IP Library Granted Patent US 9,884,039
Granted Patent B2
US 9,884,039 · App. 14/781,706 · Granted Feb 6, 2018

Pharmaceutical formulations for subcutaneous administration of furosemide

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 9,884,039
App. No.
14/781,706
Granted
Feb 6, 2018
Kind
B2
Abstract

The present teachings relate to liquid pharmaceutical formulations of furosemide, where the pharmaceutical formulations include a molar excess of tris(hydroxymethyl)aminomethane to furosemide, have a pH in the range of 7 to 8.5, and a concentration of tris(hydroxymethyl)aminomethane greater than or equal to about 50 mM. The present teachings can improve the stability of liquid pharmaceutical formulations including furosemide and the suitability of such pharmaceutical formulations for subcutaneous administration or delivery.

Claims (38)

1. A method of treating a patient with or exhibiting the symptoms of edema, hypertension or heart failure, the method comprising:

administering to a patient a liquid pharmaceutical formulation, wherein the liquid pharmaceutical formulation comprises:

furosemide, or a pharmaceutically acceptable salt, hydrate or ester thereof, wherein furosemide is the sole therapeutically active agent in the liquid pharmaceutical formulation and the amount of furosemide in the liquid pharmaceutical formulation is between about 2 mg/mL to about 15 mg/mL; and

a pharmaceutically acceptable buffer comprising

tris(hydroxymethyl)aminomethane, wherein the concentration of tris(hydroxymethyl)aminomethane in the liquid pharmaceutical formulation is in a range of about 50 mM to about 250 mM;

wherein the liquid pharmaceutical formulation is isosmotic and has a pH between about 7.2 to about 8, and the molar ratio of tris(hydroxymethyl)aminomethane to furosemide is greater than or equal to two.

2. The method of claim 1 , wherein administering comprises administering subcutaneously the pharmaceutical formulation.

3. The method of claim 2 , wherein administering subcutaneously comprises using a pump device.

4. The method of claim 3 , wherein the pump device is a patch device.

5. The method of claim 1 , wherein administering comprises administering intravenously the liquid pharmaceutical formulation.

6. A method of treating a patient with or exhibiting the symptoms of edema, hypertension or heart failure, the method comprising:

administering subcutaneously to a patient a liquid pharmaceutical formulation comprising:

furosemide, or a pharmaceutically acceptable salt, hydrate or ester thereof, wherein the liquid pharmaceutical formulation comprises about 8 mg/mL of furosemide, which is the sole therapeutically active agent; and

a pharmaceutically acceptable buffer comprising

tris(hydroxymethyl)aminomethane, wherein the concentration of tris(hydroxymethyl)aminomethane in the liquid pharmaceutical formulation is about 50 mM;

wherein the molar ratio of tris(hydroxymethyl)aminomethane to furosemide is about 2, and the liquid pharmaceutical formulation has a pH of about 7.4 and is isosmotic.

7. The method of claim 1 , wherein the amount of furosemide in the liquid pharmaceutical formulation is between about 2 mg/mL to about 10 mg/mL.

8. The method of claim 1 , wherein the amount of furosemide in the liquid pharmaceutical formulation is between about 6 mg/mL to about 10 mg/mL.

9. The method of claim 6 , wherein administering subcutaneously comprises using a pump device.

10. The method of claim 9 , wherein the pump device is a patch device.

11. A method of treating a patient with or exhibiting the symptoms of edema, hypertension or heart failure, the method comprising:

administering subcutaneously to a patient a liquid pharmaceutical formulation, wherein the liquid pharmaceutical formulation comprises:

furosemide, or a pharmaceutically acceptable salt, hydrate or ester thereof, wherein furosemide is the sole therapeutically active agent in the liquid pharmaceutical formulation and the amount of furosemide in the liquid pharmaceutical formulation is between about 2 mg/mL to about 20 mg/mL; and

a pharmaceutically acceptable buffer comprising

tris(hydroxymethyl)aminomethane, wherein the concentration of tris(hydroxymethyl)aminomethane in the liquid pharmaceutical formulation is greater than or equal to about 50 mM;

wherein the liquid pharmaceutical formulation is isosmotic and has a pH between about 7 to about 8.5, and the molar ratio of tris(hydroxymethyl)aminomethane to furosemide is greater than or equal to 1.5.

