To Evaluate the Preliminary Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Efficacy of CC-11050 in Subjects With Discoid Lupus Erythematosus and Subacute Cutaneous Lupus Erythematosus

PHASE2CompletedINTERVENTIONAL
Enrollment

48

Participants

Timeline

Start Date

October 1, 2010

Primary Completion Date

January 1, 2013

Study Completion Date

March 1, 2013

Conditions
Cutaneous Lupus Erythematosus
Interventions
DRUG

CC-11050

Cohort 1: 50 milligrams twice per day for 4 weeks Cohort 2: 100 milligrams twice per day for 8 weeks Cohort 3: 200 milligrams twice per day for 12 week

OTHER

Placebo

Trial Locations (19)

10016

NYU Langone Medical Center, New York

15213

University of Pittsburgh Medical Center, Pittsburgh

16635

Altoona Center for Clinical Research, Duncansville

17033

Penn State Hershey Dermatology, Hershey

19104

Hospital of the University of Pennsylvania, Philadelphia

30263

Central Medaphase Inc, Newnan

30322

Emory Univ. School of Medicine, Atlanta

30327

Peachtree Dermatology Associates Research Center, Atlanta

40217

DermResearch, PLLC, Louisville

44106

University Hospitals Case Medical Center, Cleveland

46256

Dawes Fretzin Clinical Research Group, LLC, Indianapolis

60611

Northwestern University, Chicago

63117

Central Dermatology, P.C., St Louis

70605

Dermatology & Advanced Aesthetics, Lake Charles

72758

Northwest Arkansas Clinical Trials Center, PLLC, Rogers

90045

Dermatology Research Associates, Los Angeles

92103

Medderm Associates, San Diego

02919

Clinical Partners, LLC, Johnston

75390-9090

UT Southwestern Medical Center Dallas, Dallas

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY