A Compassionate Use Study of Tenofovir Disoproxil Fumarate as Treatment for HIV Infection
Not Applicable
Completed
- Conditions
- HIV Infections
- Registration Number
- NCT00002453
- Lead Sponsor
- Gilead Sciences
- Brief Summary
This study allows patients who need a new anti-HIV treatment to take tenofovir disoproxil fumarate (tenofovir DF), an experimental drug. This study also looks at any side effects the drug causes.
- Detailed Description
HIV-1-infected patients who are currently receiving stable antiretroviral therapy add tenofovir DF to their regimen. Study participation lasts for approximately 48 weeks. Interested patients should contact their physicians.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 300
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
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Tenofovir Coordinating Center
🇺🇸Foster City, California, United States