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
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.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Los Angeles, California, United States
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Discussion 0
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