Silence Therapeutics PLC · NASDAQ:SLN

Silence Therapeutics — AsiaTIDES 2018

44 slides from Silence Therapeutics's conference presentation, Mar 1, 2018

  1. Slide 1: Use of Advanced siRNAs Targeted to Hepatocytes

    AsiaTIDES, 1 March 2018 Use of Advanced siRNAs Targeted to Hepatocytes for the Development of Novel Drugs to Treat Liver-related Disorders Torsten Hoffmann, PhD Chief Operating Officer

  2. Slide 2: Forward looking statements

    Forward looking statements The information contained in this presentation is being supplied and communicated to you on a Securities in the Company have not been, and will not be, registered under the United States confidential basis solely for your information and may not be reproduced, further dist

  3. Slide 3: About Silence

    About Silence © Silence Therapeutics 2018 3

  4. Slide 4: About Silence Therapeutics

    About Silence Therapeutics Only quoted European RNA Our interference player facilities Key Performance Indicators: HQ in > Net cash position of £43M at 2nd of Jan 2018 London > Market cap: £136.5M* > EV: ~ £104M* Headcount: > 42 FTE (27 in Berlin, R&D and 15 London, R&D in Berlin Corporate and R&D)

  5. Slide 5: Building a strong pipeline through a highly functional R&D organisation

    Building a strong pipeline through the creation of a highly functional R&D organisation Diverse Decision to focus on technologies GalNAc-siRNA platform Building a GalNAc-siRNA therapeutic portfolio (CRISPR, mRNA, siRNA with LNP) Outsourcing routine work 2015 2016 2017 2018 Technology- Drug Discovery

  6. Slide 6: Experienced Leadership Team

    Experienced Leadership Team: Strong background in discovery and development of RNA therapies Ali Mortazavi, Torsten Hoffmann, Ph.D. David Ellam, Chief Executive Officer Chief Operating Officer Chief Financial Officer Dmitry Samarsky, Ph.D. Laura Roca-Alonso, Ph.D. Michael Mulqueen, Chief Scientific

  7. Slide 7: Evolving modular R&D capabilities

    Evolving modular R&D capabilities In place Recently established To be established Non-clinical Drug CMC Develop- Regulatory Discovery ment Finance, Clinical Out- BD, HR, IP QA for CMC Develop- sourcing & legal ment Completed R&D reorganisation Technology > Reducing headcount and Innovation > Increas

  8. Slide 8: Pipeline

    Pipeline Building a proprietary portfolio, two projects advanced into preclinical development Our Programs 4Q 2018 Mid Mid 2019 2019 Mid 2019 Out-Licensed Programs © Silence Therapeutics 2018 8

  9. Slide 9: GalNAc conjugated siRNA technology

    GalNAc conjugated siRNA technology © Silence Therapeutics 2018 9

  10. Slide 10: siRNA mechanism of action

    siRNA mechanism of action 1 RNA interference is mRNA sequence for target gene X > A Nobel prize-winning mRNA discovery > A natural pathway that 2 can be harnessed to siRNA designed siRNA inhibit the expression specifically against target gene X of disease-causing genes without altering mRNA DNA 3 An

  11. Slide 11: GalNAc-siRNA molecules

    GalNAc-siRNA molecules Linker siRNA GalNAc gene silencing hepatocyte targeting Advantages of GalNAc-siRNA technology > GalNAc targets therapeutic siRNA molecules specifically to hepatocytes > Highly specific by targeting a single gene > Patient-friendly via infrequent subcutaneous administration > E

  12. Slide 12: GalNAc-siRNA medicines

    GalNAc-siRNA medicines Schematic structure of our therapeutic molecules: Linker Binds siRNA to delivery moiety Chemical A C G U U C G A C C G A A G U C A modifications U G C A A G C U G G C U U C A G U siRNA GalNAc (N-Acetylgalactosamine) Mediates gene silencing Mediates targeted delivery to hepatoc

  13. Slide 13: Gene silencing with GalNAc-siRNAs in hepatocytes

    Gene silencing with GalNAc-siRNAs in hepatocytes extracellular intracellular Endosomal Escape Recognition & binding GalNAc-siRNA Recycling ASGPR Receptor (ASGPR) RNAi RISC AAA Target mRNA silencing > Intracellular delivery mediated through receptor endocytosis © Silence Therapeutics 2018 13

  14. Slide 14: Platform performance

    Platform performance Platform technology: GalNAc-siRNA, able to mediate highly specific gene silencing in hepatocytes (liver) – “Specificity upon specificity” ~7,000 genes operate in the liver. We can target any of them by adapting the siRNA sequence, using the same technology Target 1 Target 2 Targ

  15. Slide 15: Advantageous properties of our medicines

    Advantageous properties of our medicines > Subcutaneous administration, patient friendly > Long duration of action (variable depending on target gene) > Well tolerated > Our GalNAc-siRNA medicines are suitable for a wide range of indications Target KD induction Trend toward recovery to baseline leve

  16. Slide 16: SLN124 for the treatment of iron overload disorders

    SLN124 for the treatment of iron overload disorders © Silence Therapeutics 2018 16

  17. Slide 17: Treatment of iron overload disorders

    Treatment of iron overload disorders GOAL > Provide an effective and safe novel treatment option for patients with iron overload conditions, such as β-Thalassemia RATIONALE > Target a key modulator in iron regulation with a GalNAc-siRNA molecule providing a highly specific, effective & safe option t

  18. Slide 18: Iron Overload Disorders

    Iron Overload Disorders Affected organs by iron overload Diseases with iron overload > β-Thalassemia > Hereditary Haemochromatosis > Myelodysplastic Syndrome > Aplastic Anaemia > Sideroblastic Anaemia If untreated, iron accumulation in organs leads to severe damage, e.g. heart, liver & endocrine org

  19. Slide 19: β-Thalassemia facts

    β-Thalassemia facts > Rare blood disorder caused by mutations in the β globin gene > Patients present with ineffective erythropoiesis and chronic haemolytic anaemia > Many β-Thalassemia intermedia and all β-Thalassemia major patients require transfusions to correct anaemia > Ineffective erythropoies

  20. Slide 20: Market opportunity for iron overload disorders

    Market opportunity for iron overload disorders β-Thalassemia intermedia & T. major (TDT) > Combination with transfusions & chelators to reduce frequency & dose 40,000 20,000 > Improve erythropoiesis and TDT NTDT reduce secondary iron overload burden β-Thalassemia intermedia (NTDT) >150,000 > Monothe

  21. Slide 21: SLN124 mechanism of action

    SLN124 mechanism of action HJV BMPR Macrophages > TMPRSS6 (Transmembrane BMP Protease, Serine 6) is a negative regulator of the Ferroportin BMP/SMAD signaling TMPRSS6 P Fe pathway Iron recycling > Inhibition of TMPRSS6 in P SMAD hepatocytes induces Hepcidin Hepcidin expression > Hepcidin reduces Iro

  22. Slide 22: Silencing TMPRSS6 lowers serum iron levels in mice

    Silencing TMPRSS6 lowers serum iron levels in mice Study design d1 d4 SC, n=4-6 mice TMPRSS6 mRNA (liver) Hepcidin mRNA (liver) Iron (serum) 4 * 40 N o r m a lis e d T M P R S S 6 m R N A N o r m a lis e d H e p c id in m R N A 1 .0 * S e r u m ir o n [µ m o l/L ] 3 30 2 ** * 20 0 .5 1 10 * 0 .0 0 0

  23. Slide 23: SLN124 lowers iron levels for at least 6 weeks in mice

    SLN124 lowers iron levels for at least 6 weeks after single administration in mice Study design d1 wk 1 wk 3 wk 6 SC, n=4 mice, 3 mg/kg TMPRSS6 mRNA (liver) Iron (serum) 40 N o r m a lis e d T M P R S S 6 m R N A 1 .0 S e ru m iro n [µ m o l/L ] 30 ** 20 0 .5 *** 10 *** *** *** 0 .0 0 1 1 3 6 w eeks

