CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 3,526 enrolled
Drug / intervention
Rituximabdrug
Likely dose
Not stated in record
Key inclusion· 4
  • Clinically Isolated Syndrome (CIS) or RRMS diagnosis
  • First DMT (treatment naïve) or second DMT of different drug class
  • Follow-up at Swedish university clinics
  • Capable of completing study assessments
Key exclusion· 1
  • Progressive forms of MS at start of therapy

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03193866
NCT03193866N/ACompleted

COMparison Between All immunoTherapies for Multiple Sclerosis. An Observational Long-term Prospective Cohort Study of Safety, Efficacy and Patient's Satisfaction of MS Disease Modulatory Treatments in Relapsing-remitting Multiple Sclerosis

Karolinska Institutet·observational·Posted Jun 21, 2017·Updated Apr 20, 2025

In Brief

An observational study evaluating Rituximab for Relapsing-remitting Multiple Sclerosis. Completed, enrolled 3,526 participants across 1 site.

Detailed Summary

The overarching goal of this study is to determine whether rituximab (RTX) offers effectiveness and safety advantages over other commonly used approved Disease-Modifying Drugs (DMT) in the largest real-world population-based structured prospective follow-up cohort of Relapsing-Remitting Multiple Sclerosis (RRMS) patients. The study will include both treatment naïve patients starting their first DMT and patients switching from a previous first line DMT (escalation/second-line).

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesSweden

Timeline

N/ACompletedFinished
201820192020202120222023202420252026
First PostedJun 21, 2017
Enrollment StartJun 2, 2017
Primary CompletionMar 31, 2022
TodayJul 2, 2026
Enrollment to primary: 4.8 yearsPosted 9.0 years ago

Interventions

Rituximabdrug

Comparisons of efficacy and safety between rituximab and all other frequently used immunomodulating drugs against multiple sclerosis