MI-CP151 was a stage 1b randomised, double-blind, placebo managed, dose-escalation, multicentre study To guage a number of intravenous doses of sifalimumab, in adult patients with dermatomyositis or polymyositis (NCT00533091). Key trial objectives were being To guage the security and tolerability of sifalimumab in dermatomyositis or polymyositis pa

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