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Clinical Trial Summary

This Phase III study was designed to evaluate the efficacy and safety of KX2-391 Ointment 1% in adult participants when applied to an area of skin containing 4-8 stable, clinically typical actinic keratosis (AK) lesions on the face or scalp.


Clinical Trial Description

This study was a double-blinded, multicenter, efficacy, and safety study of KX2-391 ointment administered topically to the face or scalp of participants with AK. The study consisted of Screening, Treatment, Follow-up, and Recurrence Follow-up Periods. Eligible participants received up to 5 consecutive days of topical treatment. Efficacy (lesion counts) and safety evaluations were performed. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03285490
Study type Interventional
Source Almirall, S.A.
Contact
Status Completed
Phase Phase 3
Start date September 15, 2017
Completion date April 24, 2019

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