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Efficacy and Safety of Patidegib Gel 2% for Preventing Basal Cell Carcinomas on the Face of Adults With Gorlin Syndrome

About

Brief Summary

The aim of this clinical study is to find out how well Patidegib Gel 2% works in preventing new basal cell carcinomas (BCCs) developing on the face of adults with Gorlin syndrome, and how safe Patidegib Gel 2% is to use.

People who take part will apply either Patidegib Gel 2% or a Vehicle Gel (with no active drug substance) to their face twice a day for a year (12 months). The number of new BCCs on the face will be compared between those who used Patidegib Gel 2% or Vehicle Gel after 12 months.

Primary Purpose
The main objective of the intervention(s) being evaluated by the clinical trial. Learn more
Prevention
Study Type
The nature of the investigation or investigational use for which clinical study information is being submitted. Learn more
Interventional
Phase
Phase 3

Eligibility

Gender
All
Healthy Volunteers
No
Minimum Age
18 Years
Maximum Age
N/A

Key Inclusion Criteria:

  • The subject must be at least 18 years old at the Screening Visit.
  • The subject must be confirmed to have a PTCH1 mutation.
  • The subject must have at least 10 BCCs on the face at Randomization (Baseline/Day 1).
  • The subject must be willing to abstain from application of any non-study topical medication (prescription or over the counter) to their facial skin for the duration of the trial, except as prescribed by the investigator.

Key Exclusion Criteria:

  • The subject has used topical treatment to the face or systemic therapies that might interfere with the evaluation of the study Investigational Product (IP).
  • The subject is known to have hypersensitivity to any of the ingredients in the IP formulation.
  • The subject has uncontrolled systemic disease.
  • The subject has been treated for invasive cancer within the past 5 years excluding chronic lymphocytic leukemia Stage 0, non-melanoma skin cancer, successfully treated melanoma in situ and Stage I melanoma, Stage I cervical cancer, or ductal carcinoma in situ of the breast.
  • Inefficacy of previous Hedgehog inhibitor therapy.
Study Stats
Protocol No.
24-5043
Category
Adolescent & Young Adults (AYA)
Melanoma (Skin Cancer)
Contact
  • April Armstrong
Location
  • UCLA Santa Monica
  • UCLA Westwood
For Providers
NCT No.
NCT06050122
For detailed technical eligibility, visit ClinicalTrials.gov.