The study is a prospective, multi-centre, observational study designed to assess the long-term effectiveness and safety of alefacept in subjects with moderate to severe chronic plaque psoriasis.
Study includes a bio-marker sub-study to determine differences in responders vs. non-responders. Additional consent is required for the sub-study.
Study Type
OBSERVATIONAL
Enrollment
64
Commercial alefacept prescribed by Physician
Unnamed facility
Edmonton, Alberta, Canada
Unnamed facility
Winnipeg, Manitoba, Canada
Unnamed facility
Assess the long-term effectiveness and safety of alefacept in subjects with moderate to severe chronic plaque psoriasis
Time frame: 8 Weeks following last dose of each treatment course throughout study
Assess the quality of life of subjects on alefacept based on completion of the Dermatology Life Quality Index
Time frame: 8 Weeks following last dose of each treatment course throughout study
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Winnipeg, Manitoba, Canada
Unnamed facility
Bathurst, New Brunswick, Canada
Unnamed facility
Quispamsis, New Brunswick, Canada
Unnamed facility
St. John's, Newfoundland and Labrador, Canada
Unnamed facility
St. John's, Newfoundland and Labrador, Canada
Unnamed facility
Halifax, Nova Scotia, Canada
Unnamed facility
Hamilton, Ontario, Canada
Unnamed facility
London, Ontario, Canada
...and 11 more locations