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We do not endorse or review these studies in any way.
Brief Title: Special Drug-use Surveillance for Kesimpta for s.c. Injection 20 mg Pen
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)
Study ID: NCT04940065
Brief Summary: This study is an uncontrolled, central registration system, open-label, multicenter observational study in patients using Kesimpta for the labeled indication.
Detailed Description: 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.
Minimum Age:
Eligible Ages: CHILD, ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
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Name: Novartis Pharmaceuticals
Affiliation: Novartis Pharmaceuticals
Role: STUDY_DIRECTOR