Satellos Bioscience Inc · TSX:MSCL

Satellos Bioscience — Investor Presentation (February 2022)

21 slides from Satellos Bioscience's investor presentation, Feb 22, 2022

  1. Slide 1: Satellos Bioscience Inc.

    Feb 22, 2022 SATELLOS BIOSCIENCE INC. Rebuilding muscle from within TM TSX: MSCL.V 1 PINK: MSCLF

  2. Slide 2: Legal Disclaimers

    2 Legal Disclaimers Certain statements in this presentation are “forward-looking statements” under applicable securities laws. Any statements that express or involve discussions with respect to predictions, expectations, beliefs, plans, projections, objectives, assumptions or future events or perfor

  3. Slide 3: Satellos: Restoring regeneration in muscle disorders

    3 Satellos: Restoring regeneration in muscle disorders Scientific leaders Massive opportunity Muscle is a regenerative organ  Experts in muscle stem cells and  Span genetic disorders to ageing role in regeneration conditions to specialty markets  Discovered polarity deficits  Musculoskeletal dis

  4. Slide 4: Satellos scientific founder: World leader in muscle stem cell research

    4 Satellos scientific founder: World leader in muscle stem cell research Muscle stem cells Regeneration failure in Duchenne defined due to progenitor deficit 2000 2009 2013 2016 Dr. Michael Rudnicki Ottawa Hosp. Res. Inst. 2007 2012 2015 2019  Order of Canada  Royal Society Fellow  Canada Res. Ch

  5. Slide 5: Seminal discoveries: Defining muscle stem cell driven cycle of regeneration

    5 Seminal discoveries: Defining muscle stem cell driven cycle of regeneration I. Muscle stem cell III. Ageing (sarcopenia) Tendon Dividing stem cell (Pax7+/Myf5-) X Too few muscle stem cells Continuous track record of seminal discoveries in muscle stem cells and regeneration II. Balanced Regeneratio

  6. Slide 6: Satellos Strategic Path

    6  Focus initially on rare diseases SATELLOS  Duchene and other dystrophies/atrophies  Massive need, limited options and high value Strategic Path  Compelling third-party evidence for Satellos approach  Then broaden to mass market indications  Ageing conditions (e.g., frailty/sarcopenia)  Mus

  7. Slide 7: Seminal discovery: Loss of polarity in Duchenne causes degeneration

    7 Seminal discovery: Loss of polarity in Duchenne causes degeneration Healthy Polarity Regeneration Regeneration Duchenne Polarity Occurs Deficit 210-12 Progenitor (Differentiation) Stem cell Stem cell (Self-renewal) Stem cell Satellos is focused on restoring regeneration 7

  8. Slide 8: Satellos approach: Correcting polarity to restore regeneration in Duchenne

    8 Satellos approach: Correcting polarity to restore regeneration in Duchenne Regeneration restored Duchenne Corrected Progenitor Stem cell We are unique in focusing on regeneration to treat Duchenne 8

  9. Slide 9: Duchenne muscular dystrophy: A failure of muscle regeneration throughout life

    9 Duchenne muscular dystrophy: A failure of muscle regeneration throughout life Progressive muscle damage Current treatments don’t in Duchenne address regeneration Gene correction  ~1 in 3,500 male births  Dystrophin gene mutated Muscle Heart inflammation function Target existing fibers Muscle Ene

  10. Slide 10: Our solution in Duchenne: Restoring stem cell driven muscle regeneration

    10 Our solution in Duchenne: Restoring stem cell driven muscle regeneration Duchenne Satellos Solution Satellos Drug Persistent damage signal triggers stem cell divisions divisions to enable regeneration Stem cell dividing Stem cell dividing Satellos discovered an imbalance in stem cell divisions Su

  11. Slide 11: Proof of Concept: Satellos treatment improves outcomes in Duchenne model

    11 Proof of Concept (POC): Satellos treatment improves outcomes in Duchenne model Mdx Q: Can divisions be reset? Mouse Stem cells imbalanced X A: Yes, divisions can be reset Mdx Drug Mouse Stem cells in balance 11

