Completed

Phase 3
Age: 12Years +
All Genders
ID00001030

A Prospective, Randomized, Comparative Study of the Safety and Efficacy of Clarithromycin Versus Rifabutin Versus the Combination of Clarithromycin Plus Rifabutin for the Prevention of Mycobacterium Avium Complex (MAC) Bacteremia or Disseminated MAC Disease in HIV-Infected Patients With CD4 Lymphocyte Counts <= 100 Cells/mm3

Led by National Institute of Allergy and Infectious Diseases (NIAID) · Updated on 2021-11-01

1100

Participants Needed

42

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

To compare the efficacy and safety of clarithromycin alone versus rifabutin alone versus the two drugs in combination for the prevention or delay of Mycobacterium avium Complex (MAC) bacteremia or disseminated MAC disease. To compare other parameters such as survival, toxicity, and quality of life among the three treatment arms. To obtain information on the incidence and clinical grade of targeted gynecologic conditions. Persons with advanced stages of HIV are considered to be at particular risk for developing disseminated MAC disease. The development of an effective regimen for the prevention of disseminated MAC disease may be of substantial benefit in altering the morbidity and possibly the mortality associated with this disease and its treatment.

CONDITIONS

Official Title

The Safety and Effectiveness of Clarithromycin and Rifabutin Used Alone or in Combination to Prevent Mycobacterium Avium Complex (MAC) or Disseminated MAC Disease in HIV-Infected Patients

Who Can Participate

Age: 12Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

Inclusion Criteria

Concurrent Medication:

Recommended:

  • PCP prophylaxis.

Allowed:

  • GM-CSF or G-CSF.
  • Erythropoietin.
  • Therapies (including antiretrovirals) available through expanded access or treatment IND programs.
  • Other non-experimental therapies available by prescription.
  • Antihistamines other than those specifically excluded.

Patients must have:

  • Evidence or diagnosis of HIV infection or a history of an AIDS-defining condition by CDC criteria.
  • CD4 count <= 100 cells/mm3 within 90 days prior to study entry.
  • Two baseline blood sample cultures negative for MAC within 30 days of study entry.
  • No suspected disseminated MAC disease, in the opinion of the clinician.

NOTE:

  • Patients with elevated GGT and/or triglycerides are allowed.

NOTE:

  • Patients may co-enroll on ACTG 081/981/181, ACTG 175, ACTG 204, ACTG 193, ACTG 241, or other acceptable protocols.

Exclusion Criteria

Co-existing Condition:

Patients with the following symptoms or conditions are excluded:

  • Known or suspected tuberculous infection or other non-tuberculous mycobacterial infection requiring chemotherapy or chemoprophylaxis (with the exception of isoniazid prophylaxis alone).

NOTE:

  • Patients may enroll who successfully completed tuberculosis (TB) treatment and have been off anti-TB drugs for more than 6 months with no symptoms of mycobacterial infection.
  • Active TB.
  • Known hypersensitivity to study drugs.
  • Malabsorption as defined by persistent diarrhea with more than 8 stools per day for > 6 weeks.

Concurrent Medication:

Excluded:

  • Frequent (more than once per month), repeated, or continuous treatment courses of quinolones, erythromycin, spiramycin, azithromycin, clarithromycin, or clindamycin.
  • Concomitant terfenadine or astemizole.

Prior Medication:

Excluded:

  • Prophylaxis with azithromycin, clarithromycin, or rifabutin for more than 4 months.
Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

Trial Site Locations

Total: 42 locations

1

Alabama Therapeutics CRS

Birmingham, Alabama, United States, 35294

Status Unknown

2

UCLA CARE Center CRS

Los Angeles, California, United States, 90095

Status Unknown

3

Children's Hosp. & Research Ctr. Oakland, Ped. Clinical Research Ctr. & Research Lab.

Oakland, California, United States, 94609

Status Unknown

4

Ucsf Aids Crs

San Francisco, California, United States

Status Unknown

5

Howard University Hosp., Div. of Infectious Diseases, ACTU

Washington D.C., District of Columbia, United States, 20059

Status Unknown

6

Univ. of Miami AIDS CRS

Miami, Florida, United States, 33136

Status Unknown

7

Univ. of Hawaii at Manoa, Leahi Hosp.

Honolulu, Hawaii, United States, 96816

Status Unknown

8

Chicago Children's CRS

Chicago, Illinois, United States, 60611

Status Unknown

9

Northwestern University CRS

Chicago, Illinois, United States, 60611

Status Unknown

10

Cook County Hosp. CORE Ctr.

