Clinical trial

Study to Evaluate Safety and Immunogenicity of the GSK Bio CMV Vaccine in…

NCT00435396 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00435396
Title Study to Evaluate Safety and Immunogenicity of the GSK Bio CMV Vaccine in CMV-seronegative Healthy Male Adult Subjects
Official title A Phase I, Open-label, Vaccination Study to Evaluate the Safety and Immunogenicity of the GSK Biologicals Recombinant CMV gB Sub-unit Vaccine GSK1492903A in CMV-seronegative Healthy Male Adult Subjects
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 1
Study type Interventional
Conditions Infections, Cytomegalovirus
Intervention type Biological
Interventions GSK Biologicals' Recombinant CMV gB Vaccine GSK1492903A
Enrollment 40
Start date Feb 22, 2007
Primary completion Aug 27, 2008
Completion Aug 27, 2008
First posted Feb 15, 2007
Last update posted May 30, 2017
Countries Belgium

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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