IP Library Granted Patent US 11,452,724
Granted Patent B2
US 11,452,724 · App. 16/855,623 · Granted Sep 27, 2022

Methods for treating amyotrophic lateral sclerosis

Inventors: Eva L. Feldman (Ann Arbor, MI); Ben Murdock (Ann Arbor, MI); Stephen Goutman (Ann Arbor, MI); Stacey Jacoby (Ann Arbor, MI)
Assignee: The Regents of the University of Michigan
A61K31/519A61P25/00A61K9/0019A61K31/133A61K31/4152A61K31/428A61K31/444A61K31/4439A61K31/51A61K31/53A61K31/7105
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Quick Facts
Patent No.
US 11,452,724
App. No.
16/855,623
Granted
Sep 27, 2022
Kind
B2
Abstract

Provided herein are methods for treating, delaying progression of, or reducing the severity of amyotrophic lateral sclerosis (ALS) in a subject through administration of therapeutically effective amounts of agents (e.g., JAK kinase inhibitors (e.g., tofacitinib)) capable of interfering with central nervous system related natural killer cell (NK) levels and function.

Claims (7)

1. A kit comprising a therapeutically effective amount of an agent capable of interfering with central nervous system related natural killer cell (NK) levels and function and instructions for administering the agent to a subject having or at risk of having ALS, wherein the agent is a JAK kinase inhibitor, wherein the agent is selected from AT9283, AZD1480, baricitinib, BMS-911543, fedratinib, filgotinib (GLPG0634), gandotinib (LY2784544), INCB039110, lestaurtinib, momelotinib (CYT0387), NS-018, pacritinib (SB1518), peficitinib (ASP015K), ruxolitinib, tofacitinib (formerly tasocitinib), and XL019.

2. The kit of claim 1 , wherein the JAK kinase inhibitor is a JAK1 kinase inhibitor, a JAK2 kinase inhibitor, and/or a JAK3 kinase inhibitor.

3. The kit of claim 1 , wherein the therapeutically effective amount is an amount sufficient to detectably reduce or ameliorate one or more symptoms of the ALS, wherein the one or more symptoms comprise difficulty lifting the front part of the foot; difficulty lifting the toes; weakness in one or both legs; weakness in one or both feet; weakness in one or both ankles; hand weakness; hand clumsiness; slurring of speech; trouble swallowing; muscle cramps; twitching in one or both arms; twitching in one or both shoulders and/or twitching of the tongue.

4. The kit of claim 1 , wherein the subject is a human subject.

5. The kit of claim 4 , wherein the subject is a human patient suffering from or at risk of suffering from ALS.

6. The kit of claim 1 , wherein the agent is formulated to be administered systemically, intravenously, intraarterially, subcutaneously, or intrathecally.

7. The kit of claim 1 , further comprising one or more of riluzole, ceftriaxone, dexpramipexole, creatine+tamoxifen, rasagiline, pioglitazone, arimoclomol, pyrimethamine, trantinoin+pioglitazone, edaravone, and an antisense molecule or interfering RNA directed against an RNA encoding superoxide dismutase.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 23, 2024
From: UNIVERSITY OF MICHIGAN
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 066364/0148 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 19, 2020
From: FELDMAN, EVA L.; MURDOCK, BEN; GOUTMAN, STEPHEN; JACOBY, STACEY
To: THE REGENTS OF THE UNIVERSITY OF MICHIGAN
Reel/Frame 052697/0336 →
Continuity (3)
Division 16539289 · Aug 13, 2019
Provisional Application 62718122 · Aug 13, 2018
Related Publication 20200253977A1 · Aug 13, 2020