Clinical trial
A Phase II, Randomized, Controlled, Double-blind, Multi-center, Study to Evaluate Safety and Immunogenicity of Two Doses, Administered Three Weeks Apart, of Two Monovalent H5N1 (Surface Antigen Adjuvanted With MF59C.1) Influenza Vaccines Containing 3.75 µg or 7.5 μg of H5N1 Influenza Antigen, in Non-elderly Adult and Elderly Subjects
NCT00914771 is registered in ClinicalTrials.gov with Novartis Vaccines as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase II, Randomized, Controlled, Double-blind, Multi-center, Study to Evaluate Safety and Immunogenicity of Two Doses, Administered Three Weeks Apart, of Two Monovalent H5N1 (Surface Antigen Adjuvanted With MF59C.1) Influenza Vaccines Containing 3.75 µg or 7.5 μg of H5N1 Influenza Antigen, in Non-elderly Adult and Elderly Subjects
- Lead sponsor
- Novartis Vaccines
- Phase
- Phase 2
- Overall status
- Completed
- Start date
- September 30, 2009
- Completion date
- December 31, 2009
- Enrollment
- 722 (actual)
- Sites
- 12
Conditions
As the registry lists them; a condition with its own page is linked.
pandemic h5n1 influenza