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Clinical Trials

Lamisil Solution, 1%

The following drug information is obtained from various newswires, published medical journal articles, and medical conference presentations.


Approval Status:

Approved March 2001

Specific Treatments:

Dermatologic infections

General Information

Lamisil Solution, 1% is a synthetic antifungal compound approved for the topical treatment of tinea (pityriasis) versicolor due to Malassezia furfur, and tinea pedis (athlete's foot), tinea cruris (jock itch), or tinea corporis (ringworm), due to Trichophyton rubrum, Trichophyton mentagrophytes, or Epidermaphyton floccosum.

Lamisil Solution, 1% is designed for one week usage and is administered to the infected area once or twice daily, depending on indication.

Clinical Results

The effectiveness of Lamisil Solution, 1% was evaluated in separate eight week placebo-controlled trials for tinea (pityriasis) versicolor, tinea pedis, and tinea corporis/cruris, involving a total of 898 subjects. In the majority of pateints, relief of symptoms began within the one week treatment period and continued improvement was recorded over the following seven weeks. (from Lamisil Solution, 1% Prescribing Information)

Side Effects

Adverse events associated with the use of terbinafine hydrochloride may include (but are not limited to) the following:

  • site irritation
  • itching
  • skin exfoliation
  • erythematous rash

Mechanism of Action

Lamisil Solution, 1% (terbinafine hydrochloride solution) is a synthetic allyamine derivative. Terbinafine hydrochloride is thought to act by inhibiting the epoxidation of squalene, thus blocking the biosysnthesis of ergosterol, an essential component of fungal cell membranes. Depending on the concentration of the drug and the fungal species being tested in vitro, terbinafine hydrochloride may be fungicidal. (from Lamisil Solution, 1% Prescribing Information)

Additional Information

For additional information on Lamisil Solution, 1%, please visit Novartis.

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