Oral terbinafine in the treatment of toenail onychomycosis: North American multicenter trial

J Am Acad Dermatol. 1997 Nov;37(5 Pt 1):740-5. doi: 10.1016/s0190-9622(97)70111-7.

Abstract

Background: Onychomycosis is an increasing problem with limited therapeutic options.

Objective: We evaluated the safety and efficacy, of oral terbinafine, a new fungicidal antimycotic, in patients with toenail onychomycosis.

Methods: A North American multicenter, double-blind, placebo-controlled study evaluated the mycologic and clinical efficacy of oral terbinafine 250 mg/day for 12 or 24 weeks in 358 patients with toenail onychomycosis.

Results: A total of 74% of patients treated with 12 or 24 weeks of terbinafine achieved a successful clinical outcome. Approximately 11% of terbinafine responders showed evidence of relapse 18 of 21 months after cessation of treatment. Terbinafine was well tolerated; most adverse events were transient and mild to moderate in severity.

Conclusion: The results of this study confirm that oral terbinafine is a safe and effective therapy for the treatment of onychomycosis.

Publication types

  • Clinical Trial
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abdominal Pain / chemically induced
  • Administration, Oral
  • Adult
  • Aged
  • Antifungal Agents / adverse effects
  • Antifungal Agents / therapeutic use*
  • Diarrhea / chemically induced
  • Double-Blind Method
  • Drug Eruptions / etiology
  • Epidermophyton / isolation & purification
  • Female
  • Follow-Up Studies
  • Humans
  • Male
  • Middle Aged
  • Naphthalenes / adverse effects
  • Naphthalenes / therapeutic use*
  • Onychomycosis / diagnosis
  • Onychomycosis / drug therapy*
  • Onychomycosis / microbiology
  • Recurrence
  • Terbinafine
  • Toes
  • Trichophyton / isolation & purification

Substances

  • Antifungal Agents
  • Naphthalenes
  • Terbinafine