IP Library Granted Patent US 8,501,678
Granted Patent B2
US 8,501,678 · App. 13/329,897 · Granted Aug 6, 2013

Variant activin receptor polypeptides and uses thereof

Inventors: Jeonghoon Sun (Thousand Oaks, CA); Lei-Ting Tony Tam (Thousand Oaks, CA); Hui-Quan Han (Thousand Oaks, CA); Keith Soo-Nyung Kwak (Thousand Oaks, CA); Xiaolan Zhou (Thousand Oaks, CA); John Lu (Culver City, CA)
Assignee: Atara Biotherapeutics, Inc.
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Quick Facts
Patent No.
US 8,501,678
App. No.
13/329,897
Granted
Aug 6, 2013
Kind
B2
Abstract

The present invention provides variant activin IIB soluble receptor polypeptides and proteins capable of binding and inhibiting the activities of activin A, myostatin, or GDF-11. The present invention also provides polynucleotides, vectors and host cells capable of producing the variant polypeptides and proteins. Compositions and methods for treating muscle-wasting and other diseases and disorders are also provided.

Claims (20)

1. A pharmaceutical composition comprising i) an isolated protein comprising a variant activin IIB receptor polypeptide (vActRIIB) wherein vActRIIB comprises a polypeptide sequence having at least 95% identity to the amino acid sequence set forth at amino acids 25 through 134 of SEQ ID NO: 18, wherein the polypeptide comprises an amino acid substitution at position 28, and wherein the polypeptide is capable of binding myostatin, activin A, or GDF-11, and ii) a chemotherapeutic agent.

2. The pharmaceutical composition of claim 1 , wherein the substitution at position 28 of the vActRIIB polypeptide is selected from the group consisting of A, F, Q, V, I, L, M, K, H, W and Y for E.

3. The pharmaceutical composition of claim 1 , wherein the substitution at position 28 of the vActRIIB polypeptide is selected from the group of amino acids consisting of A, W and Y for E.

4. The pharmaceutical composition of claim 1 , wherein the substitution at position 28 of the vActRIIB polypeptide is W.

5. The pharmaceutical composition of claim 1 , wherein the isolated protein further comprises SEQ ID NO:79.

6. The pharmaceutical composition of claim 1 , wherein the chemotherapeutic agent is a nucleoside analogue.

7. The pharmaceutical composition of claim 1 , wherein the chemotherapeutic agent is 5-fluorouracil.

8. The pharmaceutical composition of claim 1 , wherein the chemotherapeutic agent is dacarbazine.

9. A method of treating a gonadal cancer in a subject in need of such treatment comprising administering a therapeutically effective amount of the composition of claim 1 to the subject, wherein the substitution at position 28 is selected from the group of amino acids consisting of A, W, and Y for E.

10. The method of claim 9 , wherein the cancer is ovarian cancer.

11. The method of claim 9 , wherein the cancer is testicular cancer.

12. A method of reducing the size of a gonadal tumor mass in a subject in need of such treatment comprising administering an effective amount of the composition of claim 1 to the subject, wherein the substitution at position 28 is selected from the group of amino acids consisting of A, W, and Y for E.

13. The method of claim 12 , wherein the tumor mass is resulting from testicular or ovarian cancer.

14. The pharmaceutical composition of claim 1 , wherein the isolated protein further comprises SEQ ID NO:80.

15. The pharmaceutical composition of claim 1 , wherein the polypeptide sequence has at least 99% identity to the amino acid sequence set forth at amino acids 25 through 134 of SEQ ID NO: 18, and wherein the polypeptide comprises an amino acid substitution at position 28.

16. The pharmaceutical composition of claim 15 , wherein the substitution at position 28 of the vActRIIB polypeptide is W for E, and wherein the isolated protein further comprises an Fc domain linked to vActRIIB via a linker.

17. A method of reducing the size of a gonadal tumor mass in a subject in need of such treatment comprising administering to the subject: an effective amount of an isolated protein comprising a variant activin IIB receptor polypeptide (vActRIIB) wherein vActRIIB comprises a polypeptide sequence having at least 95% identity to the amino acid sequence set forth at amino acids 25 through 134 of SEQ ID NO: 18, wherein the polypeptide comprises an amino acid substitution at position 28, wherein the substitution at position 28 is selected from the group of amino acids consisting of A, W, and Y for E, and wherein the polypeptide is capable of binding myostatin, activin A, or GDF-11; and a chemotherapeutic agent.

18. The method of claim 17 , wherein the tumor mass is an ovarian tumor mass.

19. A method of treating a gonadal cancer in a subject in need of such treatment comprising administering to the subject: an effective amount of an isolated protein comprising a variant activin IIB receptor polypeptide (vActRIIB) wherein vActRIIB comprises a polypeptide sequence having at least 95% identity to the amino acid sequence set forth at amino acids 25 through 134 of SEQ ID NO: 18, wherein the polypeptide comprises an amino acid substitution at position 28, wherein the substitution at position 28 is selected from the group of amino acids consisting of A, W, and Y for E, and wherein the polypeptide is capable of binding myostatin, activin A, or GDF-11; and a chemotherapeutic agent.

20. The method of claim 19 , wherein the gonadal cancer is ovarian cancer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 8, 2012
From: SUN, JEONGHOON; TAM, LEI-TING TONY; HAN, HUI-QUAN; KWAK, KEITH SOO-NYUNG; ZHOU, XIAOLAN; LU, JOHN
To: AMGEN INC.
Reel/Frame 027827/0667 →
Continuity (5)
Continuation In Part 13080515 · Apr 5, 2011
Division 12074877 · Mar 5, 2008
Provisional Application 61065474 · Feb 11, 2008
Provisional Application 60905459 · Mar 6, 2007
Related Publication 20120328595A1 · Dec 27, 2012