SEP-RR: Retrospective Study on Registry Data to Evaluate the Impact of Ocrelizumab Used in Routine Care in Patients With RRMS
Study Details
Study Description
Brief Summary
Multiple Sclerosis (MS) is a chronic, autoimmune, neurodegenerative disease; clinical events are mainly attributed to myelin destruction and inflammatory of the central nervous system.
The diagnosis resides in clinical and radiological criteria according to 2017 McDonald criteria.
Once the diagnosis of MS has been made, treatment should be initiated promptly, in order to delay the onset of severe disability in the long-term, even more ocrelizumab are a treatment of high efficacy.
Ocrelizumab is used as a first-line or second-line treatment in Relapsing Remitting MS (RRMS) It is an anti-CD20 monoclonal antibody that provides rapid depletion of circulating CD20+ B lymphocytes by complement-dependent cytotoxicity and antibody-dependent cellular cytotoxicity.
The main objective is the retrospective evaluation of the impact of ocrelizumab on the outcome of MS.
The secondary objective is the search of predictive factors of response to treatment.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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Study Design
Outcome Measures
Primary Outcome Measures
- Retrospective study of the impact of ocrelizumab used in patients with multiple sclerosis [Files analysed retrospectively from October 01, 2018 to November 31, 2020 will be examined]]
Eligibility Criteria
Criteria
Inclusion criteria:
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Major subject (≥18 years old)
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Suffering from relapsing-remitting MS (RRMS)
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Supported in a neurology department at Strasbourg or Nancy University Hospital between 10/01/2018 and 11/31/2020.
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Treated with ocrelizumab 600mg every 6 months during the period from 01/10/2018 to 01/05/2020.
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Have had an M0, M3 / M6 and M12 MRI after initiation of treatment.
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Subject not having expressed his opposition, after information, to the reuse of his data for the purposes of this research
Exclusion criteria:
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Subject having expressed opposition to participating in the study
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Primary progressive multiple sclerosis (MS-PP), secondarily progressive (MS-SP)
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Subject not meeting all the inclusion criteria
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Impossibility of providing the subject with enlightened information (difficulties in understanding the subject, etc.)
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Subjects under safeguard of justice
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Subject under guardianship or guardianship
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Hautepierre Clinical Investigation Center - Strasbourg University Hospitals | Strasbourg | France | 67091 |
Sponsors and Collaborators
- University Hospital, Strasbourg, France
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- 8037