FOR U.S. RESIDENTS ONLY
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Penlac® provides targeted efficacy*
- Rapid mycological cure begins as early as week 12; these results were sustained throughout the entire 48-week study
- Proven efficacy demonstrated at 48 weeks
- In clinical studies, 12% or fewer patients achieved a clear or almost clear nail at the end of 48 weeks of treatment
Adapted from Penlac® Prescribing Information. Unretouched photographs. Results may vary.
Penlac® is safe and non-systemic
Penlac® safely treats onychomycosis at the site of infection
- No blood or liver function tests or monitoring are required with Penlac®
- No liver damage has been reported with Penlac® use
- No drug interactions have been reported with Penlac® use
- No serious treatment-related adverse events occurred with Penlac® during pivotal trials
| * | In 2 US pivotal trials (48 weeks each); trials were placebo-controlled, double-blind, randomized, and multicenter. |
| † | Clear nail and negative mycology in Pivotal Study 2; in Pivotal Study 1, the complete cure rate was 5.5%. |
| ‡ | ≤10% nail involvement and negative mycology in Pivotal Study 2; in Pivotal Study 1, the almost-clear rate was 6.5%. |
| § | Negative KOH and negative culture in Pivotal Study 2; in Pivotal Study 1, the mycological cure rate was 29%. |
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Penlac®, part of a comprehensive management program, includes regular removal of the unattached, infected nail by a health care professional, especially for patients with diabetes. Clinical data regarding use of systemic antifungals and Penlac® is not available to support concomitant use. Penlac® is well-tolerated: treatment-related side effects were periungual erythema (5%) and nail disorders (2%).
Patients with insulin-dependent diabetes or those with diabetic neuropathy were not included in pivotal clinical trials with Penlac®.