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Phase I Study of the Clinical Pharmacology of Azithromycin in Buffy Coat of HIV-Infected Subjects.

Primary Purpose

Bacterial Infections, HIV Infections

Status
Completed
Phase
Phase 1
Locations
United States
Study Type
Interventional
Intervention
Azithromycin
Sponsored by
Pfizer
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bacterial Infections focused on measuring Acquired Immunodeficiency Syndrome, Azithromycin, Bacterial Infections

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

Sites / Locations

  • Ctr for Phase I Research

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
June 23, 2005
Sponsor
Pfizer
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1. Study Identification

Unique Protocol Identification Number
NCT00002139
Brief Title
Phase I Study of the Clinical Pharmacology of Azithromycin in Buffy Coat of HIV-Infected Subjects.
Official Title
Phase I Study of the Clinical Pharmacology of Azithromycin in Buffy Coat of HIV-Infected Subjects.
Study Type
Interventional

2. Study Status

Record Verification Date
April 1996
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)

3. Sponsor/Collaborators

Name of the Sponsor
Pfizer

4. Oversight

5. Study Description

Brief Summary
To compare the uptake of azithromycin in white cells relative to plasma concentrations in HIV-infected patients.
Detailed Description
Patients are randomized to receive azithromycin orally or intravenously, with crossover to the alternate treatment after a 21-day wash-out period.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bacterial Infections, HIV Infections
Keywords
Acquired Immunodeficiency Syndrome, Azithromycin, Bacterial Infections

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1
Masking
None (Open Label)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Azithromycin

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility 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.
Facility Information:
Facility Name
Ctr for Phase I Research
City
Wichita
State/Province
Kansas
ZIP/Postal Code
67214
Country
United States

12. IPD Sharing Statement

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Phase I Study of the Clinical Pharmacology of Azithromycin in Buffy Coat of HIV-Infected Subjects.

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