Vaxcyte, Inc. · NASDAQ:PCVX

Vaxcyte — Technical Presentation (October 2026)

35 slides from Vaxcyte's technical presentation, Oct 5, 2026

  1. Slide 1: VAX-31 OPUS-1 Pivotal Phase 3 Adult Trial: Topline Results

    October 5, 2026 VAX-31 OPUS-1 Pivotal Phase 3 Adult Trial: Topline Results Exhibit 99.2

  2. Slide 2: Vaxcyte Leadership Team on Today's Call

    October 5, 2026 Strong Track Record in Vaccines and Biopharma Grant Pickering, MBA Chief Executive Officer, Director & Co-Founder Andrew Guggenhime, MBA President & Chief Financial Officer Jim Wassil, MS, MBA Executive VP, Chief Operating Officer & Chief Scientific Officer Luis Jodar, PhD Chief Medi

  3. Slide 3: Forward-Looking Statements

    Forward-Looking Statements October 5, 2026 This presentation contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. These statements include, but are not limited to, statements related to the potential benefits of Vaxcyte’s carrier-sparing pla

  4. Slide 4: Agenda

    October 5, 2026 Introduction and results overview Agenda OPUS-1 Study and TOPLINE results Trial Design, Disposition and Demographics Tolerability and Safety Data Immunogenicity in Adults Aged ≥50 Years and 18-49 Years Vax-31 PROGRAM Next Steps

  5. Slide 5: Introduction and Results Overview

    Introduction and Results Overview October 5, 2026

  6. Slide 6: Pneumococcal Vaccine Market is Large, Durable and Poised for Significant Growth

    October 5, 2026 Combined $8.5B Market Expected to Grow to ~$12B by 2030¹ Driven Primarily by Adult Market Expansion Pneumococcal Vaccine Market is Large, Durable and Poised for Significant Growth Future Market 2030: ~$12B Pediatric market is large, well-established, and highly durable Total Market T

  7. Slide 7: VAX-31 is Designed to Expand Protection with Broadest Disease Coverage in Adults

    VAX-31 is Designed to Expand Protection with Broadest Disease Coverage in Adults IPD² (Adults ≥50) IPD = Invasive Pneumococcal Disease; SoC = standard of care; ST = serotype. (1) Immune responses elicited by 20C are expected to be highly cross-reactive with 20B. PCV21 includes 20A and VAX-31 include

  8. Slide 8: OPUS-1 Inaugurates a More Stringent Noninferiority Standard

    LBCI >1 OPUS-1 Inaugurates a More Stringent >0.667 Noninferiority Standard, Setting a New Bar for Adult PCV Clinical Studies October 5, 2026 OPA GMR: LBCI >0.5 LBCI >0.667 Immune Response Standards for OPA GMRs OPA = opsonophagocytic activity; GMR = geometric mean ratio; NI = noninferiority; ST = se

  9. Slide 9: OPUS-1 Phase 3 Study: Statistical Framework to Define Success

    October 5, 2026 OPUS-1 Phase 3 Study: Statistical Framework to Define Success 11 serotypes shared by all 3 vaccines Noninferiority vs PCV20 and/or PCV21 (OPA GMR: LBCI >0.667)¹ 9 serotypes shared with PCV20 only Noninferiority vs PCV20 (OPA GMR: LBCI >0.667) 8 serotypes shared with PCV21 only Noninf

  10. Slide 10: OPUS-1 Topline Results: VAX-31 Met All Primary Immunogenicity Endpoints and Safety Objectives

    October 5, 2026 OPUS-1 Phase 3 Topline Results: VAX-31 Met All Primary Immunogenicity Endpoints and Safety Objectives (1) Groups 1 and 4: one-sided Hochberg-adjusted p-value <0.025 against at least one comparator, as prespecified in the protocol. (2) The 32 assessments include 31 vaccine serotypes a

  11. Slide 11: OPUS-1 Study and Topline Results

    OPUS-1 Study and Topline Results October 5, 2026

  12. Slide 12: Trial Design, Disposition and Demographics

    Trial Design, Disposition and Demographics October 5, 2026

  13. Slide 13: OPUS-1 Phase 3 Pivotal, Randomized, Double-Blind, Active-Controlled Trial

    6 Month Safety Follow-Up OPUS-1 Phase 3 Pivotal, Randomized, Double-Blind, Active-Controlled Clinical Trial in Adults Aged 18 and Older (n=4,047*) October 5, 2026 Adults aged ≥50 years (n=3,572) Adults aged 18-49 years (n=475) Screen Blood Sample Screen Randomize (3:1) Month 1 Month 6 Day 1 Blood Sa

