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NCT00106379 · ClinicalTrials.gov registry record · Phase 4
Tenofovir DF (Disoproxil Fumarate) in Combination With Emtricitabine in HIV-1 Patients
A Phase 4 study, sponsored by Gilead Sciences.
- Completed
- Registry status
- Phase 4
- Development phase
- 52
- Enrollment target
NCT00106379: Completed Phase 4 study, sponsored by Gilead Sciences.
NCT00106379 is a Phase 4 study that has completed, run by Gilead Sciences. The registered enrollment target is 52 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00106379, a Phase 4 study, has completed, sponsored by Gilead Sciences.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 52 participants
- Enrollment target
Study Summary
The purpose of this study is to provide long-term clinical safety and efficacy data for tenofovir disoproxil fumarate and emtricitabine in HIV-infected patients experiencing various degrees of renal impairment.
Interventions
- DRUG Truvada (tenofovir DF + emtricitabine)
- DRUG Emtriva (emtricitabine)
- DRUG Viread (tenofovir DF)
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 52 participants |
| Start Date | 2004-10 |
| Est. Completion | 2007-01 |
| Phase | Phase 4 |
What the finished NCT00106379 record still lists
NCT00106379 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 52 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (90% lower).
The record links to 0 conditions, and to 3 interventions - of which Truvada (tenofovir DF + emtricitabine) is the first listed.
NCT00106379 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00106379 about?
NCT00106379 is a clinical study titled "Tenofovir DF (Disoproxil Fumarate) in Combination With Emtricitabine in HIV-1 Patients". The purpose of this study is to provide long-term clinical safety and efficacy data for tenofovir disoproxil fumarate and emtricitabine in HIV-infected patients experiencing various degrees of renal impairment.
What is the current status of trial NCT00106379?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 52 participants. The study started on 2004-10. Estimated completion is 2007-01.
What interventions are being tested in trial NCT00106379?
The interventions under investigation include: Truvada (tenofovir DF + emtricitabine) (DRUG), Emtriva (emtricitabine) (DRUG), Viread (tenofovir DF) (DRUG).
Who is sponsoring clinical trial NCT00106379?
This trial is sponsored by Gilead Sciences, which has 504 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00106379's enrollment target sits among peer trials
52 1233rd of 2000 higher than 752 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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