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