IP Library Granted Patent US 11,419,839
Granted Patent B2
US 11,419,839 · App. 16/723,241 · Granted Aug 23, 2022

Therapeutic use of compounds

Inventors: Robin Simon Brooke Williams (Egham, GB); Matthew Walker (London, GB)
Assignee: UCL BUSINESS LTD
A61K31/20
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Quick Facts
Patent No.
US 11,419,839
App. No.
16/723,241
Granted
Aug 23, 2022
Kind
B2
Abstract

A compound having the formula (I) R1-COOH. R1 is an alkyl or alkenyl group having a C 7-11 backbone, optionally branched with a C 1-6 alkyl group at any C position in the backbone, or a pharmaceutically acceptable salt, amide or ester thereof. The backbone of the alkyl or alkenyl group, and/or the branched alkyl groups, are optionally interrupted by one or more heteroatoms, provided that when R1 is an alkyl group having a C 7 backbone, the branching does not consist only of a hexyl group at the a carbon of R1, or only of a methyl group at the γ carbon of R1, or of only single methyl groups at both the β and ω-1 carbons of R1, and provided that when R1 is an alkyl group having a C 8 or C 11 backbone, the branching does not consist only of a propyl group at the a carbon of R1.

Claims (5)

1. A method for treating a seizure-related disorder in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of 4-ethyloctanoic acid, wherein the therapeutically effective amount of the 4-ethyloctanoic acid is 1 to 20,000 μg/kg per dose.

2. The method according to claim 1 , wherein the seizure-related disorder is epilepsy.

3. The method according to claim 1 , wherein the therapeutically effective amount of the 4-ethyloctanoic acid is administered to the subject with one or more of a pharmaceutically acceptable carrier, a pharmaceutically acceptable adjuvant or a pharmaceutically acceptable vehicle.

4. The method according to claim 1 , wherein the therapeutically effective amount of the 4-ethyloctanoic acid is administered to the subject orally.

5. The method according to claim 1 , wherein the therapeutically effective amount of the 4-ethyloctanoic acid is administered in an orally acceptable dosage form selected from the group consisting of capsules, tablets, powders, granules, aqueous suspensions and solutions.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 5, 2022
From: WILLIAMS, ROBIN SIMON BROOKE; WALKER, MATTHEW
To: UCL BUSINESS PLC
Reel/Frame 059824/0715 →
CHANGE OF NAME Recorded May 5, 2022
From: UCL BUSINESS PLC
To: UCL BUSINESS LTD
Reel/Frame 059856/0162 →
Priority Claims (1)
GB 1020133 · Nov 26, 2010 · national
Continuity (2)
Division 13989360
Related Publication 20200268699A1 · Aug 27, 2020