IP Library › Granted Patent US 10,159,713
Granted Patent B2
US 10,159,713 · App. 15/073,364 · Granted Dec 25, 2018

Treatment of type 2 diabetes mellitus patients

Inventors: Rene Belder (Bridgewater, NJ); Peter Johnston (Barryville, NY); Francesca Lawson (Bridgewater, NJ); Lin Ping (Bridgewater, NJ); Xiaodan Wei (Bridgewater, NJ)
Assignee: Sanofi-Aventis Deutschland GmbH
A61K38/26
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Quick Facts
Patent No.
US 10,159,713
App. No.
15/073,364
Granted
Dec 25, 2018
Kind
B2
Abstract

The present invention refers to lixisenatide for use in the reduction of progression of urinary albumin excretion in a type 2 diabetes mellitus patient.

Claims (19)

1. A method of reducing urinary albumin excretion in a type 2 diabetes mellitus patient with albumunuria, said method comprising

selecting a type 2 diabetes mellitus patient with albuminuria, and administering lixisenatide or a pharmaceutically acceptable salt thereof to the patient in need thereof, thereby reducing albumin excretion in the patient.

2. The method of claim 1 , wherein the patient has microalbuminuria.

3. The method of claim 1 , wherein the patient has a urinary albumin to creatinine ratio (UACR) of ≥30 mg/g to <300 mg/g.

4. The method of claim 1 , wherein the patient has a urinary albumin to creatinine ratio (UACR) of ≥300 mg/g.

5. The method of claim 1 , wherein the patient has a glomerular filtration rate (GFR) of ≥60 mL/min/1.73 m 2 to <90 mL/min/1.73 m 2 .

6. The method of claim 1 , wherein the patient has a glomerular filtration rate (GFR) of ≥30 mL/min/1.73 m 2 to <60 mL/min/1.73 m 2 .

7. The method of claim 1 , wherein the patient has a glomerular filtration rate (GFR) of ≥15 mL/min/1.73 m 2 to <30 mL/min/1.73 m 2 .

8. The method of claim 1 , wherein the patient receives lixisenatide in combination with

an insulin or a pharmaceutically acceptable salt thereof.

9. The method of claim 1 , wherein prior to the onset of treatment with lixisenatide, the patient has a HbA1c value of 7% to 10%.

10. The method of claim 1 , wherein the patient has macroalbuminuria.

11. The method of claim 1 , wherein prior to the onset of treatment with lixisenatide, the patient's type 2 diabetes mellitus is not adequately controlled.

12. The method of claim 1 , wherein the lixisenatide is administered subcutaneously.

13. The method of claim 1 , wherein the lixisenatide is administered in a daily dose of 5 μg to 20 μg.

14. The method of claim 11 , wherein the patient's type 2 diabetes mellitus is not adequately controlled on insulin or a pharmaceutically acceptable salt thereof.

15. The method of claim 1 , wherein the patient receives lixisenatide in combination with metformin or a pharmaceutically acceptable salt thereof.

16. The method of claim 1 , wherein the patient receives lixisenatide in combination with a glinide or a pharmaceutically acceptable salt thereof.

17. The method of claim 1 , wherein the patient receives lixisenatide in combination with a sulfonylurea or a pharmaceutically acceptable salt thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 14, 2016
From: BELDER, RENE; JOHNSTON, PETER; LAWSON, FRANCESCA; PING, LIN; WEI, XIAODAN
To: SANOFI-AVENTIS DEUTSCHLAND GMBH
Reel/Frame 038913/0816 →
Priority Claims (2)
EP 15159733 · Mar 18, 2015 · regional
EP 15191585 · Oct 27, 2015 · regional
Continuity (1)
Related Publication 20160296601A1 · Oct 13, 2016
Cited By (1)
US 12,186,374