The purpose of the study is to evaluate efficacy of riliprubart compared to placebo in adult participants with CIDP whose disease is refractory to standard of care. The study duration will be for a maximum of 109 weeks including screening, treatment phases, and follow-up.
Please see section 3 of the full protocol Please see section 3 of the full protocol Please see section 3 of the full protocol
Please see section 3 of the full protocol Please see section 3 of the full protocol Please see section 3 of the full protocol
UPENN Case Test Trial 2 (Do Not Make Any Changes)
UPENN Case Test Trial 4 (Do Not Make Any Changes)
UPENN Case Test Trial 5 (Do Not Make Any Changes)
UPENN Case Test Trial 7 (Do Not Make Any Changes)
UPENN Case Test Trial 12 (Do Not Make Any Changes)
UPENN Case Test Trial 13 (Do Not Make Any Changes)
Congrats! You have your own personal workspace now.