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Search / Trial NCT00002032

Rifabutin Therapy for the Prevention of Mycobacterium Avium Complex (MAC) Bacteremia in AIDS Patients With CD4 Counts = or < 200: A Double-Blind, Placebo-Controlled Trial

Launched by PHARMACIA · Aug 30, 2001

Trial Information

Current as of March 22, 2025

Completed

Keywords

Rifabutin Aids Related Opportunistic Infections Mycobacterium Avium Intracellulare Infection Acquired Immunodeficiency Syndrome Antitubercular Agents

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria
  • Patients must have the following:
  • Diagnosis of AIDS with a case defining infection other than Mycobacterium avium complex (MAC).
  • Written informed consent.
  • Females of childbearing potential must also sign a special informed consent.
  • Exclusion Criteria
  • Co-existing Condition:
  • Patients with the following conditions or symptoms are excluded:
  • Known hypersensitivity to rifabutin, rifampin, other rifamycins, zidovudine or didanosine (ddI).
  • Previous or current infection due to Mycobacterium avium complex (MAC) disease as evaluated by two successive blood cultures and two successive stool cultures taken within 14 days prior to study initiation.
  • Concurrent Medication:
  • Excluded:
  • Antiretroviral agents other than zidovudine (AZT).
  • Didanosine (ddI).
  • Antimycobacterial therapy.
  • Rifampin.
  • Isoniazid.
  • Clofazimine.
  • Ethambutol.
  • Cycloserine.
  • Ethionamide.
  • Amikacin.
  • Ciprofloxacin.
  • Streptomycin.
  • Other investigational drugs.
  • If antimicrobial therapy is required to treat bacterial infections (= or \< 14 days), Adria Laboratories must be contacted prior to initiation of therapy.
  • Patients with the following are excluded:
  • Known hypersensitivity to rifabutin, rifampin, other rifamycins, zidovudine (AZT), or didanosine (ddI).
  • Previous or current Mycobacterium avium complex (MAC) infection.
  • Perceived patient unreliability or unavailability for frequent monitoring.
  • Prior Medication:
  • Excluded within 4 weeks of study entry:
  • Antiretroviral agents other than zidovudine (AZT) or didanosine (ddI).
  • Antimycobacterial therapy.
  • Rifampin.
  • Isoniazid.
  • Clofazimine.
  • Ethambutol.
  • Cycloserine.
  • Ethionamide.
  • Amikacin.
  • Ciprofloxacin.
  • Required:
  • Zidovudine (AZT).
  • Antipneumocystis prophylactic therapy.
  • Required for at least 4 weeks prior to study entry:
  • Zidovudine (AZT) or didanosine (ddI).
  • Antipneumocystis prophylaxis.

About Pharmacia

Pharmacia is a global biopharmaceutical company dedicated to advancing healthcare through innovative research and development. With a strong focus on delivering effective therapies for a range of medical conditions, Pharmacia harnesses cutting-edge science and technology to create solutions that enhance patient outcomes. The company is committed to conducting rigorous clinical trials that adhere to the highest ethical and scientific standards, ensuring the safety and well-being of participants while contributing to the advancement of medical knowledge. Through collaboration with healthcare professionals and regulatory bodies, Pharmacia strives to bring transformative treatments to market that address unmet medical needs and improve the quality of life for patients worldwide.

Locations

Houston, Texas, United States

Atlanta, Georgia, United States

Sylmar, California, United States

East Meadow, New York, United States

Houston, Texas, United States

Washington, District Of Columbia, United States

Roswell, Georgia, United States

New York, New York, United States

Cleveland, Ohio, United States

Columbus, Ohio, United States

Dallas, Texas, United States

Temple, Texas, United States

Dallas, Texas, United States

Irvine, California, United States

Fort Lauderdale, Florida, United States

Fort Lauderdale, Florida, United States

Hollywood, Florida, United States

Kansas City, Missouri, United States

Kansas City, Missouri, United States

Denver, Colorado, United States

Orlando, Florida, United States

Atlanta, Georgia, United States

Baltimore, Maryland, United States

Brookline, Massachusetts, United States

Brooklyn, New York, United States

Brooklyn, New York, United States

New Hyde Park, New York, United States

New York, New York, United States

New York, New York, United States

Austin, Texas, United States

El Paso, Texas, United States

San Antonio, Texas, United States

Waco, Texas, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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