Clinical Trial

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

Recruiting Phase 3
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Summary
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.
Protocol Amendment History 1 change
notable Trial sites expanded: 1 -> 7 locations 2026-04-16
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