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More info
You can access this
clinical trial
if you have
Influenza, Pandemic Influenza or Influenza A Virus, H1N1 Subtype
and you are
over 18
years old
3
This is a trial in the final phase before the treatment is released on the market.
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The purpose

The purpose of this study is to assess the safety and immunogenicity of one dose of A/H1N1 non-adjuvanted pandemic vaccine to support registration of the vaccine in India. Primary Objective: - To describe the safety profile (injection site reactions and systemic events) of the vaccine within 21 days following vaccination, and serious adverse events throughout the study in all subjects Secondary Objectives: - To describe the immune response to the vaccine 21 days after vaccination by hemagglutination inhibition (HAI) testing in all subjects - To describe the antibody persistence 6 months after vaccination by HAI testing in all subjects.

Provided treatments

  • Biological: A/H1N1 pandemic influenza vaccine (non- adjuvanted)

Locations near you

Unfortunately, there are no recruiting locations near you. Please check the list with all locations below.
Tris trial is registered with FDA with number: NCT01053143. The sponsor of the trial is Sanofi Pasteur, a Sanofi Company and it is looking for 100 volunteers for the current phase.
Official trial title:
Bridging Study on Safety and Immunogenicity of an Intramuscular Inactivated, Split Virion Swine-Origin A/H1N1 Influenza Non-Adjuvanted Vaccine in Healthy Adults in India