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MI-CP151 was a section 1b randomised, double-blind, placebo managed, dose-escalation, multicentre examine To judge a number of intravenous doses of sifalimumab, in adult patients with dermatomyositis or polymyositis (NCT00533091). Key demo goals have been To guage the safety and tolerability of sifalimumab in dermatomyositis or polymyositis people,