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NCT01376726 · ClinicalTrials.gov registry record · Phase 1

Evaluating the Safety and Immune Response to an HIV Vaccine in Healthy, HIV-Uninfected Adults Who Have Participated in Previous HIV Vaccine Clinical Trials and in Adults Who Have Not Participated in Previous HIV Vaccine Clinical Trials

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

Completed
Registry status
Phase 1
Development phase
36
Enrollment target

NCT01376726: Completed Phase 1 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

NCT01376726 is a Phase 1 study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 36 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01376726, a Phase 1 study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
Phase 1
Development phase
36 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety and immune response to an HIV vaccine in healthy, HIV-uninfected adults who have participated in a previous HIV vaccine clinical trial and in healthy, HIV-uninfected adults who have not participated in a previous HIV vaccine clinical trial.

Interventions

  • BIOLOGICAL Sub C gp140 Vaccine
  • BIOLOGICAL MF59C.1 Adjuvant

Trial Details

FieldValue
Enrollment Target 36 participants
Start Date 2011-07
Est. Completion 2014-12
Phase Phase 1

What the finished NCT01376726 record still lists

NCT01376726 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 36 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (40% lower).

The record links to 0 conditions, and to 2 interventions - of which Sub C gp140 Vaccine is the first listed.

NCT01376726 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01376726 about?

NCT01376726 is a clinical study titled "Evaluating the Safety and Immune Response to an HIV Vaccine in Healthy, HIV-Uninfected Adults Who Have Participated in Previous HIV Vaccine Clinical Trials and in Adults Who Have Not Participated in Previous HIV Vaccine Clinical Trials". The purpose of this study is to evaluate the safety and immune response to an HIV vaccine in healthy, HIV-uninfected adults who have participated in a previous HIV vaccine clinical trial and in healthy, HIV-uninfected adults who have not participated in a previous HIV vaccine clinical trial.

What is the current status of trial NCT01376726?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 36 participants. The study started on 2011-07. Estimated completion is 2014-12.

What interventions are being tested in trial NCT01376726?

The interventions under investigation include: Sub C gp140 Vaccine (BIOLOGICAL), MF59C.1 Adjuvant (BIOLOGICAL).

Who is sponsoring clinical trial NCT01376726?

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

How this trial's enrollment target compares

Where NCT01376726's enrollment target sits among peer trials

36 1210th of 2000 higher than 743 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01376726, the US trial registry maintained by the National Library of Medicine. NCT01376726 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.