Genelux Corporation · NASDAQ:GNLX

Genelux — Investor Presentation (October 2023)

38 slides from Genelux's investor presentation, Oct 10, 2023

  1. Slide 1: Redefining Immuno-Oncology

    Redefining Immuno-Oncology Corporate Presentation | October 2023

  2. Slide 2: Forward Looking Statements

    Forward Looking Statements This presentation contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as amended, and Section 21E of the Securities Exchange Act of 1934, as amended, which are subject to the “safe harbor” created by those sections, about Ge

  3. Slide 3: Highlights

    Highlights Olvi-Vec: De-risked late-stage Clinical Program Ongoing pivotal trial in late-stage Ovarian Cancer, SCLC and planned Phase 2 trial Adjuvant Maintenance NSCLC CHOICE™ Platform; Broad and Diverse Discovery Engine Library with over 500 novel vaccinia strains and 110+ transgenes Validating St

  4. Slide 4: The Most Advanced Non-local Delivery Oncolytic Immunotherapy

    The Most Advanced Non-local Delivery Oncolytic Immunotherapy Olvi-Vec: Engineered to selectively target and eliminate tumor cells while inducing a robust patient-specific immune response Physician-preferred Routes Antitumor Effect Ideal Backbone of of Delivery and Well Tolerated Combination Therapy

  5. Slide 5: Diversified Designs and Indications Exploit Competitive Advantages

    Diversified Designs and Indications Exploit Competitive Advantages Olvi-Vec Human Health Design _Preclinical Phase 1 Phase 2 Phase 3 Collaborators Ovarian Cancer {plotinum-resistont/cefcactory) Regional Route Gunchecy, Ph3 OnPrime/GOG-3076 Study Actively Enrolling GOG: (Cooperative Group) ‘Non-Small

  6. Slide 6: Selective Replication In Tumors Unleashes Immune System Against Cancer

    Selective Re lication In Tumors Unleashes Immune System Against Cancer Key Takeaways Olvi-Vec is g robust immune modulator that utilizes a triple mode of action to mount a personalized attack against cancer cells Hi iroughout the body * Kills cancer cells directly + Enhances (neo)antigen presen anon

  7. Slide 7: Olvi-Vec-Primed Immunochemotherapy: Overcoming Drug Resistance

    Olvi-Vec-Primed Immunochemotherapy: Overcoming Drug Resistance Olvi-Vec-Induced Hot Tumor Pro-therapeutic gene expression ; P emotherapy synergy > Positive regulation of T-cell activating inog=ric call death and trafficking ee i : i Depletion of suppressor cells > Expression profiles correlated to b

  8. Slide 8: Over $4 Billion in Transactions in Active Oncolytic Space

    Over $4 Billion in Transactions in Active Oncolytic Space Cs 2237S With its recent IPO, Genelux joined the public markets as a Phase 3 company pO Replimune’ Replimune completed a $225 milion offering as well as $200M in non-dilutive debt financing ‘A maturing field with Amgen launching Imiygie in 20

  9. Slide 9: Competitive Advantages of Olvi-Vec as an Oncolytic Virus

    Competi ive Advantages of Olvi-Vec as an Oncolytic Virus Key Takeaways UN Oncolytic Virus Space Olvi-Vec Key Advantages: Key Players and Assets Olvi-Vec Key Advantages * Broad spectrum of activity Genecurx> Olvi-vec + Tumor selectivity @ Target & Treat Metastatic Disease ee AMGEN Herpes é eure activ

  10. Slide 10: Creating a New Paradigm Of Oncolytic Virus Drug Development

    Creating a New Paradigm Of Oncolytic Virus Drug Development 7 completed clinical trials ~150 patients @enNevcux Our Advantage Systemic Dosing _Robust Immune and Redosing Activation Profile Target & Treat Metastatic Diseases Broad spectrum of accessible tumor types AMGEN {!} Replimune® ilere] T-VEC (

