Clinical trial

Study to Evaluate the Safety and Immunogenicity of Pandemic Monovalent (H5N1)…

NCT00309647 · GlaxoSmithKline, Industry · Completed

Key facts

NCT number NCT00309647
Title Study to Evaluate the Safety and Immunogenicity of Pandemic Monovalent (H5N1) Influenza Vaccines (Whole Virus Formulation) in Adults 18 and 60 Years of Age
Official title A Partially-blind Multi-centric Study in Adults Aged Between 18-60 Years Designed to Evaluate the Reactogenicity and Immunogenicity of 1 and 2 Doses of Pandemic Monovalent (H5N1) Influenza Vaccines (Whole Virus Formulation) Administered at Different Doses and Adjuvanted or Not
Lead sponsor GlaxoSmithKline, Industry
Status Completed
Phase Phase 1
Study type Interventional
Conditions Influenza
Intervention type Biological
Interventions Influenza Monovalent Whole virus (H5N1) adjuvanted vaccine, Influenza Monovalent Whole virus (H5N1)
Enrollment 400
Start date Mar 29, 2006
Primary completion Nov 1, 2006
Completion Nov 16, 2006
First posted Apr 3, 2006
Last update posted May 8, 2017
Countries Germany

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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