Details, Fiction and PARP-1-IN-3
MI-CP151 was a period 1b randomised, double-blind, placebo managed, dose-escalation, multicentre examine To judge a number of intravenous doses of sifalimumab, in Grownup clients with dermatomyositis or polymyositis (NCT00533091). Key demo targets were To judge the security and tolerability of sifalimumab in dermatomyositis or polymyositis patients