Clinical trial

A Phase I/II Double-Blind Controlled Trial to Determine the Safety and…

NCT00000822 · National Institute of Allergy and Infectious Diseases (NIAID), NIH · Completed

Key facts

NCT number NCT00000822
Title A Phase I/II Double-Blind Controlled Trial to Determine the Safety and Immunogenicity of HIV-1 MN rgp160 Immuno AG Vaccine Therapy in HIV-Infected Individuals With Greater Than or Equal to 500/mm3 CD4+ T Cells and 200-400/mm3 CD4+ T Cells
Official title A Phase I/II Double-Blind Controlled Trial to Determine the Safety and Immunogenicity of HIV-1 MN rgp160 Immuno AG Vaccine Therapy in HIV-Infected Individuals With Greater Than or Equal to 500/mm3 CD4+ T Cells and 200-400/mm3 CD4+ T Cells
Lead sponsor National Institute of Allergy and Infectious Diseases (NIAID), NIH
Collaborators Bristol-Myers Squibb Industry Immuno-US
Status Completed
Phase Phase 1
Study type Interventional
Conditions HIV Infections
Intervention type Biological, Drug
Interventions Ritonavir, gp160 Vaccine (Immuno-AG), Stavudine, Didanosine
Enrollment 46
Completion May 1, 1999
First posted Aug 31, 2001
Last update posted Oct 29, 2021
Countries United States

At a glance

  • 1–9 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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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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