US2017020851A1PendingUtilityA1
Treatment of progressive neurodegenerative disease with ibudilast
Est. expiryJul 11, 2027(~1 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 25/16A61P 25/14A61P 25/28A61P 25/00A61P 21/00A61K 31/437A61K 45/06A61K 9/0019A61K 9/0053A61K 9/06A61K 9/0014
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Claims
Abstract
Compositions and methods for treating progressive neurodegenerative diseases, and their associated symptoms by administration of ibudilast (3-isobutyryl-2-isopropylpyrazolo[1,5-a]pyridine).
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of treating a subject diagnosed with a myelopathy comprising administering to the subject a therapeutically effective amount of ibudilast or a pharmaceutically acceptable salt thereof.
2 . The method of claim 1 in which the ibudilast or pharmaceutically acceptable salt thereof is administered for at least 3 months.
3 . The method of claim 1 in which the ibudilast or pharmaceutically acceptable salt thereof is administered for at least six months.
4 . The method of claim 1 in which the ibudilast or pharmaceutically acceptable salt thereof is administered for at least one year.
5 . The method of claim 1 in which the ibudilast or pharmaceutically acceptable salt thereof is administered for at least two years.
6 . The method of claim 1 in which the ibudilast or pharmaceutically acceptable salt thereof is administered at least once daily.
7 . The method of claim 1 in which the ibudilast or pharmaceutically acceptable salt thereof is administered at least twice daily.
8 . The method of claim 1 in which the ibudilast or pharmaceutically acceptable salt thereof is administered at least three times daily.
9 . The method of claim 1 in which the ibudilast or pharmaceutically acceptable salt thereof is administered orally.
10 . The method of claim 1 in which the ibudilast or pharmaceutically acceptable salt thereof is administered parenterally, enterally, intravenously, intranasally, or sublingually.
11 . The method of claim 1 , in which the ibudilast or pharmaceutically acceptable salt thereof is administered through an injection.
12 . The method of claim 1 , wherein the therapeutically effective amount of ibudilast or pharmaceutically acceptable salt thereof is from about 0.1 mg to about 200 mg per day.
13 . The method of claim 1 , wherein the therapeutically effective amount of ibudilast or pharmaceutically acceptable salt thereof is from about 1 mg to about 240 mg per day.
14 . The method of claim 1 , wherein the therapeutically effective amount of ibudilast or pharmaceutically acceptable salt thereof is from about 30 mg to about 240 mg per day.
15 . The method of claim 1 , wherein the therapeutically effective amount of ibudilast or pharmaceutically acceptable salt thereof is from about 30 mg to about 180 mg per day.
16 . The method of claim 1 , in which the therapeutically effective amount of ibudilast or pharmaceutically acceptable salt thereof is selected from the group consisting of 30 mg/day, 60 mg/day, 90 mg/day, or 120 mg/day.
17 . The method of claim 1 , in which the therapeutically effective amount of ibudilast or pharmaceutically acceptable salt thereof is 60 mg/day.
18 . The method of claim 1 , wherein the therapeutically effective amount is administered as a single dose or is divided into multiple dosages.
19 . The method of claim 1 , wherein the therapeutically effective amount is administered in one, two, or three doses per day.
20 . The method of claim 1 , wherein the ibudilast or a pharmaceutically acceptable salt thereof is administered as part of a combination therapy that includes one or more other therapeutic agents.
21 . The method of claim 20 , wherein the one or more other therapeutic agents is approved and known to have a utility in the myelopathy.
22 . The method of claim 1 , wherein the subject is a human subject.
23 . A method of treating a subject diagnosed with a myelopathy comprising administering to the subject a therapeutically effective amount of ibudilast.Join the waitlist — get patent alerts
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