A Phase 1/2, First-Time-in Human (FTiH), Randomized, Observer-blind, Placebo-controlled, Dose Escalation Study to Assess Safety, Reactogenicity and Immunogenicity of a Candidate Cytomegalovirus (CMV) Vaccine Comprising Recombinant Protein and Adjuvant When Administered Intramuscularly in Healthy Adults
Latest Information Update: 23 May 2025
At a glance
- Drugs GSK 3993129A (Primary)
- Indications Cytomegalovirus infections
- Focus Adverse reactions; First in man
- Sponsors GlaxoSmithKline; GSK
Most Recent Events
- 14 May 2025 Status changed from active, no longer recruiting to completed.
- 27 Dec 2024 Planned End Date changed from 19 Jun 2029 to 6 Jun 2025.
- 27 Dec 2024 Planned primary completion date changed from 19 Jun 2029 to 6 Jun 2025.