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Streptococcus pneumoniae serotype 10A capsular antigen diphtheria CRM197 protein conjugate vaccine

Generic: Streptococcus pneumoniae serotype 10A capsular antigen diphtheria CRM197 protein conjugate vaccine·Brand: Capvaxive, Prevnar 20

Streptococcus pneumoniae serotype 10A capsular antigen diphtheria CRM197 protein conjugate vaccine: 4 clinical trials tracked.

Streptococcus pneumoniae serotype 10A capsular antigen diphtheria CRM197 protein conjugate vaccine evidence translation

What we can confirm

4 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about Streptococcus pneumoniae serotype 10A capsular antigen diphtheria CRM197 protein conjugate vaccine, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence1 indications · 2 study sponsors
Clinical Trial Registry Records (4)

A Phase 1, Randomized, Double-Blind, Comparator-Controlled Dose-Escalation Study to Evaluate the Safety, Tolerability, and Immunogenicity of V132 in Healthy Older Participants

NCT07712575Registry updated 2026-10-05·Phase 1
Recruiting

Primary endpoint: Percentage of Participants with Immediate Reactions Occurring Within 30 Minutes After Any Vaccination

InterventionalRandomizeddouble280 targetStarted 2026-08Completion 2028-0610 sites · United StatesMerck Sharp & Dohme LLC

A Randomized, Double-Blind Study to Evaluate the Safety, Tolerability, and Immunogenicity of V118 Formulation E in Healthy Adults

NCT07168915Registry updated 2026-07-15·Phase 1
Recruiting

Primary endpoint: Number of Participants With Solicited Injection-Site Adverse Events (AEs)

InterventionalRandomizeddouble126 targetStarted 2025-10Completion 2027-074 sites · United StatesMerck Sharp & Dohme LLC

A PHASE 3, RANDOMIZED, PLACEBO-CONTROLLED, DOUBLE-BLINDED TRIAL TO EVALUATE THE SAFETY, TOLERABILITY, AND IMMUNOGENICITY OF A MULTIVALENT GROUP B STREPTOCOCCUS VACCINE IN HEALTHY PREGNANT WOMEN AND THEIR INFANTS

NCT07160244Registry updated 2026-06-23·Phase 3·PFE
Recruiting

Primary endpoint: The proportion of maternal participants reporting prespecified local reactions within 7 days following study intervention

InterventionalRandomizedquadruple6,000 targetStarted 2025-08Completion 2029-0350 sites · United StatesPfizer

A Phase 1/2, Randomized, Observer-Blind, Dose-Finding, Active-Controlled, Parallel-Group, Clinical Study to Evaluate the Safety, Tolerability, and Immunogenicity of a 31-Valent Pneumococcal Conjugate Vaccine (VAX-31) in Healthy Adults Aged 50 Years and Older

NCT06151288Registry updated 2025-07-28·Phase 1/Phase 2·PCVX
Completed

Primary endpoint: Percentage of Subjects Reporting Solicited Local Reactions Within 7 Days After Vaccination (Redness, Swelling, and Pain at Injection Site) in Each Age Group

InterventionalRandomizedquadruple1,015 enrolledStarted 2023-11Completion 2024-0725 sites · United StatesVaxcyte, Inc.