This protocol relates to a phase II randomized double blind, placebo controlled study of the AS101 topical application for the treatment of mild to moderate Psoriasis.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
4% AS101 Cream or Placebo cream, twice a day for 12 weeks
Hadassah Medical Organization
Jerusalem, Israel
To evaluate the percentege of patients in which modified PASI (mPASI) score reduction of more than 66% from Baseline whithin 12-week treatment period is achieved
Time frame: 12 weeks treatment and 3 month follow up
The main secondary endpoints are to evaluate safety, tolerability of topical AS010 treatment and long term remission of psoriasis.
Time frame: 12 weeks treatment and 3 month follow up
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