Clinical Trials Directory

Trials / Completed

CompletedNCT00928785

Study Comparing a Tdap-IPV Combined Vaccine With a Tetanus Monovalent Vaccine in Healthy Adults

A Randomised, Comparative, Multicentre Clinical Trial of the Immunogenicity and Safety of Tdap-IPV Vaccine and a Tetanus Monovalent Vaccine in Healthy Adults 18 Years of Age and Older

Status
Completed
Phase
Phase 3
Study type
Interventional
Enrollment
52 (actual)
Sponsor
Sanofi Pasteur, a Sanofi Company · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to demonstrate that a combined adult Tdap-IPV vaccine (REPEVAX®) will provide similar rapid antibody responses against tetanus toxoid as a tetanus toxoid vaccine alone in healthy adults.

Conditions

Interventions

TypeNameDescription
BIOLOGICALREPEVAX1 dose of 0.5 mL at Day 0
BIOLOGICALMonovalent Tetanus vaccine1 dose of 0.5 mL at Day 0

Timeline

Start date
2009-07-01
Primary completion
2009-12-01
Completion
2009-12-01
First posted
2009-06-26
Last updated
2017-09-11

Locations

9 sites across 2 countries: France, Germany

Source: ClinicalTrials.gov record NCT00928785. Inclusion in this directory is not an endorsement.