Cel-sci Corporation · AMEX:CVM

Cel-sci — Investor Presentation (October 2023)

24 slides from Cel-sci's investor presentation, October 2023

  1. Slide 1: Multikine Pre-Surgical Cancer Therapy

    Leukocyte Interleukin, Injection For Head And Neck Cancer Multikine™ Pre-Surgical Cancer Therapy Pre-surgical, Tumor responses Longer local therapy before surgery life NYSE: CVM SLIDE 1

  2. Slide 2: Forward Looking Statements

    Forward Looking Statements SLIDE 2

  3. Slide 3: Equity Summary

    Equity Summary CEL-SCI Corporation NYSE American: CVM Clinical Trial Stage Completed 928-patient, global, multicenter, Phase 3 cancer immunotherapy study Market Capitalization ~$65 million Avg. Daily Trading Volume ~ 1 million shares per day Shares Outstanding ~ 47.25 million shares; completely clea

  4. Slide 4: What Is Multikine? Multikine Treatment Regimen

    What Is Multikine?  Multikine is a true first line immunotherapy — 3 weeks before surgery.  It is a mixture of cytokines and biological molecules.  Multikine induces a local immune anti-tumor attack before the immune system has been compromised by treatment or disease. Multikine Treatment Regimen

  5. Slide 5: Why are we confident in gaining approval of our drug?

    Why are we confident in gaining approval of our drug? Simply put: OUR DATA 928 patients in 20 countries Completed Pivotal 100 hospitals, 20 countries, $100+ million Phase 3 Randomized Controlled Good Clinical Practices and fully audited data Trial Results presented at ASCO, ESMO, ECHMO, AHNS SLIDE 5

  6. Slide 6: Excellent Safety Profile

    Excellent Safety Profile  No Multikine-related deaths.  Multikine-related adverse events before surgery were local and resolved after surgery.  Adverse event rates in the Multikine and control groups were not significantly different. SLIDE 6

  7. Slide 7: Our Data: Multikine Leads To Better Survival

    Our Data: Multikine Leads To Better Survival Multikine 73% vs 45% Control SLIDE 7

  8. Slide 8: Our Data: Multikine Leads To Better Survival

    Our Data: Multikine Leads To Better Survival 60% Risk of death, 55% Reduction in death risk 5-year risk of death 50% 40% Control Multikine cut the 5-year risk 30% Risk of death, 27% of death IN HALF in the target population 20% Multikine 10% 0% SLIDE 8

  9. Slide 9: We Know How Multikine Works And Can Target This

    We Know How Multikine Works And Can Target This 1. 2. 3. Multikine leads to Pre-surgical responses Therefore, Multikine pre-surgical responses. lead to better survival. leads to better survival. SLIDE 9

  10. Slide 10: Multikine Leads To Pre-Surgical Responses

    Multikine Leads To Pre-Surgical Responses >30% reduction in Reductions (PSR) tumor dimensions Stage IV to III, Downstages (PSD) Stage III to II SLIDE 10

  11. Slide 11: Multikine Leads To Pre-Surgical Responses

    Multikine Leads To Pre-Surgical Responses SLIDE 11

  12. Slide 12: Pre-Surgical Responses Lead To Better Survival

    Pre-Surgical Responses Lead To Better Survival SLIDE 12

  13. Slide 13: Therefore, Multikine Leads To Better Survival

    Therefore, Multikine Leads To Better Survival Multikine 73% vs 45% Control SLIDE 13

  14. Slide 14: Higher Response Rates In The Target Population

    Higher Response Rates In The Target Population SLIDE 14

  15. Slide 15: Positive Results In The Target Population

    Positive Results In The Target Population  73% survival for Multikine vs 45% in the control, at 5 years  28% jump in 5-year absolute survival  5-year risk of death cut from 55% to 27%  Statistically significant p = 0.0015  Hazard ratio = 0.35 (95% CIs [0.19, 0.66])  Tumor reduction rate >13% 

  16. Slide 16: Positive Results In The Target Population

    Positive Results In The Target Population  The target population are patients who present with: • No nodal involvement and no extracapsular spread (via PET scan) • Low PD-L1 tumor expression (defined as TPS<10, via biopsy) (Note, this differentiates Multikine from high PD-L1 checkpoint inhibitors.)

  17. Slide 17: Bottom Line: The Data Proves That Multikine Works

    Bottom Line: The Data Proves That Multikine Works 1. 2. 3. Multikine leads to Pre-surgical Therefore, pre-surgical responses lead to Multikine leads to responses. better survival. better survival. SLIDE 17

  18. Slide 18: CEL-SCI Plans To Seek Immediate Approval

    CEL-SCI Plans To Seek Immediate Approval  Europe, UK, Canada, USA  Seeking approval based on current data  Goal: get approval first, then do confirmatory study if required  Submissions filed 3Q23-1Q24  Certification of manufacturing plant completed by 1Q24  Earliest informal indication of like

  19. Slide 19: Top-Tier Physician Consultants

    Top-Tier Physician Consultants Barbara Burtness, MD • Anthony N. Brady Professor of Medicine (Medical Oncology) at Yale School of Medicine • Chief Translational Research Officer, Yale Cancer Center • Chief, Head and Neck Cancers/Sarcoma and Co-Leader, Developmental Therapeutics, Yale Cancer Center •

  20. Slide 20: Top-Tier Physician Consultants

    Top-Tier Physician Consultants Marshall Posner, MD • Consultant for CEL-SCI since 2005 • Principal Investigator and Chair of the IDMC in CEL-SCI’s Phase 3 study • Director, Head and Neck Oncology, Mt. Sinai NY • Co-Leader, Cancer Clinical Investigation Program, Tisch Cancer Institute • More than 250

  21. Slide 21: State-Of-The-Art Manufacturing Facility

    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 no loss of

  22. Slide 22: CEL-SCI's Value Proposition

    CEL-SCI’s Value Proposition Initial capacity 12,000 treatments per year, if approved Cancer drugs $65 million that save lives market cap are worth many billions. ~$150,000 per treatment SLIDE 22

  23. Slide 23: Upcoming Catalysts

    Upcoming Catalysts Complete the commissioning of our manufacturing facility Potential Commercialization in Canada as Early as 2024 • We are preparing application for NOC/C approval as they suggested, hopeful to file 1Q24 • If NOC/C granted, then possible to begin commercialization in Canada late 202

  24. Slide 24: Thank you.

    Thank you. Pre-surgical, Tumor responses Longer local therapy before surgery life NYSE: CVM SLIDE 24

CEL-SCI — Investor Presentation (October 2023) on 6ix