The purpose of the study is to evalute the efficacy, safety and tolerability of rozanolixizumab for treatment of adult participants with myelin oligodendrocyte glycoprotein (MOG) antibody-associated disease (MOGAD).
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
For Part A: Time from randomization to first independently centrally adjudicated relapse (TTFR) during the DB Treatment Period
Timeframe: Baseline (Week 1) to EDB/EWD Visit (until a confirmed relapse or up to approximately 132 weeks; in isolated cases this can be up to approximately 204 weeks)
For Part B: Incidence of treatment-emergent adverse events (TEAEs) during OLE Treatment Period
Timeframe: OLE Treatment Period (OLE Week 1) to EOS/EWD Visit (up to OLE Week 52)
For Part B: Incidence of treatment-emergent adverse events (TEAEs) leading to permanent withdrawal of investigational medicinal product (IMP) during OLE Treatment Period
Timeframe: OLE Treatment Period (OLE Week 1) to EOS/EWD Visit (up to OLE Week 52)