A randomized trial to assess once-daily topical treatment of tinea corporis with butenafine, a new antifungal agent - 11/09/11
Abstract |
Background: Tinea corporis treatment usually requires topical application of an antifungal agent for 2 to 3 weeks. Objective: We evaluated short-term treatment of tinea corporis with butenafine hydrochloride, a new benzylamine with in vitro fungicidal activity. Methods: Patients (n = 78) were randomly selected to apply butenafine or its cream vehicle alone once daily for 14 days and were periodically assessed until day 42. Results: Butenafine recipients had significantly higher rates of mycologic cure beginning at day 7 (64% vs 9%) with continued improvements through day 42 (88% vs 17%). They also had higher rates of effective treatment (mycologic cure and 90% to 100% symptom improvement) at day 7 (33% vs 0%) with increasing rates through day 42 (81% vs 14%). Conclusion: Butenafine provides rapid and persistent antifungal activity and symptom relief in patients with tinea corporis. Significant effects were observed within 7 days of therapy initiation, and increasing effectiveness was observed 4 weeks after therapy. (J Am Acad Dermatol 1997;37:231-5.)
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Supported by Penederm Inc., Foster City, Calif. |
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Reprint requests: Donald L. Greer, PhD, Department of Dermatology, LSU Medical Center, 1542 Tulane Ave., New Orleans, LA 70112. |
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0190-9622/97/$5.00 + 0 16/1/82015 |
Vol 37 - N° 2P1
P. 231-235 - août 1997 Retour au numéroBienvenue sur EM-consulte, la référence des professionnels de santé.
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