Clinical Trials Directory

Trials / Completed

CompletedNCT00325260

Non-Inferiority Study Comparing the Subunit Vaccines Influvac and Agrippal in China

A Randomized, Endpoint-Blind, Parallel Group Study to Demonstrate the Non-Inferiority of the Subunit Influenza Vaccine Influvac® to the Subunit Influenza Vaccine Agrippal® in Healthy Children, Adults and Elderly in China.

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
900 (planned)
Sponsor
Solvay Pharmaceuticals · Industry
Sex
All
Age
3 Years
Healthy volunteers
Accepted

Summary

In the study Influvac will be compared to Agrippal, another subunit influenza vaccine that is already on the market in China. The main objective of the study is to show that both vaccines are comparable with regard to efficacy. In addition, safety and efficacy data with Influvac will be assessed in the Chinese population.

Conditions

Interventions

TypeNameDescription
BIOLOGICALInfluvac; subunit influenza vaccine

Timeline

Start date
2006-03-01
First posted
2006-05-12
Last updated
2006-11-01

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT00325260. Inclusion in this directory is not an endorsement.

Non-Inferiority Study Comparing the Subunit Vaccines Influvac and Agrippal in China (NCT00325260) · Clinical Trials Directory