Clinical trial
A Phase II, 24-Week, Open-Label Study Designed to Evaluate the Pharmacokinetics, Safety, Tolerability, and Efficacy of Novel Combination Therapy With Videx (Didanosine), Zerit (Stavudine), Viramune (Nevirapine), and MKC-442 (With or Without Hydroxyurea) for the Treatment of HIV-1 Infection in Non-Nucleoside Reverse Transcriptase Inhibitor Naive Patients Who Failed Previous Protease Inhibitor Treatment
NCT00002418 is registered in ClinicalTrials.gov with Bristol-Myers Squibb as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Phase II, 24-Week, Open-Label Study Designed to Evaluate the Pharmacokinetics, Safety, Tolerability, and Efficacy of Novel Combination Therapy With Videx (Didanosine), Zerit (Stavudine), Viramune (Nevirapine), and MKC-442 (With or Without Hydroxyurea) for the Treatment of HIV-1 Infection in Non-Nucleoside Reverse Transcriptase Inhibitor Naive Patients Who Failed Previous Protease Inhibitor Treatment
- Lead sponsor
- Bristol-Myers Squibb
- Phase
- Phase 2
- Overall status
- Terminated
- Start date
- Not reported
- Completion date
- Not reported
- Enrollment
- 25
- Sites
- 5
Conditions
As the registry lists them; a condition with its own page is linked.