- Vaxcyte reported that enrollment is complete in the OPUS-1 Phase 3 trial of VAX-31 with about 4,000 participants and the OPUS-2 Phase 3 trial with about 1,300 participants.
- OPUS-1 is a randomized, double-blind, active-controlled noninferiority study comparing VAX-31 with Capvaxive (PCV21) and Prevnar 20 (PCV20) in pneumococcal-naïve adults ages 50 and older, with a separate cohort ages 18–49.
- Participants ages 50 and older were randomized 1:1:1 to VAX-31, PCV21, or PCV20, while adults ages 18–49 were randomized 3:1 to VAX-31 or PCV20.
- Topline safety, tolerability, and immunogenicity results from OPUS-1 are expected in the fourth quarter of 2026.
- OPUS-2 is evaluating concomitant administration of VAX-31 with a seasonal influenza vaccine, with results expected in the first half of 2027.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Vaxcyte Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603230830PRIMZONEFULLFEED9676418) on March 23, 2026, and is solely responsible for the information contained therein.