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Study of a Single Dose of a 21-valent Pneumococcal Conjugate Vaccine in Children and Adolescents With Sickle Cell Disease

StatusRecruiting
PhasePhase 3
SponsorSanofi
Started2026-01-20
View on ClinicalTrials.gov ↗
The purpose of this study is to measure whether PCV21 vaccine (investigational pneumococcal vaccine) is safe and can help the body to develop germ-fighting agents called "antibodies" (immunogenicity) compared with 20vPCV (licensed pneumococcal vaccine) when given as a single dose to children aged 2 to 17 years with sickle cell disease who had received or not a previous vaccination with pneumococcal conjugate or pneumococcal polysaccharide vaccine.

Amendment history 1 change detected by DataLookout

2026-04-16
minor
Trial sites expanded: 1 → 7 locations
Trial Details
NCT Number NCT07247188
Lead Sponsor Sanofi
Conditions Sickle Cell Disease
Enrollment 100 participants
Start Date 2026-01-20
Primary Completion 2027-01-07 (estimated)
Study Completion 2027-01-07 (estimated)
Updated on ClinicalTrials.gov 2026-04-15