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NCT00472719 · ClinicalTrials.gov registry record · Phase 1

Safety of and Immune Response to a DNA HIV Vaccine Followed By Boosting With One of Two Serotypes of Adenoviral Vector HIV Vaccine in Healthy Adults

A Phase 1 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Completed
Registry status
Phase 1
Development phase
17
Enrollment target

NCT00472719 is a Phase 1 study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 17 participants.

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The verdict

NCT00472719, a Phase 1 study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
Phase 1
Development phase
17 participants
Enrollment target

Study Summary

The purpose of this study is to determine the safety of and immune response to an experimental DNA HIV vaccine followed by boosting with either an experimental adenoviral vector HIV vaccine of serotype 5 or 35 in HIV uninfected adults. This study will also determine the safety of and immune response to an adenoviral vector HIV vaccine of serotype 5 followed by a booster of an adenoviral vector of serotype 35, or vice versa, in HIV uninfected adults.

Interventions

  • BIOLOGICAL VRC-HIVADV027-00-VP
  • BIOLOGICAL VRC-HIVADV038-00-VP
  • BIOLOGICAL VRC-HIVDNA044-00-VP

Trial Details

FieldValue
Enrollment Target 17 participants
Start Date 2007-08
Est. Completion 2013-01
Phase Phase 1

What the Registry Record Tells You About NCT00472719

The ClinicalTrials.gov registry entry for NCT00472719 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 17 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which VRC-HIVADV027-00-VP is the first listed.

NCT00472719 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00472719 about?

NCT00472719 is a clinical study titled "Safety of and Immune Response to a DNA HIV Vaccine Followed By Boosting With One of Two Serotypes of Adenoviral Vector HIV Vaccine in Healthy Adults". The purpose of this study is to determine the safety of and immune response to an experimental DNA HIV vaccine followed by boosting with either an experimental adenoviral vector HIV vaccine of serotype 5 or 35 in HIV uninfected adults. This study will also determine the safety of and immune response...

What is the current status of trial NCT00472719?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 17 participants. The study started on 2007-08. Estimated completion is 2013-01.

What interventions are being tested in trial NCT00472719?

The interventions under investigation include: VRC-HIVADV027-00-VP (BIOLOGICAL), VRC-HIVADV038-00-VP (BIOLOGICAL), VRC-HIVDNA044-00-VP (BIOLOGICAL).

Who is sponsoring clinical trial NCT00472719?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.