MI-CP151 was a period 1b randomised, double-blind, placebo managed, dose-escalation, multicentre analyze To judge numerous intravenous doses of sifalimumab, in Grownup patients with dermatomyositis or polymyositis (NCT00533091). Major demo goals have been To guage the protection and tolerability of sifalimumab in dermatomyositis or polymyositis cli
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