Clinical trial

Safety and Effectiveness of the Oral HIV Entry Inhibitor Vicriviroc in HIV…

NCT00082498 · National Institute of Allergy and Infectious Diseases (NIAID), NIH · Completed

Key facts

NCT number NCT00082498
Title Safety and Effectiveness of the Oral HIV Entry Inhibitor Vicriviroc in HIV Infected Patients
Official title Phase II, Randomized, Double-Blind Study of the Safety and Efficacy of Vicriviroc (An Orally Administered HIV-1 Entry Inhibitor) in HIV-Infected, Treatment-Experienced Subjects
Lead sponsor National Institute of Allergy and Infectious Diseases (NIAID), NIH
Collaborators Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections
Status Completed
Phase Phase 2
Study type Interventional
Conditions HIV Infections
Intervention type Drug
Interventions SCH-D (vicriviroc), Placebo
Enrollment 119
Start date May 1, 2004
Primary completion Dec 1, 2005
Completion Jan 1, 2011
First posted May 12, 2004
Last update posted Nov 1, 2021
Countries United States

At a glance

  • 10–99 Study sites
  • No 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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