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Valneva — Investor Presentation (April 2026)

25 slides from Valneva's investor presentation, April 2026

  1. Slide 1: A Leading Specialty Vaccine Company

    A Leading Specialty Vaccine Company April 2026

  2. Slide 2: Disclaimer

    Disclaimer This presentation does not contain or constitute an offer of, or the solicitation of an offer Certain information and statements included in this presentation are not historical facts to buy or subscribe for, Valneva SE shares to any person in the USA or in any jurisdiction to but are for

  3. Slide 3: A Leading Specialty Vaccine Company

    Cash-Generating Specialty Vaccines Business: Proprietary travel vaccines: IXIARO®, DUKORAL®, IXCHIQ® A Leading Specialty Vaccine Company: Blockbuster Opportunity: Focused on vaccines that Lyme disease vaccine partnered with Pfizer showed strong efficacy in Phase 3 make a difference trial; Pfizer is

  4. Slide 4: Our Strategy as a Leading Vaccine Biotech Company

    Our Strategy as a Leading Vaccine Biotech Company Contributing to a world in which no one dies or suffers from a vaccine preventable disease Fully Leverage … Maximize Integrated Biotech Drive R&D Upside Model Commercial Growth Augment clinical pipeline to achieve Create value with proven R&D Provide

  5. Slide 5: Proprietary Commercial Portfolio of Differentiated Vaccines

    Proprietary Commercial Portfolio of Differentiated Vaccines Differentiated vaccines Brand Indication Differentiation Key Markets Valneva direct markets: US, CA, UK, Only vaccine approved in U.S./Europe FR, Nordics, BE, NL, AT Active immunization against Japanese Requirement for U.S. military encepha

  6. Slide 6: Vaccine Sales Fuel Strategic Investments into R&D

    Vaccine Sales Fuel Strategic Investments into R&D Continued Growth of Proprietary vaccines drives revenue quality, margin expansion with strategic reduction in third-party product (3PP) sales2 Lean and Efficient € 163m € 145m – € 160m1 Commercial Infrastructure € 158m IXCHIQ® Highly experienced team

  7. Slide 7: Valneva's Current R&D Portfolio

    Valneva’s Current R&D Portfolio Program Design/Description Pre-Clinical Phase 1 Phase 2 Phase 3 World’s most clinically advanced LB6V / VLA15: Lyme vaccine candidate; protein Lyme disease subunit-based Clinical VLA1553: Post-marketing efficacy studies Programs Chikungunya underway; live-attenuated v

  8. Slide 8: LB6V / VLA15 World's leading Lyme Disease Vaccine Candidate

    LB6V / VLA15 World’s leading Lyme Disease Vaccine Candidate

  9. Slide 9: Lyme Disease Represents A Major Medical Need And Market Opportunity

    Lyme Disease Represents A Major Medical Need And Market Opportunity No vaccine is currently available to prevent Lyme disease in humans Commercial opportunity for Valneva Annual Burden of Disease U.S. : ~476K cases Europe : >132K cases Severe Manifestations3 10-30% cases develop • Lyme carditis • Ly

  10. Slide 10: Lyme Disease Incidence in United States

    Lyme Disease Incidence in United States 2002 2012 2022 Focal areas of high incidence Expansion of high incidence Continued expansion of high (>10 cases/100,000 persons) in areas northward towards incidence areas, particularly the northeast and central Canada and southward into expansion into neighbo

  11. Slide 11: World's Leading Vaccine Candidate Against Lyme Disease

    World’s Leading Vaccine Candidate Against Lyme Disease The only Lyme disease program in advanced clinical development today Vaccine Market Key Highlights Opportunity Milestones Multivalent, recombinant proteins Exclusive, worldwide Reported strong efficacy in partnership2 Phase 3 trial4 Targets six

  12. Slide 12: Phase 3: Vaccination Completed; First Data Readout Upcoming

    Phase 3: Vaccination Completed; First Data Readout Upcoming Pfizer aims to submit regulatory applications in U.S. and Europe in 20261 Tick Season 2023 Tick Season 2024 Tick Season 2025 VLA15 Cohort 1 Placebo Month 0 2 5-9 6-10 13 18 19 25 Primary series Booster VLA15 Efficacy Cohort 2 Read-out Place

