MI-CP151 was a stage 1b randomised, double-blind, placebo managed, dose-escalation, multicentre research To guage many intravenous doses of sifalimumab, in adult sufferers with dermatomyositis or polymyositis (NCT00533091). Main demo goals were being to evaluate the protection and tolerability of sifalimumab in dermatomyositis or polymyositis suffe
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