There is an unmet medical need for safe, effective oral therapy for moderate-to-severe psoriasis. CC-10004 will be evaluated in a controlled setting of a clinical study. The information obtained from the study will aid in the design of future clinical trials and to establish the safety and efficacy of CC-10004.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
260
To compare the clinical efficacy of 2 oral doses of CC-10004 with placebo when taken for 12 weeks in subjects with moderate-to-severe plaque-type psoriasis
Time frame: 12 weeks
To evaluate the safety of CC-10004 compared with placebo in subjects with moderate-to-severe placque-type psoriasis
Time frame: 12 weeks
To evaluate the effects of CC-10004 compared to placebo on the quality of life in subjects with moderate-to-severe plaque-type psoriasis.
Time frame: 12 weeks
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Division of Dermatology and Cutaneous Science
Edmonton, Alberta, Canada
Division of Dermatology
Vancouver, British Columbia, Canada
Duronder C.P. Inc
Moncton, New Brunswick, Canada
Eastern Canada Cutaneous Research Associates
Halifax, Nova Scotia, Canada
Ultranova Skincare
Barrie, Ontario, Canada
Dermatrials Research
Hamilton, Ontario, Canada
The Lynde Center for Dermatology
Markham, Ontario, Canada
North Bay Dermatology Centre
North Bay, Ontario, Canada
K. Papp Clinical Research
Waterloo, Ontario, Canada
Innovaderm
Montreal, Quebec, Canada
...and 21 more locations