US2021154160A1PendingUtilityA1

Method of Treating a Disorder of Cognitive Performance or Memory

Assignee: GRESPO ABPriority: Sep 19, 2012Filed: Jan 29, 2021Published: May 27, 2021
Est. expirySep 19, 2032(~6.2 yrs left)· nominal 20-yr term from priority
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
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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-modified
I 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.

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