Revive Therapeutics Ltd. · CSE:RVV

Revive Therapeutics — Investor Presentation (November 2020)

17 slides from Revive Therapeutics's investor presentation, November 2020

  1. Slide 1: A Specialty Life Sciences Company: Corporate Presentation

    A SPECIALTY LIFE SCIENCES COMPANY Corporate Presentation November 2020 US: RVVTF Revive Therapeutics Ltd. | Office: 1-888-901-0036 | E-mail: [email protected]

  2. Slide 2: Forward Looking Statements

    FORWARD LOOKING STATEMENTS Certain statements contained in this presentation constitute forward-looking information within the meaning of securities laws. Forward- looking information may relate to our future outlook and anticipated events or results and may include statements regarding our future f

  3. Slide 3: Revive Therapeutics

    REVIVE THERAPEUTICS Bucillamine Specialty life sciences company FDA approved Phase 3 clinical Developing novel Psilocybin focused on repurposing drugs trial for Bucillamine in the and Cannabidiol therapeutics Psilocybin for rare disorders and treatment of COVID-19 for various CNS and infectious dise

  4. Slide 4: Pharmaceutical Strategy

    PHARMACEUTICAL STRATEGY Targeting FDA Designations: Clinical development of Targeting Rare Novel Uses, Orphan, Fast track, Psilocybin, Cannabidiol Disorders and Formulations, and Breakthrough and Bucillamine Infectious Diseases Delivery System therapy © COPYRIGHT 2020. Revive Therapeutics Ltd. ALL R

  5. Slide 5: Patent Portfolio

    PATENT PORTFOLIO Title USPTO No. Status Use of Bucillamine in the Treatment of Infectious Diseases, including COVID-19 62/991,996 Provisional patent filed Use of Bucillamine in the Treatment of Gout US9662305 Issued on May 30, 2017 US 8642088 Issued on February 4, 2014 Drug Delivery System US 954542

  6. Slide 6: Product Pipeline

    PRODUCT PIPELINE Focus on Infectious Diseases, Psychedelics and Rare Disorders Stage of Product Indication Regulatory Status Development Infectious Diseases Phase 3 FDA approved Bucillamine (COVID-19) (COVID-19) for Phase 3 Methamphetamine CTA with University of Psilocybin Phase 1 Use Disorder Wisco

  7. Slide 7: Infectious Disease Opportunity

    INFECTIOUS DISEASE OPPORTUNITY Received FDA approval for Focus on Bucillamine in Revive’s clinical history Bucillamine (BUC) scientific FDA Phase 3 clinical trial the treatment of with Bucillamine rationale as an intervention for for COVID-19 infectious diseases COVID-19 (see Appendix) • Well-known

  8. Slide 8: Psychedelics Opportunity

    PSYCHEDELICS OPPORTUNITY Acquired Psilocin Pharma Corp. • Derrick Welch, Founder with 14 years of HC experience; 5 years in Cannabis • Worked with Xanthic Bio Pharma and Green Growth Brands • Developed water Soluble THC and CBD products (Beverages, effervescent tablets) Novel Psilocybin formulations

  9. Slide 9: Formulation & Delivery Technology

    FORMULATION & DELIVERY TECHNOLOGY Delivering naturally extracted and synthetic psychedelics and cannabinoids DELIVERY SYSTEM Combines Tannin (antibacterial, antifungal, antioxidant, wound healing) and Chitosan (blood-clotting and antimicrobial) composites Releases (rapid, controlled, sustained), imp

  10. Slide 10: Liver Disease Opportunity

    LIVER DISEASE OPPORTUNITY Focus on Autoimmune Hepatitis (AIH) AIH - rare disease (~76k patients in US) Obtained FDA orphan drug status for CBD in the treatment of AIH causing liver inflammation Drawbacks of current therapies (steroids): Severe side effects in 13%, relapse after drug Seeking to file

  11. Slide 11: Strategic Partners

    STRATEGIC PARTNERS Acquired March 2020 R&D partnership Infectious Diseases CRO Psychedelic pharma Psychedelic pharma License of cannabidiol for treatment License of cannabinoid of Autoimmune Hepatitis delivery technology © COPYRIGHT 2020. Revive Therapeutics Ltd. ALL RIGHTS RESERVED. 11

  12. Slide 12: Milestones

    MILESTONES Q4 Q1 Q2 2020 2021 2021 • Patient enrollment of Phase 3 study of • Continued patient enrollment and ongoing • Continued patient enrollment and ongoing Bucillamine in the treatment of COVID-19 updates from Phase 3 clinical study of Bucillamine updates from Phase 3 clinical study of Bucilla

  13. Slide 13: Peer Comparison (Market Caps)

    PEER COMPARISON (MARKET CAPS) $3.5B $1.4B $635M $475M $50M © COPYRIGHT 2020. Revive Therapeutics Ltd. ALL RIGHTS RESERVED. 13

  14. Slide 14: Team

    TEAM Management Clinical & Regulatory Board of Directors • Michael Frank • Dr. Kelly McKee, Jr., MD, MPH • Michael Frank Chairman and CEO Chief Scientific Officer, Chairman and CEO Consultant • Carmelo Marrelli • William Jackson Chief Financial Officer • Dr. Onesmo Mpanju, PhD Director FDA Regulator

  15. Slide 15: Stock Information

    STOCK INFORMATION Ticker 52-Week High/Low Market Cap RVV (CSE) | RVVTF (US) CAD $0.395 / $0.025 CAD ~ $50,000,000 Share Price Capital Structure CAD $0.215 (November 18, 2020) 240,526,239 common shares © COPYRIGHT 2020. Revive Therapeutics Ltd. ALL RIGHTS RESERVED. 15

  16. Slide 16: Appendix – Bucillamine Scientific Rationale for COVID-19

    APPENDIX – BUCILLAMINE SCIENTIFIC RATIONALE FOR COVID-19 Current antiviral interventions for influenza have exhibited modest efficacy, especially in improving mortality in at-risk populations, such as the elderly.1,2 Novel antivirals have been plagued by poor oral bioavailability and lack of efficac

  17. Slide 17: Appendix – Bucillamine Scientific Rationale for COVID-19 (References)

    APPENDIX – BUCILLAMINE SCIENTIFIC RATIONALE FOR COVID-19 References 1. Muthuri SG, Venkatesan S, Myles PR et al. Effectiveness of neuraminidase inhibitors in reducing mortality in patients admitted to hospital with influenza A H1N1pdm09 virus infection: a meta-analysis of individual participant data

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