  13. Slide 13: LB6V (formerly VLA15) Demonstrates Strong Efficacy in Phase 3

    LB6V (formerly VLA15) Demonstrates Strong Efficacy in Phase 31 Results strengthen confidence - Pfizer planning regulatory submissions in U.S. and Europe Vaccine Efficacy Safety Pre-specified Analysis Vaccine candidate was well tolerated Efficacy (95% CI) (Season 2) 28 days post-dose 4 73% (16, 94) N

  14. Slide 14: VLA15 is a Compelling Opportunity in an Underserved Market

    VLA15 is a Compelling Opportunity in an Underserved Market First-Mover Differentiated Compelling Strategic Fit Attractive Advantage in Highly Product Profile Target Population with Pfizer’s Vaccine Commercial Receptive Market and Use Case Franchise Dynamics Only Lyme disease Proven MoA with Broad ad

  15. Slide 15: Valneva's and Pfizer's Collaboration to Co-Develop and Commercialize LB6V

    Valneva’s and Pfizer’s Collaboration to Co-Develop and Commercialize LB6V Established April 2020 June 2022; Equity Investment of $95 Million by Pfizer; Updated Phase 3 cost split 40/60% (Valneva/Pfizer)* Rationale Maximize Lyme disease opportunity by leveraging Pfizer’s outstanding development and c

  16. Slide 16: IXCHIQ / VLA1553 A Highly Differentiated single-shot Chikungunya Vaccine

    IXCHIQ® / VLA1553 A Highly Differentiated single-shot Chikungunya Vaccine

  17. Slide 17: Chikungunya: A Major Public Health Threat

    Chikungunya: A Major Public Health Threat Mosquito-transmitted outbreak disease with potentially debilitating consequences • Often causes large, explosive outbreaks • Affecting up to 75% of the local population1 • Substantial quality-of-life and health-economic impact2 • Nearly half (43%) of those i

  18. Slide 18: IXCHIQ: Focused on Confirming Efficacy/Safety and Expanding Access

    IXCHIQ®: Focused on Confirming Efficacy/Safety and Expanding Access Robust clinical program supported by CEPI grant Pilot Vaccination Campaign Ongoing (Brazil) To serve as the basis for post-marketing commitment studies • Launched in February 2026 with partner Instituto Butantan in select municipali

  19. Slide 19: S4V2 World's Most Clinically Advanced Tetravalent Shigella Vaccine Candidate

    S4V2 World’s Most Clinically Advanced Tetravalent Shigella Vaccine Candidate

  20. Slide 20: S4V2: Opportunity to Develop First-in-Class Vaccine for a Life-Threatening Disease

    S4V2: Opportunity to Develop First-in-Class Vaccine for a Life-Threatening Disease Tetravalent bioconjugate vaccine with potential to cover up to ~85% of shigellosis infections1 Vaccine Market Key Highlights Opportunity Milestones World’s most clinically advanced Global market expected to exceed Pha

  21. Slide 21: Commercial Assessment of Shigella vaccine

    Commercial Assessment of Shigella vaccine Shigella vaccine market estimated to peak at ~€500 million1 Children in endemic Traveler (~23%) Military (<1%) countries (~76%) 20-50% 30-100% 70-90% Recommendation (OOP-reimbursement) (Med-high risk destinations) (Med-high risk destinations Acceptance 30% 1

  22. Slide 22: Financial Guidance & Outlook

    Financial Guidance & Outlook

  23. Slide 23: Valneva Remains Solidly Funded with Strong Financial Outlook

    Valneva Remains Solidly Funded with Strong Financial Outlook 2026 Guidance Financial Outlook Product Sales: €145 - €160 million1; Commercial Continued growth and cash flows from proprietary business expected to remain cash-flow positive commercialized vaccines Total Revenues: €155 - €170 million Foc

  24. Slide 24: Our Next Phase as a Leading Vaccine Biotech Company

    Our Next Phase as a Leading Vaccine Biotech Company Potential LB6V Success Would Offer Strategic Growth Opportunities Leverage core strengths in vaccine development to deliver greater long-term value Key initiatives: Build scale in R&D pipeline post-VLA15 exit • Strategic in-licensing/M&A to augment

  25. Slide 25: Thank you

    Thank you Merci Danke Tack valneva

Valneva — Investor Presentation (April 2026) on 6ix