A Phase II/III Study of Cysteamine (Mercaptoethylamine) and Zidovudine for the Treatment of HIV Disease
Launched by MYLAN LABORATORIES · Aug 30, 2001
Trial Information
Current as of March 27, 2025
Completed
Keywords
ClinConnect Summary
Patients receive high or low doses of cysteamine plus AZT or placebo plus AZT. The target dose of cysteamine is determined by titration of the dose over a 6-week period, after which the patient receives 24 additional weeks of treatment. An initial cohort of 36 patients will be enrolled in a 10-week pilot phase. Accrual will be temporarily suspended while data from the pilot phase is assessed.
Gender
ALL
Eligibility criteria
- • Inclusion Criteria
- Concurrent Medication:
- Allowed:
- • Chemoprophylaxis for Pneumocystis carinii pneumonia, candidiasis, Mycobacterium tuberculosis, and herpes as prescribed by the investigator.
- • Recombinant erythropoietin and G-CSF if clinically indicated.
- Patients must have:
- • Documented HIV infection.
- • CD4 count 300 - 500 cells/mm3.
- • Prior AZT therapy for at least 3 months but less than 12 months prior to study entry.
- • No past or current AIDS-defining opportunistic infection.
- • Exclusion Criteria
- Co-existing Condition:
- Patients with the following symptoms or conditions are excluded:
- • Kaposi's sarcoma requiring systemic therapy.
- • Active malignancy other than basal cell carcinoma or in situ cervical carcinoma.
- Concurrent Medication:
- Excluded:
- • Antiretroviral therapy other than AZT.
- • Immunosuppressive drugs.
- • Investigational HIV drugs/therapies other than study drug.
- • Interferon.
- • Steroids.
- • Hematopoietins.
- • Cytotoxic chemotherapy including Adriamycin, bleomycin, and vincristine.
- Concurrent Treatment:
- Excluded:
- • Radiation therapy.
- Patients with the following prior condition are excluded:
- • History of treatment-limiting intolerance to 500-600 mg AZT daily as manifested by the same recurrent grade 3 toxicity or any prior grade 4 toxicity.
- Prior Medication:
- Excluded:
- • Prior antiretroviral therapy other than AZT.
- Required:
- • AZT for at least 3 months but no more than 12 months prior to study entry.
About Mylan Laboratories
Mylan Laboratories, now part of Viatris, is a global pharmaceutical company committed to providing access to high-quality medicines. With a robust portfolio that includes generic and specialty pharmaceuticals, Mylan focuses on delivering affordable healthcare solutions across various therapeutic areas. The company is dedicated to innovation and the development of complex generics, biosimilars, and over-the-counter products. Mylan’s commitment to rigorous clinical trials ensures the safety and efficacy of its offerings, making it a trusted partner in improving patient outcomes worldwide.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
New Orleans, Louisiana, United States
Dallas, Texas, United States
Stony Brook, New York, United States
Tampa, Florida, United States
Winston Salem, North Carolina, United States
Cranston, Rhode Island, United States
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Discussion 0
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