Expired Study
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Foster City, California 94404


Purpose:

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.


Study summary:

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.


Criteria:

Inclusion Criteria You may be eligible for this study if you: - Are HIV-positive. - Have a viral load greater than or equal to 10,000 copies/ml. - Have a CD4 count less than or equal to 50 cells/mm3, or have a CD4 count greater than 50 and no more than 200 cells/mm3 with an opportunistic (AIDS-related) infection within 90 days of study entry. (Patients with a CD4 count above 200 cells/mm3 may be considered depending on drug supply.) - Are at least 18 years old. - Agree to use barrier methods of birth control (such as condoms) while on the study and for 30 days afterward. - Have a life expectancy of at least one year. Exclusion Criteria You will not be eligible for this study if you: - Have a history of a serious kidney or bone disease. - Have severe nausea, vomiting, or trouble taking medications by mouth. - Are pregnant or breast-feeding. - Abuse alcohol or other substances that your doctor thinks would interfere with taking this medicine. - Are taking any medicines that interfere with kidney functions.


NCT ID:

NCT00002453


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Foster City, California 94404
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: September 26, 2017

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