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NCT00002418 · ClinicalTrials.gov registry record · Phase 2

The Safety and Effectiveness of Didanosine Plus Stavudine Plus Nevirapine Combined With MKC-442 in HIV-Infected Patients Who Have Not Had Success With Protease Inhibitors

A Phase 2 study, sponsored by Bristol-Myers Squibb.

Terminated
Registry status
Phase 2
Development phase
25
Enrollment target

NCT00002418: Clinical Trial Phase 2 study, sponsored by Bristol-Myers Squibb.

NCT00002418 is a Phase 2 study that was terminated before completion, run by Bristol-Myers Squibb. The registered enrollment target is 25 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00002418, a Phase 2 study, was terminated before completion, sponsored by Bristol-Myers Squibb.

TERMINATED
Registry status
Phase 2
Development phase
25 participants
Enrollment target

Study Summary

The purpose of this study is to see if it is safe and effective to give a new anti-HIV drug combination to HIV-infected patients who have never taken nonnucleoside reverse transcriptase inhibitors (NNRTIs) and who have failed to respond to protease inhibitors (PIs). The drug combination will contain didanosine (ddI) plus stavudine (d4T) plus nevirapine (NVP) plus MKC-442. Hydroxyurea (HU) may be added.

Interventions

  • DRUG Hydroxyurea
  • DRUG Stavudine
  • DRUG Didanosine
  • DRUG Nevirapine
  • DRUG Emivirine

Trial Details

FieldValue
Enrollment Target 25 participants
Phase Phase 2
Bristol-Myers Squibb

1,025 total trials

Why NCT00002418 stopped before completion

NCT00002418 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 25 participants, a relatively small participant target, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (81% lower).

The record links to 0 conditions, and to 5 interventions - of which Hydroxyurea is the first listed.

NCT00002418 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00002418 about?

NCT00002418 is a clinical study titled "The Safety and Effectiveness of Didanosine Plus Stavudine Plus Nevirapine Combined With MKC-442 in HIV-Infected Patients Who Have Not Had Success With Protease Inhibitors". The purpose of this study is to see if it is safe and effective to give a new anti-HIV drug combination to HIV-infected patients who have never taken nonnucleoside reverse transcriptase inhibitors (NNRTIs) and who have failed to respond to protease inhibitors (PIs). The drug combination will contain...

What is the current status of trial NCT00002418?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 25 participants.

What interventions are being tested in trial NCT00002418?

The interventions under investigation include: Hydroxyurea (DRUG), Stavudine (DRUG), Didanosine (DRUG), Nevirapine (DRUG), Emivirine (DRUG).

Who is sponsoring clinical trial NCT00002418?

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 NCT00002418's enrollment target sits among peer trials

25 1719th of 2000 higher than 245 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT00002418, the US trial registry maintained by the National Library of Medicine. NCT00002418 (small enrollment · none site footprint · terminated) retrieved and formatted by PlainTrial, see methodology.