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Terminated Phase 1 Interventional

Study Evaluating Vaccine in Adults With HIV

ClinicalTrials.gov ID: NCT00195312

Public ClinicalTrials.gov record NCT00195312. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 24, 2026, 9:51 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

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.

Study identification

NCT ID
NCT00195312
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Enrollment
91 participants

Conditions and interventions

Conditions

Interventions

  • HIV-1 gag DNA (formulated with bupivacaine) Biological
  • IL-15 DNA (formulated with bupivacaine) Biological
  • IL-12 DNA (formulated with bupivacaine) Biological
  • Sodium chloride injection USP (0.9%) Biological

Biological

Eligibility (public fields only)

Age range
18 Years to 50 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jul 31, 2005
Primary completion
Not listed
Completion
Jul 31, 2007
Last update posted
Dec 4, 2007

2005 – 2007

United States locations

U.S. sites
6
U.S. states
5
U.S. cities
6
Facility City State ZIP Site status
Not listed Birmingham Alabama 35294
Not listed Denver Colorado 80262
Not listed Orlando Florida 32803
Not listed Boston Massachusetts 02215
Not listed Austin Texas 78705
Not listed Dallas Texas 75246

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00195312, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Dec 4, 2007 · Synced Jul 24, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00195312 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →