Document 1093 DOCN M94A1093 TI Human leukocyte alpha-interferon in cream for the treatment of genital herpes. A placebo-controlled, double-blind study. DT 9412 AU Syed TA; Lundin S; Kahlon BM; Ahmad SA; Kahlon RC; Dept. of Clinical Physiology, University Hospital Malmo,; University of Lund, Sweden. SO Int Conf AIDS. 1994 Aug 7-12;10(2):210 (abstract no. PB0852). Unique Identifier : AIDSLINE ICA10/94371482 AB OBJECTIVE: The study was conducted to evaluate the clinical efficacy of human leukocyte alpha-interferon in cream containing 2 x 10(6) IU/g to cure patients afflicted with first episodes of genital herpes. METHODS: Patients (n = 60) aged 18-40 years (mean 22.8 years) with culture-proven herpes simplex genitalis, harboring 752 lesions (mean 12.3 number) were randomly allocated into two parallel groups, (active/placebo). Each patient received a 40 g tube with instructions to apply the test medication on their lesions thrice daily for five consecutive days, (max. 15 topical applications per week). Study was scheduled for 16 weeks, with (4 weeks active treatment). Patients were examined on weekly basis. A completely re-epitheliazed lesion with persistent erythema was evaluated as healed or cured. RESULTS: Leukocyte alpha-interferon cream treated patients had significantly shorter mean duration of viral shedding/healing than placebo recipients, 7 days vs. 15 days (p < 0.01), and so the number of cured patients, 24/30 (80%) vs. 5/30 (17%) p < 0.001, with no complaint of adverse symptoms. CONCLUSION: Leukocyte alpha-interferon (2 x 10(6) IU/g) in hydrophilic cream is more efficacious than placebo and can be considered a home-based reliable treatment to cure genital herpes in males. DE Administration, Topical Adolescence Adult Double-Blind Method Herpes Genitalis/*DRUG THERAPY Human Interferon-alpha/*ADMINISTRATION & DOSAGE Ointments CLINICAL TRIAL MEETING ABSTRACT RANDOMIZED CONTROLLED TRIAL SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).