Status:

COMPLETED

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)

Lead Sponsor:

Merck Sharp & Dohme LLC

Conditions:

Neoplasms, Glandular and Epithelial

Diphtheria

Eligibility:

All Genders

11-17 years

Phase:

PHASE3

Brief Summary

Data from this study are expected to demonstrate that Gardasil (V501, Human Papillomavirus \[Types 6, 11, 16, 18\] Recombinant Vaccine), when administered concomitantly with a combined diphtheria, tet...

Eligibility Criteria

Inclusion

  • Must be healthy boys or girls, 11-17 years of age
  • Must be a virgin with no intention of becoming sexually active during the study period
  • Must have been properly vaccinated against diphtheria, tetanus, pertussis and polio

Exclusion

  • Must not have received a vaccine against diphtheria, tetanus, pertussis and polio in the past 5 years
  • Must not have received any prior human papillomavirus (HPV) vaccine

Key Trial Info

Start Date :

May 1 2006

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

May 1 2007

Estimated Enrollment :

843 Patients enrolled

Trial Details

Trial ID

NCT00337428

Start Date

May 1 2006

End Date

May 1 2007

Last Update

November 16 2016

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