  11. Slide 11: Phase 1b: Anti-tumor Activity as Monotherapy Leading into Combination

    hase 1b: Anti-tumor Activity as Monotherapy Leading into Combination Key Clinical Takeaways IN + mPFS of 6.1 months median 4 prior lines; 5%Cl: 2.2-NA) for the six patients in Cohort 1 virus monotherapy - the dose used in Ph2- + SOC-AURELIA regimen (1-2 prior lines; mPFS: 6.7 mos) + ELAHARE (1-3 pri

  12. Slide 12: Completed Phase 2 Tested Olvi-Vec Immunochemotherapy

    Completed Phase 2 Tested Olvi-Vec Immunochemothera Olvi-Vec Primed Immunochemotherapy in Heavily Pretreated Patients With Platinum-Resistant or Platinum-Refractory Ovarian Cancer Data Presentations Reveucicreena 7) puaioulsnaaGon aan Sater Det Antal eetne cesta n=27 Gynecologic Cancer Society Oral P

  13. Slide 13: Key Clinical Takeaways

    Key Clinical Takeaways Promising ORR and PFS, and clinical reversal of platinum resistance and refractoriness among patients with PRROC + All patients had documented progressive disease at enrollment * Overall response rate in 27 patients was 54% with 7.6- month median duration of response * Histori

  14. Slide 14: Demonstrated Deep and Durable Tumor Shrinkage

    Demonstrated Deep and Durable Tumor Shrinkage Key Clinical Takeaways Refractory patients performed as well as resistant patients Tumor Shrinkage * Overall, 86% of PRROC patients showed tumor reduction, with 91% of Platinum-refractory patients showing tumor reduction + Four patients had 100% reductio

  15. Slide 15: Olvi-Vec-Primed Immunochemotherapy Overcomes “Refractoriness”

    Olvi-Vec-Primed Immunochemotherapy Overcomes “Refractoriness” Exemplary platinum-refractory patients, after platinum re-challenge, achieved PFS exceeding any prior lines 15B-01; ‘Stage IIIB papillary serous ECOG: 0 BRCA negative PD-Li negative Stage Il grade serous ECOG: 0 BRCA negative PD-L1 negati

  16. Slide 16: Durable Benefit of Overall Survival via Clinically-Validated Endpoint

    Durable Benefit of Overall Survival via Clinically-Validated Endpoint Key Clinical Takeaways IN 20% long-term survivors consistent with commercially successful immunotherapies + Historical data in 4th line and beyond shows a median overall survival of only 9.8 months » Onamedian Sth line of treatmen

  17. Slide 17: “Allcomers” Approach May Reset Life Clock of Heavily Pre-treated Patients

    “Allcomers” Approach May Reset Life Clock of Heavily Pre-treated Patients Key Trial Takeaways IN Olvi-Vec addresses a broad and underserved pool of patients * Olvi-Vec trial inclusion criteria allows patients regardless of i) tumor biomarkers, ii) platinum refractory tumors, or (iii) number of prior

  18. Slide 18: Phase 3 Pivotal Trial Design Founded on Phase 2 Trial Design & Results

    Phase 3 Pivotal Trial Design Founded on Phase 2 Trial Design & Results Trial design intends to replicate previous data showing anti-tumor activity of Olvi-Vec and reversal of platinum resistance in the tumor microenvironment Key Inclusion Criteri Multi-center, randomized open-label 86 + High-grade s

  19. Slide 19: Systemic administration demonstrated dose-dependent OS benefit

    Systemic administration demonstrated dose-dependent OS benefit IN Key Trial Takeaways Demonstrated feasibility and clinical benefit of multiple lv cycles * Median 5 prior lines of therapy * Regimen: various dosing levels and schedules iret over 4-6 months, + Well tolerated: noMTD reached with one DL

  20. Slide 20: Systemic Administration + Chemo Generated Encouraging Data

    tration + Chemo Generated Encouraging Data Systemic Admi N adverttath | eeuane ° Expanded Access Program Key Trial Takeaways Recurrent metastatic cervical cancer | High-grade pancreatic cancer with lung mets lung & liver mets Anti-tumor effect of IV ‘Case Report (Pt 8214-06) Report (PLAZIA-O4) Immun

  21. Slide 21: Genelux has Partnered with Newsoara BioPharma Co., Ltd

    Genelux has Partnered with Newsoara BioPharma Co., Ltd NEWSGARA HIGHLIGHTS 7 5 ENELUX NEWSGARA GREhER Pipelines Phase IIb/III Indications Phase II $850 Million Valuation Top 10 Blue-chip Biotech Investors 2023 Benny Li, PhD Founder and Chief Executive Officer 20+ yrs. global and China local pharma F

  22. Slide 22: Validating Industry Collaboration with Newsoara BioPharma Co., Ltd

    Validating Industry Collaboration with Newsoara BioPharma Co,, Ltd Key Takeaways IN > Newsoara will fund the US-based Genelux Phase 2 trial in NSCLC. - Newsoara has development and commercialization rights in Greater China + Interim readout for one or more systemic administration trials expected as

  23. Slide 23: V2ACT Therapeutics LLC: Joint Venture between GNLX and TVAX BioMedical

    V2ACT Therapeutics LLC: Joint Venture between GNLX and TVAX BioMedical Key Trial Takeaways iN V2ACT Therapeutics is a joint venture between Genelux Corporation and TVAX Biomedical, Inc. established to develop and test V2ACT. V2ACT Immunothera| Vaccination increases the numbers of neoantigen-specific

  24. Slide 24: Estimated Billion Dollar Plus annual Olvi-Vec Commercial Opportunity (US)

    Estimated Billion Dollar Plus annual Olvi-Vec Commercial Opportunity (us) Ovarian Cancer Market? Ovarian Cancer ee q Non-Small Cell Lung Cancer ‘$1.8B jn 2022, expected CAG Additional revenue drivers: eo © > Re-treatment > Front-Line therapy > Additional Indications, i.e.: ~236,511 women in the US c

  25. Slide 25: Integrated R&D and Manufacturing Capabilities For Phase 3 And Launch

    Integrated R&D and Manufacturing Capabilities For Phase 3 And Launch Large-Scale cGMP Manufacturing _— iN Process to Optimize Production ‘ey Takeaways Headquarters ‘wanifacturnic Foal Westlake Village, CA, USA D; + Established and equipped an al ‘cS wage. Geta orpchy Pa conti folied 7) Kir Manufactu

  26. Slide 26: Commercial Strategy

    Commercial Strategy Partnerships Self-Manufacturing Patients Reimbursement Leverage partnership Large-Scale cGMP Population without Compelling Value with GOG Foundation Manufacturing Standard of Care Proposition for Payors + Preeminent US-based * Control of Production + PRROC patients lack ° Sipiffe

  27. Slide 27: CHOICE Platform Library: 500+ Vectors with 110+ Transgenes

    Choice Platform Library: 500+ Vectors with 110+ Transgenes Engineered and selected clonal isolated (non-GMO) viral strains identified from in vitro and in vivo selection criteria Virus-encoded transgenes Therapeutic Well Growth & Differentiation Regulators Hormones Genes Metastasis Suppressor Genes

  28. Slide 28: Intellectual Property: Market Exclusivity & Freedom to Operate

    Intellectual Property: Market Exclusivity & Freedom to Operate Patent Portfolio: 33 issued patents; 7 pending Olvi-Vec covered by Composition of Matter (2031) and Manufacturing (2038) St ng IP = Olvi-Vec: Worldwide operating freedom; Regulatory No third-party royalties due Designations Long Duration

