drugset / Trial / NCT07653100

A Phase 3 Study in India to Describe the Safety and Immunogenicity of RSVpreF

NCT07653100

Phase 3 Not yet recruiting 540 enrolled Pfizer
RandomizedParallel-groupDouble-blindPrevention

Summary

The purpose of this phase 3 multicenter, double-blinded, placebo-controlled study in India is to learn about the safety and immunogenicity of RSVpreF in adults.

Timeline

Start
2026-06-22
Primary completion
2027-01-25
Completion
2027-01-25

Drugs

EvaluationDrugModalityDoseRoute
Subject RSVpreF Vaccine