IP Library › Granted Patent US 9,173,881
Granted Patent B2
US 9,173,881 · App. 14/335,657 · Granted Nov 3, 2015

Therapeutic compositions containing macitentan

Inventor: Martine Clozel (Binningen, CH)
Assignee: ACTELION PHARMACEUTICALS LTD.
A61K31/4965A61K31/343A61K31/506A61K31/5575A61K31/5578A61K45/06
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Quick Facts
Patent No.
US 9,173,881
App. No.
14/335,657
Granted
Nov 3, 2015
Kind
B2
Abstract

The invention relates to a product containing the compound of formula (I) below or a pharmaceutically acceptable salt of this compound, in combination of at least one compound having prostacyclin receptor (IP) agonist properties, or a pharmaceutically acceptable salt thereof.

Claims (21)

1. A method for the treatment of a disease selected from hypertension, pulmonary hypertension, diabetic arteriopathy, heart failure, erectile dysfunction, angina pectoris and pulmonary fibrosis, comprising administering an effective amount of the compound of formula (I)

in free or pharmaceutically acceptable salt form, in combination with an effective amount of at least one compound having prostacyclin receptor (IP) agonist properties selected from 2-{4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}-N-(methylsulfonyl)acetamide and {4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}acetic acid, in free or pharmaceutically acceptable salt form.

2. The method according to claim 1 , wherein the compound having prostacyclin receptor (IP) agonist properties is {4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}acetic acid, in free or pharmaceutically acceptable salt form.

3. The method according to claim 1 , wherein the compound having prostacyclin receptor (IP) agonist properties is 2-{4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}-N-(methylsulfonyl)acetamide, in free or pharmaceutically acceptable salt form.

4. The method according to claim 1 , wherein the compound of formula (I) and the compound having prostacyclin receptor (IP) agonist properties are administered simultaneously, separately or over a period of time.

5. The method according to claim 1 , wherein the disease is pulmonary hypertension.

6. The method according to claim 1 , wherein the disease is pulmonary arterial hypertension.

7. The method according to claim 6 , wherein the compound of formula (I) is in free form.

8. The method according to claim 7 , wherein the compound of formula (I) and the compound having prostacyclin receptor (IP) agonist properties are administered simultaneously.

9. The method according to claim 7 , wherein the compound of formula (I) and the compound having prostacyclin receptor (IP) agonist properties are administered separately.

10. The method according to claim 7 , wherein the compound of formula (I) and the compound having prostacyclin receptor (IP) agonist properties are administered over a period of time.

11. The method according to claim 6 , wherein the compound of formula (I) and the prostacyclin receptor (IP) agonist are administered orally.

12. The method according to claim 1 , wherein the compound of formula (I) and the prostacyclin receptor (IP) agonist are administered orally.

13. A method for the treatment of pulmonary arterial hypertension comprising administering an effective amount of the compound of formula (I)

in free or pharmaceutically acceptable salt form, in combination with an effective amount of 2-{4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}-N-(methylsulfonyl)acetamide, in free or pharmaceutically acceptable salt form.

14. The method according to claim 13 , wherein the compound of formula (I) and 2-{4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}-N-(methylsulfonyl)acetamide are administered simultaneously.

15. The method according to claim 13 , wherein the compound of formula (I) and 2-{4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}-N-(methylsulfonyl)acetamide are administered separately.

16. The method according to claim 13 , wherein the compound of formula (I) and 2-{4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}-N-(methylsulfonyl)acetamide are administered over a period of time.

17. The method according to claim 13 , wherein the compound of formula (I) is administered once a day.

18. The method according to claim 13 , wherein 2-{4-[(5,6-diphenylpyrazin-2-yl)(isopropyl)amino]butoxy}-N-(methylsulfonyl)acetamide is administered twice a day.

19. The method according to claim 13 wherein the compound of formula (I) and the prostacyclin receptor (IP) agonist are administered orally.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 20, 2014
From: CLOZEL, MARTINE
To: ACTELION PHARMACEUTICALS LTD.
Reel/Frame 033980/0325 →
Priority Claims (1)
WO PCT/IB2008/053252 · Aug 13, 2008 · international
Continuity (2)
Continuation 13058639
Related Publication 20140329824A1 · Nov 6, 2014