CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 769 enrolled
Drug / intervention
Tetanus, Reduced Diphtheria Toxoid and Acellular Pertussis (ADACEL®) +1 morebiological
Likely dose
Tetanus, Reduced Diphtheria Toxoid and Acellular Pertussis (ADACEL®) 0.5 mlfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00712959
NCT00712959Phase 4Completed

Immune Responses in Adults to Revaccination With Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine Adsorbed (ADACEL®) 10 Years After a Previous Dose

Sanofi Pasteur, a Sanofi Company·interventional·Posted Jul 10, 2008·Updated Apr 30, 2014

In Brief

A Phase 4 clinical trial evaluating Tetanus, Reduced Diphtheria Toxoid and Acellular Pertussis (ADACEL®) for Pertussis and 2 related conditions. Completed, enrolled 769 participants across 7 sites.

Detailed Summary

The purpose of this study is to collect additional immunogenicity and safety data on re-dosing with Tdap vaccine (ADACEL®) in a continuing effort to address the public health need to establish broader population immunity against pertussis, as well as diphtheria and tetanus. Primary Objective: * To assess immune response to Tdap vaccine (ADACEL®) one month after booster vaccination.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada
Collaborators--

Timeline

Phase 4CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJul 10, 2008
Enrollment StartJun 1, 2008
Primary CompletionSep 1, 2009
Study CompletionDec 1, 2009
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 18.0 years ago

Interventions

Tetanus, Reduced Diphtheria Toxoid and Acellular Pertussis (ADACEL®)biological

0.5 ml, IM

Tetanus, Reduced Diphtheria Toxoid and Acellular Pertussis (ADACEL®)biological

0.5 mL, IM