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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 adult clients with dermatomyositis or polymyositis (NCT00533091). Major trial aims had been To guage the safety and tolerability of sifalimumab in dermatomyositis or polymyositis sufferers, w