Expired Study
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Peapack, New Jersey 07977


Purpose:

The purpose of this study is to compare the safety and effectiveness of giving HIV-infected patients delavirdine (DLV) plus zidovudine (ZDV) plus 2 doses of indinavir (IDV) or ZDV plus IDV plus lamivudine (3TC). This study also examines how the body processes DLV when it is given in combination with other drugs.


Study summary:

In this multicenter, open-label study, 45 HIV-1-positive patients receive either combination drug therapy with delavirdine (DLV), zidovudine (ZDV), and indinavir (IDV) or combination drug therapy with ZDV, lamivudine (3TC), and IDV. NOTE: Patients are treated for 24 weeks and may opt to continue on study for 24 additional weeks, if HIV-1 RNA is less than 5,000 copies/ml or at the investigator's discretion.


Criteria:

Inclusion Criteria Patients must have: - HIV-1 positive. - CD4 count above 50. - HIV-1 RNA greater than 20,000. Prior Medication: Allowed: Less than 1 month prior treatment with zidovudine. Exclusion Criteria Prior Medication: Excluded: - Prior 3TC, protease inhibitors, or non-nucleoside reverse transcriptase inhibitors. - Prior ZDV of greater than 1 month total duration. Prior Treatment: Excluded: - Lamivudine. - Protease inhibitors. - Non-nucleoside reverse transcriptase inhibitors.


NCT ID:

NCT00002400


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Peapack, New Jersey 07977
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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