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| Sponsored by: |
National Institute of Allergy and Infectious Diseases (NIAID) |
|---|---|
| Information provided by: | National Institute of Allergy and Infectious Diseases (NIAID) |
| ClinicalTrials.gov Identifier: | NCT00000641 |
Purpose
To compare the effectiveness and toxicity of two combination drug treatment programs for the treatment of disseminated Mycobacterium avium infection in HIV seropositive patients. [Per 03/06/92 amendment: to evaluate the efficacy of azithromycin when given in conjunction with either ethambutol or clofazimine as maintenance therapy.] Disseminated M. avium infection is the most common systemic bacterial infection complicating AIDS in the United States. The prognosis of patients with disseminated M. avium is extremely poor, particularly when it follows other opportunistic infections or is associated with anemia. Test tube studies and clinical data indicate that the best treatment program may include clofazimine, ethambutol, a rifamycin derivative, and ciprofloxacin. Test tube and animal studies indicate that amikacin is a bactericidal (bacteria destroying) drug that works better when used with ciprofloxacin. Its role in treatment programs is a key issue because of toxicity and because it must be administered parenterally (by injection or intravenously).
| Condition | Intervention | Phase |
|---|---|---|
|
Mycobacterium Avium-Intracellulare Infection HIV Infections |
Drug: Ciprofloxacin hydrochloride Drug: Ethambutol hydrochloride Drug: Amikacin sulfate Drug: Azithromycin Drug: Rifampin Drug: Clofazimine |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Open Label |
| Official Title: | A Phase II/III Trial of Rifampin, Ciprofloxacin, Clofazimine, Ethambutol, and Amikacin in the Treatment of Disseminated Mycobacterium Avium Infection in HIV-Infected Individuals. |
| Estimated Enrollment: | 90 |
Disseminated M. avium infection is the most common systemic bacterial infection complicating AIDS in the United States. The prognosis of patients with disseminated M. avium is extremely poor, particularly when it follows other opportunistic infections or is associated with anemia. Test tube studies and clinical data indicate that the best treatment program may include clofazimine, ethambutol, a rifamycin derivative, and ciprofloxacin. Test tube and animal studies indicate that amikacin is a bactericidal (bacteria destroying) drug that works better when used with ciprofloxacin. Its role in treatment programs is a key issue because of toxicity and because it must be administered parenterally (by injection or intravenously).
Patients undergo an initial 2-week observation period (days 1 - 14) during which time baseline evaluations are performed and type and severity of symptoms are monitored. Eligible patients are randomized on day 15 to one of two treatment programs: (1) ciprofloxacin, clofazimine, ethambutol, and rifampin (all taken orally), or (2) the same four drugs plus amikacin. Only patients for whom blood cultures obtained on either day 1 or day 14/15 are positive by week 6 continue on study drugs. Patients receive combination therapy for 24 weeks. Patients may have an indwelling central venous catheter in place for long-term administration of intravenous drug. PER 03/06/92 AMENDMENT: Newly enrolled patients who demonstrate a complete or partial clinical response at the end of study week 10 (8 weeks of drug therapy) discontinue their current regimen and begin maintenance therapy with azithromycin plus either ethambutol or clofazimine for an additional 24 weeks. Patients who do not demonstrate a response at study week 10 are discontinued from all study therapy. Patients enrolled on earlier versions of the protocol who have surpassed study week 16 (14 weeks of drug therapy) continue treatment with their originally assigned regimen through study week 26; those who have not surpassed study week 16 are considered for inclusion in the maintenance phase of the study.
Eligibility| Ages Eligible for Study: | 13 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Concurrent Medication:
Allowed:
Concurrent Treatment:
Allowed:
Patients must have the following:
Prior Medication:
Allowed:
Exclusion Criteria
Co-existing Condition:
Patients with the following symptoms or conditions are excluded:
Treatment Phase:
Maintenance Phase:
Concurrent Medication:
Excluded:
Patients with the following are excluded:
Prior Medication:
Excluded:
History of unreliable drug intake.
Contacts and Locations
Show 38 Study Locations| Study Chair: | DM Parenti | |
| Study Chair: | J Ellner |
More Information
| Study ID Numbers: | ACTG 135 |
| Study First Received: | November 2, 1999 |
| Last Updated: | July 29, 2008 |
| ClinicalTrials.gov Identifier: | NCT00000641 |
| Health Authority: | United States: Federal Government |
|
Rifampin Mycobacterium avium-intracellulare Infection Drug Evaluation Drug Therapy, Combination Ethambutol |
Clofazimine Acquired Immunodeficiency Syndrome Amikacin Azithromycin Ciprofloxacin |
|
Bacterial Infections Sexually Transmitted Diseases, Viral Amikacin Acquired Immunodeficiency Syndrome Clofazimine Immunologic Deficiency Syndromes Mycobacterium Infections, Atypical Mycobacterium avium-intracellulare Infection Virus Diseases Ciprofloxacin |
Rifampin Gram-Positive Bacterial Infections HIV Infections Azithromycin Sexually Transmitted Diseases Mycobacterium Infections Ethambutol Mycobacterium avium complex infection Retroviridae Infections |
|
Anti-Inflammatory Agents Anti-Infective Agents Communicable Diseases Slow Virus Diseases Molecular Mechanisms of Pharmacological Action Physiological Effects of Drugs Infection Anti-Bacterial Agents Sensory System Agents Therapeutic Uses Anti-Inflammatory Agents, Non-Steroidal Analgesics Nucleic Acid Synthesis Inhibitors |
RNA Virus Infections Immune System Diseases Enzyme Inhibitors Pharmacologic Actions Actinomycetales Infections Antibiotics, Antitubercular Analgesics, Non-Narcotic Lentivirus Infections Peripheral Nervous System Agents Antitubercular Agents Antirheumatic Agents Central Nervous System Agents Leprostatic Agents |
