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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 is a Phase 4 study that has completed, run by Gilead Sciences. The registered enrollment target is 52 participants.

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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

FieldValue
Enrollment Target 52 participants
Start Date 2004-10
Est. Completion 2007-01
Phase Phase 4

Sponsor

Gilead Sciences

504 total trials

What the Registry Record Tells You About NCT00106379

The ClinicalTrials.gov registry entry for NCT00106379 describes a study currently listed as completed, categorized as Phase 4. The registered enrollment target is 52 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Gilead Sciences, which has 504 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which Truvada (tenofovir DF + emtricitabine) is the first listed.

NCT00106379 reports 0 study locations.

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.

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.