IP Library › Granted Patent US 12,605,366
Granted Patent B2
US 12,605,366 · App. 17/596,356 · Granted Apr 21, 2026

Telmisartan for the treatment of hypertension in dogs

Inventors: Anne Michelle Traas (Saint Joseph, MO); Amanda Erickson Coleman (Bogart, GA); Bianca Natália Ferreira De Moura Lourenco (Athens, GA); Kate Elizabeth Creevy (College Station, TX); Scott Alan Brown (Winterville, GA)
A61K31/4184A61K45/06A61P9/12
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Quick Facts
Patent No.
US 12,605,366
App. No.
17/596,356
Granted
Apr 21, 2026
Kind
B2
Abstract

The present invention relates to telmisartan or a pharmaceutically acceptable salt thereof as a medicament for the treatment of hypertension in dogs, wherein the therapeutically effective amount of telmisartan is administered in a daily dosage amount that is varied over a treatment period.

Claims (15)

1 . A method for the treatment of hypertension in a dog in need of such treatment, wherein the dog has a systolic blood pressure (SBP) greater than 140 mmHg and the method comprises administration of a therapeutically effective amount of telmisartan or a pharmaceutically acceptable salt thereof to the dog, wherein the therapeutically effective amount of telmisartan is administered in a daily dosage amount that is varied over a treatment period, the daily dosage amount of telmisartan for a first period of time during the treatment period is at least 1.0 mg/kg of body weight, and the daily dosage amount of telmisartan is increased for a second period of time subsequent the first period of time during the treatment period and in which an identified urinary protein-to-creatinine concentration (UPC) ratio is at least 0.5.

2 . The method according to claim 1 , wherein the hypertension is associated with systemic chronic kidney disease (CKD), elevated urinary protein-to-creatinine ratio (UPC) levels and/or hyperthyroidism.

3 . The method according to claim 1 , which comprises administration of an effective amount of the sodium or potassium salt of telmisartan.

4 . Telmisartan according to claim 1 , wherein the hypertension is idiopathic hypertension.

5 . The method according to claim 1 , wherein the daily therapeutically effective amount of telmisartan ranges from 1.0 to 10.0 mg/kg of body weight.

6 . The method according to claim 1 , wherein the daily dosage amount of telmisartan is increased for the second period of time by an incremental amount ranging from 0.25 to 2.50 mg/kg of body weight.

7 . The method according to claim 6 , wherein the daily dosage amount of telmisartan for a first period of time during the treatment period is 1.0 to 1.5 mg/kg of body weight, and the daily dosage amount of telmisartan for the second period of time is 1.75 to 4.0 mg/kg of body weight.

8 . The method according to claim 1 , wherein the daily dosage amount of telmisartan is decreased after the second period of time by an incremental amount ranging from 0.25 to 2.50 mg/kg of body weight.

9 . The method according to claim 1 , wherein the daily dosage amount of telmisartan is decreased after the second period of time based upon measuring the systolic blood pressure (SBP) value measured for the dog.

10 . The method according to claim 9 , wherein daily dosage amount of telmisartan is decreased when the systolic blood pressure (SBP) value measured for the dog decreases after the second period of time by at least 10 mmHg or at least 20 mmHg or by 10 to 150 mmHg, 10 to 100 mmHg, 10 to 80 mmHg, 10 to 50 mmHg, 10 to 30 mmHg, 10 to 20 mmHg, 20 to 150 mmHg, 20 to 100 mmHg, 20 to 80 mmHg, 20 to 50 mmHg, or 20 to 30 mmHg in relation to a baseline SBP value measured for the dog prior to the first period of time.

11 . The method according to claim 1 , wherein the method further comprises administration of at least one other drug to such dog in need of such a treatment.

12 . The method according to claim 11 , wherein the other drug is selected from the group consisting of calcium channel blockers, cardiotonic-calcium sensitizing agents and ACE inhibitors.

13 . The method according to claim 12 , wherein the other drug is selected from the group consisting of amlodipine, pimobendan, levosimendan, ramipril, benazepril and enalapril.

14 . The method according to claim 1 , wherein the hypertension of the dog in need of such treatment is non-refractory to the treatment with ACE inhibitors.

15 . A method for the treatment of hypertension in a dog in need of such treatment, wherein the dog has a systolic blood pressure (SBP) greater than 140 mmHg and the method comprises administration of a therapeutically effective amount of telmisartan or a pharmaceutically acceptable salt thereof to the dog, wherein the therapeutically effective amount of telmisartan is administered in a daily dosage amount that is varied over a treatment period, a first daily dosage amount of telmisartan is administered for a first period of time during the treatment period, and a second daily dosage amount of telmisartan is administered for a second period of time subsequent the first period of time during the treatment period and based upon a change in an identified urinary protein-to-creatinine concentration (UPC) ratio determined for the dog.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 21, 2025
From: BOEHRINGER INGELHEIM ANIMAL HEALTH INC.
To: BOEHRINGER INGELHEIM VETMEDICA GMBH
Reel/Frame 070584/0787 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2022
From: TRAAS, ANNE MICHELLE
To: BOEHRINGER INGELHEIM ANIMAL HEALTH USA INC.
Reel/Frame 059675/0647 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 22, 2022
From: COLEMAN, AMANDA ERICKSON; FERREIRA DE MOURA LOURENCO, BIANCA NATÁLIA; CREEVY, KATE ELIZABETH; BROWN, SCOTT ALAN
To: UNIVERSITY OF GEORGIA RESEARCH FOUNDATION, INC.
Reel/Frame 059676/0651 →
Continuity (2)
Provisional Application 62871749 · Jul 9, 2019
Related Publication 20220226290A1 · Jul 21, 2022
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