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The Safety and Effectiveness of Rifabutin, Combined With Clarithromycin or Azithromycin, in HIV-Infected Patients

Primary Purpose

Mycobacterium Avium-intracellulare Infection, HIV Infections

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Clarithromycin
Azithromycin
Rifabutin
Sponsored by
National Institute of Allergy and Infectious Diseases (NIAID)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Mycobacterium Avium-intracellulare Infection focused on measuring Rifabutin, Mycobacterium avium-intracellulare Infection, Drug Interactions, Azithromycin, Clarithromycin

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria Concurrent Medication: Allowed: Primary or secondary PCP prophylaxis with TMP/SMX, dapsone, or aerosolized pentamidine. Any approved therapy for antiretroviral treatment, or antiretroviral therapy available through FDA-sanctioned treatment IND or treatment protocol. Patients must have: AMENDED (PART B): Either HIV infection OR no HIV infection. CD4 count unspecified. ORIGINAL: Documented HIV infection. CD4 count < 200 cells/mm3 within 90 days prior to study entry. Exclusion Criteria Co-existing Condition: Patients with the following symptoms and conditions are excluded: Known Mycobacterium avium-intracellulare (MAI) bacteremia or presence of a clinical syndrome compatible with MAI (i.e., fevers, weight loss, elevated LDH and alkaline phosphatase). Fever = or > 38.5 deg C (100.4 deg F) within 7 days prior to study entry. Concurrent Medication: Excluded: Acute or chronic use of phenobarbital, carbamazepine, rifampin, dilantin, fluconazole, itraconazole, ketoconazole, ciprofloxacin, beta-blockers, or clarithromycin. Oral contraceptives. Acute therapy for an AIDS-related opportunistic infection or malignancy, or other acute medical illness, or infection. Maintenance therapy for CMV, cryptococcal meningitis, or toxoplasmosis. Cytotoxic chemotherapy. Patients with the following prior conditions are excluded: History of intolerance or hypersensitivity to study drugs, other macrolide antibiotics, or rifampin. Three or more loose bowel movements per day within 3 months prior to study entry. Unintentional weight loss >= 5 percent of body weight within 3 months prior to study entry. Prior Medication: Excluded: Rifabutin within 30 days prior to study entry. Clarithromycin or azithromycin within 14 days prior to study entry. Acute therapy for an AIDS-related opportunistic infection or malignancy, or other acute medical illness, or infection within 28 days prior to study entry. Prior Treatment: Excluded: Blood transfusions within 1 month prior to study entry.

Sites / Locations

  • Univ of Arizona / Health Science Ctr
  • Palo Alto Veterans Affairs Health Care System
  • Davies Med Ctr
  • Denver Public Health Dept
  • Georgetown Univ Med Ctr
  • Tulane Univ Med School
  • Univ of Maryland at Baltimore / Veterans Adm
  • Washington Univ School of Medicine
  • Univ of North Carolina School of Medicine
  • Univ of Rhode Island / Roger Williams Med Ctr
  • Med College of Virginia / School of Pharmacy

Outcomes

Primary Outcome Measures

Secondary Outcome Measures

Full Information

First Posted
November 2, 1999
Last Updated
October 29, 2012
Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
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1. Study Identification

Unique Protocol Identification Number
NCT00001023
Brief Title
The Safety and Effectiveness of Rifabutin, Combined With Clarithromycin or Azithromycin, in HIV-Infected Patients
Official Title
Evaluation of the Safety, Tolerance and Pharmacokinetics of Rifabutin/Clarithromycin Combination and Rifabutin/Azithromycin Combination in HIV-Infected Patients
Study Type
Interventional

2. Study Status

Record Verification Date
October 2012
Overall Recruitment Status
Completed
Study Start Date
undefined (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
July 1998 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)

4. Oversight

5. Study Description

Brief Summary
PER 03/10/94 AMENDMENT: PART B. To determine whether there is an effect on plasma drug levels of azithromycin and rifabutin as measured by changes in the plasma concentration-time curve (AUC) when these drugs are taken concomitantly. ORIGINAL PRIMARY: To gain preliminary information about the safety and tolerance of clarithromycin and azithromycin in combination with rifabutin (three potential agents against Mycobacterium avium-intracellulare) in HIV-infected patients with CD4 counts < 200 cells/mm3. ORIGINAL SECONDARY: To determine whether there is an effect on the pharmacokinetics of the macrolide antibiotics or rifabutin when these drugs are taken concomitantly. To monitor the effect of rifabutin therapy on dapsone serum levels in patients taking dapsone for PCP prophylaxis. To monitor the effect of macrolide/rifabutin combination therapies on AZT or ddI serum levels. Two new macrolide antibiotics, clarithromycin and azithromycin, and rifabutin (a rifamycin derivative) have all demonstrated in vitro and in vivo activity against Mycobacterium avium-intracellulare, a common systemic bacterial infection complicating AIDS. Further information is needed, however, regarding the clinical and pharmacokinetic interaction of these drugs used in combination.
Detailed Description
Two new macrolide antibiotics, clarithromycin and azithromycin, and rifabutin (a rifamycin derivative) have all demonstrated in vitro and in vivo activity against Mycobacterium avium-intracellulare, a common systemic bacterial infection complicating AIDS. Further information is needed, however, regarding the clinical and pharmacokinetic interaction of these drugs used in combination. AMENDED 03/10/94 (Part B): Approximately 38 HIV-infected or uninfected subjects are randomized to receive azithromycin or rifabutin (Groups 3 and 4) daily for 14 days, followed by a combination regimen of both drugs for 4 additional weeks. Patients are followed weekly. Pharmacokinetic sampling will be performed on days 14, 15, and 42-45. ORIGINAL: Sixty-eight patients are randomly assigned to one of four groups (17 patients per group). They receive either clarithromycin or azithromycin in combination with rifabutin on one of two different dosing schedules. Patients receive medication for 6 weeks and undergo follow-up weekly during drug administration and at week 8.

