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Lot-to-lot Consistency Study of a 21-valent Pneumococcal Conjugate Vaccine in Healthy Infants From 2 Months of Age

← catalyst calendar

NCT07348692 · readout in 292 d

Sponsored by Sanofi (industry) · SNY — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · Quadruple · Prevention
Enrollment
2,195estimated
Sites
19
Countries
Honduras, Puerto Rico, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-01-20actualWhen the study began enrolling
Primary completion2027-06-07estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-05-29estimatedThe whole study's end, after follow-up
First posted2026-01-16actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-05-22actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Conditions

  • Pneumococcal Immunization
  • Healthy Volunteers

Interventions

  • Biological: PCV21 vaccine — also filed as 515
  • Biological: 20vPCV licensed vaccine — also filed as Prevnar 20™

Primary outcome

what the primary-completion date above is the date OF
For all participants: Serotype specific Immunoglobulin g (IgG) Geometric Mean Concentration (GMC)
measured 30 days after the third dose of PCV21 vaccine

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