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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 is a Phase 2 study that was terminated before completion, run by Bristol-Myers Squibb. The registered enrollment target is 25 participants.

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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

Sponsor

Bristol-Myers Squibb

1,025 total trials

What the Registry Record Tells You About NCT00002418

The ClinicalTrials.gov registry entry for NCT00002418 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.

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

NCT00002418 reports 0 study locations.

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.

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.