Effectiveness and Safety of Two Forms of Stavudine in HIV-Infected Patients
The Safety and Antiviral Efficacy of Stavudine Extended Release Formulation as Compared to Stavudine Immediate Release Formulation, Each as Part of Potent Antiretroviral Combination Therapy
Sponsor: Bristol-Myers Squibb
Listed as NCT00005918, this PHASE3 trial focuses on HIV Infections and remains completed. Sponsored by Bristol-Myers Squibb, it has been updated 8 times since 2000, reflecting limited change activity. This study is part of the global effort to build evidence for infectious disease interventions.
Status Flow
Change History
8 versions recorded-
Sep 2025 — Present [monthly]
Completed PHASE3
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Sep 2024 — Sep 2025 [monthly]
Completed PHASE3
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Jul 2024 — Sep 2024 [monthly]
Completed PHASE3
-
Apr 2022 — Jul 2024 [monthly]
Completed PHASE3
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Jan 2021 — Apr 2022 [monthly]
Completed PHASE3
▶ Show 3 earlier versions
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Jun 2018 — Jan 2021 [monthly]
Completed PHASE3
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Feb 2017 — Jun 2018 [monthly]
Completed PHASE3
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Jan 2017 — Feb 2017 [monthly]
Completed PHASE3
First recorded
Jun 2000
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- Bristol-Myers Squibb
For direct contact, visit the study record on ClinicalTrials.gov .
Study Locations
Almada, Portugal , Altamonte Springs, United States , Antella, Italy , Bangkok, Thailand , Barcelona, Spain , Bari, Italy , Belo Horizonte-MG, Brazil , Bergamo, Italy , Bordeaux, France , Botucatu-SP, Brazil and 53 more locations