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Search / Trial NCT00002026

Treatment and Suppression of Hairy Leukoplakia in ARC Patients With Oral Acyclovir (ACV)

Launched by GLAXO WELLCOME · Aug 30, 2001

Trial Information

Current as of March 23, 2025

Completed

Keywords

Aids Related Opportunistic Infections Leukoplakia, Oral Herpesvirus 4, Human Acyclovir Aids Related Complex

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria
  • Concurrent Medication:
  • Allowed:
  • Topical antifungal therapy.
  • Patient must have:
  • Newly diagnosed clinical and histological hairy leukoplakia.
  • Positive HIV antibody by licensed ELISA or Western blot.
  • Exclusion Criteria
  • Co-existing Condition:
  • Patients with AIDS or a history of intolerance or allergy to acyclovir are excluded.
  • Concurrent Medication:
  • Excluded within 2 weeks of study entry:
  • Systemic antifungal treatment.
  • * Excluded within 6 weeks of study entry:
  • Immunomodulators.
  • Systemic antiviral treatment.
  • Patients with AIDS or a history of intolerance or allergy to acyclovir are excluded.
  • Prior Medication:
  • Excluded within 2 weeks of study entry:
  • Systemic antifungal.
  • * Excluded within 6 weeks of study entry:
  • Immunomodulators.
  • Systemic antiviral treatment.
  • * Excluded within 8 weeks of study entry:
  • Zidovudine (AZT) or other antiretroviral therapy.

About Glaxo Wellcome

Glaxo Wellcome, a leading global biopharmaceutical company, is dedicated to advancing healthcare through innovative research and development of new therapies. With a strong focus on addressing unmet medical needs, Glaxo Wellcome combines scientific excellence with a commitment to improving patient outcomes across various therapeutic areas, including respiratory, infectious diseases, and oncology. The company is recognized for its robust clinical trial portfolio, leveraging cutting-edge technology and collaborative partnerships to drive the development of transformative treatments. Glaxo Wellcome upholds the highest ethical standards in clinical research, ensuring patient safety and integrity throughout the trial process.

Locations

Los Angeles, California, United States

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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