CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 20 enrolled
Drug / intervention
ingenol mebutate gel 0.015%drug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02866695
NCT02866695Phase 4Completed

Safety and Efficacy of Ingenol Mebutate Gel 0.015% for Treatment of Actinic Keratosis on the Face in Solid Organ Transplant Recipients

University of California, San Francisco·interventional·Posted Aug 15, 2016·Updated Mar 9, 2022

In Brief

A Phase 4 clinical trial evaluating ingenol mebutate gel 0.015% for Actinic Keratosis. Completed, enrolled 20 participants across 1 site.

Detailed Summary

This is a single arm, open-label interventional study of ingenol mebutate 0.015% in solid organ transplant recipients. The investigators plan to treat 20 subjects, 10 kidney transplant recipients and 10 lung transplant recipients. The investigators have selected these two populations as the represent the spectrum of solid organ transplantation: kidney transplant recipients are the largest transplant population, but have lower levels of immunosuppression and skin cancer risk. Lung transplant recipients have the highest burden of skin cancer and actinic keratoses.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
2017201820192020202120222023202420252026
First PostedAug 15, 2016
Enrollment StartOct 6, 2016
Primary CompletionJul 2, 2018
TodayJul 2, 2026
Enrollment to primary: 1.7 yearsPosted 9.9 years ago

Interventions

ingenol mebutate gel 0.015%drug

ingenol mebutate gel 0.015% to be applied on treatment area