IP Library Granted Patent US 11,213,508
Granted Patent B2
US 11,213,508 · App. 16/751,677 · Granted Jan 4, 2022

Compositions comprising urolithins and uses thereof for the stimulation of insulin secretion

Inventors: Gerard Cros (Montpellier, FR); Alan Crozier (Glasgow, GB); Margherita Dall'asta (Parma, IT); Daniele Del Rio (Parma, IT); Richard Magous (Lunel, FR); Catherine Oiry (Pignan, FR)
Assignees: Universite de Montpellier; University de Parma; Ecole Nationale Supérieure de Chimie de Montpellier
A61K31/37A61K31/255A61K38/26A23V2002/00
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Quick Facts
Patent No.
US 11,213,508
App. No.
16/751,677
Granted
Jan 4, 2022
Kind
B2
Abstract

The present invention relates to a composition comprising urolithin A, urolithin B, urolithin C, urolithin D, or a combination thereof, for the stimulation of insulin secretion, and to the use of a compound chosen among urolithin A, urolithin B, urolithin C, urolithin D, or a combination thereof, intended for the stimulation of insulin secretion. The present invention also relates to a composition comprising an effective amount of urolithin B, urolithin C, urolithin D, or a combination thereof, for the treatment or the prevention of diabetes mellitus, and in particular for the treatment or the prevention of type 2 diabetes, and to the use of a compound chosen among urolithin B, urolithin C, urolithin D, and a combination thereof, intended for the treatment or the prevention of diabetes mellitus, and in particular of type 2 diabetes.

Claims (15)

1. A composition comprising urolithin C and a second compound able to stimulate insulin secretion selected from the group consisting of sulfonylureas, GLP-1 analogs, and DPP4 inhibitors.

2. The composition of claim 1 , wherein the compound able to stimulate insulin secretion is a sulfonylurea.

3. The composition of claim 2 , wherein the compound able to stimulate insulin secretion is a sulfonylurea selected from the group consisting of Metahexamide, Glibenclamide (Glyburide), Carbutamide, Acetohexamide, Chlorpropamide, Tolbutamide, Tolazamide, Glipizide, Gliclazide, Glibornuride, Gliquidone, Glisoxepide, Glyclopyramide, and Glimepiride.

4. The composition of claim 3 , wherein the compound able to stimulate insulin secretion is Glibenclamide.

5. The composition of claim 1 , wherein the compound able to stimulate insulin secretion is a GLP-1 analog.

6. The composition of claim 5 , wherein the compound able to stimulate insulin secretion is a GLP-1 analog selected from the group consisting of exenatide and liraglutide.

7. The composition of claim 6 , wherein the compound able to stimulate insulin secretion is exenatide.

8. The composition of claim 1 , wherein the compound able to stimulate insulin secretion is a DPP4 inhibitor.

9. The composition of claim 8 , wherein the compound able to stimulate insulin secretion is a DPP4 inhibitor selected from the group consisting of Alogliptin, Gemigliptin, Linagliptin, Saxagliptin, Sitagliptin, and Vildagliptin.

10. A pharmaceutical formulation for the treatment of diabetes mellitus comprising an effective amount of the composition of claim 1 in a pharmaceutically acceptable vehicle.

11. A food product or a nutritional supplement for the stimulation of insulin secretion comprising an effective amount of the composition of claim 1 and a nutritionally acceptable vehicle.

12. A swallowable tablet, chewable tablet, effervescent tablet, capsule, pill, powder, granule, oral solution, oral suspension, sublingual dosage form, or buccal dosage form, comprising the composition of claim 1 and a carrier that is acceptable for nutritional usage.

13. A pharmaceutical formulation, food product, or a nutritional supplement comprising the composition of claim 1 for the treatment of a patient chosen from among the group consisting of a prediabetic patient, a patient whose fasting glycemia is comprised between 1 and 1.25 g L −1 and a patient whose post-prandial glycemia is comprised between 1.40 and 1.99 g L −1 .

14. A pharmaceutical formulation, food product, or a nutritional supplement comprising the composition of claim 1 for the treatment of a diabetic patient, a patient whose fasting glycemia is equal or superior to 1.26 g·L −1 and a patient whose post-prandial glycemia is equal or superior to 2 g·L −1 .

15. A combination product comprising the components of the composition of claim 1 , provided for simultaneous, separate or sequential use.

Assignments (2)
MERGER Recorded Jun 14, 2021
From: ECOLE NATIONALE SUPERIEURE DE CHIMIE
To: ECOLE NATIONALE SUPERIEURE DE CHIMIE DE MONTPELLIER
Reel/Frame 056531/0193 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 10, 2021
From: CROS, GÉRARD; CROZIER, ALAN; DALL'ASTA, MARGHERITA; DEL RIO, DANIELE; MAGOUS, RICHARD; OIRY, CATHERINE
To: CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE (CNRS); UNIVERSITE DE MONTPELLIER; UNIVERSITY DE PARMA; ECOLE NATIONALE SUPERIEURE DE CHIMIE
Reel/Frame 055219/0883 →
Priority Claims (1)
EP 13306415 · Oct 15, 2013 · regional
Continuity (2)
Division 15029384
Related Publication 20200155504A1 · May 21, 2020