Relapsing-remitting Multiple Sclerosis Clinical Trial
Official title:
Special Drug-use Surveillance for Kesimpta for s.c. Injection 20 mg Pen (Relapsing-remitting Multiple Sclerosis and Active Secondary Progressive Multiple Sclerosis)
This study is an uncontrolled, central registration system, open-label, multicenter observational study in patients using Kesimpta for the labeled indication.
This is a primary data collection-based special drug-use surveillance to be conducted in accordance with the GPSP ordinance. Observational period will last 24 months from the start of treatment with Kesimpta. ;
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