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NCT00046176 · ClinicalTrials.gov registry record · Phase 3

A HIV Study Of A Fixed-Dose Combination Tablet In Antiretroviral Experienced Patients

A Phase 3 study, sponsored by ViiV Healthcare.

Completed
Registry status
Phase 3
Development phase
240
Enrollment target

NCT00046176: Completed Phase 3 study, sponsored by ViiV Healthcare.

NCT00046176 is a Phase 3 study that has completed, run by ViiV Healthcare. The registered enrollment target is 240 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (69% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00046176, a Phase 3 study, has completed, sponsored by ViiV Healthcare.

COMPLETED
Registry status
Phase 3
Development phase
240 participants
Enrollment target

Study Summary

This study is a 48-week study designed to evaluate the safety and efficacy of a fixed-dose combination tablet administered once-a-day versus the individual tablets administered twice-a-day within 3-drug combination regimens in ART (antiretroviral)-experienced HIV-1 infected patients.

Interventions

  • DRUG lamivudine
  • DRUG abacavir/lamivudine
  • DRUG abacavir

Trial Details

FieldValue
Enrollment Target 240 participants
Start Date 2002-08-26
Est. Completion 2004-05-17
Phase Phase 3
ViiV Healthcare

182 total trials

What the finished NCT00046176 record still lists

NCT00046176 is an interventional study that assigns participants to a tested intervention. The registered 240 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (69% lower).

The record links to 0 conditions, and to 3 interventions - of which lamivudine is the first listed.

NCT00046176 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00046176 about?

NCT00046176 is a clinical study titled "A HIV Study Of A Fixed-Dose Combination Tablet In Antiretroviral Experienced Patients". This study is a 48-week study designed to evaluate the safety and efficacy of a fixed-dose combination tablet administered once-a-day versus the individual tablets administered twice-a-day within 3-drug combination regimens in ART (antiretroviral)-experienced HIV-1 infected patients.

What is the current status of trial NCT00046176?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 240 participants. The study started on 2002-08-26. Estimated completion is 2004-05-17.

What interventions are being tested in trial NCT00046176?

The interventions under investigation include: lamivudine (DRUG), abacavir/lamivudine (DRUG), abacavir (DRUG).

Who is sponsoring clinical trial NCT00046176?

This trial is sponsored by ViiV Healthcare, which has 182 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00046176's enrollment target sits among peer trials

240 1273rd of 2000 higher than 710 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT00046176, the US trial registry maintained by the National Library of Medicine. NCT00046176 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.