Clinical trial

Concomitant Use of Gardasil (V501, Human Papillomavirus [Types 6, 11, 16, 18]…

NCT00337428 · Merck Sharp & Dohme LLC, Industry · Completed

Key facts

NCT number NCT00337428
Title Concomitant Use of Gardasil (V501, Human Papillomavirus [Types 6, 11, 16, 18] Recombinant Vaccine) With Combined Diptheria, Tetanus, Pertussis and Poliomyelitis Vaccine in Adolescents (V501-024)(COMPLETED)
Official title An Open-Label, Randomized, Multicenter Study of the Safety, Tolerability, and Immunogenicity of Gardasil (V501) Given Concomitantly With REPEVAX™ in Healthy Adolescents 11-17 Years of Age
Lead sponsor Merck Sharp & Dohme LLC, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Neoplasms, Glandular and Epithelial, Diphtheria, Tetanus, Whooping Cough, Poliomyelitis
Intervention type Biological
Interventions Comparator: Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) Recombinant (qHPV) Vaccine from Current Manufacturing Facility (CMF), 18) Recombinant (qHPV) Vaccine from Future Manufacturing Facility (FMF), Comparator: REPEVAX™ (Concomitant), Comparator: REPEVAX™ (Non-Concomitant)
Enrollment 843
Start date May 1, 2006
Primary completion May 1, 2007
Completion May 1, 2007
First posted Jun 16, 2006
Last update posted Nov 16, 2016

At a glance

  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies