 2013 2013 2012 2011 In EUR k (unconsolidated*) (consolidated) Earnings, Financial and Net Assets Position Revenues 0 0 0 6 21 Operating profit/loss -11,267 -9,701 -9,651 -10,558 -14,269 Net loss for the period -11,437 -9,807 -9,929 -18,720 -16,307 Equity (end of the year)

  14. Slide 14: Details of the Financial Results (according to IFRS)

    Details of the Financial Results (according to IFRS) Net loss net loss  Net loss in line with expectations  Operating loss primarily driven by R&D expenses  Increase in operating expenses reflects operating loss EUR 11,267 k primarily IPO preparation costs and post-listing financial loss EUR 170

  15. Slide 15: Operational Review

    Operational Review Pipeline Update PQ912  In 2014 prepared for a Phase 2a study (SAPHIR).  In preceding Phase 1 study with healthy young and elderly volunteers was shown to be safe and well tolerated and revealed high QC-inhibition.  First QC-inhibitor being tested in humans.  SAPHIR is a random

  16. Slide 16: Operational Review

    Operational Review PBD-C06  Monoclonal antibody targeting pGlu-Abeta, currently in preclinical stage  Successfully humanized and also de-immunized PQ1565  Second QC-inhibitor with attractive drug-like properties, currently in preclinical stage  Regulatory toxicology studies in preparation, produ

  17. Slide 17: The Probiodrug Share

    The Probiodrug Share KEY FIGURES AS OF 31 DECEMBER 2014 SHAREHOLDERS  ISIN: DE0007921835  WKN: 792183  Ticker Symbol: PBD  Type of shares: Bearer shares  Number of shares: 6,765,898  Stock exchange: Euronext Amsterdam  Liquidity Provider: Kempen & Co.  First trading day: 27 October 2014  IP

  18. Slide 18: Content

    Content 1. Corporate introduction 2. Results 2014 3. Outlook 4. Q & A 18

  19. Slide 19: Outlook 2015

    Outlook 2015 The mid-term focus of Probiodrug’s business activities can be summarised as follows:  Further preclinical and clinical testing of the development candidate PQ912, in particular execution of the first patient study in a Phase 2a “SAPHIR” trial in 2015/2016  Securing further supporting

  20. Slide 20: Anticipated news flow (selection)

    Anticipated news flow (selection)  PQ912 CTA submission for Phase 2 ✔ 2014  PQ912 First patient enrolled ✔  PQ912 Publication of complete Phase 1 results 2015  PBD-C06 Results in inflammatory part of AD pathology in animal model  PQ912 Assessment of potential in Down syndrome  PBD-C06 start of

  21. Slide 21: Financial Calendar

    Financial Calendar  13 May 2015 Interim Management Statement Q1 2015  10 June 2015 Annual General Meeting of Shareholders in Berlin  27 August 2015 Interim Report, half year results 2015  19 November 2015 Interim Management Statement Q3 2015 21

  22. Slide 22: Content

    Content 1. Corporate introduction 2. Results 2014 3. Outlook 4. Q & A 22

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