Longeveron Inc. · NASDAQ:LGVN

Longeveron — Investor Presentation (December 2023)

30 slides from Longeveron's investor presentation, Dec 6, 2023

  1. Slide 1: A Regenerative Medicine Company

    Cell-Based Therapies A Regenerative Medicine Company August 2023

  2. Slide 2: Forward Looking Statements

    Forward Looking Statements Certain statements in this presentation that are not historical facts are forward-looking statements made pursuant to the safe harbor provisions of the Private Securities Litigation Reform Act of 1995, which reflect management's current expectations, assumptions, and estim

  3. Slide 3: Our Mission: Deliver Regenerative Medical Therapies for Unmet Medical Needs

    Our Mission: Deliver Regenerative Medical Therapies for Unmet Medical Needs Lomecel-B™ -- A Pipeline in a Product Three Clinical-Stage Programs Allogeneic medicinal signaling cells (MSCs) isolated • Hypoplastic Left Heart Syndrome: from bone marrow of healthy young adults (Open-label Ph. 1 data led

  4. Slide 4: Longeveron Overview

    Longeveron Overview Leader in development of MSCs for therapeutic indications Well-characterized allogeneic MSC (Lomecel-B™) product in Phase 2 trials Robust clinical pipeline with clinical efficacy signals in multiple indications with large unmet need: Alzheimer’s Disease, Aging-Related Frailty, an

  5. Slide 5: Lomecel-B™: Multiple Mechanisms of Action (MOA)

    Lomecel-B™ : Multiple Mechanisms of Action (MOA) Pro-vascular, Pro-regenerative and Anti-inflammatory: Repairs Tissue and Promotes Healing LOMECEL-B ™ Anti- Cell-cell Interactions Exosome and Mitochondrial inflammatory (stem cells) MicroRNA Release Transfer (somatic Key Advantages: Cytokines cells)

  6. Slide 6: Robust Clinical Pipeline

    Robust Clinical Pipeline Indication Geography Phase 1 Phase 2 Phase 3 Hypoplastic Left Phase 2 trial actively U.S. enrolling. Heart Syndrome 2b Single-Dose Trial complete; data Aging-Related U.S. & Japan announced Q3 2021. Frailty Ongoing Phase 2 trial in Japan. Ongoing Phase 2a trial; enrollment Al

  7. Slide 7: Lomecel-B™ for Hypoplastic Left Heart Syndrome

    Lomecel-B™ for Hypoplastic Left Heart Syndrome

  8. Slide 8: Large Unmet Need in Hypoplastic Left Heart Syndrome

    Large Unmet Need in Hypoplastic Left Heart Syndrome • HLHS is a rare congenital heart defect in which the left side of the heart fails to normally develop • Children with HLHS require 3 staged open-heart surgeries in order to survive – these surgeries reconfigure the heart so that the right side of

  9. Slide 9: Lomecel-B™: Hypoplastic Left Heart Syndrome (HLHS)

    Lomecel-B™: Hypoplastic Left Heart Syndrome (HLHS) Clinical Approach • Lomecel-B™ administered directly into heart Glenn: Redirects ‒ Injected into cardiac tissue of right ventricle during Stage II surgery at Blood to PA (St II – 4 mo.) approximately 4 months of age (“Glenn or Hemi-Fontan Procedure”

  10. Slide 10: Advantages of Lomecel-B™ in HLHS

    Advantages of Lomecel-B™ in HLHS • Findings in studies of adults using MSCs: ‒ Boosts ejection fraction (EF) in patients with dilated cardiomyopathy (DCM) • EF increased by 8.0 percentage points (95% CI: 2.8 to 13.2 percentage points; p = 0.004) ‒ Reduces ventricular chamber size in adults with DCM,

