A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Evaluate the Safety and Efficacy of Ravulizumab in Complement-Inhibitor-Naïve Adult Patients with Generalized Myasthenia Gravis IND 140,115 STUDY NUMBER: ALXN1210-MG-306

    Not Recruiting
Updated on 18 June 2021
mycophenolate mofetil
cholinesterase inhibitors
serologic test
myasthenia gravis
generalized myasthenia gravis
repetitive nerve stimulation
acetylcholinesterase inhibitors
edrophonium chloride
edrophonium chloride test
anticholinesterase agents


To assess the efficacy of ravulizumab compared with placebo in the treatment of gMG based on the improvement in the Myasthenia Gravis-Activities of Daily Living (MG-ADL) profile.
To assess the efficacy of ravulizumab compared with placebo in the treatment of gMG based on the improvement in the Quantitative Myasthenia Gravis (QMG) total score.


There are no medical benefits that can be guaranteed to the patient for the patient’s taking part in this research study. The patient’s willingness to take part, however, may help doctors better understand and/or treat others who have the patient’s condition. Information gained from this study may benefit others. No guarantees have been made to the patient as to the results of this research study.

Condition Myasthenia Gravis generalised
Clinical Study IdentifierTX220311
Last Modified on18 June 2021

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