MI-CP151 was a period 1b randomised, double-blind, placebo managed, dose-escalation, multicentre analyze To guage many intravenous doses of sifalimumab, in Grownup patients with dermatomyositis or polymyositis (NCT00533091). Major demo targets were to evaluate the security and tolerability of sifalimumab in dermatomyositis or polymyositis patients,
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To blind the investigate staff only animal quantity not therapy teams have been used when investigators produced measurements or conducted Investigation, one example is flowcytometry Examination, survival or ultrasound measurements. Main info are noted in data file S1.Thanks to generous benefactors, your reward now may have 5X the influence to prog
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