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NCT00005918 · ClinicalTrials.gov registry record · Phase 3

Effectiveness and Safety of Two Forms of Stavudine in HIV-Infected Patients

A Phase 3 study, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 3
Development phase
730
Enrollment target

NCT00005918: Completed Phase 3 study, sponsored by Bristol-Myers Squibb.

NCT00005918 is a Phase 3 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 730 participants, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00005918, a Phase 3 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 3
Development phase
730 participants
Enrollment target

Study Summary

The purpose of this study is to compare the safety and effectiveness of 2 forms of stavudine (d4T). One form is taken once a day (extended release) and the other form is taken twice a day (immediate release).

Interventions

  • DRUG Lamivudine
  • DRUG Efavirenz
  • DRUG Stavudine

Trial Details

FieldValue
Enrollment Target 730 participants
Start Date 2000-06
Est. Completion 2002-04
Phase Phase 3
Bristol-Myers Squibb

1,025 total trials

What the finished NCT00005918 record still lists

NCT00005918 is an interventional study that assigns participants to a tested intervention. The registered 730 participants enrollment target is mid-sized for trials with a published cap, roughly in line with the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target.

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

NCT00005918 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00005918 about?

NCT00005918 is a clinical study titled "Effectiveness and Safety of Two Forms of Stavudine in HIV-Infected Patients". The purpose of this study is to compare the safety and effectiveness of 2 forms of stavudine (d4T). One form is taken once a day (extended release) and the other form is taken twice a day (immediate release).

What is the current status of trial NCT00005918?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 730 participants. The study started on 2000-06. Estimated completion is 2002-04.

What interventions are being tested in trial NCT00005918?

The interventions under investigation include: Lamivudine (DRUG), Efavirenz (DRUG), Stavudine (DRUG).

Who is sponsoring clinical trial NCT00005918?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00005918's enrollment target sits among peer trials

730 489th of 2000 higher than 1,512 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 NCT00005918, the US trial registry maintained by the National Library of Medicine. NCT00005918 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.