US2022249481A1PendingUtilityA1
Treating neural disease with tyrosine kinase inhibitors
Est. expiryMay 2, 2032(~5.8 yrs left)· nominal 20-yr term from priority
Inventors:Charbel Moussa
A61K 31/506A61P 25/16A61P 25/28A61K 31/496A61K 45/06
72
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
Provided herein are methods of treating or preventing a neurodegenerative disease, a myodegenerative disease or a prion disease in a subject comprising administering a tyrosine kinase inhibitor.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method of treating Lewy Body disease in a subject in need thereof, comprising: selecting a subject with Lewy Body disease or at risk for Lewy Body disease; and administering to the subject an effective amount of a tyrosine kinase inhibitor or a pharmaceutically acceptable salt thereof, wherein the tyrosine kinase inhibitor is not Gleevec, and wherein the tyrosine kinase inhibitor or a pharmaceutically acceptable salt thereof crosses the blood brain barrier.
2 . The method of claim 1 , wherein the tyrosine kinase inhibitor is selected from the group consisting of nilotinib or a pharmaceutically acceptable salt thereof, bosutinib or a pharmaceutically acceptable salt thereof, and a combination thereof.
3 . The method of claim 1 , wherein the effective amount of the tyrosine kinase inhibitor or a pharmaceutically acceptable salt thereof is less than about 10 mg/kg.
4 . The method of claim 1 , wherein the tyrosine kinase inhibitor or a pharmaceutically acceptable salt thereof is administered daily.
5 . The method of claim 1 , further comprising administering a second therapeutic agent to the subject.
6 . A method of inhibiting or preventing toxic protein aggregation in a neuron of a subject with Lewy Body disease, comprising contacting the neuron in the subject with an effective amount of a tyrosine kinase inhibitor or a pharmaceutically acceptable salt thereof, wherein the tyrosine kinase inhibitor is not Gleevec, and wherein the tyrosine kinase inhibitor or a pharmaceutically acceptable salt thereof crosses the blood brain barrier.
7 . The method of claim 6 , wherein the tyrosine kinase inhibitor is selected from the group consisting of nilotinib or a pharmaceutically acceptable salt thereof, bosutinib or a pharmaceutically acceptable salt thereof, and a combination thereof.
8 . The method of claim 6 , wherein the protein is selected from the group consisting of alpha-synuclein and insoluble Parkin.
9 . The method of claim 6 , wherein the effective amount of the tyrosine kinase inhibitor or a pharmaceutically acceptable salt thereof is less than about 10 mg/kg.Join the waitlist — get patent alerts
Track US2022249481A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.