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Search / Trial NCT00002110

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

Drug Therapy, Combination Aids Related Complex Zidovudine Cysteamine

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.

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

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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