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Completed Phase 1Phase 2 Interventional Results available

Safety and Efficacy of Escalating Doses of LEO 43204 Applied Once Daily for Two Consecutive Days on Approximately 250 cm2 on Trunk and Extremities in Subjects With Actinic Keratosis

ClinicalTrials.gov ID: NCT02120456

Public ClinicalTrials.gov record NCT02120456. 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 22, 2026, 12:48 AM EDT

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

Brief summary

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

Part 1: To identify Maximum Tolerated Dose (MTD) levels of LEO 43204 after once daily treatment for two consecutive days Part 2: To evaluate the efficacy of LEO 43204 in two doses after once daily treatment for two consecutive days compared to vehicle

Study identification

NCT ID
NCT02120456
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
LEO Pharma
Industry
Enrollment
224 participants

Conditions and interventions

Interventions

Drug

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
May 2014 (Type not available)
Primary completion
May 2015 (Actual)
Completion
May 2015 (Actual)
Last update posted
Mar 6, 2025

2014 – 2015

United States locations

U.S. sites
13
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Omni Dermatology Phoenix Arizona 85018 —
Torrance Clinical Research Institute Inc. Lomita California 90717 —
Dermatology Cosmetic Laser Medical Associates of La Jolla, Inc. San Diego California 92121 —
Dermatology Associates and Research Coral Gables Florida 33134 —
Leavitt Medical Associates of Florida Ormond Beach Florida 32174 —
Deaconess Clinic, Inc. Evansville Indiana 47713 —
Hudson Dermatology, LLC Evansville Indiana 47714 —
Indiana Clinical Trials Center Plainfield Indiana 46168 —
DermAssociates, PC Rockville Maryland 20850 —
Great Lakes Research Group, Inc. Bay City Michigan 48706 —
The Dermatology Group, P.C. Verona New Jersey 07044 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213 —
Pflugerville Dermatology Clinical Research Center, Inc. Pflugerville Texas 78660 —

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 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02120456, 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 Mar 6, 2025 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02120456 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →