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Clinical Trial Summary

This was a US-based, observational cross-sectional study with primary data collection via questionnaires directly administered to patients with MS receiving KESIMPTA and care partners of patients with MS (formal or informal)receiving KESIMPTA.


Clinical Trial Description

The study aimed to enroll ninety-four (94) patients/care partners. The time period for enrollment was dependent on the uptake of KESIMPTA in the real-world. Data collected for the study was obtained directly from the patient/care partner within the web-based database: De-identified data was stored on a secure server and transferred for analysis. Responses from the patient and care partner surveys were pooled for analysis of study endpoints. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05334472
Study type Observational
Source Novartis
Contact
Status Completed
Phase
Start date November 24, 2021
Completion date February 15, 2023

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