The Efficacy and Safety of CC-10004 in Chronic Cutaneous Sarcoidosis

PHASE2/PHASE3CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

November 30, 2008

Primary Completion Date

December 31, 2011

Study Completion Date

December 31, 2011

Conditions
SarcoidosisCutaneous Sarcoidosis
Interventions
DRUG

CC-100004

After the screening period, subjects will receive CC-10004 20mg by mouth BID for 84 days. The 84-day duration of treatment is expected to provide adequate time to assess the short-term efficacy and safety of CC-10004 in a population of subjects with chronic cutaneous sarcoidosis.

Trial Locations (1)

45220

University of Cincinnati, Cincinnati

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Celgene Corporation

INDUSTRY

collaborator

Medical University of South Carolina

OTHER

lead

University of Cincinnati

OTHER