MI-CP151 was a phase 1b randomised, double-blind, placebo managed, dose-escalation, multicentre research To judge many intravenous doses of sifalimumab, in adult people with dermatomyositis or polymyositis (NCT00533091). Principal demo objectives were To guage the protection and tolerability of sifalimumab in dermatomyositis or polymyositis suffere
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