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MI-CP151 was a phase 1b randomised, double-blind, placebo controlled, dose-escalation, multicentre review to evaluate various intravenous doses of sifalimumab, in adult clients with dermatomyositis or polymyositis (NCT00533091). Major demo targets had been To guage the safety and tolerability of sifalimumab in dermatomyositis or polymyositis client
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