US2021206869A1PendingUtilityA1
Methods for treating progressive multiple sclerosis
Est. expirySep 16, 2028(~2.1 yrs left)· nominal 20-yr term from priority
A61B 5/055A61K 39/00C07K 2317/24A61K 2039/505G01N 2800/7095A61K 2039/55A61P 25/00A61K 2039/545C07K 16/2887C07K 2317/76G06Q 99/00A61P 37/00A61K 2039/507A61P 37/06A61K 39/3955A61K 45/06G01N 2800/52A61K 9/0019G01N 33/686A61P 37/02C07K 2317/565A61P 25/28A61P 29/00
69
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Claims
Abstract
The present invention concerns methods for treating progressive multiple sclerosis (MS) in a patient, and an article of manufacture with instructions for such use.
Claims
exact text as granted — not AI-modified1 . A method of treating progressive multiple sclerosis in a patient comprising administering to the patient an effective amount of an anti-CD20 antibody, wherein treatment is based upon the patient having one or more characteristics selected from the group consisting of (a) an age less than about 55 years, (b) one or more gadolinium staining lesions, (c) at least about a one point increase in Expanded Disability Status Scale (EDSS) over two years prior to starting treatment, and (d) a Multiple Sclerosis Severity Score (MSSS) greater than about 5 points.
2 - 38 . (canceled)
39 . A method of treating multiple sclerosis in a patient comprising administering an effective amount of ocrelizumab to the patient to provide an initial ocrelizumab exposure of between about 0.3 to about 0.6 grams followed by a second ocrelizumab exposure of between about 0.3 to about 0.6 grams, the second exposure not being provided until from about 16 to 60 weeks from the initial exposure, and each of the ocrelizumab exposures is provided to the patient as one or two doses of ocrelizumab.
40 - 46 . (canceled)
47 . An article of manufacture comprising:
(a) a container comprising ocrelizumab; and (b) a package insert with instructions for treating multiple sclerosis in a patient, wherein the instructions indicate that an amount of ocrelizumab is administered to the patient that is effective to provide an initial ocrelizumab exposure of between about 0.3 to about 0.6 grams followed by a second ocrelizumab exposure of between about 0.3 to about 0.6 grams, the second exposure not being administered until from about 16 to 60 weeks from the initial exposure, and each of the ocrelizumab exposures is provided to the patient as one or two doses of ocrelizumabJoin the waitlist — get patent alerts
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