A Study of Azithromycin Plus Pyrimethamine in the Treatment of a Brain Infection in Patients With AIDS
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Purpose
To evaluate the effectiveness and toxicity of oral azithromycin and pyrimethamine as acute therapy for toxoplasmic encephalitis in AIDS patients. To assess the toxicity and effectiveness of azithromycin alone as maintenance therapy.
Encephalitis caused by Toxoplasma gondii is the most frequent cause of focal central nervous system infection in patients with AIDS. Untreated, the encephalitis is fatal. Standard treatment for toxoplasmic encephalitis is associated with serious adverse effects. Thus, alternative treatments are needed.
| Condition | Intervention | Phase |
|---|---|---|
|
Toxoplasmosis, Cerebral HIV Infections |
Drug: Azithromycin Drug: Pyrimethamine Drug: Leucovorin calcium |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Primary Purpose: Treatment |
| Official Title: | A Dose-Escalation, Phase I/II Study of Oral Azithromycin and Pyrimethamine for the Treatment of Toxoplasmic Encephalitis in Patients With AIDS |
| Estimated Enrollment: | 45 |
Encephalitis caused by Toxoplasma gondii is the most frequent cause of focal central nervous system infection in patients with AIDS. Untreated, the encephalitis is fatal. Standard treatment for toxoplasmic encephalitis is associated with serious adverse effects. Thus, alternative treatments are needed.
Patients with toxoplasmosis are given azithromycin at doses starting at the lowest dose for the first cohort, an intermediate dose for the second cohort, and a higher dose for the third cohort. Subsequent cohorts may receive azithromycin in increased dosage, if needed to determine the MTD. All patients also receive pyrimethamine. Folinic acid is also provided for as long as patients receive pyrimethamine. Patients are evaluated for clinical response to treatment at days 3, 7, and 14, and weekly for 6 weeks. Maintenance treatment with azithromycin continues for an additional 24 weeks. Patients who complete the study period without relapse or significant toxicity are offered continued therapy by the drug company and are followed for survival and relapse on a monthly basis for 1 year. After the MTD is determined, a subsequent cohort may be added for special studies.
Eligibility| Ages Eligible for Study: | 13 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Concurrent Medication:
Allowed:
- Aerosolized pentamidine for prophylaxis against Pneumocystis carinii pneumonia (PCP).
- Allowed during maintenance period (weeks 7 - 24):
- Zidovudine and other antiretrovirals available through treatment IND mechanisms, ganciclovir, and maintenance doses of amphotericin (other investigational therapies require permission from the study chair), steroids for the treatment of acute PCP.
- Isoniazid (INH) only for patients already on INH.
Patients must have the following:
- HIV infection or belong to high-risk group. Presumptive or definite diagnosis of toxoplasmic encephalitis.
- Each patient, or his/her appropriate family member, or legal designee must be able to understand and sign a written informed consent, in accordance with the local practices at each site.
Exclusion Criteria
Co-existing Condition:
Patients with the following conditions or symptoms are excluded:
- History of cerebral toxoplasmosis or toxoplasmosis infection in any other organ or tissue.
- Coma.
- More than 72 hours of treatment for current episode of toxoplasmic encephalitis prior to study entry.
- Central nervous system (CNS) lymphoma.
- Cerebral Kaposi's sarcoma.
- Active hepatitis or clinical jaundice.
- History of serious hypersensitivity or intolerance to any of the study drugs.
- Serum or cerebrospinal fluid (CSF) positive for cryptococcus antigen or culture.
- Malignancies requiring use of cytotoxic chemotherapy.
- Inability to take oral therapy reliably.
- Malabsorption syndrome.
Concurrent Medication:
Excluded:
- Opportunistic infection requiring either acute treatment or maintenance therapy with azithromycin, erythromycin or other macrolides, sulfonamides, amphotericin, dapsone, ganciclovir, antifolates, and other investigational agents except erythropoietin. For first 6 weeks of treatment, patients may not receive treatment with erythromycin (or other macrolides), sulfonamides, immunomodulators with the exception of alpha interferon, lymphocyte replacement, cytotoxic chemotherapy, dapsone, ganciclovir, rifampicin, coumadin, antiretrovirals, and investigational agents other than erythropoietin.
Patients with the following are excluded:
- Negative HIV antibodies by a federally licensed ELISA, unless there is documentation of a previously positive HIV culture or p24 antigen.
- Infections of the central nervous system.
- Malignancies requiring the use of cytotoxic chemotherapy.
- Any medical or social condition that, in the opinion of the investigator, would adversely affect participation and/or compliance in this study.
Contacts and Locations| United States, California | |
| Los Angeles County - USC Med Ctr | |
| Los Angeles, California, United States, 90033 | |
| United States, Florida | |
| Univ of Miami School of Medicine | |
| Miami, Florida, United States, 331361013 | |
| United States, Massachusetts | |
| Univ of Massachusetts Med Ctr | |
| Worcester, Massachusetts, United States, 01655 | |
| United States, New York | |
| Bronx Veterans Administration / Mount Sinai Hosp | |
| Bronx, New York, United States, 10468 | |
| Bronx Municipal Hosp Ctr/Jacobi Med Ctr | |
| Bronx, New York, United States, 10461 | |
| Montefiore Med Ctr / Bronx Municipal Hosp | |
| Bronx, New York, United States, 10467 | |
| Nassau County Med Ctr | |
| East Meadow, New York, United States, 11554 | |
| Cornell Univ Med Ctr | |
| New York, New York, United States, 10021 | |
| Bellevue Hosp / New York Univ Med Ctr | |
| New York, New York, United States, 10016 | |
| SUNY - Stony Brook | |
| Stony Brook, New York, United States, 117948153 | |
| United States, South Carolina | |
| Julio Arroyo | |
| West Columbia, South Carolina, United States, 29169 | |
| Study Chair: | Luft B | |
| Study Chair: | Remington J |
More Information
Additional Information:
Publications:
| ClinicalTrials.gov Identifier: | NCT00000966 History of Changes |
| Other Study ID Numbers: | ACTG 156 |
| Study First Received: | November 2, 1999 |
| Last Updated: | August 25, 2008 |
| Health Authority: | Unspecified |
Keywords provided by National Institute of Allergy and Infectious Diseases (NIAID):
|
Toxoplasmosis Toxoplasma Pyrimethamine Leucovorin Drug Evaluation |
Drug Therapy, Combination Encephalitis Administration, Oral Acquired Immunodeficiency Syndrome Azithromycin |
Additional relevant MeSH terms:
|
HIV Infections Acquired Immunodeficiency Syndrome Encephalitis Toxoplasmosis Toxoplasmosis, Cerebral Lentivirus Infections Retroviridae Infections RNA Virus Infections Virus Diseases Sexually Transmitted Diseases, Viral Sexually Transmitted Diseases Immunologic Deficiency Syndromes Immune System Diseases Slow Virus Diseases Central Nervous System Viral Diseases |
Brain Diseases Central Nervous System Diseases Nervous System Diseases Central Nervous System Infections Coccidiosis Protozoan Infections Parasitic Diseases Brain Abscess Abscess Suppuration Infection Central Nervous System Protozoal Infections Central Nervous System Parasitic Infections Leucovorin Levoleucovorin |
ClinicalTrials.gov processed this record on June 18, 2013