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Last Updated: 09/18/2022

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Phase I, Open Label Study Designed to Evaluate the Safety and Efficacy of a 1% Topical Formulation of KM-001 in the Treatment of Type I Punctate Palmoplantar Keratoderma or Pachyonychia Congenital Diseases

Summary: In this phase 1 open label study, up to 10 eligible patients with type I punctate palmoplantar keratoderma or pachyonychia congenital will be recruited to be treated twice daily, for 12 weeks, with 1% topical KM-001.~Treatment safety and efficacy will be assessed in the clinic on Days 7, 21, 42, 56, 70 and 84 after initiation of treatment. In between visits, safety will also be assessed by phone o...
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Last Updated: 09/18/2022