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MI-CP151 was a period 1b randomised, double-blind, placebo managed, dose-escalation, multicentre examine To guage various intravenous doses of sifalimumab, in Grownup patients with dermatomyositis or polymyositis (NCT00533091). Primary trial objectives have been To judge the safety and tolerability of sifalimumab in dermatomyositis or polymyositis