HIV Infections Clinical Trial
Official title:
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
NCT number | NCT00002032 |
Other study ID # | 048A |
Secondary ID | 087023-999 |
Status | Completed |
Phase | N/A |
First received | November 2, 1999 |
Last updated | June 23, 2005 |
The primary objectives of this trial are: To compare the safety of oral rifabutin versus placebo in the treatment of Mycobacterium avium complex (MAC) bacteremia in AIDS patients with CD4 counts less than or equal to 200 cells/mm3. To investigate the incidence of MAC in these patients. A secondary objective is to compare clinical response, quality of life (Karnofsky), and survival between these two groups.
Status | Completed |
Enrollment | 750 |
Est. completion date | |
Est. primary completion date | |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
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. |
Masking: Double-Blind, Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
United States | AIDS Research Consortium of Atlanta | Atlanta | Georgia |
United States | Grady Memorial Hosp / Hughs Spalding Med Ctr | Atlanta | Georgia |
United States | Central Texas Med Foundation | Austin | Texas |
United States | Johns Hopkins School of Medicine | Baltimore | Maryland |
United States | CRI of New England | Brookline | Massachusetts |
United States | Brooklyn Veterans Administration | Brooklyn | New York |
United States | Maimonides Med Ctr | Brooklyn | New York |
United States | Univ Hosp of Cleveland / Case Western Reserve Univ | Cleveland | Ohio |
United States | Ohio State Univ Med Ctr | Columbus | Ohio |
United States | Nelson Tebedo Community Clinic | Dallas | Texas |
United States | Univ of Texas Southwestern Med Ctr of Dallas | Dallas | Texas |
United States | Denver Public Health Dept | Denver | Colorado |
United States | Nassau County Med Ctr | East Meadow | New York |
United States | Texas Tech Health Sciences Ctr | El Paso | Texas |
United States | Ctr for Special Immunology | Fort Lauderdale | Florida |
United States | TheraFirst Med Ctrs Inc | Fort Lauderdale | Florida |
United States | Mem Hosp Hollywood | Hollywood | Florida |
United States | Baylor College of Medicine | Houston | Texas |
United States | Houston Clinical Research Network | Houston | Texas |
United States | Ctr for Special Immunology | Irvine | California |
United States | Research Med Ctr | Kansas City | Missouri |
United States | Univ of Missouri at Kansas City School of Medicine | Kansas City | Missouri |
United States | Long Island Jewish Med Ctr | New Hyde Park | New York |
United States | Chelsea Village Med Ctr | New York | New York |
United States | Community Research Initiative | New York | New York |
United States | Mem Sloan - Kettering Cancer Ctr | New York | New York |
United States | VP Med Services / HHCS Research Institute Inc | Orlando | Florida |
United States | Dr Winkler Weinberg | Roswell | Georgia |
United States | Univ TX San Antonio Health Science Ctr | San Antonio | Texas |
United States | Olive View Med Ctr | Sylmar | California |
United States | Scott and White Hosp | Temple | Texas |
United States | Dr Scott Lea | Waco | Texas |
United States | Veterans Administration Med Ctr | Washington | District of Columbia |
Lead Sponsor | Collaborator |
---|---|
Pharmacia |
United States,
Dautzenberg B, Castellani P, Truffot-Pernot CH, Leng B, Sassella D. Bacteriological assessment of rifabutin versus placebo for M. avium bacteremia in AIDS patients. Int Conf AIDS. 1996 Jul 7-12;11(1):117 (abstract no MoB1359)
Moore RD, Chaisson RE. Survival analysis of two controlled trials of rifabutin prophylaxis against Mycobacterium avium complex in AIDS. AIDS. 1995 Dec;9(12):1337-42. — View Citation
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