Chicago, Illinois, United States, 60612

Status Unknown

11

Rush Univ. Med. Ctr. ACTG CRS

Chicago, Illinois, United States, 60612

Status Unknown

12

Indiana Univ. School of Medicine, Infectious Disease Research Clinic

Indianapolis, Indiana, United States, 46202

Status Unknown

13

Methodist Hosp. of Indiana

Indianapolis, Indiana, United States, 46202

Status Unknown

14

Univ. of Iowa Healthcare, Div. of Infectious Diseases

Iowa City, Iowa, United States, 52242

Status Unknown

15

Johns Hopkins Adult AIDS CRS

Baltimore, Maryland, United States, 21287

Status Unknown

16

Massachusetts General Hospital ACTG CRS

Boston, Massachusetts, United States, 02114

Status Unknown

17

Bmc Actg Crs

Boston, Massachusetts, United States, 02118

Status Unknown

18

Beth Israel Deaconess - East Campus A0102 CRS

Boston, Massachusetts, United States, 02215

Status Unknown

19

Beth Israel Deaconess Med. Ctr., ACTG CRS

Boston, Massachusetts, United States, 02215

Status Unknown

20

Hennepin County Med. Ctr., Div. of Infectious Diseases

Minneapolis, Minnesota, United States, 55415

Status Unknown

21

University of Minnesota, ACTU

Minneapolis, Minnesota, United States, 55455

Status Unknown

22

St. Louis ConnectCare, Infectious Diseases Clinic

St Louis, Missouri, United States

Status Unknown

23

Washington U CRS

St Louis, Missouri, United States

Status Unknown

24

Univ. of Nebraska Med. Ctr., Durham Outpatient Ctr.

Omaha, Nebraska, United States, 68198

Status Unknown

25

SUNY - Buffalo, Erie County Medical Ctr.

Buffalo, New York, United States, 14215

Status Unknown

26

NY Univ. HIV/AIDS CRS

New York, New York, United States, 10016

Status Unknown

27

Memorial Sloan-Kettering Cancer Ctr.

New York, New York, United States, 10021

Status Unknown

28

Beth Israel Med. Ctr. (Mt. Sinai)

New York, New York, United States, 10029

Status Unknown

29

Cornell University A2201

New York, New York, United States

Status Unknown

30

Univ. of Rochester ACTG CRS

Rochester, New York, United States, 14642

Status Unknown

31

Bronx-Lebanon Hosp. IMPAACT CRS

The Bronx, New York, United States, 10457

Status Unknown

32

Unc Aids Crs

Chapel Hill, North Carolina, United States, 27599

Status Unknown

33

Carolinas HealthCare System, Carolinas Med. Ctr.

Charlotte, North Carolina, United States, 28203

Status Unknown

34

Regional Center for Infectious Disease, Wendover Medical Center CRS

Greensboro, North Carolina, United States, 27401

Status Unknown

35

Univ. of Cincinnati CRS

Cincinnati, Ohio, United States, 45267

Status Unknown

36

Case CRS

Cleveland, Ohio, United States, 44106

Status Unknown

37

MetroHealth CRS

Cleveland, Ohio, United States, 44109

Status Unknown

38

The Ohio State Univ. AIDS CRS

Columbus, Ohio, United States, 43210

Status Unknown

39

Hosp. of the Univ. of Pennsylvania CRS

Philadelphia, Pennsylvania, United States, 19104

Status Unknown

40

The Children's Hosp. of Philadelphia IMPAACT CRS

Philadelphia, Pennsylvania, United States, 19104

Status Unknown

41

University of Washington AIDS CRS

Seattle, Washington, United States, 98122

Status Unknown

42

Mbeya Med. Research Program, Mbeya Referral Hosp. CRS

Mbeya, Tanzania

Status Unknown

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How is the study designed?

Study Type

INTERVENTIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

TREATMENT

Number of Arms

0

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Published Research Related To This Trial

Comparison of gynecologic history and laboratory results in HIV-positive women with CD4+ lymphocyte counts between 200 and 500 cells/microl and below 100 cells/microl.

D H Watts, C Spino, L Zaborski...

https://pubmed.ncbi.nlm.nih.gov/10225227

Clarithromycin or rifabutin alone or in combination for primary prophylaxis of Mycobacterium avium complex disease in patients with AIDS: A randomized, double-blind, placebo-controlled trial. The AIDS Clinical Trials Group 196/Terry Beirn Community Programs for Clinical Research on AIDS 009 Protocol Team.

C A Benson, P L Williams, D L Cohn...

https://pubmed.ncbi.nlm.nih.gov/10762562

Impact of prophylaxis for Mycobacterium avium complex on bacterial infections in patients with advanced human immunodeficiency virus disease.

J S Currier, P Williams, J Feinberg...

https://pubmed.ncbi.nlm.nih.gov/11340534