Clinical trial

Safety and Immunogenicity of Two Adjuvanted and One Non-adjuvanted H5N1…

NCT00382187 · Novartis Vaccines, Industry · Completed

Key facts

NCT number NCT00382187
Title Safety and Immunogenicity of Two Adjuvanted and One Non-adjuvanted H5N1 Influenza Vaccine in Adults
Official title A Phase II, Randomized, Controlled, Observer-blind, Single-Center Study to Evaluate Safety and Immunogenicity of Two Doses, Administered Three Weeks Apart, and a Six Month Booster Dose of Two Surface Antigen Adjuvanted With MF59C.1 Influenza Vaccines Containing 7.5 Micrograms or 15 Micrograms of…
Lead sponsor Novartis Vaccines, Industry
Status Completed
Phase Phase 2
Study type Interventional
Conditions Influenza
Intervention type Biological
Interventions MF59 adjuvanted H5N1 influenza vaccine
Enrollment 40
Start date Nov 1, 2006
Primary completion Jan 1, 2008
Completion Jan 1, 2008
First posted Sep 28, 2006
Last update posted Dec 1, 2016
Countries Italy

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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