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Published on: December 9, 2015
Ocrelizumab initiation in patients with MS: A multicenter observational study
Erik Ellwardt1, Leoni Rolfes2, Julia Klein2
1From the Focus Program Translational Neurosciences (FTN) and Immunology (FZI) (E.E., K.P., F.Z., S.B.), Rhine Main Neuroscience Network (rmn), Department of Neurology, University Medical Center of the Johannes Gutenberg University Mainz; Department of Neurology (L.R., T.R., H.W.), University of Muenster; Department of Neurology (J.K., M.S., C.W.), Faculty of Medicine and University Hospital Cologne, University of Cologne; and Department of Neurology (S.G.M.), Institute of Translational Neurology, University of Muenster, Germany. erik.ellwardt@unimedizin-mainz.de.
Ocrelizumab effectively stabilizes both treatment-naive and previously treated patients with multiple sclerosis (MS). This B cell-depleting antibody offers a viable treatment option for MS management, with generally well-tolerated short-term side effects.
Area of Science:
- Neurology
- Immunology
- Clinical Trials
Background:
- Multiple sclerosis (MS) is a chronic autoimmune disease affecting the central nervous system.
- B cell-depleting therapies, such as ocrelizumab, have emerged as significant treatment options for MS.
- Real-world data on ocrelizumab's efficacy and safety in diverse MS populations are crucial.
Purpose of the Study:
- To evaluate the real-world effectiveness and safety of ocrelizumab in patients with multiple sclerosis.
- To assess ocrelizumab's impact on disease course in both treatment-naive and previously treated MS patients.
- To provide Class IV evidence for ocrelizumab as a therapeutic option in MS management.
Main Methods:
- Retrospective data collection from 210 patients with MS across three major neurology centers.
- Analysis of patient characteristics, including disease type, prior treatments, and ocrelizumab administration.
- Evaluation of clinical outcomes such as relapse rates, disability progression, and documented side effects.
Main Results:
- Ocrelizumab treatment stabilized disease in 13% of relapsing MS patients (annualized relapse rate 0.17) and 5% of all MS patients showed disability progression.
- Twenty-six percent of patients had primary progressive MS (PPMS), while 74% had relapsing-remitting (RRMS) or active secondary progressive MS (aSPMS).
- Treatment was generally well-tolerated, with short-term side effects including infusion reactions and mild infections.
Conclusions:
- Ocrelizumab demonstrates efficacy in stabilizing both treatment-naive and pretreated patients with MS.
- The findings support ocrelizumab as a valuable treatment option, potentially following therapies like natalizumab or fingolimod.
- Further long-term studies are necessary to fully ascertain the safety profile and confirm these real-world findings.
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