CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 395 enrolled
Drug / intervention
Ingenol mebutate gel +1 moredrug
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/NCT01820260
NCT01820260Phase 2Completed

Safety and Efficacy of Escalating Doses of Ingenol Mebutate Once Daily for Two or Three Consecutive Days When Used on Full Face, Full Balding Scalp or Approximately 250 cm2 on the Chest in Subjects With Actinic Keratosis

LEO Pharma·interventional·Posted Mar 28, 2013·Updated Mar 13, 2025

In Brief

A Phase 2 clinical trial evaluating Ingenol mebutate gel and placebo for Actinic Keratosis. Completed, enrolled 395 participants across 1 site.

Detailed Summary

To identify the Maximum Tolerated Dose levels of ingenol mebutate gel after once daily treatment for 2 or 3 consecutive days and to evaluate efficacy of ingenol mebutate gel in different doses after once daily treatment for 2 or 3 consecutive days compared to vehicle gel

Study Details

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

Timeline

Phase 2CompletedFinished
20132014201520162017201820192020202120222023202420252026
First PostedMar 28, 2013
Enrollment StartApr 1, 2013
Primary CompletionAug 1, 2014
TodayJul 2, 2026
Enrollment to primary: 1.3 yearsPosted 13.3 years ago

Interventions

Ingenol mebutate geldrug

placebodrug