  12. Slide 12: Proof of Concept: Satellos treatment improves outcomes in Duchenne model

    12 Proof of Concept (POC): Satellos treatment improves outcomes in Duchenne model Mdx Enhanced Muscle Quality Q: Can divisions be reset? Mouse  Bigger muscle Stem cells imbalanced  Less fibrosis (green)  Larger fibers (black) X Untreated Treated Diaphragm Enhanced Muscle Performance A: Yes, divis

  13. Slide 13: Third party evidence: Regeneration cited as modifier in dogs

    13 Third party evidence: Regeneration cited as modifier in muscular dystrophy dogs Vieira et al, 2015 Jagged-1 Rescues Disease Dystrophy Phenotype  Colony of dystrophin deficient dogs  Some dogs had normal muscular function  Mutation mapped to Jagged1  Precise MOA never fully determined by autho

  14. Slide 14: Third party evidence: Nationwide researchers identify polarity as modifier

    14 Third party evidence: Nationwide researchers identify polarity as potential disease modifier Some boys continue to walk more than 10 years longer than peers  Analyzed 419 dystrophin null boys for factors associated with ambulation  Mutation enhancing stem cell polarity (via PARD6G) identified a

  15. Slide 15: Numerous Dystrophies may have polarity deficits

    15 Dystrophin Associated Protein Complex Numerous Ullrich CMD & Collagen Dystrophies Bethlem Myopathy MDC1A may have Laminin LGMD2C-F polarity deficits α-Dystroglycanopathies α-DG Sarco α β у δ Sarcoglycan β-DG span complex • Mutations in DAPC result in Caveolin-3 muscular dystrophy LGMD1C • Satello

  16. Slide 16: Near term priorities to build value in lead program

    16 Near term priorities to build value in lead program 2022 Q1 Q2 Q3 Q4 Output: Multiple candidates suitable for Proof Design / advance drug candidates and file IP of Concept (POC) testing and optimization Evaluate / select lead drug candidates Pre-IND Studies Utility: Precedent in Duchenne for biom

  17. Slide 17: Medium term value deliverables

    17 Medium term value deliverables: Ph II trials in lead program and 2nd program clinic ready Q1/22 Q2/22 Q3/22 Q4/22 Q1/23 Q2/23 Q3/23 Q4/23 Q1/24 Q2/24 Lead Duchenne program in Phase II trials Delivered by Q2/24 Follow-on indication in Phase II trials  Pre-IND studies completed, and Delivered by Q

  18. Slide 18: Leadership

    18 Leadership Frank Gleeson, MBA Michael Rudnicki, PhD, OC, FRS Sridhar Narayan, PhD, MBA Geoffrey Mackay Adam Mostafa William Jarosz, JD Board Member and CEO Chief Scientific Officer VP – Drug Discovery Chair — Board of Directors Board Member and Chair – Board Member and CEO – Audit Committee AmpB

  19. Slide 19: Value potential is significant: Attractive market capitalizations in muscle space

    19 Value potential is significant: Attractive market capitalizations in muscle space Phase 3 / Commercial 36 – 60 months US$2.5BN US$7.3BN US$0.6BN Phase 1 - 2 Trials 18 – 36 months US$0.1BN US$0.6BN US$0.4BN US$0.8BN Pre-IND/IND 12 – 18 months US$20M Development Stages Timeline Goals PEER COMPANIES

  20. Slide 20: Cap Table and Key Professional Providers

    20 SATELLOS (TSX: MSCL.V; PINK: MSCLF) Cap Table and Key Professional Providers KEY PROVIDERS CAPITAL TABLE  Legal: Borden Ladner Gervais, LLP Common Shares 32,995,548  David Henry, LLB, Partner Warrants 2,162,762  Accounting: PricewaterhouseCoopers Stock options 2,847,252  Craig McMillan, CPA,

  21. Slide 21: Summary

    21  Transformative science in area of broad medical need  Initial focus on rare, lethal disease ‒ Duchenne Summary  Strong founding group and leadership team  Huge potential upside on near term deliverables  Plan for NASDAQ financing in 2022 Satellos Bioscience Inc. 65 Front Street East, Suite

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