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A Study to Evaluate the Use of Stavudine (d4T) to Treat AIDS Dementia Complex

Phase 3
Completed
Conditions
AIDS Dementia Complex
HIV Infections
Registration Number
NCT00002246
Lead Sponsor
Bristol-Myers Squibb
Brief Summary

The purpose of this study is to see if adding stavudine (d4T) to anti-HIV drug regimens (with or without zidovudine, ZDV) can improve symptoms of AIDS Dementia Complex (ADC, problems involving the brain or spinal cord) in HIV-positive patients.

Detailed Description

In this open-label, multicenter, multinational study, ZDV is replaced with d4T in ZDV-containing regimens, or d4T is added to non-ZDV-containing regimens in 20 patients experiencing ADC. Patients are defined as having failed treatment if they progress by one ADC stage on the MSK (Memorial Sloan Kettering) rating scale on study (i.e., from Stage 1 to 2 or Stage 2 to 3). Patients are evaluated on a weekly basis until the dementia deterioration is confirmed to be caused by HIV-1. The effect of d4T-containing regimens is assessed for the following parameters: neurological status, survival, AIDS-defining conditions, CSF (cerebrospinal fluid) and plasma viral load, CSF and blood immunological markers, blood CD4 cell counts, and viral resistance. This study also assesses the pharmacokinetics of d4T in the CSF and in the blood.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

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Exclusion Criteria

Not provided

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Study & Design

Study Type
INTERVENTIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (5)

AIDS ReSEARCH Alliance

πŸ‡ΊπŸ‡Έ

West Hollywood, California, United States

Mount Sinai Hosp

πŸ‡ΊπŸ‡Έ

New York, New York, United States

Charing Cross and Westminster Med School

πŸ‡¬πŸ‡§

London SW 10, United Kingdom

National Centre in HIV Epidemiology and Clinical Research

πŸ‡¦πŸ‡Ί

Sydney, Australia

HIV Neurobehavioral Research Ctr

πŸ‡ΊπŸ‡Έ

San Diego, California, United States

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