US2020038382A1PendingUtilityA1
Methods of treating glioblastoma multiforme using ibudilast
Est. expiryDec 22, 2036(~10.4 yrs left)· nominal 20-yr term from priority
A61K 31/437A61K 45/06A61K 31/495A61K 31/4704A61P 35/00Y02A50/465Y02A50/30
61
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Compositions and methods for treating glioblastoma or recurrent glioblastoma and its associated symptoms by administration of ibudilast (3-isobutyryl-2-isopropylpyrazolo[1,5-a]pyridine) or a pharmaceutically acceptable salt thereof.
Claims
exact text as granted — not AI-modified1 . A method of treating a patient diagnosed with glioblastoma or suffering from recurrent glioblastoma comprising administering to the patient a therapeutically effective amount of ibudilast or a pharmaceutically acceptable salt thereof, as part of a combination therapy comprising one or more other therapeutic agent selected from carmustine, bevacizumab, procarbazine, hydroxyurea, irinotecan, lomustine, nimotuzumab, sirolimus, mipsagargin, cabozantinib, onartuzumab, patupilone (Epothilone B), recombinant oncolytic poliovirus (PVS-RIPO), or any combination of one or more of the foregoing.
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 at least once daily.
4 . The method of claim 1 in which the ibudilast or pharmaceutically acceptable salt thereof is administered orally.
5 . The method of claim 1 , wherein the therapeutically effective amount of ibudilast or a pharmaceutically acceptable salt thereof is from 0.1 mg to 720 mg per day.
6 . The method of claim 1 , wherein the therapeutically effective amount is administered as a single dose or is divided into two, three, or four doses.
7 .- 10 . (canceled)
11 . A method of treating a patient suffering from recurrent glioblastoma comprising administering to the patient a therapeutically effective amount of ibudilast or a pharmaceutically acceptable salt thereof, as part of a combination therapy comprising one or more other therapeutic agent selected from carmustine, bevacizumab, procarbazine, hydroxyurea, irinotecan, lomustine, nimotuzumab, sirolimus, mipsagargin, cabozantinib, onartuzumab, patupilone (Epothilone B), recombinant oncolytic poliovirus (PVS-RIPO), or any combination of one or more of the foregoing.
12 . The method of claim 11 in which the ibudilast or pharmaceutically acceptable salt thereof is administered for at least 3 months.
13 . The method of claim 11 in which the ibudilast or pharmaceutically acceptable salt thereof is administered at least once daily.
14 . The method of claim 11 in which the ibudilast or pharmaceutically acceptable salt thereof is administered orally.
15 . The method of claim 11 , wherein the therapeutically effective amount of ibudilast or a pharmaceutically acceptable salt thereof is from 0.1 mg to 720 mg per day.
16 . The method of claim 11 , wherein the therapeutically effective amount is administered as a single dose or is divided into two, three, or four doses.
17 .- 20 . (canceled)Join the waitlist — get patent alerts
Track US2020038382A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.