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Clinical Trial Summary

This is a multicenter, randomized, double-blind, stratified, vehicle-controlled study of the efficacy and safety of Patidegib Topical Gel, 2%, applied topically twice daily to the face of adult participants with non-Gorlin HF-BCC (high-frequency basal cell carcinoma). Participants will be randomized (1:1) to receive either Patidegib Topical Gel, 2%, or Vehicle for 9 months. Randomization will be stratified by gender. The primary endpoint is the number of nSEB (surgically eligible basal cell carcinoma) that develop on the face over the 9 month period. The primary end point will be assessed by imaging and tracking of BCCs consistently throughout the study in order to identify nSEBs.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04155190
Study type Interventional
Source Sol-Gel Technologies, Ltd.
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Status Terminated
Phase Phase 2
Start date December 20, 2019
Completion date April 23, 2021