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MI-CP151 was a period 1b randomised, double-blind, placebo controlled, dose-escalation, multicentre examine To judge numerous intravenous doses of sifalimumab, in adult patients with dermatomyositis or polymyositis (NCT00533091). Primary trial targets had been To judge the safety and tolerability of sifalimumab in dermatomyositis or polymyositis su

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