Actinic Keratosis Clinical Trial
Official title:
A Randomized Phase 2 Proof-of-Concept Study to Evaluate the Efficacy and Safety of Topical Bimiralisib Application in Participants Suffering From Actinic Keratosis on the Face and/or Scalp and/or Back of Hands Over a 2 and 4-week Treatment Period
The aim of the study is to evaluate efficacy and safety of bimiralisib gel treatment for treatment of actinic keratosis (AK) on the face and/or scalp and/or back of hands
This is a multi-center, randomized, open label, parallel group study. The study products will be applied to the target lesions for a duration of 2 or 4 weeks of treatment. The study consists of the following periods: - Screening (up to 30 days) - Treatment (2 or 4 weeks) - Follow-Up (4 weeks) Participants will be randomized to one of two groups (1:1): - Arm A: Topical bimiralisib gel treatment for 2 weeks - Arm B: Topical bimiralisib gel treatment for 4 weeks ;
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