  14. Slide 14: ~97% of Vaccinated Subjects Included in Immunogenicity Evaluable Population

    ~97% of Vaccinated Subjects Included in Immunogenicity Evaluable Population Study Disposition October 5, 2026 ≥50 YEARS 18-49 YEARS* Total Enrolled1 N = 3,572 Total Enrolled1 N = 475 VAX-31 N = 1,194 PCV20 N = 1,195 PCV21 N = 1,183 N = 1,194 N = 1,195 N = 1,183 N = 1,147 N = 1,162 N = 1,151 VAX-31 N

  15. Slide 15: Population Demographics in Adults Aged 50 Years and Older

    Population Demographics in Adults Aged 50 Years and Older October 5, 2026 VAX-31 PCV20 PCV21 Safety Immunogenicity Safety Immunogenicity Safety Immunogenicity Number of Subjects 1194 1147 1195 1162 1183 1151 Median Age, Years (range) 60.0 (50, 97) 60.0 (50, 97) 60.0 (50, 86) 60.5 (50, 86) 60.0 (50,

  16. Slide 16: Population Demographics in Adults Aged 18-49

    Well-Balanced Across Cohorts and Similar for the Safety and Immunogenicity Populations Population Demographics in Adults Aged 18-49 October 5, 2026 18-49 YEARS SAFETY POPULATION VAX-31 RECIPIENTS (IEP) VAX-31 PCV20 18-49 Years 50-64 Years Number of Subjects 354 120 348 763 Median Age, Years (range)

  17. Slide 17: Tolerability and Safety Data

    Tolerability and Safety Data October 5, 2026

  18. Slide 18: Local and Systemic Solicited AEs in Adults Aged 50 Years and Older

    Local and Systemic Solicited AEs in Adults Aged 50 Years and Older October 5, 2026 VAX-31 was Well-Tolerated and Consistent with PCV20 and PCV21, Majority of AEs Resolved Within 48 Hours AEs = adverse events. Grade 1 Grade 2 Grade 3 VAX-31 PCV20 PCV21 ADULTS ≥50 YEARS

  19. Slide 19: Local and Systemic Solicited AEs Similar to PCV20 in Adults Aged 18-49

    Local and Systemic Solicited AEs Similar to PCV20 in Adults Aged 18-49 October 5, 2026 AEs = adverse events. VAX-31 was Well-Tolerated and Consistent with PCV20, Majority of AEs Resolved Within 48 Hours Grade 1 Grade 2 Grade 3 VAX-31 PCV20 ADULTS 18-49 YEARS

  20. Slide 20: Overall Safety Profile Similar to PCV20 and PCV21

    Overall Safety Profile Similar to PCV20 and PCV21 October 5, 2026 AEs = adverse events; MAAE = medically attended adverse event; NOCI = new onset of chronic illness; SAE = serious adverse event; Discontinuation = subject discontinued from the study due to an AE. (1) All four deaths were assessed as

  21. Slide 21: Immunogenicity Data In Adults Aged ≥50 Years and 18-49 Years

    Immunogenicity Data In Adults Aged ≥50 Years and 18-49 Years October 5, 2026

  22. Slide 22: VAX-31 vs PCV20 & PCV21 on Common 11 STs

    VAX-31/PCV20 VAX-31/PCV21 11 STs in Common With PCV20 and PCV21 October 5, 2026 VAX-31 vs PCV20 & PCV21 on Common 11 STs ST = serotype; OPA = opsonophagocytic activity; GMR = geometric mean ratio; LBCI = lower bound of the 2-sided 95% CI. (1) SAP criterion: lower bound of the 95% CI of the OPA GMR >

  23. Slide 23: STs in Common With Only PCV20 and Only PCV21

    9 STs in Common With Only PCV20 and 8 STs Common With Only PCV21 October 5, 2026 ST = serotype; OPA = opsonophagocytic activity; GMR = geometric mean ratio; LBCI = lower bound of the 2-sided 95% CI. VAX-31 vs PCV20: Shared 9 STs GMR: Met 9 of 9 ST OPA GMR Comparisons vs PCV20 and 8 of 8 vs PCV21 Per

