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NCT01260727 · ClinicalTrials.gov registry record · Phase 1
Evaluating the Safety of and Immune Response to an HIV Vaccine Followed by Booster, Administered by Two Devices, in HIV-Uninfected Adults
A Phase 1 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).
- Completed
- Registry status
- Phase 1
- Development phase
- 92
- Enrollment target
NCT01260727: Completed Phase 1 study, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).
NCT01260727 is a Phase 1 study that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 92 participants, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (53% higher). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01260727, a Phase 1 study, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 92 participants
- Enrollment target
Study Summary
The purpose of this study is to evaluate the safety of and immune response to an HIV vaccine, administered using two different devices, followed by a vaccine boost, in healthy, HIV-uninfected adults.
Interventions
- BIOLOGICAL PENNVAX-G DNA Vaccine
- BIOLOGICAL MVA-CMDR Vaccine
- BIOLOGICAL Placebo PENNVAX-G Vaccine
- BIOLOGICAL Placebo MVA-CMDR Vaccine
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 92 participants |
| Start Date | 2010-02 |
| Est. Completion | 2015-06 |
| Phase | Phase 1 |
What the finished NCT01260727 record still lists
NCT01260727 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 92 participants, a relatively small participant target, above the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (53% higher).
The record links to 0 conditions, and to 4 interventions - of which PENNVAX-G DNA Vaccine is the first listed.
NCT01260727 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01260727 about?
NCT01260727 is a clinical study titled "Evaluating the Safety of and Immune Response to an HIV Vaccine Followed by Booster, Administered by Two Devices, in HIV-Uninfected Adults". The purpose of this study is to evaluate the safety of and immune response to an HIV vaccine, administered using two different devices, followed by a vaccine boost, in healthy, HIV-uninfected adults.
What is the current status of trial NCT01260727?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 92 participants. The study started on 2010-02. Estimated completion is 2015-06.
What interventions are being tested in trial NCT01260727?
The interventions under investigation include: PENNVAX-G DNA Vaccine (BIOLOGICAL), MVA-CMDR Vaccine (BIOLOGICAL), Placebo PENNVAX-G Vaccine (BIOLOGICAL), Placebo MVA-CMDR Vaccine (BIOLOGICAL).
Who is sponsoring clinical trial NCT01260727?
This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01260727's enrollment target sits among peer trials
92 625th of 2000 higher than 1,375 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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