  11. Slide 11: Lomecel-B™: Hypoplastic Left Heart Syndrome (HLHS)

    Lomecel-B™: Hypoplastic Left Heart Syndrome (HLHS) Positive ELPIS 1 (Phase 1b) Trial Results (N=10) • Open-label study provided sufficient initial safety data to warrant randomized, controlled trial of Lomecel-B™ in HLHS (ELPIS II) ‒ No SAEs attributed to treatment • No transplants required in the 1

  12. Slide 12: Long-term Survival in HLHS from ELPIS I Trial of Lomecel-B™

    Long-term Survival in Hypoplastic Left Heart Syndrome (HLHS) from ELPIS I Trial of Lomecel-B™™ TM Results from ELPIS I trial showed 100% survival (transplant-free) In Lomecel-B™ treated patients at up to 5 years. In SVR historically matched controls, 5-year mortality was ~20% The NIH/NHLBI Pediatric

  13. Slide 13: ELPIS II: Ongoing Phase 2 Trial of Lomecel-B™ in HLHS

    Lomecel-B™: Hypoplastic Left Heart Syndrome (HLHS) ELPIS II: Ongoing Phase 2 Trial of Lomecel-B™ in HLHS • Total population = 38 patients • Randomized, controlled study comparing best medical care to the same treatment with addition of Lomecel-B™ (5-minute additional procedure during surgery) • Prim

  14. Slide 14: Lomecel-B™ for Aging-Related Frailty

    Lomecel-B™ for Aging-Related Frailty

  15. Slide 15: Aging-Related Frailty: Diminishing Health, Independence and QoL

    Aging-Related Frailty*: Diminishing Health, Independence and QoL Frailty Etiology of Aging-Related • Age-associated decline in reserve and function Frailty across multiple physiologic systems leading to inability to cope with stressors • Characterized by mobility disability, weakness, fatigue, weigh

  16. Slide 16: Lomecel-B™ for Aging-Related Frailty

    Lomecel-B™ for Aging-Related Frailty Phase 2b Study Aging-Related Frailty Study (N=143) • Designed to determine whether there was a dose response to a single infusion of Lomecel-B™ in Results (graphs on next slide) aging-related frailty • There was a statistically significant • There were 5 treatmen

  17. Slide 17: Lomecel-B™ Improved 6MWT Walking Distance

    Lomecel-B™ Improved 6MWT Walking Distance Statistically-significant dose response at 180 days. * Change from baseline; p<0.05 # Versus placebo; p<0.05 ** Change from baseline; p<0.01 ## Versus placebo; p<0.01 17

  18. Slide 18: Japan Clinical Trial Strategy Offers Fast Track for Regenerative Medicine

    Lomecel-B™ for Aging-Related Frailty Japan Clinical Trial Strategy Offers Fast Track for Regenerative Medicine Regenerative Medicine (Gene and Cell Therapies) The Act on the Safety of Regenerative Medicine (ASRM) The Act on Pharmaceuticals and Medical Devices (PMDA) • Comprises all medical technolog

  19. Slide 19: Clinical Trial in Japan (N=45)

    Lomecel-B™ for Aging-Related Frailty Clinical Trial in Japan (N=45) • Primary Objective ‒ Safety • Japanese National Center for Geriatrics and Gerontology-sponsored trial ‒ NCGG (Nagoya) and Juntendo University (Tokyo) selected as clinical sites Tokyo • Amended protocol accepted by PMDA on August 8,

  20. Slide 20: Lomecel-B™ for Alzheimer's Disease

    Lomecel-B™ for Alzheimer’s Disease

  21. Slide 21: Lomecel-B™ for Alzheimer's Disease: Targeting CNS Inflammation

    Lomecel-B™ for Alzheimer’s Disease: Targeting CNS Inflammation • Previous therapies have targeted either amyloid plaques (b-secretase inhibitors and anti-amyloid antibodies) or neurofibrillary tangles (antibodies) with little evidence of improvement of disease state • Increasingly inflammation is re

