Trial Profile

A Phase 1, First-Time-in-Human (FTiH), Observer-blind, Randomized, Controlled Study to Evaluate the Safety, Reactogenicity and Immune Response of Various Doses of an mRNA-based Respiratory Syncytial Virus (RSV) Investigational Vaccine in Healthy Participants 18-45 Years of Age

Status: Active, no longer recruiting

Phase of Trial: Phase I

Latest Information Update: 25 Jun 2025

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At a glance

Drugs MRNA-based-respiratory-syncytial-virus-vaccine-GlaxoSmithKline (Primary)
Indications Respiratory syncytial virus infections
Focus Adverse reactions; First in man
Sponsors GSK

18 Jun 2025 Planned End Date changed from 24 Aug 2026 to 20 Apr 2026.
18 Jun 2025 Planned primary completion date changed from 24 Aug 2026 to 20 Apr 2026.
05 Mar 2025 Planned End Date changed from 17 Jul 2026 to 24 Aug 2026.

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