Compositions and methods for treating pulmonary hypertension

Patent metadata

Field	Value
Publication number	US-11219666-B2
Application number	US-202017002292-A
Country	US
Kind code	B2
Filing date	Aug 25, 2020
Priority date	Jul 15, 2016
Publication date	Jan 11, 2022
Grant date	Jan 11, 2022

Abstract

In some aspects, the disclosure relates to GDF/BMP antagonists and methods of using GDF/BMP antagonists to treat, prevent, or reduce the progression rate and/or severity of pulmonary hypertension (PH), particularly treating, preventing or reducing the progression rate and/or severity of one or more PH-associated complications. The disclosure also provides methods of using a GDF/BMP antagonist to treat, prevent, or reduce the progression rate and/or severity of a variety of conditions including, but not limited to, pulmonary vascular remodeling, pulmonary fibrosis, and right ventricular hypertrophy. The disclosure further provides methods of using a GDF/BMP antagonist to reduce right ventricular systolic pressure in a subject in need thereof.

First claim

We claim:

1. A method of treating pulmonary arterial hypertension, comprising subcutaneously administering to a patient in need thereof an effective amount of a polypeptide comprising an amino acid sequence that is at least 90% identical to the amino acid sequence of SEQ ID NO: 32, wherein the polypeptide binds to activin and/or GDF11, and wherein the patient has Functional Class II or Class III pulmonary hypertension in accordance with the World Health Organization's functional classification system for pulmonary hypertension.

2. The method of claim 1 , wherein the polypeptide is a polypeptide comprising an amino acid sequence that is at least 95% identical to the amino acid sequence of SEQ ID NO: 32.

3. The method of claim 1 , wherein the polypeptide is a polypeptide comprising an amino acid sequence that is at least 99% identical to the amino acid sequence of SEQ ID NO: 32.

4. The method of claim 1 , wherein the polypeptide is a polypeptide comprising the amino acid sequence of SEQ ID NO: 32.

5. The method of claim 1 , wherein the polypeptide is a polypeptide consisting of the amino acid sequence of SEQ ID NO: 32.

6. The method of claim 1 , wherein the polypeptide is part of a homodimer protein complex.

7. The method of claim 1 , wherein the polypeptide is glycosylated.

8. The method of claim 1 , wherein the patient has resting pulmonary arterial pressure of at least 25 mmHg.

9. The method of claim 1 , wherein the method decreases pulmonary arterial pressure in the patient.

10. The method of claim 9 , wherein the method decreases the pulmonary arterial pressure by at least 5 mmHg.

11. The method of claim 9 , wherein the method decreases the pulmonary arterial pressure by at least 7 mmHg.

12. The method of claim 1 , wherein the method increases the patient's 6-minute walk distance.

13. The method of claim 12 , wherein the method increases the patient's 6-minute walk distance by at least 40 meters.

14. The method of claim 1 , wherein the method decreases ventricle hypertrophy in the patient.

15. The method of claim 1 , wherein the method decreases smooth muscle hypertrophy in the patient.

16. The method of claim 1 , wherein the method decreases pulmonary arteriole muscularity in the patient.

17. The method of claim 1 , wherein the method decreases pulmonary vascular resistance in the patient.

18. The method of claim 17 , wherein the method decreases pulmonary vascular resistance in the patient by at least 10%.

19. The method of claim 1 , wherein the patient has been treated with one or more vasodilators.

20. The method of claim 1 , wherein the patient has been treated with one or more agents selected from the group consisting of: phosphodiesterase type 5 inhibitors, soluble guanylate cyclase stimulators, prostacyclin receptor agonist, and endothelin receptor antagonists.

21. The method of claim 20 , wherein the one or more agents is selected from the group consisting of: bosentan, sildenafil, beraprost, macitentan, selexipag, epoprostenol, treprostinil, iloprost, ambrisentan, and tadalafil.

22. The method of claim 1 , wherein the method delays clinical worsening of pulmonary arterial hypertension.

23. The method of claim 22 , wherein the method delays clinical worsening of pulmonary arterial hypertension in accordance with the World Health Organization's functional classification system for pulmonary hypertension.

24. The method of claim 23 , wherein the method delays clinical worsening of pulmonary hypertension by delaying the progression from Functional Class II to Class III as recognized by the World Health Organization.

25. The method of claim 23 , wherein the method delays clinical worsening of pulmonary hypertension by delaying the progression from Functional Class III to Class IV as recognized by the World Health Organization.

26. The method of claim 1 , wherein the polypeptide is formulated into a pharmaceutical composition.

27. The method of claim 26 , wherein the pharmaceutical composition comprises a sterile injectable solution.

28. The method of claim 27 , wherein the sterile injectable solution comprises a sterile powder which is reconstituted with an acceptable solution.

29. The method of claim 28 , wherein the acceptable solution is water.

Assignees

• Acceleron Pharma Inc

Inventors

• Kumar Ravindra
• Knopf John

Classifications

• A61K38/17 Primary

  from animals; from humans {(enzyme inhibitors A61K38/005)} · CPC title

• C07K14/71

  for growth factors; for growth regulators · CPC title

• A61K38/1875 Primary

  Bone morphogenic factor; Osteogenins; Osteogenic factor; Bone-inducing factor · CPC title

• A61K38/45

  Transferases (2) · CPC title

• A61K38/1796 Primary

  for hormones (for neuromediators A61K38/1787) · CPC title