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MI-CP151 was a section 1b randomised, double-blind, placebo managed, dose-escalation, multicentre analyze to evaluate several intravenous doses of sifalimumab, in adult sufferers with dermatomyositis or polymyositis (NCT00533091). Principal demo aims were being To guage the protection and tolerability of sifalimumab in dermatomyositis or polymyosit