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An Open-Label Study of the Use of Azithromycin in Patients With Symptomatic Disseminated Mycobacterium Avium-Intracellulare Complex (MAC) Infection Failing Current Therapy

Primary Purpose

Mycobacterium Avium-Intracellulare Infection, HIV Infections

Status
Completed
Phase
Not Applicable
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 Mycobacterium Avium-Intracellulare Infection focused on measuring Mycobacterium avium-intracellulare Infection, Acquired Immunodeficiency Syndrome, Azithromycin

Eligibility Criteria

1 Day - undefined (Child, Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria Patients must have: Disseminated MAC as defined by current (within the last month) positive blood, bone marrow, or liver biopsy culture for MAC, and considered symptomatic (fever, night sweats, anorexia, weight loss, fatigue, or malaise). At least 2 months of prior treatment with available combination MAC therapy or less than 2 months of such accompanied by unacceptable adverse effects. Life expectancy of more than 2 weeks. Approval of eligibility from Pfizer Clinical Monitor. Consent of parent or guardian if under legal age of consent. NOTE: Patients who have completed acute treatment with azithromycin for MAC in protocol 066-131 or 066-148 will be exempt from inclusion criteria 1 and 2 and can continue therapy through this protocol if their physician feels they have benefitted from prior azithromycin therapy. Exclusion Criteria Co-existing Condition: Patients with the following symptoms and conditions are excluded: Known hypersensitivity or intolerance to macrolide antibiotics. Inability to take oral medications or current condition that is likely to interfere with absorption (e.g., gastrectomy). Concurrent Medication: Excluded: Other MAC therapy instituted during the first 2 months of the study. Other investigational drugs, with the exception of those available through a Treatment IND program. Patients with the following prior conditions are excluded: History of hypersensitivity or intolerance to azithromycin. Prior Medication: Excluded: Other investigational drugs within 7 days of enrollment, with the exception of Treatment IND drugs (such as ddC).

Sites / Locations

  • Pfizer Central 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
NCT00002089
Brief Title
An Open-Label Study of the Use of Azithromycin in Patients With Symptomatic Disseminated Mycobacterium Avium-Intracellulare Complex (MAC) Infection Failing Current Therapy
Official Title
An Open-Label Study of the Use of Azithromycin in Patients With Symptomatic Disseminated Mycobacterium Avium-Intracellulare Complex (MAC) Infection Failing Current Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
July 1998
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 evaluate the efficacy and safety of azithromycin given chronically for the treatment of Mycobacterium avium (MAC) bacteremia in patients failing or intolerant of current available MAC therapy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Mycobacterium Avium-Intracellulare Infection, HIV Infections
Keywords
Mycobacterium avium-intracellulare Infection, Acquired Immunodeficiency Syndrome, Azithromycin

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
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
1 Day
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patients must have: Disseminated MAC as defined by current (within the last month) positive blood, bone marrow, or liver biopsy culture for MAC, and considered symptomatic (fever, night sweats, anorexia, weight loss, fatigue, or malaise). At least 2 months of prior treatment with available combination MAC therapy or less than 2 months of such accompanied by unacceptable adverse effects. Life expectancy of more than 2 weeks. Approval of eligibility from Pfizer Clinical Monitor. Consent of parent or guardian if under legal age of consent. NOTE: Patients who have completed acute treatment with azithromycin for MAC in protocol 066-131 or 066-148 will be exempt from inclusion criteria 1 and 2 and can continue therapy through this protocol if their physician feels they have benefitted from prior azithromycin therapy. Exclusion Criteria Co-existing Condition: Patients with the following symptoms and conditions are excluded: Known hypersensitivity or intolerance to macrolide antibiotics. Inability to take oral medications or current condition that is likely to interfere with absorption (e.g., gastrectomy). Concurrent Medication: Excluded: Other MAC therapy instituted during the first 2 months of the study. Other investigational drugs, with the exception of those available through a Treatment IND program. Patients with the following prior conditions are excluded: History of hypersensitivity or intolerance to azithromycin. Prior Medication: Excluded: Other investigational drugs within 7 days of enrollment, with the exception of Treatment IND drugs (such as ddC).
Facility Information:
Facility Name
Pfizer Central Research
City
Groton
State/Province
Connecticut
ZIP/Postal Code
06340
Country
United States

12. IPD Sharing Statement

Learn more about this trial

An Open-Label Study of the Use of Azithromycin in Patients With Symptomatic Disseminated Mycobacterium Avium-Intracellulare Complex (MAC) Infection Failing Current Therapy

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