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Completed Phase 2 Interventional Results available

A Dose-Finding Study of GSK2894512 Cream in Subjects With Atopic Dermatitis (AD)

ClinicalTrials.gov ID: NCT02564055

Public ClinicalTrials.gov record NCT02564055. 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 Sep 1, 2026, 5:32 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

Study 203121: A Randomized, Blinded, Vehicle-Controlled, Dose-Finding Study of GSK2894512 Cream for the Treatment of Atopic Dermatitis

Brief summary

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

This study will evaluate the efficacy and safety of two concentrations (0.5 percent \[%\] and 1%) and two application frequencies (once a day and twice a day) of GSK2894512 cream for the topical treatment in adolescent and adult subjects with atopic dermatitis. Results from this study will be considered when selecting the most appropriate concentration of GSK2894512 cream and application frequency in future clinical studies. This is a multicenter (United States, Canada, and Japan), randomized, double-blind (sponsor-unblind), vehicle-controlled, 6-arm, parallel-group, dose-finding study in adolescent and adult subjects with atopic dermatitis. Two concentrations of GSK2894512 cream (0.5% and 1%) and a vehicle control cream will be equally randomized and evaluated following application to all atopic dermatitis lesions (except on the scalp) once daily (evening) or twice daily (morning and evening) for 12 weeks. This study will consist of 3 periods: up to 4 weeks screening, 12 weeks double-blind treatment, and 4 weeks post-treatment follow-up. The total duration of subject participation will be approximately 16 to 20 weeks. Approximately 270 adolescent and adult males and females subjects with atopic dermatitis will be screened in order to have at least 228 randomized subjects (38 subjects for each of the 6 treatment groups) and approximately 204 evaluable subjects overall. Approximately 30 subjects will be randomized in Japan to achieve at least 24 evaluable Japanese subjects.

Study identification

NCT ID
NCT02564055
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
247 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years to 65 Years
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
Nov 30, 2015
Primary completion
Dec 31, 2016
Completion
Jan 11, 2017
Last update posted
Nov 19, 2017

2015 – 2017

United States locations

U.S. sites
36
U.S. states
22
U.S. cities
33
Facility City State ZIP Site status
GSK Investigational Site Fort Smith Arkansas 72916
GSK Investigational Site Fresno California 93720-2933
GSK Investigational Site Irvine California 92697
GSK Investigational Site Los Angeles California 90045
GSK Investigational Site Oceanside California 92056
GSK Investigational Site Santa Ana California 92701
GSK Investigational Site Denver Colorado 80220
GSK Investigational Site North Logan Connecticut 06032
GSK Investigational Site Atlanta Georgia 30342
GSK Investigational Site Chicago Illinois 60611
GSK Investigational Site West Dundee Illinois 60118
GSK Investigational Site Indianapolis Indiana 46256
GSK Investigational Site New Albany Indiana 47150
GSK Investigational Site Overland Park Kansas 66215
GSK Investigational Site New Orleans Louisiana 70115
GSK Investigational Site Andover Massachusetts 01810
GSK Investigational Site Bay City Michigan 48706
GSK Investigational Site West Bloomfield Michigan 48322
GSK Investigational Site Fridley Minnesota 55432
GSK Investigational Site Saint Joseph Missouri 64506
GSK Investigational Site New York New York 10022
GSK Investigational Site High Point North Carolina 27262
GSK Investigational Site Cincinnati Ohio 45255
GSK Investigational Site Philadelphia Pennsylvania 19103
GSK Investigational Site Pittsburgh Pennsylvania 15213
GSK Investigational Site Cranston Rhode Island 2910
GSK Investigational Site Greer South Carolina 29650
GSK Investigational Site Dallas Texas 75230
GSK Investigational Site Dallas Texas 75231
GSK Investigational Site Houston Texas 77004
GSK Investigational Site Houston Texas 77056
GSK Investigational Site San Antonio Texas 78218
GSK Investigational Site San Antonio Texas 78229
GSK Investigational Site Webster Texas 77598
GSK Investigational Site Norfolk Virginia 23507
GSK Investigational Site Seattle Washington 98101

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 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02564055, 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 Nov 19, 2017 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02564055 live on ClinicalTrials.gov.

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