IP Library Granted Patent US 9,968,625
Granted Patent B2
US 9,968,625 · App. 14/830,558 · Granted May 15, 2018

Synthetic or recombinant fucosylated oligosaccarides for use in the treatment of infections

Inventor: Stefan Jennewein (Bad Honnef, DE)
Assignee: Jennewein Biotechnologie GmbH
A61K31/702A61K31/715
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Quick Facts
Patent No.
US 9,968,625
App. No.
14/830,558
Granted
May 15, 2018
Kind
B2
Abstract

The present invention relates to synthetic fucosylated oligosaccharide for use in the treatment or prophylaxis of an infection with a Norwalk-like Virus or Rotavirus of a mam-mal, wherein the synthetic fucosylated oligosaccharide comprises a non-reducing end and an reducing end, wherein the reducing end comprises a first carbohydrate unit consisting of a galactose (Gal) linked via a β1-4 glycosidic bond to a glucose (Glc), and wherein the non-reducing end comprises a second carbohydrate unit linked via a β1-3 glycosidic bond to the first carbohydrate unit of the reducing end, and wherein the second carbohydrate unit comprises a) at least one or more of a fucose (Fucose) and a Galactose (Gal), and b) at least one or more of a N-acetylglucosamine (GlcNAc) or a N-acetylgalactosamine (GalNAc).

Claims (23)

1. A fucosylated oligosaccharide for treating or inhibiting an Norwalk-like Virus or Rotavirus infection in a mammal, wherein the fucosylated oligosaccharide comprises a non-reducing end and a reducing end, wherein the reducing end comprises a first carbohydrate unit consisting of a galactose (Gal) linked via a β1-4 glycosidic bond to a glucose (Glc), and wherein the non-reducing end comprises a second carbohydrate unit linked via a β1-3 glycosidic bond to the first carbohydrate unit of the reducing end, and wherein the second carbohydrate unit comprises a) at least one or more of a fucose (Fuc) and a galactose (Gal), and b) at least one or more of a N-acetylglucosamine (GlcNAc) or a N-acetylgalactosamine (GalNAc), and wherein the second carbohydrate unit is:

GlcNAcα1-3 (Fucα1-2)Galβ1-3GlcNAc

Galβ1-3(Fucα1-2)Galβ1-3GlcNAc

or

Fucα1-2Galβ1-4GalNAc.

2. The fucosylated oligosaccharide of claim 1 , wherein the fucosylated oligosaccharide is:

GlcNAcα1-3 (Fucα1-2)Galβ1-3GlcNAcβ1-3Galβ1-4Glc.

3. The fucosylated oligosaccharide of claim 1 , wherein the fucosylated oligosaccharide is Galβ1-3(Fucα1-2)Galβ1-3GlcNAcβ1-3Galβ1-4Glc.

4. The fucosylated oligosaccharide of claim 1 , wherein the fucosylated oligosaccharide is Fucα1-2Galβ1-4GalNAcβ1-3Galβ1-4Glc.

5. A composition comprising two or more of:

GlcNAcα1-3 (Fucα1-2)Galβ1-3GlcNAcβ1-3Galβ1-4Glc;

Galβ1-3(Fucα1-2)Galβ1-3GlcNAcβ1-3Galβ1-4Glc; and

Fucα1-2Galβ1-4GalNAcβ1-3Galβ1-4Glc.

6. A composition comprising the fucosylated oligosaccharide of claim 1 , and one or both of Fucα1-2Galβ1-3GlcNAcβ1-3Galβ1-4Glc and Galβ1-4(Fucα1-3)GlcNAcβ1-3Galβ1-4Glc.

7. A pharmaceutical composition comprising at least one of the fucosylated oligosaccharides of claim 1 , and a pharmaceutically acceptable carrier.

8. A synthetic nutrition composition comprising at least one of the fucosylated oligosaccharides of claim 1 .

9. A method for treating a Norwalk-like Virus infection in a mammal, comprising administering a therapeutically effective amount of the fucosylated oligosaccharide of claim 1 to the mammal, thereby treating the Norwalk-like virus infection in the mammal.

10. A method for treating a Norwalk-like Virus infection in a mammal, comprising administering a therapeutically effective amount of the fucosylated oligosaccharide of claim 2 to the mammal, thereby treating the Norwalk-like virus infection in the mammal.

11. A method for treating a Norwalk-like Virus infection in a mammal, comprising administering a therapeutically effective amount of the fucosylated oligosaccharide of claim 3 to the mammal, thereby treating the Norwalk-like virus infection in the mammal.

12. A method for treating a Norwalk-like Virus infection in a mammal, comprising administering a therapeutically effective amount of the fucosylated oligosaccharide of claim 4 to the mammal, thereby treating the Norwalk-like virus infection in the mammal.

13. A method for treating a Norwalk-like Virus infection in a mammal, comprising administering a therapeutically effective amount of the composition of claim 5 to the mammal, thereby treating the Norwalk-like virus infection in the mammal.

14. A method for treating a Norwalk-like Virus infection in a mammal, comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 7 to the mammal, thereby treating the Norwalk-like virus infection in the mammal.

15. A method for treating a Norwalk-like Virus infection in a mammal, comprising administering a therapeutically effective amount of the synthetic nutrition composition of claim 8 to the mammal, thereby treating the Norwalk-like virus infection in the mammal.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2025
From: CHR. HANSEN HMO GMBH
To: CHR. HANSEN A/S
Reel/Frame 070396/0299 →
CHANGE OF NAME Recorded Jun 22, 2021
From: JENNEWEIN BIOTECHNOLOGIE GMBH
To: CHR. HANSEN HMO GMBH
Reel/Frame 057701/0507 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 25, 2016
From: JENNEWEIN, STEFAN
To: JENNEWEIN BIOTECHNOLOGIE GMBH
Reel/Frame 039823/0925 →
Priority Claims (1)
EP 13156224 · Feb 21, 2013 · regional
Continuity (2)
Continuation PCTEP2014052912 · Feb 14, 2014
Related Publication 20150352133A1 · Dec 10, 2015