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Evaluation of the Therapeutic Benefit of r-metHuIFN- Gamma in AIDS Patients With Disseminated Mycobacterium Avium-Intracellulare (MAI) Infection: A Multi-Centered Pilot Study

Evaluation of the Therapeutic Benefit of r-metHuIFN- Gamma in AIDS Patients With Disseminated Mycobacterium Avium-Intracellulare (MAI) Infection: A Multi-Centered Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00002037
Enrollment
15
Registered
2001-08-31
Start date
Unknown
Completion date
Unknown
Last updated
2005-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mycobacterium Avium-Intracellulare Infection, HIV Infections

Keywords

AIDS-Related Opportunistic Infections, Mycobacterium avium-intracellulare Infection, Interferon-gamma, Recombinant, Acquired Immunodeficiency Syndrome

Brief summary

To examine the effectiveness of subcutaneous gamma interferon in reducing severity of Mycobacterium avium- intracellulare (MAI) bacillemia episodes in AIDS patients in an open-label dose-randomized multi-center pilot clinical investigation. To evaluate the safety of gamma interferon given by subcutaneous injection (SC) in the AIDS patient in the presence and absence of AZT therapy.

Interventions

Sponsors

Amgen
Lead SponsorINDUSTRY

Study design

Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Patients must have: * Diagnosis of AIDS and persistent Mycobacterium avium- intracellulare (MAI) bacillemia. * Life expectancy of at least 3 months. * Baseline chest X-ray and EKG (electrocardiogram).

Exclusion criteria

Co-existing Condition: Patients with the following conditions or symptoms are excluded: * Known hypersensitivity to interferons or other exogenous lymphokine. * History of cardiac abnormality or disease. * History of hypertension. Patients with the following are excluded: * Known hypersensitivity to interferons or other exogenous lymphokine. * History of cardiac abnormality or disease. * History of hypertension. Prior Medication: Excluded within 4 weeks of study entry: * Corticosteroids. * Anti-inflammatory medication (except aspirin). * Changes in the dose of anti-mycobacterial drugs. * Immune agents. Prior Treatment: Excluded within 4 weeks of study entry: * Radiotherapy. Risk Behavior: Excluded: * Intravenous drug abuse.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026