TrialSignal
Clinical trial intelligence report
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
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT06573281-Jul 28, 2026
NCT ID
NCT06573281
Status
ACTIVE_NOT_RECRUITING
Phase
Phase 1
Sponsor
GlaxoSmithKline
Executive brief
Investment-Ready Snapshot
GlaxoSmithKline (GSK) is advancing an mRNA-based vaccine targeting Respiratory Syncytial Virus (RSV) in a Phase 1 clinical trial. The trial aims to evaluate the safety, reactogenicity, and immune response of various vaccine formulations in healthy adults aged 18-45. Given the significant unmet medical need for effective RSV vaccines, particularly in vulnerable populations such as infants and the elderly, successful outcomes could position GSK favorably in a competitive landscape that includes other mRNA vaccine developers. The trial's active status, despite not currently recruiting, indicates ongoing commitment to this asset, with potential implications for future partnerships or licensing opportunities. The market for RSV vaccines is expected to grow, driven by increasing awareness and demand for preventive measures against respiratory infections.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06573281
Indication
Respiratory Syncytial Virus Infections
Modality
vaccine
Target
Respiratory Syncytial Virus (RSV) through mRNA technology
Intervention
Investigational RSV vaccine 1, Investigational RSV vaccine 2, Investigational RSV vaccine 3, Investigational RSV vaccine 4, Investigational RSV vaccine 5, Investigational RSV vaccine 6, Placebo
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.