IP Library Granted Patent US 11,260,107
Granted Patent B2
US 11,260,107 · App. 16/657,287 · Granted Mar 1, 2022

Methods and compositions for treating ulcers

Inventor: Kenneth M. Attie (Boston, MA)
Assignee: ACCELERON PHARMA INC.
A61K38/179A61K38/1793A61K47/6811A61P7/06A61P17/02C07K14/475A61K31/16A61K31/17A61K31/4196A61K31/4422A61K38/00A61K38/1816A61K38/45A61K45/06C07K14/71C07K14/715C07K16/22C07K19/00C07K2317/31C07K2317/52C07K2317/76C07K2319/30C07K2319/31C07K2319/32C07K2319/90C12Y207/1103
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Quick Facts
Patent No.
US 11,260,107
App. No.
16/657,287
Granted
Mar 1, 2022
Kind
B2
Abstract

The present disclosure provides compositions and methods for treating or preventing ulcers in subjects having low red blood cell levels and/or hemoglobin levels (e.g, anemia). In some embodiments, the compositions of the disclosure may be used to treat or prevent ulcers associated with anemia.

Claims (21)

1. A method for treating a cutaneous ulcer in a subject that has sickle-cell disease, comprising administering to the subject an ActRIIB polypeptide, wherein the polypeptide comprises an amino acid sequence that is at least 85% identical to the sequence of amino acids 29-109 of SEQ ID NO: 1.

2. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 90% identical to the sequence of amino acids 29-109 of SEQ ID NO: 1, wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.

3. The method of claim 1 , wherein the polypeptide is a fusion protein further comprising an immunoglobulin Fc domain.

4. The method of claim 3 , wherein the fusion protein further comprises a linker domain positioned between the polypeptide and the immunoglobulin Fc domain.

5. The method of claim 1 , wherein the polypeptide comprises one or more amino acid modifications selected from: a glycosylated amino acid, a PEGylated amino acid, a farnesylated amino acid, an acetylated amino acid, a biotinylated amino acid, and an amino acid conjugated to a lipid moiety.

6. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 95% identical to amino acids 29-109 of SEQ ID NO: 1, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.

7. The method of claim 1 , wherein the polypeptide comprises amino acids 29-109 of SEQ ID NO: 1, but wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.

8. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 85% identical to the sequence of amino acids 25-131 of SEQ ID NO: 1, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.

9. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 90% identical to the sequence of amino acids 25-131 of SEQ ID NO: 1, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.

10. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 95% identical to the sequence of amino acids 25-131 of SEQ ID NO: 1, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.

11. The method of claim 1 , wherein the polypeptide comprises amino acids 25-131 of SEQ ID NO: 1, but wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.

12. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 85% identical to SEQ ID NO: 44, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.

13. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 90% identical to SEQ ID NO: 44, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.

14. The method of claim 1 , wherein the polypeptide comprises an amino acid sequence that is at least 95% identical to SEQ ID NO: 44, and wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.

15. The method of claim 1 , wherein the polypeptide comprises the amino acid sequence of SEQ ID NO: 44, but wherein the polypeptide comprises an acidic amino acid at the position corresponding to position 79 of SEQ ID NO: 1.

16. The method of claim 1 , wherein the polypeptide inhibits signaling by GDF8 in a cell-based assay.

17. The method of claim 1 , wherein the polypeptide inhibits signaling by GDF11 in a cell-based assay.

18. The method of claim 1 , wherein the amino acid at the position corresponding to position 79 of SEQ ID NO: 1 is an aspartic acid.

19. The method of claim 1 , wherein the amino acid at the position corresponding to position 79 of SEQ ID NO: 1 is a glutamic acid.

20. The method of claim 1 , wherein the polypeptide binds GDF8.

21. The method of claim 1 , wherein the polypeptide binds GDF11.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 7, 2020
From: ATTIE, KENNETH M.
To: ACCELERON PHARMA INC.
Reel/Frame 051435/0418 →
Continuity (5)
Division 15818974 · Nov 21, 2017
Division 14738761 · Jun 12, 2015
Provisional Application 62045808 · Sep 4, 2014
Provisional Application 62012109 · Jun 13, 2014
Related Publication 20200109193A1 · Apr 9, 2020