Clinical trial
Post-Licensure Safety Surveillance Study of Routine Use of PENTACEL® Diphtheria and Tetanus Toxoids and Acellular Pertussis Adsorbed, Inactivated Poliovirus and Haemophilus b Conjugate (Tetanus Toxoid Conjugate) Vaccine
NCT00804284 is registered in ClinicalTrials.gov with Sanofi Pasteur, a Sanofi Company as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Post-Licensure Safety Surveillance Study of Routine Use of PENTACEL® Diphtheria and Tetanus Toxoids and Acellular Pertussis Adsorbed, Inactivated Poliovirus and Haemophilus b Conjugate (Tetanus Toxoid Conjugate) Vaccine
- Lead sponsor
- Sanofi Pasteur, a Sanofi Company
- Phase
- Observational
- Overall status
- Completed
- Start date
- September 30, 2008
- Completion date
- January 31, 2015
- Enrollment
- 62,538 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
diphtheria, haemophilus influenzae, pertussis, tetanus