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Terminated Phase 2 Interventional

A Research Study to Assess if CC-930 is Safe in Treating Subjects With Discoid Lupus Erythematosus

ClinicalTrials.gov ID: NCT01466725

Public ClinicalTrials.gov record NCT01466725. 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, 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.

Official title

A Phase 2, Pilot, Multicenter, Randomized, Placebo-Controlled Sequential, Ascending Dose Study to Characterize the Safety, Tolerability, Pharmacokinetic and Pharmacodynamic Activity of CC-930 in Subjects With Recalcitrant Discoid Lupus Erythematosus (DLE)

Brief summary

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

The purpose of the study is to assess if CC-930 is safe and tolerable in treating subjects with Discoid Lupus Erythematosus. Pharmacokinetic and pharmacodynamics will also be evaluated.

Study identification

NCT ID
NCT01466725
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Celgene
Industry
Enrollment
5 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 64 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 1, 2011 (Actual)
Primary completion
Jul 30, 2012 (Actual)
Completion
Jul 30, 2012 (Actual)
Last update posted
Nov 19, 2019

2011 – 2012

United States locations

U.S. sites
19
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
UAB Dermatology Birmingham Alabama 35233 —
The Regents of the University of California Irvine California 92697 —
Medical Faculty Associates Washington D.C. District of Columbia 20037 —
Advanced Pharma, CR, LLC Miami Florida 33136 —
University of Miami - Department of Dermatology Miami Florida 33136 —
Rush Medical Center Chicago Illinois 60612 —
North Shore University Health System Skokie Illinois 60077 —
SIU School of Medicine Springfield Illinois 62702 —
Tulane University School of Medicine New Orleans Louisiana 70112 —
John Hopkins University Baltimore Maryland 21205 —
Boston Cancer Center Boston Massachusetts 02118 —
University of Minnesota-Department of Dermatology Minneapolis Minnesota 55455 —
University of Rochester Medical Center Rochester New York 14623 —
Ohio State Univ Medical Center, Division of Dermatology Columbus Ohio 43221 —
Rhode Island Hospital University Dermatology, Inc. Providence Rhode Island 02903 —
Medical University of South Carolina Charleston South Carolina 29425 —
Dermatology and Research Dallas Texas 75230 —
University of Texas Dermatology Houston Texas 77030 —
Sun Research Institute San Antonio Texas 78215 —

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 NCT01466725, 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, 2019 · Synced Oct 31, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01466725 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →