Ocrelizumab versus placebi in primary progressive multiplesclerosis
In the phase 3 trial 732 patients were randomly assigned with primary progressive multiple sclerosis in a 2:1 ratio to receive intravenous ocrelizumab or placebo every 24 weeks for at least 120 weeks and until a prespecified number of confirmed disability progression events had occurred.Neoplasms occurred in 2.3% of patients who received ocrelizumab and in 0.8% of patients who received placebo. Among patients with primary progressive multiple sclerosis, ocrelizumab was associated with lower rates of clinical and MRI progression than placebo..
Medienart: |
Artikel |
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Erscheinungsjahr: |
2017 |
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Erschienen: |
2017 |
Enthalten in: |
Zur Gesamtaufnahme - volume:376 |
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Enthalten in: |
The New England journal of medicine - 376(2017), 3, Seite 209 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Kappos, L [VerfasserIn] |
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BKL: | |
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Themen: |
Care and treatment |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
OLC1991145217 |
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520 | |a In the phase 3 trial 732 patients were randomly assigned with primary progressive multiple sclerosis in a 2:1 ratio to receive intravenous ocrelizumab or placebo every 24 weeks for at least 120 weeks and until a prespecified number of confirmed disability progression events had occurred.Neoplasms occurred in 2.3% of patients who received ocrelizumab and in 0.8% of patients who received placebo. Among patients with primary progressive multiple sclerosis, ocrelizumab was associated with lower rates of clinical and MRI progression than placebo. | ||
650 | 4 | |a Comparative analysis | |
650 | 4 | |a Diagnosis | |
650 | 4 | |a Monoclonal antibodies | |
650 | 4 | |a Multiple sclerosis | |
650 | 4 | |a Health aspects | |
650 | 4 | |a Care and treatment | |
650 | 4 | |a Placebos | |
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650 | 4 | |a Usage | |
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