IP Library Granted Patent US 10,758,545
Granted Patent B2
US 10,758,545 · App. 15/579,546 · Granted Sep 1, 2020

Methods to treat neurological diseases

Inventors: Justin Ichida (Los Angeles, CA); Shaoyu Lin (Monterey Park, CA); Yichen Li (Oxford, GB); Yingxiao Shi (Los Angeles, CA)
Assignee: University of Southern California
A61K31/5377A61K31/27A61K45/06A61P25/28
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Quick Facts
Patent No.
US 10,758,545
App. No.
15/579,546
Granted
Sep 1, 2020
Kind
B2
Abstract

Disclosed is a method of treating a subject who has a neurological disease. The neurological disease may be associated with altered C9ORF72 protein activity. In one aspect, the method includes a step of administering an effective dose of a pharmaceutical composition to a subject in need thereof, thereby rescuing the defects associated with altered C9ORF72 protein activity. Also described are methods for identifying a compound for inhibiting motor neuron degeneration.

Claims (11)

1. A method of treating a subject having amyotrophic lateral sclerosis or frontotemporal dementia, comprising:

administering to the subject an effective dose of a PIKFYVE kinase inhibitor selected from the croup consisting of apilimod and YM201636,

wherein the treatment results in an alleviation, reduction, amelioration or improvement in the subject's condition,

and wherein the subject has reduced C9ORF72 gene activity.

2. The method of claim 1 , wherein the subject's C9ORF72 gene comprises a (GGGGCC) n repeat expansion located between exons 1a and 1b of the C9ORF72 gene, wherein n is an integer greater than 25.

3. The method of claim 2 , wherein the subject is haploinsufficient for the C9ORF72 gene.

4. The method of claim 3 , wherein the haploinsufficiency results in a 50% or greater reduction in C9ORF72 protein activity.

5. The method of claim 2 , wherein the C9ORF72 gene product comprises a dipeptide repeat resulting from the (GGGGCC) n expansion.

6. The method of claim 5 , wherein the dipeptide repeat is cytotoxic.

7. The method of claim 2 , wherein the expansion is a gain-of-function or loss-of function mutation.

8. The method of claim 1 , wherein the amyotrophic lateral sclerosis or frontotemporal dementia are associated with neuronal hyperexcitability.

Assignments (2)
CONFIRMATORY LICENSE Recorded Feb 9, 2024
From: UNIVERSITY OF SOUTHERN CALIFORNIA
To: THE UNITED STATES GOVERNMENT
Reel/Frame 066550/0844 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 21, 2020
From: ICHIDA, JUSTIN; LIN, SHAOYU; LI, YICHEN; SHI, YINGXIAO
To: UNIVERSITY OF SOUTHERN CALIFORNIA
Reel/Frame 052729/0111 →
Continuity (2)
Provisional Application 62184732 · Jun 25, 2015
Related Publication 20180161335A1 · Jun 14, 2018
Cited By (1)
US 12,486,274