  29. Slide 29: Accomplished Leadership Team

    Accomplished Leadership Team j Board of Directors Executive Team THOMAS ZINDRICK, JD agen acvamnics Chairman of the Board — Writ vers Squats JAMES L. TYREE, MBA e Lead independent Sector Thee anes Thomas Zindrick, JD Lourie Zak Paul Scigalla, MD, PhD Sean Ryder, JD MARY MIRABELLI, MBA cant Chief Exe

  30. Slide 30: Genelux Has Executed on Multiple Milestones and is Positioned for the Future

    Genelux Has Executed on Multiple Milestones and is Positioned for the Future Executed Milestones IN Executed on go public strategy i) and follow on with $60M raised oO Initiation of Phase 3 Trial in oO PRROC , Phase 2 results published in JAMA Oncology r) Collaboration and License agreement with New

  31. Slide 31: Expected Operating Runway into 1Q 2026

    Expected Operating Runway into 1Q 2026 Capitalization Summary Analyst Coverage Stock Symbol GNLX Bruce Jackson M.S,, MBA Share Price!) $28.89 * Kemp Dolliver CFA Shares Outstanding 25.98M res Outstanding * Jason McCarthy, Ph.D. Market Capitalization $750M Cash & Equivalents”) $28.40M aiken pot ca Ma

  32. Slide 32: Highlights

    Highlights Olvi-Vec: De-risked late-stage Clinical Program Ongoing pivotal trial in late-stage Ovarian Cancer, SCLC and planned Phase 2 trial Adjuvant Maintenance NSCLC CHOICE™ Platform; Broad and Diverse Discovery Engine Library with over 500 novel vaccinia strains and 110+ transgenes 7 Validating

  33. Slide 33: Appendix

    HeNELUXx Redefining Immuno-Oncology Corporate Presentation | October 2023 Appendix

  34. Slide 34: Accomplished Clinical Advisory Board

    Accom lished Clinical Advisory Board Robert Holloway, MD CHAIRMAN Cie aca cio arian ae Robert Coleman, MD Member Albert A. Mendivil, MD Member Deputy oer of hs Univers of Thomas J. Herzog. MD Cineiesicaenr| Toate Chief Executive Officer Protersorand olsen orector, rivers comprehensive ‘Caneet Costar

  35. Slide 35: Olvi-Vec Demonstrates Monotherapy Oncolysis and Immune Activation

    Olvi-Vec Demonstrates Monotherapy Oncolysis and Immune Activation (VIRO-15: monotherapy) Key Takeaways iN (PL#15A01) (PLAS A-11) Elimination of Cancer Cells after Increased Lymphocyte infiltrationin different cavities Olvi-Vec monotherapy shows decreased tumor cells and increase immune activation pe

  36. Slide 36: CD8+ T-cells: Infiltrating Lymphocytes are Prognostic for Response/Survival

    CD8+ T-cells: infiltrating Lymphocytes are Prognostic for Response/Survival Pt# 15A-16 Pt# 15A-18 Pt# 45A-23 —_ Pan] ae BSc Se eae cos+ co4+ cD8+ co4+ cose 7 rostolw-vec (prior to subsequent chemotherapy) Endogenous TiLs (intrar tumoral and stromal) are very low in ovarian cancer Pti 15A-16 Ptit 15A

  37. Slide 37: VIRO-15: Monotherapy

    (MRO-15: manatherapy} Tanta tamorantigen presentation Long-lasting, Tumor-specific T cell response corresponds to tumor reduction IN Off-the-Shelf Personalized Medicine: Single Agent generates Individualized Results Key Takeaways * Olvi-Vec induces favorable & long-lasting Tumor-specific T-cell Resp

  38. Slide 38: Olvi-Vec: Ideal Backbone for Combination Therapy

    Olvi-Vec: Ideal Backbone for Combination Thera Converts Tumor Microenvironment to Inflammatory “Hot Spot” NCT01443260/TUE Study 6 zg es Induction of acute inflammatory 3 i, cytokines 5, (ThI-type related) ra 52) VIRO-I5 Study 31 zy Baseline Massive inflammatory response after cycle 1 of vieus treatm

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