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Completed Phase 3 Interventional Results available

LEO 80185 in the Treatment of Psoriasis Vulgaris on the Non-scalp Regions of the Body (Trunk and/or Limbs)

ClinicalTrials.gov ID: NCT01188928

Public ClinicalTrials.gov record NCT01188928. 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, 5:45 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 Study Comparing Once Daily Treatment With Calcipotriol 50 mcg/g Plus Betamethasone 0.5 mg/g (as Dipropionate) Topical Suspension With Betamethasone 0.5 mg/g (as Dipropionate) in the Topical Suspension Vehicle, Calcipotriol 50 mcg/g in the Topical Suspension Vehicle and the Topical Suspension Vehicle Alone in Subjects With Psoriasis Vulgaris on Non-scalp Regions of the Body (Trunk and/or Limbs)

Brief summary

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

The purpose of this study is to compare the efficacy and safety of Calcipotriol 50 Mcg/g Plus Betamethasone 0.5 mg/g (as Dipropionate) Topical Suspension with the active components when used individually as monotherapy in the topical suspension vehicle (betamethasone dipropionate in the topical suspension vehicle, calcipotriol in the topical suspension vehicle) and with the topical suspension vehicle alone in the treatment of psoriasis vulgaris on the non-scalp regions of the body (trunk and/or limbs) in a large phase 3 study. This comparison will ensure a more informed assessment of the benefit/risk ratio of Calcipotriol 50 Mcg/g Plus Betamethasone 0.5 mg/g (as Dipropionate) Topical Suspension while also establishing the optimal treatment duration in psoriasis vulgaris on the non-scalp regions of the body (trunk and/or limbs).

Study identification

NCT ID
NCT01188928
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
LEO Pharma
Industry
Enrollment
1,152 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
Sep 2010 (Type not available)
Primary completion
Mar 2011 (Actual)
Completion
Mar 2011 (Actual)
Last update posted
Mar 10, 2025

2010 – 2011

United States locations

U.S. sites
59
U.S. states
23
U.S. cities
53
Facility City State ZIP Site status
Horizon Research Group, Inc Mobile Alabama 36606 —
Burke Pharmaceutical Research Hot Springs Arkansas 71913 —
Advanced Clinical Research Institute Anaheim California 92801 —
DBA Torrance Clinical Research Lomita California 90717 —
Dermatology Specialists, Inc. Oceanside California 92056 —
Skin Surgery Medical Group, Inc. San Diego California 92117 —
Walter Nahm, MD, Ph.D., Inc San Diego California 92123 —
Coastal Medical Research Group, Inc. San Luis Obispo California 93401 —
Clinical Science Institute Santa Monica California 90404 —
Dermatology Research Centers Santa Monica California 90404 —
Colorado Medical Research Center, Inc. Denver Colorado 80120 —
Horizons Clinical Research Center, LLC Denver Colorado 80220 —
Visions Clinical Research Boynton Beach Florida 33472 —
Dermatology Associates and Research Coral Gables Florida 33134 —
North Florida Dermatology Associates, PA Jacksonville Florida 32204 —
International Dermatology Research, Inc. Miami Florida 33144 —
Ameriderm Research Ormond Beach Florida 32174 —
Palm Beach Research Center West Palm Beach Florida 33409 —
Atlanta Dermatology, Vein & Research Center Alpharetta Georgia 30022 —
Peachtree Dermatology Associates Atlanta Georgia 30327 —
Dermatologic Surgery Specialists, PC Macon Georgia 31217 —
Gwinnett Clinical Research Center, Inc Snellville Georgia 30078 —
Altman Dermatology Associates Arlington Hts Illinois 60005 —
Glazer Dermatology Buffalo Grove Illinois 60089 —
Deaconess Clinic, Inc. Evansville Indiana 47713 —
Hudson Dermatology Evansville Indiana 47714 —
Dawes Fretzin Clinical Research Group Indianapolis Indiana 46256 —
Indiana Clinical Trials Center Plainfield Indiana 46168 —
Dermatology Specialists Louisville Kentucky 40202 —
Owensboro Dermatology Associates Owensboro Kentucky 42303 —
Lawrence J. Green, MD, LLC Rockville Maryland 20850 —
David Fivenson, MD Dermatology, PLC Ann Arbor Michigan 48103 —
Great Lakes Research Group, Inc Bay City Michigan 48706 —
Michigan Center for Research Corp., Clinton Township Michigan 48038 —
Henry Ford Health System Detroit Michigan 48202 —
Hamzavi Dermatology Fort Gratiot Michigan 48059 —
Somerset Skin Centre Troy Michigan 48084 —
Grekin Skin Institute Warren Michigan 48088 —
Minnesota Clinical Study Center Fridley Minnesota 55432 —
Karl G. Heine, M. D. Dermatology Henderson Nevada 89052 —
Psoriasis Treatment Center of Central NJ East Windsor New Jersey 08520 —
Anderson & Collins Clinical Research, Inc. Edison New Jersey 08817 —
The Dermatology Group, PC Verona New Jersey 07044 —
Academic Dermatology Associates Albuquerque New Mexico 87106 —
Mount Sinai School of Medicine New York New York 10029 —
Derm Research Center of New York Stony Brook New York 11790 —
Triangle Medical Research Associates, LLC Cary North Carolina 27518 —
Haber Dermatology and Cosmetic Surgery South Euclid Ohio 44118 —
Oregon Dermatology and Research Center Portland Oregon 97210 —
King-Maceyko Dermatology Associates Johnstown Pennsylvania 15905 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15213 —
J&S Studies, Inc. College Station Texas 77845 —
Division of Dermatology, Baylor Research Institute Dallas Texas 75246 —
Centre for Clinical Studies Houston Texas 77030 —
Clinical Trials of Texas, Inc. San Antonio Texas 78229 —
Dermatology Clinical Research Center of San Antonio San Antonio Texas 78229 —
Progressive Clinical Research, P.A. San Antonio Texas 78229 —
Dermatology Research Center, Inc. Salt Lake City Utah 84117 —
Premier Clinical Research Spokane Washington 99204 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01188928, 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 10, 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 NCT01188928 live on ClinicalTrials.gov.

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