Clinical trial

Study Evaluating Vaccine in Adults With HIV

NCT00195312 · Wyeth is now a wholly owned subsidiary of Pfizer, Industry · Terminated

Key facts

NCT number NCT00195312
Title Study Evaluating Vaccine in Adults With HIV
Official title A Phase 1 Multicenter, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Safety and Immunogenicity of an HIV-1 Gag DNA Vaccine Administered Alone or With Escalating Doses of IL-12 DNA or IL-15 DNA Molecular Adjuvants to HIV-1 Positive Adults Receiving Stable HAART.
Lead sponsor Wyeth is now a wholly owned subsidiary of Pfizer, Industry
Status Terminated
Phase Phase 1
Study type Interventional
Conditions HIV Infections
Intervention type Biological
Interventions HIV-1 gag DNA (formulated with bupivacaine), IL-15 DNA (formulated with bupivacaine), IL-12 DNA (formulated with bupivacaine), Sodium chloride injection USP (0.9%)
Enrollment 91
Start date Aug 1, 2005
Completion Aug 1, 2007
First posted Sep 19, 2005
Last update posted Dec 5, 2007
Countries Germany, Sweden, United States

At a glance

  • 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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