  24. Slide 24: Sustained iron reduction in non-human primates

    Sustained reduction of circulating iron levels after single administration in non-human primates Study design Day 1 8 22 29 43 57 71 SC, n=4 Cynomolgus monkeys Iron (plasma) P la s m a Ir o n [ % P r e d o s e ] 125 100 V e h ic l e 75 1 m g /k g S L N 1 2 4 50 3 m g /k g S L N 1 2 4 1 0 m g /k g S

  25. Slide 25: SLN124 in hereditary haemochromatosis model - 1/2

    Therapeutic activity of SLN124 in a disease model for hereditary haemochromatosis (HFE-/- mice) - 1/2 Study design Collaboration with d1 wk 3 Prof. Dr. Martina Muckenthaler SC, n=6-7 HFE-/- mice Heidelberg University, Germany TMPRSS6 mRNA (liver) Hepcidin (serum) Iron (serum) 2 .0 800 *** N o r m a

  26. Slide 26: SLN124 in hereditary haemochromatosis model - 2/2

    Therapeutic activity of SLN124 in a disease model for hereditary haemochromatosis (HFE-/- mice) - 2/2 Collaboration with Prof. Dr. Martina Muckenthaler Heidelberg University, Germany Transferrin Saturation Haemoglobin Mean corpuscular volume M e a n c o r p u s c u la r v o lu m e [ µ m ] 3 19 60 %

  27. Slide 27: SLN124 in β-Thalassemia disease model

    SLN124 normalizes ROS species & improves RBC parameters in b-Thalassemia disease model Study design Collaboration with d1 wk 2 wk 5 Prof. J. Vadolas & Dr. Grigoriadis Monash Medical Centre/Melbourne, Australia SC, n=6-8 Hbbth3/+ mice Reactive oxygen species (ROS) Reticulocyte proportion Haematocrit

  28. Slide 28: SLN124 development timelines – key milestones

    SLN124 development timelines – key milestones Candidate Pilot batch release Sterile nomination manufacture GMP release 2017 2018 2019 Q2 Q3 Q4 Q1 Q2 Q3 Q4 Q1 Start DRF Start GLP tox KOL meeting IND/CTA filing EIH On track for CTA filing 15 months after candidate selection © Silence Therapeutics 2018

  29. Slide 29: SLN124 - Summary

    SLN124 - Summary > Highly potent, selective and long acting GalNAc-siRNA > Efficacious in lowering blood iron and well tolerated in healthy mice and non-human primates after single subcutaneous administration > Demonstrated therapeutic efficacy in clinically relevant animal disease models > Currentl

  30. Slide 30: SLN226 for the treatment of alcohol use disorder

    SLN226 for the treatment of alcohol use disorder © Silence Therapeutics 2018 30

  31. Slide 31: SLN226 for the treatment of alcohol use disorder

    SLN226 for the treatment of alcohol use disorder GOAL > Provide an effective & safe novel treatment option for patients with alcohol use disorder (AUD) RATIONALE > Target ALDH2, a validated target for alcohol aversion therapy, with a GalNAc-siRNA molecule providing a highly specific, effective & saf

  32. Slide 32: Alcohol use disorder facts - 1/2

    Alcohol use disorder facts - 1/2 Long term effects of alcohol abuse Consequences of alcohol abuse > Liver damage > Cardiovascular complications > Gastrointestinal damage > Central & peripheral neurological symptoms > Anxiety, depression, suicidal tendencies > Negative impact on social life Alcohol a

  33. Slide 33: Alcohol use disorder facts - 2/2

    Alcohol use disorder facts - 2/2 > Chronic alcohol abuse leads to alcoholic liver disease (ALD) – spectrum of conditions including hepatitis and cirrhosis which may eventually require liver transplantation > One third of all liver transplants due to ALD (~4,000 per year); 6-month abstinence rule whi

  34. Slide 34: Market opportunity of SLN226 (US & Europe)

    Market opportunity of SLN226 (US & Europe) Patients urgently requiring abstinence > 20-33% liver transplants due to alcohol abuse alone or in 40,000 combination with viral infection Requiring abstinence > Potentially a similar number of patients on the waiting list needing abstinence support 8,000,0

  35. Slide 35: SLN226 mechanism of action

    SLN226 mechanism of action > Alcohol dehydrogenase 2 (ALDH2) is the key alcohol metabolizing enzyme > Liver is the key organ for ethanol detoxification by ALDH2 > ALDH2 is rate limiting enzyme in the ethanol metabolic pathway Ethanol Validated target ADH > Clinically: ALDH inhibitors Acetaldehyde e.

