Expired Study
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Wichita, Kansas 67214


Purpose:

To compare the uptake of azithromycin in white cells relative to plasma concentrations in HIV-infected patients.


Study summary:

Patients are randomized to receive azithromycin orally or intravenously, with crossover to the alternate treatment after a 21-day wash-out period.


Criteria:

Inclusion Criteria Concurrent Medication: Allowed: - Antiretroviral agents, provided regimen has been stable for at least 1 month. Patients must have: - HIV infection. - CD4 count <= 200 cells/mm3. - No active opportunistic infection (pending discussion with Pfizer Clinician). Prior Medication: Allowed: - Prior antiretroviral agents. Exclusion Criteria Co-existing Condition: Patients with the following symptoms or conditions are excluded: - Active intercurrent illness (pending discussion with the Pfizer Clinician). - Allergies to macrolide antibiotics. - Signs and symptoms of severe illness that would preclude treatment. Patients with the following prior conditions are excluded: - History of clinically significant allergic, hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, or neurological disease. - Clinically important change in baseline status within 4 weeks prior to study entry. - Condition affecting drug absorption (e.g., ulcers, gastrectomy, HIV-associated enteropathies) within 4 weeks prior to study entry. Prior Medication: Excluded: - Investigational drugs including treatment IND drugs within 4 weeks prior to study entry. Known drug or alcohol dependence.


NCT ID:

NCT00002139


Primary Contact:

N/A


Backup Contact:

N/A


Location Contact:

Wichita, Kansas 67214
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: October 23, 2017

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