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Clinical Trial Summary

This is a non-interventional, cross-sectional, multicentric, and nationwide study, based on primary and secondary data collection.


Clinical Trial Description

The present study aims to characterize the use of subcutaneous ofatumumab in a real-world setting. Specifically, the investigation will assess the effectiveness, safety, and treatment adherence associated with subcutaneous ofatumumab in individuals with relapsing forms of multiple sclerosis (RMS) within the Spanish healthcare system. The study will use primary and secondary data collection. Primary data collection includes information collected using PRO, clinical-reported outcomes (ClinRO), scales or tests and the interview during the study visit. Secondary data collection includes existing data from electronic medical records (EMR) or paper-based medical records, collected as part of the routine follow-up of patients with RMS in the clinical practice. Baseline will be defined as the date of ofatumumab initiation. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06251986
Study type Observational
Source Novartis
Contact Novartis Pharmaceuticals
Phone +41613241111
Email novartis.email@novartis.com
Status Recruiting
Phase
Start date February 26, 2024
Completion date June 15, 2025

See also
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