IP Library Granted Patent US 12,121,517
Granted Patent B2
US 12,121,517 · App. 18/213,601 · Granted Oct 22, 2024

Combination of zibotentan and dapagliflozin for the treatment of endothelin related diseases

Inventors: Peter Greasley (Mölndal, SE); Christine Ahlström (Mölndal, IL); Stanko Skrtic (Mölndal, SE); Robert Menzies (Mölndal, SE); Anne-Kristina Mercier (Mölndal, SE); Mikael Sunnåker (Mölndal, SE)
Assignee: ASTRAZENECA AB
A61K31/497A61K31/7034A61P13/12
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,121,517
App. No.
18/213,601
Granted
Oct 22, 2024
Kind
B2
Abstract

The present disclosure relates to the endothelin receptor antagonist (ERA) zibotentan in combination with the sodium-dependent glucose cotransporter 2 (SGLT-2) inhibitor dapagliflozin for use in the treatment of certain endothelin related diseases.

Claims (24)

1. A method of reducing UACR and reducing the incidence of cardiovascular or renal death in a human patient with chronic kidney disease, the method comprising administering to the patient in need thereof, a combination of zibotentan, N-(3-methoxy-5-methylpyrazin-2-yl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]pyridine-3-sulfonamide,

or a pharmaceutically acceptable salt thereof, and dapagliflozin.

2. The method according to claim 1 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered once daily in combination with dapagliflozin.

3. The method according to claim 2 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered at a dose of about 5 mg and dapagliflozin is administered at a dose of 10 mg.

4. The method according to claim 2 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered at a dose of about 1.5 mg and dapagliflozin is administered at a dose of 10 mg.

5. The method according to claim 2 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered at a dose of about 0.25 mg and dapagliflozin is administered at a dose of 10 mg.

6. The method according to claim 2 , wherein the patient is a chronic kidney disease patient classified as a stage 1-4 patient having an eGFR 20-60 ml/min/1.73 m 2 .

7. The method according to claim 6 , wherein the human patient is a chronic kidney disease patient classified as a stage 3-4 patient.

8. A method of reducing UACR to <300 mg/g in a human patient with chronic kidney disease, the method comprising administering to the patient in need thereof, a combination of zibotentan, N-(3-methoxy-5-methylpyrazin-2-yl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]pyridine-3-sulfonamide,

or a pharmaceutically acceptable salt thereof, and dapagliflozin.

9. The method according to claim 8 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered once daily in combination with dapagliflozin.

10. The method according to claim 9 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered at a dose of about 5 mg and dapagliflozin is administered at a dose of 10 mg.

11. The method according to claim 9 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered at a dose of about 1.5 mg and dapagliflozin is administered at a dose of 10 mg.

12. The method according to claim 9 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered at a dose of about 0.25 mg and dapagliflozin is administered at a dose of 10 mg.

13. The method according to claim 9 , wherein the patient is a chronic kidney disease patient classified as a stage 1-4 patient having an eGFR 20-60 ml/min/1.73 m 2 .

14. The method according to claim 13 , wherein the human patient is a chronic kidney disease patient classified as a stage 3-4 patient.

15. A method of reducing the risk of UACR progressing to ≥3000 mg/g in a human patient with chronic kidney disease, the method comprising administering to the patient in need thereof, a combination of zibotentan, N-(3-methoxy-5-methylpyrazin-2-yl)-2-[4-(1,3,4-oxadiazol-2-yl)phenyl]pyridine-3-sulfonamide,

or a pharmaceutically acceptable salt thereof, and dapagliflozin.

16. The method according to claim 15 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered once daily in combination with dapagliflozin.

17. The method according to claim 16 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered at a dose of about 5 mg and dapagliflozin is administered at a dose of 10 mg.

18. The method according to claim 16 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered at a dose of about 1.5 mg and dapagliflozin is administered at a dose of 10 mg.

19. The method according to claim 16 , where zibotentan, or a pharmaceutically acceptable salt thereof, is administered at a dose of about 0.25 mg and dapagliflozin is administered at a dose of 10 mg.

20. The method according to claim 16 , wherein the patient is a chronic kidney disease patient classified as a stage 1-4 patient having an eGFR 20-60 ml/min/1.73 m 2 .

21. The method according to claim 20 , wherein the human patient is a chronic kidney disease patient classified as a stage 3-4 patient.

Continuity (4)
Continuation 17371162 · Jul 9, 2021
Provisional Application 63196793 · Jun 4, 2021
Provisional Application 63050147 · Jul 10, 2020
Related Publication 20230364077A1 · Nov 16, 2023
Cited By (1)
US 12,409,174