US2020155616A1PendingUtilityA1

Use of akkermansia for treating metabolic disorders

Assignee: UNIV CATHOLIQUE LOUVAINPriority: Nov 19, 2012Filed: Dec 10, 2019Published: May 21, 2020
Est. expiryNov 19, 2032(~6.3 yrs left)· nominal 20-yr term from priority
A61P 25/00A61P 9/00A61P 1/16A61P 25/28A61P 3/10A61P 35/00A61P 43/00A61P 3/00A61K 35/74A61P 19/02A61K 35/741A61P 3/06A61P 9/12A61K 9/0053A61P 11/00A61P 9/10A61P 37/02A61P 3/04A61P 37/04A61P 11/06Y02A50/481A61K 2300/00A61P 37/00A61P 29/00A61K 45/06Y02A50/30
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Claims

Abstract

The present invention relates to Akkermansia muciniphila or fragments thereof for treating a metabolic disorder in a subject in need thereof. The present invention also relates to a composition, a pharmaceutical composition and a medicament comprising Akkermansia muciniphila or fragments thereof for treating a metabolic disorder. The present invention also relates to the use of Akkermansia muciniphila or fragments thereof for promoting weight loss in a subject in need thereof.

Claims

exact text as granted — not AI-modified
1 - 17 . (canceled) 
     
     
         18 . A method for treating a metabolic disorder in a subject in need thereof, the method comprising orally administering a composition comprising a therapeutically effective amount of bacteria comprising substantially purified  Akkermansia  to the subject wherein the substantially purified  Akkermansia  comprises at least 50% of a strain of  Akkermansia.    
     
     
         19 . The method according to  claim 18 , wherein said metabolic disorder is obesity. 
     
     
         20 . The method according to  claim 18 , wherein said metabolic disorder is selected from the group consisting of metabolic syndrome, insulin-deficiency, insulin-resistance related disorder, diabetes mellitus, glucose intolerance, abnormal lipid metabolism, atherosclerosis, hypertension, stroke, non-alcoholic fatty liver disease, dyslipidemia, high cholesterol, elevated triglycerides, sleep apnea, osteoarthritis, neurodegenerative disorder, inflammatory disorder, immune disorder, atherogenic dyslipidemia, and heart disease. 
     
     
         21 . The method according to  claim 18 , wherein viable cells of the  Akkermansia  are administered to the subject. 
     
     
         22 . The method according to  claim 18 , wherein the composition is administered one or more times. 
     
     
         23 . The method according to  claim 18 , wherein the  Akkermansia  is co-administered with another probiotic strain and/or with one or more prebiotics. 
     
     
         24 . The method according to  claim 23 , wherein the  Akkermansia  is co-administered with another probiotic strain. 
     
     
         25 . The method according to  claim 23 , wherein the  Akkermansia  is co-administered with one or more prebiotics. 
     
     
         26 . The method according to  claim 18 , wherein said metabolic disorder is selected from the group consisting of obesity, insulin-deficiency, and insulin-resistance related disorders. 
     
     
         27 . The method according to  claim 18 , wherein the bacteria consist essentially of  Akkermansia.    
     
     
         28 . The method according to  claim 18 , wherein if the bacteria comprise a mixture of bacterial strains, then at least 50% of the bacterial strains in the composition are  Verrucomicrobia, Bacteroidetes, Firmicutes , or  Proteobacteria.    
     
     
         29 . The method according to  claim 18 , wherein the bacteria further comprise substantially purified  Clostridiales.    
     
     
         30 . The method according to  claim 18 , wherein the bacteria further comprise substantially purified  Clostridium.    
     
     
         31 . The method according to  claim 18 , wherein the  Akkermansia  is lyophilized. 
     
     
         32 . The method according to  claim 18 , wherein the composition comprises a coating, wherein the coating does not fully degrade until after it exits the stomach of the subject. 
     
     
         33 . The method according to  claim 18 , wherein the composition comprises a mixture of bacterial strains selected from the group consisting of  Verrucomicrobia, Bacteroidetes, Firmicutes , and  Proteobacteria.    
     
     
         34 . The method according to  claim 18 , wherein the bacteria further comprise substantially purified  Firmicutes.    
     
     
         35 . The method according to  claim 18 , wherein the composition comprises a coating. 
     
     
         36 . The method according to  claim 22 , wherein the composition is administered to the subject at least three times a week. 
     
     
         37 . The method according to  claim 18 , wherein the  Akkermansia  is non-viable.

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