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NCT00365612 · ClinicalTrials.gov registry record · Phase 4

Single Tablet Regimen (STR) Simplification Study for HIV-1 Infected Patients

A Phase 4 study, sponsored by Gilead Sciences.

Completed
Registry status
Phase 4
Development phase
300
Enrollment target

NCT00365612: Completed Phase 4 study, sponsored by Gilead Sciences.

NCT00365612 is a Phase 4 study that has completed, run by Gilead Sciences. The registered enrollment target is 300 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (42% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00365612, a Phase 4 study, has completed, sponsored by Gilead Sciences.

COMPLETED
Registry status
Phase 4
Development phase
300 participants
Enrollment target

Study Summary

To compare the effectiveness (efficacy, safety \& tolerability) of a Single Tablet Regimen of efavirenz/emtricitabine/tenofovir DF to subjects continuing on unmodified HAART as measured by the proportion of patients who maintain viral load (HIV-1 RNA) \<200 copies/mL at Week 48.

Interventions

  • DRUG Efavirenz (EFV), Emtricitabine (FTC), Tenofovir DF (TDF)

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2006-07
Est. Completion 2008-01
Phase Phase 4
Gilead Sciences

504 total trials

What the finished NCT00365612 record still lists

NCT00365612 is an interventional study that assigns participants to a tested intervention. The registered 300 participants enrollment target is mid-sized for trials with a published cap, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (42% lower).

The record links to 0 conditions, and to 1 intervention - of which Efavirenz (EFV), Emtricitabine (FTC), Tenofovir DF (TDF) is the first listed.

NCT00365612 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00365612 about?

NCT00365612 is a clinical study titled "Single Tablet Regimen (STR) Simplification Study for HIV-1 Infected Patients". To compare the effectiveness (efficacy, safety \& tolerability) of a Single Tablet Regimen of efavirenz/emtricitabine/tenofovir DF to subjects continuing on unmodified HAART as measured by the proportion of patients who maintain viral load (HIV-1 RNA) \<200 copies/mL at Week 48.

What is the current status of trial NCT00365612?

This trial is currently completed. It is a Phase 4 study. The enrollment target is 300 participants. The study started on 2006-07. Estimated completion is 2008-01.

What interventions are being tested in trial NCT00365612?

The interventions under investigation include: Efavirenz (EFV), Emtricitabine (FTC), Tenofovir DF (TDF) (DRUG).

Who is sponsoring clinical trial NCT00365612?

This trial is sponsored by Gilead Sciences, which has 504 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00365612's enrollment target sits among peer trials

300 269th of 2000 higher than 1,709 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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Source: ClinicalTrials.gov NCT00365612, the US trial registry maintained by the National Library of Medicine. NCT00365612 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.