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Suppression of Frequently Recurring Genital Herpes — A Placebo-Controlled Double-Blind Trial of Oral Acyclovir

List of authors.
  • Stephen E. Straus, M.D.,
  • Howard E. Tariff, M.D.,
  • Mindell Seidlin, M.D.,
  • Susan Bachrach, R.N.,
  • Lloyd Lininger, Ph.D.,
  • John J. DiGiovanna, M.D.,
  • Karl A. Western, M.D.,
  • Holly A. Smith,
  • Sandra Nusinoff Lehrman, M.D.,
  • Teresa Creagh-Kirk, M.S.,
  • and David W. Alling, M.D.

Abstract

We studied 35 otherwise healthy adults with frequently recurring genital herpes (≥1 episode per month), in a double-blind trial comparing oral acyclovir with placebo capsules for suppression of recurrent infection. The patients were treated for 125 days unless herpes recurred. Among 32 evaluable patients, there were significantly fewer recurrences during acyclovir treatment (4 of 16) than during placebo treatment (16 of 16, P<0.001). The mean duration of therapy was significantly longer for patients receiving acyclovir than for those receiving placebo (114.9 vs. 24.8 days, P<0.001). Of 19 patients who had recurrences in the blind trial, only 2 had recurrences when given acyclovir in a second, open-study phase. All patients had recurrences after completing acyclovir treatment. The therapy was well tolerated, with minimal gastrointestinal upset and one hypersensitivity reaction. Studies of the viral isolates demonstrated that lesions developing in patients receiving acyclovir contained drug-resistant virus. Later recurrences in these patients were associated with drug-sensitive virus.

We conclude that oral acyclovir suppresses genital herpes in patients with frequent recurrences, but the potential for problems with drug resistance and the long-term safety need to be more fully explored. (N Engl J Med 1984; 310:1545–50.)

Funding and Disclosures

We are indebted to Carol Crout and Karen Leighty for assistance in manuscript preparation and editing; to Ralph Wright for supervising the outpatient clinic; to George Grimes and James Wilson for coordinating and monitoring the proper distribution of study drugs; to Paulo de Miranda for performing the urinary acyclovir assays; to M. Nixon Ellis, Cornelia Dekker, and Paul Keller for acyclovir sensitivity and thymidine kinase determinations; and to Gerald Macks of the National Institutes of Health Medical Information System Project for assistance with computerized compilation of laboratory data.

Author Affiliations

From the Laboratory of Clinical Investigation and the Office of the Director, National Institute of Allergy and Infectious Diseases, the Clinical Center, and the Dermatology Branch, National Cancer Institute, National Institutes of Health, Bethesda, Md., and the Burroughs Wellcome Co., Research Triangle Park, N.C. Address reprint requests to Dr. Straus at the Medical Virology Section, Laboratory of Clinical Investigation. Bldg. 10, Km. 11N–113, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda. MD 20205.

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