Cel-sci Corporation · AMEX:CVM

Cel-sci — Investor Presentation (June 2024)

25 slides from Cel-sci's investor presentation, June 2024

  1. Slide 1: Multikine First In Class Immunotherapy Cancer Therapy

    Multikine™ “First In Class Immunotherapy” Cancer Therapy First Indication: Head & Neck Cancer Neoadjuvant Immunotherapy June 2024 NYSE American: CVM 1

  2. Slide 2: Forward Looking Statements

    Forward Looking Statements This presentation contains “forward-looking statements” standards; our expectations regarding federal, state by applicable laws and regulations, we undertake no within the meaning of the Private Securities Litigation and foreign regulatory requirements; the therapeutic obl

  3. Slide 3: Company Overview

    Company Overview → We are developing the first pre-surgical cancer drug in head and neck cancer. We believe Multikine will become the standard of care once successful. → After testing 750 patients we have identified the patient population where we believe Multikine provides a large survival benefit.

  4. Slide 4: What is unique about Multikine?

    What is unique about Multikine? → Multikine is a cancer immunotherapy. It is a controlled mixture of natural cytokines and biological molecules that is given right after diagnosis, before surgery, radiation and chemotherapy have damaged the immune system. → This approach is unique compared to normal

  5. Slide 5: Multikine Mechanism of Action

    These studies support Multikine’s three-part mechanism of action, which is (1) to overcome Multikine Mechanism of Action suppression of the local immune system by the tumor; (2) to enable a local antitumor immune response to occur; and (3) to break down the tumor’s tolerances to such an attack. This

  6. Slide 6: CD4 Increased In Multikine Treated Patients (Phase 2, Tímár 2005)

    CD4 Increased In Multikine Treated Patients (Phase 2, Tímár 2005) OUR FOUNDATION: MULTIKINE’S MECHANISM OF ACTION Figure 3 CD4 Increased In Multikine Treated Patients (Phase 2, Tímár 2005) You can see the effect of Multikine clearly under the microscope. One of the clearest examples is from a Phase

  7. Slide 7: Tumor Cell Death Without And With Multikine

    Tumor Cell Death Without And With Multikine Without Multikine With Multikine How the Tumor Defense Mechanisms Can How Multikine May Circumvent T cells Circumvent An Anti-tumor Immune Response T cells The Tumor Defense Mechanisms! LYMPH LYMPH NODE NODE T DC cells DC T Kill Tumor DC cells (GzmB, PFN;

  8. Slide 8: What is the Target Population?

    What is the Target Population? The 212 patient confirmatory study will focus on these Kaplan-Meier Overall Survival for Multikine target population (n=114) in the Phase 3 study patients: → Newly diagnosed locally advanced primary head and neck cancer 5-year survival patients with no lymph node invol

  9. Slide 9: Why N0, PET Scan, and Low PD-L1?

    Why N0, PET Scan, and Low PD-L1? Why N0 (no cancer found in the regional lymph nodes)? ↪ The immune system needs the lymph nodes to work. If nodes are damaged by disease, then the immune system is less effective. Patients with “N0” can mount the strongest immune attack. Why PET scan? ↪ PET Scan prov

  10. Slide 10: In the Target Population: Improved Survival In Patients

    In the Target Population: Improved Survival In Patients Kaplan-Meier Overall Survival for Multikine target population (n=114) in the Phase 3 study Data Presented at European Society for Medical Oncology in October 2023 No safety signals or toxicities vs standard of care 73% survival for Multikine vs

  11. Slide 11: The Multikine Treatment Regimen

    The Multikine Treatment Regimen Multikine would be added to the current standard of care, delivered locally via injections around the tumor and adjacent lymph nodes for three weeks, 5 days per week before surgery: 11 SLIDE 1

  12. Slide 12: Our Registration Study Design

    Our Registration Study Design Stage 1: Treatment Period Stage 2: Follow-up period Treatment Arm Multikine treatment first then standard of care n=106 Randomized 1:1 between the Assess overall survival as the treatment arm and the control arm. primary efficacy endpoint, and then histopathology biomar

  13. Slide 13: Increased Pre-Surgical Tumor Responses Lead to Increased Survival

    Increased Pre-Surgical Tumor Responses Appear to Lead to Increased Survival Across All Patients in the Phase 3 Trial p < 0.005 80% .........................................................................................................................................................................