  24. Slide 24: Unique VAX-31 STs and 20B

    3 Unique VAX-31 STs and 20B October 5, 2026 ST = serotype; OPA = opsonophagocytic activity; GMR = geometric mean ratio; LBCI = lower bound of the 2-sided 95% CI. (1) With Hochberg multiplicity analysis per protocol. (2) VAX-31 includes serotype 20C; 20B is being evaluated in clinical studies to demo

  25. Slide 25: Immunobridging Comparison in 18-49-Year-Olds vs 50-64-Year-Olds

    October 5, 2026 Met Prespecified Primary Endpoint Across All 32 STs¹ (OPA GMR With LBCI >0.667) ST = serotype; OPA = opsonophagocytic activity; GMR = geometric mean ratio; LBCI = lower bound of the 2-sided 95% CI. (1) The 32 assessments include 31 vaccine serotypes and cross-reactive 20B. GMR: GMR:

  26. Slide 26: VAX-31 Met Noninferiority Criterion for 20/20 STs vs PCV20 and 17/19 vs PCV21

    0.667 VAX-31 Met Noninferiority Criterion for 20/20 STs vs PCV20 and 17/19 STs vs PCV21 Comparator-Specific Assessments: VAX-31 Immune Responses vs PCV20 and PCV21 October 5, 2026 VAX-31 vs PCV20: Common 20 STs ST = serotype; OPA = opsonophagocytic activity; GMR = geometric mean ratio; LBCI = lower

  27. Slide 27: VAX-31 Data Support Potential Best-in-Class Adult PCV Profile

    VAX-31 Data Support Potential Best-in-Class Adult PCV Profile with Broadest Coverage Relative to SoC; Advancing Toward BLA Submission October 5, 2026 SoC = standard of care; BLA = Biologics License Application; ST = serotype. (1) % of IPD caused in individuals ≥50 yrs of age in the U.S. in 2022-2024

  28. Slide 28: VAX-31 Program Next Steps

    VAX-31 Program Next Steps October 5, 2026

  29. Slide 29: OPUS Phase 3 Program Serves as Cornerstone of Planned BLA Submission

    October 5, 2026 OPUS-1 PIVOTAL TRIAL (N=4,047) Topline results reported; complete data set to be published MANUFACTURING CONSISTENCY STUDY (e.g. lot-to-lot) (N=TBD) OPUS-2: CONCOMITANT ADMINISTRATION WITH SEASONAL INFLUENZA VACCINE (N=1,390) Enrollment complete; topline results anticipated 1H 2027 O

  30. Slide 30: Foundation to Support Expected U.S. Commercial Launch

    Establish commercial manufacturing readiness, including: Existing supply chain sufficient to meet demand for U.S. adult launch Expanding commercial-scale capacity to support future U.S. demand Foundation to Support Expected U.S. Commercial Launch October 5, 2026 Medical affairs and commercial infras

  31. Slide 31: Pipeline of Vaccines with Multiple Near-Term Milestones

    Announce safety, tolerability and immunogenicity data from the OPUS-2 and OPUS-3² trials in the first half of 2027 Pipeline of Vaccines with Multiple Near-Term Milestones October 5, 2026 Guidance as of October 5, 2026. OPUS-2 is a Phase 3 trial evaluating concomitant administration of VAX-31 with a

  32. Slide 32: Vaxcyte

    VAXCYTE pritecl humanbind

  33. Slide 33: Appendix

    Appendix October 5, 2026

  34. Slide 34: VAX-31 Demonstrated Robust OPA GMT Immune Responses

    VAX-31 Demonstrated Robust OPA GMT Immune Responses October 5, 2026 IgG = immunoglobulin G; GMT = geometric mean titer; OPA = opsonophagocytic activity; ST = serotype. (1) VAX-31 includes serotype 20C; 20B is being evaluated in clinical studies to demonstrate cross-protection. For further detail on

  35. Slide 35: VAX-31 Demonstrated Robust IgG GMC Responses

    VAX-31 Demonstrated Robust IgG GMC Responses October 5, 2026 IgG = immunoglobulin G; GMC = Geometric Mean Concentration; OPA = opsonophagocytic activity; ST = serotype. (1) VAX-31 includes serotype 20C; 20B is being evaluated in clinical studies to demonstrate cross-protection. For further detail on

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