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Terminated Phase 3 Interventional Results available

Extension Study of Patidegib Topical Gel, 2% in Subjects With Gorlin Syndrome (Basal Cell Nevus Syndrome)

ClinicalTrials.gov ID: NCT04308395

Public ClinicalTrials.gov record NCT04308395. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 4:15 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Multicenter, Open-Label Extension Study of Patidegib Topical Gel, 2% in Subjects With Gorlin Syndrome (Basal Cell Nevus Syndrome)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a multicenter, open label extension study evaluating the safety of Patidegib Topical Gel, 2%, applied topically twice daily to the face of adult subjects with Gorlin syndrome.

Study identification

NCT ID
NCT04308395
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Sol-Gel Technologies, Ltd.
Industry
Enrollment
108 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 3, 2020 (Actual)
Primary completion
Jul 14, 2021 (Actual)
Completion
Jul 14, 2021 (Actual)
Last update posted
Sep 24, 2024

2020 – 2021

United States locations

U.S. sites
17
U.S. states
15
U.S. cities
17
Facility City State ZIP Site status
PellePharm Investigative Site Fremont California 94538 —
PellePharm Investigative Site Newport Beach California 92660 —
Yale University New Haven Connecticut 06519 —
Pellepharm Investigative Site Miami Florida 33125 —
PellePharm Investigative Site Ormond Beach Florida 32174 —
PellePharm Investigative Site Chicago Illinois 60637 —
Laser & Skin Surgery Center of Indiana Indianapolis Indiana 46260 —
Pellepharm Investigative Site Ann Arbor Michigan 48109 —
University of Minnesota Minneapolis Minnesota 55455 —
Saint Louis University St Louis Missouri 63104 —
Columbia University Irving Medical Center New York New York 10032 —
Duke University Medical Center Durham North Carolina 27710 —
Cleveland Clinic Cleveland Ohio 44195 —
Oregon Health and Science University Portland Oregon 97239 —
Penn State Health Milton S. Hershey Medical Center Hershey Pennsylvania 17033 —
MD Anderson Cancer Center Houston Texas 77030 —
University of Utah, Midvalley Dermatology Murray Utah 84107 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 20 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT04308395, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 24, 2024 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT04308395 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →