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MI-CP151 was a section 1b randomised, double-blind, placebo managed, dose-escalation, multicentre examine To guage a number of intravenous doses of sifalimumab, in Grownup patients with dermatomyositis or polymyositis (NCT00533091). Key demo targets had been To guage the security and tolerability of sifalimumab in dermatomyositis or polymyositis cl