ClinicalTrials.gov record
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 May 6, 2026, 9:54 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)

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

  • CC-930 Drug
  • Placebo Drug

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
Oct 31, 2011
Primary completion
Jul 29, 2012
Completion
Jul 29, 2012
Last update posted
Nov 18, 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 18, 2019 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01466725 live on ClinicalTrials.gov.

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