Details, Fiction and Z-LEHD-fmk
MI-CP151 was a period 1b randomised, double-blind, placebo controlled, dose-escalation, multicentre analyze To guage many intravenous doses of sifalimumab, in adult clients with dermatomyositis or polymyositis (NCT00533091). Major demo aims were To guage the security and tolerability of sifalimumab in dermatomyositis or polymyositis patients, when