NexMed, Inc.

NexMed Announces Decision for NM100060

Published in Medical Letter on the CDC and FDA, September 14th, 2008

NexMed, Inc. (Nasdaq: NEXM), a developer of products based on the NexACT(R) drug delivery technology, announced that based on First Interpretable Results of Phase III clinical studies for NM100060, a topical application of terbinafine formulated with NexACT(R) for the treatment of onychomycosis, the decision has been taken not to submit a New Drug Application with the Food and Drug Administration at this time.

The two NM100060 clinical studies were randomized, double-blind and placebo-controlled, and designed to assess the efficacy, safety and tolerability of NM100060 in patients with mild to moderate toenail onychomycosis (nail fungus). No significant adverse event was...

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Source: Medical Letter on the CDC and FDA (2008-09-14)

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