CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 58 enrolled
Drug / intervention
Patients elected to take licensed drugs. The vaccine was not provided for evaluation +3 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00238459
NCT00238459N/ACompleted

Immunopathogenesis of Acute and Early HIV Infection and the Role of HIV-Specific CD4 T Cell Responses and the Effect of Their Enhancement by Potent Antiretroviral Drugs and an HIV Vaccine Adequate Vaccine Was Not Provided.

National Institute of Allergy and Infectious Diseases (NIAID)·observational·Posted Oct 13, 2005·Updated Nov 20, 2013

In Brief

An observational study evaluating Patients elected to take licensed drugs. The vaccine was not provided for evaluation, multiple licensed drugs not randomized, and 2 other interventions for HIV Infections. Completed, enrolled 58 participants across 2 sites in 2 countries.

Detailed Summary

The purpose of this study is to determine the role of HIV-specific CD4 T cell responses and immune responses dependent upon these CD4 responses that develop when antiretroviral drugs are started during acute or recent HIV infection, whether these CD4 responses can be enhanced with a therapeutic HIV vaccine (HIV-1 immunogen), and what pattern of HIV-specific immune responses is associated with control of HIV upon discontinuation of antiretroviral drugs during an analytical therapeutic interruption. Participants will be treatment-naive adults with acute or early HIV infection who will choose to start or not start anti-HIV drugs at the beginning of the study. NOTE: In August 2007 we were notified by the manufacturer of the candidate vaccine that they were no longer making the vaccine, and that the vaccine would no longer be available. Unfortunately too few participants have received either the vaccine or placebo to conclude anything about efficacy. No safety problems occurred.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
ConditionsHIV Infections
CountriesCanada, United States
Collaborators--

Timeline

N/ACompletedFinished
20052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 13, 2005
Enrollment StartJul 1, 2005
Primary CompletionMar 1, 2011
Study CompletionOct 1, 2013
TodayJul 2, 2026
Enrollment to primary: 5.7 yearsPosted 20.7 years ago

Interventions

Patients elected to take licensed drugs. The vaccine was not provided for evaluationdrug

Note:In August 2007 we were notified by the manufacturer that the experimental vaccine was no longer being made and would no longer be available for this study. Too few participants have received the vaccine or placebo to conclude anything about potential efficacy

multiple licensed drugs not randomizeddrug

multiple licensed antiretroviral drugs; not randomizeddrug

Intended vaccine not provided, Licensed drugs provided, but were not investigatedother