US2021154160A1PendingUtilityA1
Method of Treating a Disorder of Cognitive Performance or Memory
Est. expirySep 19, 2032(~6.2 yrs left)· nominal 20-yr term from priority
Inventors:Stefan Pierzynowski
A61K 45/06A61P 25/14C12Y 302/01001A61K 38/47A61P 25/24A61K 38/465A61K 38/54A61P 21/00A61P 25/00A61K 31/194A61K 38/48A61P 25/16A61P 3/02A61P 43/00A61K 31/198A61P 25/18A61P 25/28A61P 25/22A61P 9/10A61P 27/02
60
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Claims
Abstract
A composition comprising alpha-ketoglutaric acid or a pharmaceutically acceptable salt thereof (AKG), and one or more enzymes selected from a group consisting of a lipase, a protease and an amylase, and medical uses thereof in, neurological and/or neurodegenerative disease, neurological trauma, depression or chronic fatigue syndrome.
Claims
exact text as granted — not AI-modifiedI claim:
1 . A method of treating a disorder of cognitive performance or memory, comprising orally administering to a subject in need thereof a composition comprising:
a. alpha-ketoglutaric acid or a pharmaceutically acceptable salt thereof (AKG); and b. a lipase, a protease and an amylase.
2 . The method according to claim 1 , wherein the composition comprises: 200-20000 USP units of lipase per mmol AKG, 500-50000 USP units of protease per mmol AKG and 200-20000 USP units of amylase per mmol AKG.
3 . The method according to claim 2 , wherein the lipase is a Burkholderia cepacia lipase, preferably as cross-linked lipase crystals, the protease is an Aspergillus melleus protease and the amylase is an Aspergillus oryzae amylase.
4 . The method according to claim 2 , wherein the lipase is a pancrelipase lipase, the protease is a pancrelipase protease and the amylase is a pancrelipase amylase.
5 . The method according to claim 1 , said method comprising orally administering an amount of the composition containing about 12-240 mmol AKG to a subject per day.
6 . The method according to claim 2 , said method comprising orally administering an amount of the composition containing about 12-240 mmol AKG to a subject per day.
7 . The method according to claim 6 , said method comprising orally administering an amount of the composition containing about 24-120 mmol AKG to a subject per day.
8 . The method according to claim 7 , said method comprising orally administering an amount of the composition containing about 36-120 mmol AKG to a subject per day.
9 . The method according to claim 8 , said method comprising orally administering an amount of the composition containing about 60-120 mmol AKG to a subject per day.
10 . The method according to claim 1 , said method comprising administering an amount of the composition containing 1-10 g AKG to a patient per day.
11 . The method according to claim 2 , said method comprising administering an amount of the composition containing 1-10 g AKG to a patient per day.
12 . The method according to claim 1 , being a method of treating a disorder of cognitive performance.
13 . The method according to claim 1 , being a method of treating a disorder of memory.
14 . The method according to claim 1 , wherein the disorder of cognitive performance or memory is mild cognitive impairment (MCI).
15 . The method according to claim 8 , being a method of treating a disorder of cognitive performance.
16 . The method according to claim 8 , being a method of treating a disorder of memory.
17 . The method according to claim 1 , wherein the AKG comprises Ca-AKG, Na-AKG, ornithine-AKG, arginine AKG, or a combination thereof.
18 . The method according to claim 1 , wherein the composition is administered encapsulated in a protective enteric coating.
19 . The method according to claim 8 , wherein the composition is administered encapsulated in a protective enteric coating.Join the waitlist — get patent alerts
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