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Completed Phase 1 Interventional

Safety of and Immune Response to an Investigational HIV-1 Vaccine With or Without Interleukin-12 (IL-12) in HIV-1 Infected Adults

ClinicalTrials.gov ID: NCT01266616

Public ClinicalTrials.gov record NCT01266616. 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 Sep 3, 2026, 3:49 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 I Randomized, Partially Double-Blind, Placebo-Controlled, Dose-Escalation Study to Evaluate the Safety and Immunogenicity of a Cytokine Enhanced HIV-1 Multi-Antigen (HIV MAG) pDNA Vaccine Delivered Intramuscularly Followed by in Vivo Electroporation (IM/EP) or Intramuscularly in HIV-1 Infected Adults Receiving ART

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Therapeutic HIV vaccines are designed to control HIV infection by boosting the body's natural immune response. There are currently no FDA-approved therapeutic HIV vaccines. This study will test whether giving an HIV-1 vaccine together with or without interleukin 12 (IL-12) is safe and effective. This study will also test a new way of giving the vaccine called electroporation (EP).

Study identification

NCT ID
NCT01266616
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
62 participants

Conditions and interventions

Conditions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
18 Years to 55 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
Feb 28, 2011
Primary completion
Sep 30, 2012
Completion
Mar 31, 2013
Last update posted
Oct 31, 2021

2011 – 2013

United States locations

U.S. sites
13
U.S. states
8
U.S. cities
11
Facility City State ZIP Site status
UCLA CARE Center CRS Los Angeles California 90035
Stanford AIDS Clinical Trials Unit CRS Palo Alto California 94304-5350
Ucsf Hiv/Aids Crs San Francisco California 94110
University of Colorado Hospital CRS Aurora Colorado 80045
Massachusetts General Hospital Clinical Research Site (MGH CRS) CRS Boston Massachusetts 02114
Brigham and Women's Hospital Therapeutics Clinical Research Site (BWH TCRS) CRS Boston Massachusetts 02115
Washington University Therapeutics (WT) CRS St Louis Missouri 63110
Trillium Health ACTG CRS Rochester New York 14607
Univ. of Rochester ACTG CRS Rochester New York 14642
Cincinnati CRS Cincinnati Ohio 45219
Penn Therapeutics Crs Philadelphia Pennsylvania 19104
University of Pittsburgh CRS Pittsburgh Pennsylvania 15213-2582
Houston AIDS Research Team CRS Houston Texas 77030

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01266616, 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 Oct 31, 2021 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01266616 live on ClinicalTrials.gov.

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