Clinical trial

Safety, Tolerability and Immune Response to LC002, an Experimental Therapeutic…

NCT00270205 · National Institute of Allergy and Infectious Diseases (NIAID), NIH · Completed

Key facts

NCT number NCT00270205
Title Safety, Tolerability and Immune Response to LC002, an Experimental Therapeutic Vaccine, in Adults Receiving HAART
Official title A Phase I/II, Randomized, Double-Blind Study to Evaluate the Safety, Tolerability, and Immunogenicity of LC002, a DermaVir Vaccine, in HIV-1-Infected Subjects Currently Under Treatment With Highly Active Antiretroviral Therapy (HAART)
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 1/Phase 2
Study type Interventional
Conditions HIV Infections
Intervention type Biological
Interventions LC002 standard vaccination, LC002 high-dose vaccination, LC002 placebo vaccination
Enrollment 28
Start date Jan 1, 2006
Primary completion Sep 1, 2010
Completion Sep 1, 2010
First posted Dec 26, 2005
Last update posted Nov 4, 2021
Countries United States

At a glance

  • 1–9 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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