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MI-CP151 was a section 1b randomised, double-blind, placebo controlled, dose-escalation, multicentre analyze To guage numerous intravenous doses of sifalimumab, in adult clients with dermatomyositis or polymyositis (NCT00533091). Major trial targets had been To judge the safety and tolerability of sifalimumab in dermatomyositis or polymyositis indi

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