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A Phase 2, Randomized, Double-Blind, Active-Controlled, Dose-Finding Clinical Study to Evaluate the Safety, Tolerability, and Immunogenicity of VAX-31 in Healthy Infants Given 4 Doses at 2, 4, 6, and 12-15 Months of Age Concomitantly With Routine Pediatric Vaccines

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Trial Profile

A Phase 2, Randomized, Double-Blind, Active-Controlled, Dose-Finding Clinical Study to Evaluate the Safety, Tolerability, and Immunogenicity of VAX-31 in Healthy Infants Given 4 Doses at 2, 4, 6, and 12-15 Months of Age Concomitantly With Routine Pediatric Vaccines

Status: Recruiting
Phase of Trial: Phase II

Latest Information Update: 10 Dec 2024

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At a glance

  • Drugs VAX 31 (Primary) ; PCV 20
  • Indications Pneumococcal infections
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors Vaxcyte

    • Most Recent Events

    • 03 Dec 2024 Status changed from planning to recruiting, according to Vaxcyte media release.
    • 03 Dec 2024 According to a Vaxcyte media release, this trial has been initiated and the first study participants have been dosed. The company expects topline data from the booster dose approximately 9 months after the announcement of topline data of the primary three-dose immunization series (in mid-2026).
    • 23 Sep 2024 New trial record

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