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MI-CP151 was a phase 1b randomised, double-blind, placebo controlled, dose-escalation, multicentre analyze To guage various intravenous doses of sifalimumab, in adult sufferers with dermatomyositis or polymyositis (NCT00533091). Main trial targets were To guage the security and tolerability of sifalimumab in dermatomyositis or polymyositis individu