An open-label, multicentre study to evaluate the efficacy and safety of one course of weekly intramuscular administration of Amevive in Taiwan patients with chronic plaque psoriasis
The purpose of the present study is to establish the efficacy and safety of one course of once weekly 15 mg intramuscular (IM) administration of AMEVIVE in an alternate study population and to address the issue of peak time to response by measuring the proportion of patients achieving a ≥ 75% reduction in PASI at any time after completion of treatment.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
ECT
Masking
NONE
Enrollment
40
To determine TRR75 of one course of once weekly 15 mg intramuscular (IM) administration of AMEVIVE
To determine TRR50, Quality of Life (QOL), the safety and tolerability
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