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Clinical Trial Summary

This study is an uncontrolled, central registration system, open-label, multicenter observational study in patients using Kesimpta for the labeled indication.


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04940065
Study type Observational
Source Novartis
Contact
Status Active, not recruiting
Phase
Start date June 30, 2021
Completion date October 27, 2025

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