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
Rifabutin, Mycobacterium avium-intracellulare Infection, Drug Interactions, Azithromycin, Clarithromycin

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Allocation
Randomized
Enrollment
91 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Clarithromycin
Intervention Type
Drug
Intervention Name(s)
Azithromycin
Intervention Type
Drug
Intervention Name(s)
Rifabutin

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Concurrent Medication: Allowed: Primary or secondary PCP prophylaxis with TMP/SMX, dapsone, or aerosolized pentamidine. Any approved therapy for antiretroviral treatment, or antiretroviral therapy available through FDA-sanctioned treatment IND or treatment protocol. Patients must have: AMENDED (PART B): Either HIV infection OR no HIV infection. CD4 count unspecified. ORIGINAL: Documented HIV infection. CD4 count < 200 cells/mm3 within 90 days prior to study entry. Exclusion Criteria Co-existing Condition: Patients with the following symptoms and conditions are excluded: Known Mycobacterium avium-intracellulare (MAI) bacteremia or presence of a clinical syndrome compatible with MAI (i.e., fevers, weight loss, elevated LDH and alkaline phosphatase). Fever = or > 38.5 deg C (100.4 deg F) within 7 days prior to study entry. Concurrent Medication: Excluded: Acute or chronic use of phenobarbital, carbamazepine, rifampin, dilantin, fluconazole, itraconazole, ketoconazole, ciprofloxacin, beta-blockers, or clarithromycin. Oral contraceptives. Acute therapy for an AIDS-related opportunistic infection or malignancy, or other acute medical illness, or infection. Maintenance therapy for CMV, cryptococcal meningitis, or toxoplasmosis. Cytotoxic chemotherapy. Patients with the following prior conditions are excluded: History of intolerance or hypersensitivity to study drugs, other macrolide antibiotics, or rifampin. Three or more loose bowel movements per day within 3 months prior to study entry. Unintentional weight loss >= 5 percent of body weight within 3 months prior to study entry. Prior Medication: Excluded: Rifabutin within 30 days prior to study entry. Clarithromycin or azithromycin within 14 days prior to study entry. Acute therapy for an AIDS-related opportunistic infection or malignancy, or other acute medical illness, or infection within 28 days prior to study entry. Prior Treatment: Excluded: Blood transfusions within 1 month prior to study entry.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
R Hafner
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
H Standiford
Official's Role
Study Chair
Facility Information:
Facility Name
Univ of Arizona / Health Science Ctr
City
Tucson
State/Province
Arizona
ZIP/Postal Code
85724
Country
United States
Facility Name
Palo Alto Veterans Affairs Health Care System
City
Palo Alto
State/Province
California
ZIP/Postal Code
94304
Country
United States
Facility Name
Davies Med Ctr
City
San Francisco
State/Province
California
ZIP/Postal Code
94114
Country
United States
Facility Name
Denver Public Health Dept
City
Denver
State/Province
Colorado
ZIP/Postal Code
802044507
Country
United States
Facility Name
Georgetown Univ Med Ctr
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20007
Country
United States
Facility Name
Tulane Univ Med School
City
New Orleans
State/Province
Louisiana
ZIP/Postal Code
701122699
Country
United States
Facility Name
Univ of Maryland at Baltimore / Veterans Adm
City
Baltimore
State/Province
Maryland
ZIP/Postal Code
21201
Country
United States
Facility Name
Washington Univ School of Medicine
City
St Louis
State/Province
Missouri
ZIP/Postal Code
63108
Country
United States
Facility Name
Univ of North Carolina School of Medicine
City
Chapel Hill
State/Province
North Carolina
ZIP/Postal Code
275997215
Country
United States
Facility Name
Univ of Rhode Island / Roger Williams Med Ctr
City
Providence
State/Province
Rhode Island
ZIP/Postal Code
02908
Country
United States
Facility Name
Med College of Virginia / School of Pharmacy
City
Richmond
State/Province
Virginia
ZIP/Postal Code
232980533
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
11302832
Citation
Hafner R, Bethel J, Standiford HC, Follansbee S, Cohn DL, Polk RE, Mole L, Raasch R, Kumar P, Mushatt D, Drusano G; DATRI 001B Study Group. Tolerance and pharmacokinetic interactions of rifabutin and azithromycin. Antimicrob Agents Chemother. 2001 May;45(5):1572-7. doi: 10.1128/AAC.45.5.1572-1577.2001.
Results Reference
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The Safety and Effectiveness of Rifabutin, Combined With Clarithromycin or Azithromycin, in HIV-Infected Patients

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