Study of Apremilast in Atopic or Contact Dermatitis

PHASE2CompletedINTERVENTIONAL
Enrollment

10

Participants

Timeline

Start Date

June 30, 2009

Primary Completion Date

March 31, 2010

Study Completion Date

March 31, 2010

Conditions
Atopic DermatitisAllergic Contact Dermatitis
Interventions
DRUG

Apremilast

Apremilast is being evaluated at daily doses of 20 mg by mouth (PO) twice daily (BID) for 12 weeks of treatment (treatment phase) in subjects with recalcitrant plaque-type Atopic Dermatitis (AD) or Allergic Contact Ddermatitis (ACD).

Trial Locations (1)

02111

Tufts Medical Center, Department of Dermatology, Boston

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Celgene Corporation

INDUSTRY

lead

Tufts Medical Center

OTHER

NCT00931242 - Study of Apremilast in Atopic or Contact Dermatitis | Biotech Hunter | Biotech Hunter