12. The method of claim 11 , wherein the molar ratio of tris(hydroxymethyl)aminomethane to furosemide is greater than or equal to two.

13. The method of claim 11 , wherein the concentration of tris(hydroxymethyl)aminomethane in the liquid pharmaceutical formulation is in a range of about 50 mM to about 250 mM.

14. The method of claim 12 , wherein the concentration of tris(hydroxymethyl)aminomethane in the liquid pharmaceutical formulation is in a range of about 50 mM to about 250 mM.

15. The method of claim 11 , wherein the liquid pharmaceutical formulation has a pH between about 7.2 to about 8.

16. The method of claim 12 , wherein the liquid pharmaceutical formulation has a pH between about 7.2 to about 8.

17. The method of claim 13 , wherein the liquid pharmaceutical formulation has a pH between about 7.2 to about 8.

18. The method of claim 13 , wherein the liquid pharmaceutical formulation has a pH between about 7.2 to about 8.

19. The method of claim 11 , wherein the amount of furosemide in the liquid pharmaceutical formulation is between about 2 mg/mL to about 15 mg/mL.

20. The method of claim 12 , wherein the amount of furosemide in the liquid pharmaceutical formulation is between about 2 mg/mL to about 15 mg/mL.

21. The method of claim 13 , wherein the amount of furosemide in the liquid pharmaceutical formulation is between about 2 mg/mL to about 15 mg/mL.

22. The method of claim 15 , wherein the amount of furosemide in the liquid pharmaceutical formulation is between about 2 mg/mL to about 15 mg/mL.

23. The method of claim 18 , wherein administering subcutaneously comprises using a pump device.

Assignments (11)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 5, 2026
From: SCPHARMACEUTICALS INC.
To: MANNKIND CORPORATION
Reel/Frame 075534/0523 →
PATENT SECURITY AGREEMENT Recorded Nov 11, 2025
From: SCPHARMACEUTICALS INC.
To: WILMINGTON TRUST, NATIONAL ASSOCIATION, AS COLLATERAL AGENT
Reel/Frame 073569/0001 →
RELEASE OF SECURITY INTEREST Recorded Oct 8, 2025
From: PERCEPTIVE CREDIT HOLDINGS IV, LP
To: SCPHARMACEUTICALS INC.
Reel/Frame 072511/0726 →
SECURITY INTEREST Recorded Aug 13, 2024
From: SCPHARMACEUTICALS INC.
To: PERCEPTIVE CREDIT HOLDINGS IV, LP
Reel/Frame 068261/0702 →
RELEASE OF SECURITY INTEREST Recorded Aug 9, 2024
From: OAKTREE FUND ADMINISTRATION, LLC, AS ADMINISTRATIVE AGENT
To: SCPHARMACEUTICALS INC.
Reel/Frame 068244/0093 →
SECURITY INTEREST Recorded Oct 13, 2022
From: SCPHARMACEUTICALS INC.
To: OAKTREE FUND ADMINISTRATION, LLC
Reel/Frame 061419/0196 →
RELEASE OF SECURITY INTEREST Recorded Oct 13, 2022
From: SLR INVESTMENT CORP. (F/K/A SOLAR CAPITAL LTD.)
To: SCPHARMACEUTICALS INC.
Reel/Frame 061419/0151 →
INTELLECTUAL PROPERTY SECURITY AGREEMENT Recorded Sep 17, 2019
From: SCPHARMACEUTICALS INC.
To: SOLAR CAPITAL LTD., AS AGENT
Reel/Frame 050399/0462 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 5, 2016
From: MUNTENDAM, PIETER
To: SCPHARMACEUTICALS INC.
Reel/Frame 040522/0437 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 5, 2016
From: LARSEN, GLENN R.; MICHAELS, SCOTT A.
To: SCPHARMACEUTICALS, LLC
Reel/Frame 040522/0479 →
CHANGE OF NAME Recorded Dec 5, 2016
From: SCPHARMACEUTICALS LLC
To: SCPHARMACEUTICALS INC.
Reel/Frame 040831/0092 →