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Search / Trial NCT00002315

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

Herpes Zoster Acyclovir Acquired Immunodeficiency Syndrome Aids Related Complex Antiviral Agents

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.

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

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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