IP Library Granted Patent US 11,844,776
Granted Patent B2
US 11,844,776 · App. 16/303,629 · Granted Dec 19, 2023

Composition for treatment and/or prevention of peripheral nerve disorder

Inventor: Shinji Hirotsune (Osaka, JP)
Assignees: OSAKA CITY UNIVERSITY; SENJU PHARMACEUTICAL CO., LTD.
A61K31/27A61K9/0019A61K31/341A61K31/351A61K31/4402A61P25/02
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Quick Facts
Patent No.
US 11,844,776
App. No.
16/303,629
Granted
Dec 19, 2023
Kind
B2
Abstract

The present invention provides a means for treating and/or preventing peripheral nerve disorder by facilitating regeneration of peripheral nerves. Specifically, the present invention provides a composition for treating and/or preventing peripheral nerve disorder comprising a compound represented by the general formula (I): wherein R 1 is lower alkyl substituted with lower alkoxy, lower alkyl substituted with a heterocyclic group, a heterocyclic group, or a group represented by the formula (IIa): R 4 O—R 5 m   (IIa) wherein R 4 is lower alkyl, R 5 is lower alkylene, and m is an integer of 1 to 6; R 2 is lower alkyl optionally substituted with phenyl; and R 3 is lower alkyl optionally substituted with halogen, lower alkoxy, or phenyl; condensed polycyclic hydrocarbon; or hydrogen.

Claims (11)

1. A method for promoting peripheral nerve regeneration to treat a peripheral nerve disorder, comprising

(i) selecting a subject suffering from a peripheral nerve disorder comprising a severed peripheral nerve or a degenerated peripheral nerve that has degenerated over time after damage, and (ii) administrating to the subject in need of treatment for the peripheral nerve disorder a therapeutically effective amount of a compound represented by the formula:

wherein the administering is commenced after the onset of a symptom of the peripheral nerve disorder in the subject, and

wherein administering the compound is effective to promote peripheral nerve regeneration.

2. The method according to claim 1 , wherein the compound is administered by oral administration, injection, or intravenous drip.

3. The method according to claim 1 , wherein the compound is administered at a dose of from 0.1 to 2,000 mg per day.

4. The method according to claim 1 , wherein the peripheral nerve disorder is at least one selected from the group consisting of mechanical or entrapment neuropathy, metabolic neuropathy, infectious neuropathy, and drug-induced peripheral nerve disorders.

5. The method according to claim 4 , wherein the entrapment neuropathy is at least one member selected from the group consisting of cubital tunnel syndrome, sciatic nerve paralysis, peroneal nerve paralysis, and tarsal tunnel syndrome.

6. The method according to claim 3 , wherein the compound is administered in 1, 2, or 3 doses per day.

7. The method according to claim 1 , wherein the peripheral nerve disorder comprises a severed peripheral nerve, and administering the compound is effective to promote peripheral nerve regeneration of the severed peripheral nerve.

8. The method according to claim 1 , wherein the peripheral nerve disorder comprises a degenerated peripheral nerve that has degenerated over time after damage, and administering the compound is effective to promote peripheral nerve regeneration of the degenerated peripheral nerve.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 21, 2018
From: HIROTSUNE, SHINJI
To: OSAKA CITY UNIVERSITY; SENJU PHARMACEUTICAL CO., LTD.
Reel/Frame 047618/0155 →
Priority Claims (1)
JP 2016-102878 · May 23, 2016 · national
Continuity (1)
Related Publication 20190314320A1 · Oct 17, 2019