A Comparison of 882C87 Versus Acyclovir in the Treatment of Herpes Zoster in Patients With Weakened Immune Systems
Launched by GLAXO WELLCOME · Aug 30, 2001
Trial Information
Current as of March 21, 2025
Completed
Keywords
ClinConnect Summary
Patients are randomized to receive either 882C87 or acyclovir with corresponding placebos for 14 days, with two hundred patients in each of the two groups. They are stratified by presence or absence of HIV infection. Patients undergo 6 months of follow-up.
Gender
ALL
Eligibility criteria
- • Inclusion Criteria
- Patients must have:
- • Acute localized herpes zoster or rash present less than 72 hours, verified by clinical diagnosis.
- • Immunocompromised condition primarily as a result of documented HIV infection, malignancy, chemotherapy or radiation therapy, solid organ or bone marrow transplant, or chronic immunosuppressive therapy.
- • Life expectancy of at least 6 months.
- • Ability to cooperate with the requirements of the study.
- • Exclusion Criteria
- Co-existing Condition:
- Patients with the following symptoms or conditions are excluded:
- • Evidence of cutaneous or visceral dissemination (more than 20 discrete lesions outside adjacent dermatomes).
- • Acute, life-threatening condition.
- • Significant malabsorption syndrome or other gastrointestinal dysfunction that may severely reduce drug absorption.
- • Intolerance of oral medication.
- Concurrent Medication:
- Excluded:
- • Tricyclic antidepressants or anti-epileptics.
- • Topical applications to the zoster lesions that would obscure evaluation.
- • Fluorouracil and flucytosine.
- • Systemic therapy with agents with antiherpetic activity (from 2 weeks prior to first dose to day 28 of study).
- • Probenecid or other drugs likely to affect elimination of study drugs (from 2 days prior to first dose to day 14 of the study).
- • Capsaicin (Zostrix).
- • Warfarin (Coumadin) during 14 days of treatment.
- Patients with the following prior conditions are excluded:
- • History of intolerance, hypersensitivity, or severe drug reaction to acyclovir.
- Prior Medication:
- Excluded:
- • Systemic therapy with agents with antiherpetic activity (including interferon) within the past 2 weeks.
- • Probenecid or other drugs likely to affect the elimination of 882C87 or acyclovir within the past 48 hours.
- • Drugs likely to interact with 882C87 (e.g., fluorouracil or flucytosine) within the past 7 days.
- • Zoster immune globulin or zoster immune plasma within the previous month. History of alcohol or drug abuse within the previous 6 months or current methadone 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
Dallas, Texas, United States
Los Angeles, California, United States
Redwood City, California, United States
San Francisco, California, United States
Providence, Rhode Island, United States
Portland, Oregon, United States
Houston, Texas, United States
Sunnyvale, California, United States
St. Louis, Missouri, United States
New Orleans, Louisiana, United States
Birmingham, Alabama, United States
Birmingham, Alabama, United States
Tucson, Arizona, United States
Trumbull, Connecticut, United States
Dubuque, Iowa, United States
Albuquerque, New Mexico, United States
High Point, North Carolina, United States
Wilmington, North Carolina, United States
Eugene, Oregon, United States
Providence, Rhode Island, United States
Nashville, Tennessee, United States
Nassau Bay, Texas, United States
Tacoma, Washington, United States
Milwaukee, Wisconsin, United States
Rhinelander, Wisconsin, United States
People applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
Discussion 0
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