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Search / Trial NCT00002267

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 21, 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 obtained, which must include a statement that treatment may involve risks to the embryo or fetus, which are currently unforeseeable, if the subject becomes pregnant.
  • 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

San Francisco, California, United States

Chicago, Illinois, United States

Chicago, Illinois, United States

Miami, Florida, United States

San Francisco, California, United States

Philadelphia, Pennsylvania, United States

Montreal, Quebec, Canada

New Orleans, Louisiana, United States

Minneapolis, Minnesota, United States

Newark, New Jersey, United States

Milwaukee, Wisconsin, United States

Albuquerque, New Mexico, United States

Annandale, Virginia, United States

Redwood City, California, United States

Vancouver, British Columbia, Canada

Ottawa, Ontario, Canada

Montreal, Quebec, Canada

Philadelphia, Pennsylvania, United States

Toronto, Ontario, Canada

San Francisco, California, United States

Montreal, Quebec, Canada

Phoenix, Arizona, United States

San Diego, California, United States

Columbia, South Carolina, United States

Berkeley, California, United States

Toronto, Ontario, Canada

Rochester, New York, United States

Hamilton, Ontario, Canada

Beverly Hills, California, United States

San Francisco, California, United States

Santa Rosa, California, United States

Tarzana, California, United States

Miami, Florida, United States

Detroit, Michigan, United States

St Paul, Minnesota, United States

Reno, Nevada, United States

Sante Fe, New Mexico, United States

Albany, New York, United States

Buffalo, New York, United States

Calgary, Alberta, Canada

Edmonton, Alberta, Canada

Halifax, Nova Scotia, Canada

Toronto, Ontario, Canada

People applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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