Clinical trial

Safety of and Immune Response to a Novel Human Papillomavirus Vaccine in HIV…

NCT00339040 · National Institute of Allergy and Infectious Diseases (NIAID), NIH · Completed

Key facts

NCT number NCT00339040
Title Safety of and Immune Response to a Novel Human Papillomavirus Vaccine in HIV Infected Children
Official title Phase II Safety and Immunogenicity Study of Quadrivalent Human Papillomavirus (Types 6, 11, 16, 18) L1 Virus-Like Particle (VLP) Vaccine in HIV Infected Children 7 to 12 Years of Age
Lead sponsor National Institute of Allergy and Infectious Diseases (NIAID), NIH
Collaborators Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD) NIH
Status Completed
Phase Phase 2
Study type Interventional
Conditions HIV Infections, Sexually Transmitted Diseases
Intervention type Biological, Other
Interventions Quadrivalent human papillomavirus (types 6, 11, 16, 18) L1 virus-like particle (VLP) or Quadrivalent human papillomavirus vaccine (QHPV), Placebo/QHPV
Enrollment 130
Start date Oct 1, 2006
Primary completion Aug 1, 2009
Completion Aug 1, 2009
First posted Jun 20, 2006
Last update posted Nov 5, 2021
Countries Puerto Rico, United States

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

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

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

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