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
| Type | Name | Description |
|---|---|---|
| BIOLOGICAL | REPEVAX | 1 dose of 0.5 mL at Day 0 |
| BIOLOGICAL | Monovalent Tetanus vaccine | 1 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.