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Completed Phase 2 Interventional Results available

A Phase 2, Double-blind, Placebo-controlled Study of the Efficacy and Safety of Belumosudil in Subjects With Moderate/Severe Chronic Plaque Psoriasis

ClinicalTrials.gov ID: NCT02852967

Public ClinicalTrials.gov record NCT02852967. 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 31, 2026, 7:50 AM 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 2 Study, Randomized, Double-blind, Placebo-controlled, Dose-finding Study to Evaluate the Efficacy, Tolerability, and Safety of Belumosudil in Subjects With Moderate/Severe Chronic Plaque Psoriasis Who Are Candidates for Systemic Therapy or Phototherapy

Brief summary

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

This is a phase 2, randomized, placebo-controlled, 2-period study to evaluate the safety, tolerability, and efficacy of belumosudil in adult subjects with moderate to severe chronic plaque psoriasis who are candidates for systemic therapy or phototherapy.

Study identification

NCT ID
NCT02852967
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Kadmon Corporation, LLC
Industry
Enrollment
110 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 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
Sep 14, 2016 (Actual)
Primary completion
Feb 13, 2019 (Actual)
Completion
Feb 13, 2019 (Actual)
Last update posted
Mar 16, 2022

2016 – 2019

United States locations

U.S. sites
14
U.S. states
11
U.S. cities
14
Facility City State ZIP Site status
Alliance Dermatology and Mohs Center Phoenix Arizona 85032 —
University of California, Irvine - Dermatology Clinical Research Center Irvine California 92697 —
Dermatology Research Associates Los Angeles California 90045 —
Renstar Medical Research Ocala Florida 34471 —
Dawes Fretzin Dermatology Group Indianapolis Indiana 46256 —
Dermatology Specialists Research New Albany Indiana 40202 —
Dermatology Specialists Research Louisville Kentucky 40202 —
Metro Boston Clinical Partners Brighton Massachusetts 02135 —
Psoriasis Treatment Center of Central New Jersey East Windsor New Jersey 08520 —
Sadick Research Group New York New York 10075 —
Oregon Dermatology and Research Center Portland Oregon 97210 —
Tennessee Clinical Research Center Nashville Tennessee 37215 —
Suzanne Bruce and Associates Katy Texas 77056 —
Austin Institute for Clinical Research 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02852967, 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 16, 2022 · Synced Oct 31, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02852967 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →