Expired Study
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Whitehouse Station, New Jersey 08889


Purpose:

The purpose of this study is to see if it is safe and effective to give indinavir sulfate plus stavudine to HIV-infected patients who have already been treated with zidovudine.


Criteria:

Inclusion Criteria Concurrent Medication: Allowed: - Prophylaxis with aerosolized pentamidine, topical antifungals, TMP / SMX, dapsone, or isoniazid. Patients must have: - HIV infection. - CD4 count 50 - 500 cells/mm3. - Prior AZT use for more than 6 months OR documented intolerance to AZT with more than 6 months use of another anti-HIV therapy other than d4T or any protease inhibitor. - No active opportunistic infection or visceral Kaposi's sarcoma. NOTE: - Patients with hemophilia may be enrolled at discretion of investigator. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: - Symptomatic neuropathy. - Acute hepatitis. Concurrent Medication: Excluded: - Antiretrovirals other than specified in protocol. - Chronic therapy for an active opportunistic infection. - Immunosuppressive therapy. Prior Medication: Excluded: - Any prior protease inhibitor or d4T. - Any nucleoside analogs within 2 weeks prior to study entry. - Investigational agents or immunomodulators within 30 days prior to study entry. Required: - More than 6 months of prior AZT unless intolerant, in which case more than 6 months of another anti-HIV therapy (other than protease inhibitors or d4T).


NCT ID:

NCT00002354


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Whitehouse Station, New Jersey 08889
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: September 20, 2017

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