drugset / Trial / NCT05393037

Safety and Immunogenicity of V116 in Adults Living With Human Immunodeficiency Virus (HIV) (V116-007, STRIDE-7)

NCT05393037

Phase 3 Completed 313 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindPrevention

Summary

This study will evaluate the safety, tolerability, and immunogenicity of a pneumococcal 21-valent conjugate vaccine (V116) in persons living with human immunodeficiency virus (HIV), for the prevention of pneumococcal disease caused by the serotypes in the vaccine.

Timeline

Start
2022-07-13
Primary completion
2023-07-13
Completion
2024-01-25

Drugs

EvaluationDrugModalityDoseRoute
Comparator Pneumovax 23 Vaccine 0.5 ml Intramuscular
Comparator V114 Vaccine 0.5 ml Intramuscular
Subject V116 Vaccine 0.5 ml Intramuscular