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Spots Global Cancer Trial Database for An Study of Patidegib Topical Gel, 2%, for the Reduction of Disease Burden of Persistently Developing Basal Cell Carcinomas in Patients With Non-Gorlin High Frequency BCC

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Trial Identification

Brief Title: An Study of Patidegib Topical Gel, 2%, for the Reduction of Disease Burden of Persistently Developing Basal Cell Carcinomas in Patients With Non-Gorlin High Frequency BCC

Official Title: A Multicenter, Randomized, Double Blind, Vehicle-controlled, Phase 2 Efficacy and Safety Study of Patidegib Topical Gel, 2%, for the Reduction of Disease Burden of Persistently Developing Basal Cell Carcinomas (BCCs) in Patients With Non-Gorlin High Frequency BCC

Study ID: NCT04155190

Study Description

Brief 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.

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Axiom Research, LLC, Apple Valley, California, United States

Axiom Research, LLC, Colton, California, United States

Center for Dermatology Clinical Research, Inc., Fremont, California, United States

Dermatology Research Associates, Los Angeles, California, United States

The Dermatology Center of Newport, Newport Beach, California, United States

Palm Beach Dermatology Research, Delray Beach, Florida, United States

Leavitt Medical Associates of Florida, Ormond Beach, Florida, United States

PellePharm Investigative Site, Saint Augustine, Florida, United States

The Indiana Clinical Trials Center, Plainfield, Indiana, United States

Grekin Skin Institute, Warren, Michigan, United States

PellePharm Investigative Site, Henderson, Nevada, United States

Skin Laser and Surgery Specialists of NY&NJ, Hackensack, New Jersey, United States

Duke University Medical Center, Durham, North Carolina, United States

University of Utah, Murray, Utah, United States

Contact Details

Name: VP, Clinical Operations

Affiliation: PellePharm, Inc.

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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