IP Library › Granted Patent US 11,844,789
Granted Patent B2
US 11,844,789 · App. 17/453,566 · Granted Dec 19, 2023

Animal treatments

Inventors: David Rock (California, MO); Mark Ridall (Skillman, NJ)
Assignee: NewMarket Pharmaceuticals LLC
A61K31/4439A61K9/0053A61K31/135A61K31/137A61K31/155A61K31/341A61K31/403A61K31/4164A61K31/4174A61K31/44A61K31/5415A61K31/635A61K31/7048C07D307/52C07D401/12
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Quick Facts
Patent No.
US 11,844,789
App. No.
17/453,566
Granted
Dec 19, 2023
Kind
B2
Abstract

Compositions and methods for the treatment and control of various conditions in an animal which comprises administering to said animal an effective amount of an immediate release composition of about 0.5% to 50% wt/wt of active ingredient together with excipients to a total of about 100%, wherein said composition dissolves in a relatively short period of time, e.g., 75 seconds or less, 5 seconds or less, or 3 seconds or less, upon administration to said animal.

Claims (28)

1. A method of treating pulmonary edema, congestive heart failure, or exercise-induced pulmonary hemorrhage in an animal in need thereof, the method comprising:

determining a dose of furosemide required; and

administering orally to a pre-gastric mucosal cell of the animal a Direct Systemic Introduction (DSI) composition comprising the furosemide;

wherein the DSI composition in the animal's oral cavity is dissolved in less than about 75 seconds; and

wherein the required dose of the furosemide is determined by greater than 50% of the administered furosemide being detected in the animal's circulatory system via the pre-gastric mucosal cells lining the animal's alimentary canal prior to the animal's secretory stomach.

2. The method according to claim 1 , wherein the DSI composition is dissolved in less than about 30 seconds.

3. The method according to claim 1 , wherein the DSI composition is dissolved in less than about 5 seconds.

4. The method according to claim 1 , wherein the animal is human.

5. The method according to claim 1 , wherein the animal is an equine.

6. The method according to claim 1 , wherein the DSI composition provides an immediate release of furosemide.

7. The method according to claim 1 , wherein the DSI composition is in the form of a tablet comprising about 50 mg to about 450 mg of furosemide.

8. The method according to claim 1 , wherein the DSI composition is formulated to provide about 0.10 mg/kg to about 2.0 mg/kg of furosemide per body weight of the animal.

9. The method according to claim 1 , wherein the DSI composition is formulated to provide about 0.25 mg/kg to about 1.5 mg/kg of furosemide per body weight of the animal.

10. The method according to claim 1 , wherein the DSI composition is formulated to provide about 0.50 mg/kg to about 1.0 mg/kg of furosemide per body weight of the animal.

11. The method according to claim 1 , wherein the DSI composition further comprises at least one excipient.

12. A method of promoting diuresis or treating an allergic reaction in an animal in need thereof, the method comprising:

determining a dose of furosemide required; and

administering orally to a pre-gastric mucosal cell of the animal a Direct Systemic Introduction (DSI) composition comprising the furosemide,

wherein the DSI composition in the animal's oral cavity is dissolved in less than about 75 seconds, and

wherein the required dose of furosemide is determined by greater than 50% of the administered furosemide being detected in the animal's circulatory system via the pre-gastric mucosal cells lining the animal's alimentary canal prior to the animal's secretory stomach.

13. The method according to claim 12 , wherein the DSI composition is dissolved in less than about 30 seconds.

14. The method according to claim 12 , wherein the DSI composition is dissolved in less than about 5 seconds.

15. The method according to claim 12 , wherein the animal is human.

16. The method according to claim 12 , wherein the animal is an equine.

17. The method according to claim 12 , wherein the DSI composition provides an immediate release of the furosemide.

18. The method according to claim 12 , wherein the DSI composition is in the form of a tablet comprising about 50 mg to about 450 mg of furosemide.

19. The method according to claim 12 , wherein the DSI composition is formulated to provide about 0.10 mg/kg to about 2.0 mg/kg of furosemide per body weight of the animal.

20. The method according to claim 1 , wherein the DSI composition is formulated to provide about 0.25 mg/kg to about 1.5 mg/kg of furosemide per body weight of the animal; or wherein the DSI composition is formulated to provide about 0.50 mg/kg to about 1.0 mg/kg of furosemide per body weight of the animal.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 8, 2023
From: ROCK, DAVID; RIDALL, MARK
To: NEWMARKET PHARMACEUTICALS, LLC
Reel/Frame 064519/0117 →
Continuity (6)
Continuation 16886093 · May 28, 2020
Continuation 16014290 · Jun 21, 2018
Continuation 14275019 · May 12, 2014
Continuation 13343692 · Jan 4, 2012
Provisional Application 61437763 · Jan 31, 2011
Related Publication 20220054470A1 · Feb 24, 2022