  36. Slide 36: ALDH2 GalNAc-siRNA induces hepatic acetaldehyde accumulation in mice

    ALDH2 GalNAc-siRNA treatment induces hepatic acetaldehyde accumulation in mice Study design d1 -4 h EtOH d10 SC, n=6 mice ALDH2 mRNA (liver) ALDH enzymatic activity (liver) Acetaldehyde (liver) 1 .5 1 .5 150 A c e ta ld e h y d e le v e ls in liv e r [n g /m g ] A ld e h y d d e h y d r o g e n a s

  37. Slide 37: Liver expression of ALDH1 isoenzymes upon ALDH2 silencing

    Liver expression of ALDH1 isoenzymes upon ALDH2 silencing in mice Study design d1 -4 h EtOH d10 SC, n=6 mice ALDH2 mRNA (liver) ALDH1B1 mRNA (liver) ALDH1A1 mRNA (liver) 1 .5 2 .0 N o r m a lis e d A L D H 1 B 1 m R N A N o r m a lis e d A L D H 1 A 1 m R N A N o r m a lis e d A L D H 2 m R N A 1 .0

  38. Slide 38: SLN226 reduces ALDH2 mRNA for at least 6 weeks

    SLN226 reduces ALDH2 mRNA in liver for at least 6 weeks after single administration in mice Study design d1 d10 d20 d30 d40 SC, n=5 mice, -4 h EtOH ALDH2 mRNA (liver) N o r m a lis e d A L D H 2 m R N A 1 .0 0 .5 0 .0 3 33 10 3 3 10 3 3 10 3 3 10 m g /k g CTRL ALDH2 CTRL ALDH2 CTRL ALDH2 CTRL ALDH2

  39. Slide 39: Potential of SLN226 as compared to Disulfiram

    Potential of SLN226 as compared to Disulfiram Reduced side effect potential (1) Hepatocyte-specific GalNAc formulation (reduction of cardio- & neurotoxic adverse effects) (2) ALDH2-specific targeting (Disulfiram inhibits ~20 off-target enzymes)  Improved safety profile Higher therapy success rate (

  40. Slide 40: SLN226 development timelines – key milestones

    SLN226 development timelines – key milestones Pilot batch release Sterile manufacture KOL meeting GMP release 2017 2018 2019 Q4 Q1 Q2 Q3 Q4 Q1 Q2 Q3 Candidate Start DRF Start GLP tox nomination IND/CTA filing* EIH* On track for IND/CTA filing in Q2 / 2019 *potentially with partner © Silence Therapeu

  41. Slide 41: SLN226 - Summary

    SLN226 - Summary > Highly potent, selective and long acting GalNAc-siRNA > Induces acetaldehyde accumulation in mice after single subcutaneous administration > Currently in preclinical development with plans to enter clinical development in Q2 2019* > Studies initiated to show therapeutic efficacy i

  42. Slide 42: Pipeline

    Pipeline Building a proprietary portfolio, two projects advanced into preclinical development Our Programs 4Q 2018 Mid Mid 2019 2019 Mid 2019 Out-Licensed Programs © Silence Therapeutics 2018 42

  43. Slide 43: R&D with focus on portfolio and innovation

    R&D with focus on portfolio and innovation Technology Innovation Drug Discovery & Development > Improve performance of our > Build a proprietary therapeutic GalNAc-siRNA molecules portfolio by applying validated > Strengthen and broaden IP portfolio siRNA technologies > Expand RNAi horizons beyond >

  44. Slide 44: Acknowledgements

    Acknowledgements Silence Preclinical Drug Discovery Team Ute Schaeper, Steffen Schubert & Ulrich Zügel Silence Technology Innovation Team Marie W. Lindholm & Dmitry Samarsky Silence Drug Development Team Manuela Aleku, Christian Frauendorf & Jens-Uwe Künstler Collaboration with Prof. Dr. Martina Muc

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