  14. Slide 14: Higher PSR/PSD Rates in the Target Population

    Higher PSR/PSD Rates in the Target Population 14 SLIDE 1

  15. Slide 15: Safety Observed Across the Entire Patient Population

    Safety Observed Across the Entire 750 Patient Population No Multikine-related systemic AEs (Adverse Effects) or SAEs (Serious Adverse Effects). No Multikine-related delays of surgery. No Multikine-related interference with post-surgical treatment. No Multikine-related deaths. 15

  16. Slide 16: Why Do We Believe Our Confirmatory Study Will Be Successful?

    These studies support Multikine’s three-part mechanism of action, which is (1) to overcome Why Do We Believe Our Confirmatory Study Will Be Successful? suppression of the local immune system by the tumor; (2) to enable a local antitumor immune response to occur; and (3) to break down the tumor’s tol

  17. Slide 17: Multikine Partners

    Multikine Partners 1 Teva Pharmaceuticals Orient EuroPharma Ergomed MD Anderson International pharmaceutical company Taiwan based pharmaceutical company Leading Clinical Research Organization for radiation qualification (CRO) for head and neck cancer 1. Represents partners from our previously comple

  18. Slide 18: Dedicated State-of-the-Art Manufacturing Facility

    Dedicated State-of-the-Art Manufacturing Facility cGMP and BSL-1 facility near Washington, DC, USA → Built specifically for Multikine → State-of-the art facility → Over 73,000 ft2 of Manufacturing and R&D space available → About 45,000 ft2 fully developed → Proprietary automated cold fill to ensure

  19. Slide 19: The CEL-SCI Team

    The CEL-SCI Team Geert Kersten, Esq. Eyal Talor, PhD Giovanni Selvaggi, MD Chief Executive Officer & Director Chief Scientific Officer since 2009 CEL-SCI Medical Advisor since 1995 Inventor / developer of Multikine® since 2024 Experience in investment banking 30 years at CEL-SCI in R&D, CMO at Xcove

  20. Slide 20: Board of Directors

    Board of Directors Robert Watson Geert R. Kersten, Esq. Chairman of the Board of Directors Director and Chief Executive Officer Mr. Watson has been a director of CEL-SCI since December 2017. Geert Kersten has served in his current leadership role at CEL-SCI He is an accomplished business leader with

  21. Slide 21: Top-Tier Physician Consultants

    Top-Tier Physician Consultants Barbara Burtness, MD Marshall Posner, MD Anthony N. Brady Professor of Medicine (Medical Oncology) Consultant for CEL-SCI since 2005 at Yale School of Medicine Principal Investigator and Chair of the IDMC in CEL-SCI’s Phase 3 study Chief Translational Research Officer,

  22. Slide 22: Opinion of a Key Opinion Leader

    Opinion of a Key Opinion Leader “ in Head and Neck Cancer? Multikine in the curative setting is unique. The confirmatory study is an opportunity to improve overall survival in the eligible patient population without increasing toxicity. It is a potential game changer in the management of oral cavity

  23. Slide 23: Opinion of a Key Opinion Leader

    Opinion of a Key Opinion Leader “ in Head and Neck Cancer? As a surgical oncologist who has treated oropharyngeal cancer for 45 years, and witnessed the results of our often failure to control the disease (whether by surgery, radiation , chemotherapy or any combination of all three), I was impressed

  24. Slide 24: Investment Highlights and Milestones

    Investment Highlights and Milestones Addressing Our belief Strong FDA approval Enrollment an unmet on the survival data pathway commences medical need clinical trial The goal of the No drug is approved as a Confirmatory study of Enrollment expected to Given the results of the confirmatory study is p

  25. Slide 25: Thank you!

    Thank you! NYSE American: CVM

CEL-SCI — Investor Presentation (June 2024) on 6ix