  22. Slide 22: Lomecel-B™ for AD

    Lomecel-B™ for AD Phase 1b Randomized and placebo-controlled trial (N=33) Results (graphs on next slide) • Designed to study safety (primary objective) of • There were no SAEs attributed to treatment single infusion of Lomecel-B™ in mild AD with Lomecel-B™ and most AEs were related patients to the p

  23. Slide 23: Low Dose Lomecel-B™: Slower Decline in Cognition (MMSE)

    Low Dose Lomecel-B™: Slower Decline in cognition (MMSE) in Phase 1b Trial than placebo Worsening Worsening Number of participants Number of participants Placebo 8 8 8 7 Placebo 8 8 8 7 20M Lomecel-B™ 15 15 15 13 20M Lomecel-B™ 15 15 15 13 100M Lomecel- 100M Lomecel- B™ 10 10 10 8 B™ 10 10 10 7 * 20M

  24. Slide 24: Phase 2a Alzheimer's Disease Study Design Ongoing

    Phase 2a Alzheimer’s Disease Study Design Ongoing Treatment: 41 weeks Primary Objective: Safety placebo Exploratory Endpoints: Topline data single dose of Lomecel-B™ include cognitive measures 48 patients 25 million cells anticipated such as MMSE, Clinical with by October Dementia Rating Scale with

  25. Slide 25: Experienced and Successful Leadership

    Experienced and Successful Leadership Wa’el Hashad Joshua M. Hare, MD Lisa Locklear Nataliya Agafonova, MD Paul Lehr CO-FOUNDER & EVP & CHIEF GENERAL COUNSEL & CHIEF EXECUTIVE OFFICER CHIEF MEDICAL OFFICER CHIEF SCIENCE OFFICER FINANCIAL OFFICER SECRETARY › 35+ years as an executive › A pioneer and

  26. Slide 26: Near-term Milestones

    Near-term Milestones 2023 Full data from the Phase 1 ELPIS I trial published in the European Heart Journal Open First patient to enroll in Japan Phase 2 Aging-Related Frailty Trial Long-term survival data disclosed from ELPIS I trial Topline data from Phase 2a Alzheimer’s Disease trial anticipated b

  27. Slide 27: Longeveron Overview

    Longeveron Overview Leader in development of MSCs for therapeutic indications Well-characterized allogeneic MSC (Lomecel-B™) product in Phase 2 trials Robust clinical pipeline with clinical efficacy signals in multiple indications with large unmet need: Alzheimer’s Disease, Aging-Related Frailty, an

  28. Slide 28: Thank You

    Thank You Website www.longeveron.com Chief Financial Officer Lisa Locklear llocklear@longeveron.com Investor Relations Mike Moyer LifeSci Advisors (617) 308-4306 mmoyer@lifesciadvisors.com Social Media Converge Miami 1951 NW 7th AVENUE @LGVNSocial Suite 520 Miami, FL 33136 @Longeveron 844-470-2550 @

  29. Slide 29: U.S Market Opportunity: Large Markets with Unmet Medical Needs

    U.S Market Opportunity: Large Markets with Unmet Medical Needs Hypoplastic Left Heart Syndrome Aging-Related Frailty Alzheimer’s Disease (HLHS) Patient Population 1,0003 8.1 million1 5.8 million2 Market Potential Up to $1B6 ~$4 – 8B4 ~$5-10B5 1 Company estimate based on US Census Bureau Population >

  30. Slide 30: Phase 2a Alzheimer's Disease Study Design (N=48) Ongoing

    Phase 2a Alzheimer’s Disease Study Design (N=48) Ongoing Clinical Screening Infusions (randomized, blinded): Follow-Up Visits Day 0, Week 4, Week 8 & Week 12 Major Eligibility Criteria Day 0, Week 4, 8 & 12: • 60-85 year old male or female Safety N=12 • Clinically diagnosed with mild Group 1 AD acco

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