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Brief Title: Study on the Safety and Efficacy of Bimiralisib Gel in Participants Suffering From Actinic Keratosis
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
Study ID: NCT06319794
Brief Summary: 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
Detailed Description: 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
Minimum Age: 50 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University Hospital Basel / Department of Dermatology, Basel, , Switzerland
CHUV centre hospitalier universitaire vaudois / Department of Dermatology and Venereology, Lausanne, , Switzerland