IP Library Granted Patent US 9,168,312
Granted Patent B2
US 9,168,312 · App. 14/152,692 · Granted Oct 27, 2015

Growth hormone polypeptides and methods of making and using same

Inventors: Volker Schellenberger (Palo Alto, CA); Joshua Silverman (Sunnyvale, CA); Willem P. Stemmer (Los Gatos, CA); Chia-wei Wang (Milpitas, CA); Nathan Geething (Santa Clara, CA); Jeffrey L. Cleland (San Carlos, CA); Benjamin Spink (San Carlos, CA)
Assignee: Amunix Operating Inc.
A61K47/48246A61K38/27C07K14/001C07K14/61A61K38/00C07K2319/00C07K2319/31C07K2319/75
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Quick Facts
Patent No.
US 9,168,312
App. No.
14/152,692
Granted
Oct 27, 2015
Kind
B2
Abstract

The present invention relates to compositions comprising growth hormone linked to extended recombinant polypeptide (XTEN), isolated nucleic acids encoding the compositions and vectors and host cells containing the same, and methods of making and using such compositions in treatment of growth hormone-related diseases, disorders, and conditions.

Claims (22)

1. An isolated fusion protein, comprising the growth hormone (GH) sequence of SEQ ID NO:1 linked to an extended recombinant polypeptide (XTEN), wherein the fusion protein has at least 90% sequence identity to the sequence of SEQ ID NO: 757.

2. The isolated fusion protein of claim 1 , wherein the fusion protein has at least 99% sequence identity to the sequence of SEQ ID NO: 757.

3. The isolated fusion protein of claim 1 , comprising the sequence of SEQ ID NO: 757.

4. The isolated fusion protein of claim 1 , wherein the binding affinity of the fusion protein to the growth hormone receptor is reduced as compared to the binding affinity of the corresponding GH that lacks the XTEN.

5. The isolated fusion protein of claim 4 , wherein the binding affinity of the fusion protein to the growth hormone receptor is reduced by at least about 3-fold compared to GH not linked to XTEN.

6. The isolated fusion protein of claim 4 , wherein the binding affinity of the fusion protein to the growth hormone receptor is reduced by at least 10-fold as compared to the binding affinity of the corresponding GH that lacks the XTEN.

7. The isolated fusion protein of claim 4 , wherein the fusion protein with reduced binding affinity exhibits reduced receptor-mediated clearance.

8. The isolated fusion protein of claim 7 , wherein the fusion protein with reduced binding affinity has a corresponding increase in half-life of at least about 3-fold compared to the corresponding GH that is not linked to the XTEN.

9. A pharmaceutical composition comprising the isolated fusion protein of claim 1 , and a pharmaceutically acceptable carrier.

10. A method of producing a fusion protein comprising a growth hormone (GH) fused to one or more extended recombinant polypeptides (XTEN), comprising:

(a) providing a host cell comprising a recombinant poly-nucleotide molecule encoding the fusion protein of claim 1 ;

(b) culturing the host cell under conditions permitting the expression of the fusion protein; and recovering the fusion protein.

11. The method of claim 10 , wherein the polynucleotide is codon optimized for enhanced expression of said fusion protein in the host cell.

12. The method of claim 10 , wherein the host cell is a prokaryotic cell.

13. The method of claim 10 , wherein the isolated fusion protein is recovered from the host cell cytoplasm.

14. A method of treating a growth-hormone related condition in a subject, comprising administering to the subject a therapeutically effective amount of a fusion protein of claim 1 wherein the growth-hormone related condition is selected from growth-hormone deficiency, Turner's Syndrome, Prader-Willi Syndrome, idiopathic short stature, AIDS wasting, multiple sclerosis, Crohn's disease, ulcerative colitis, and muscular dystrophy.

15. The method of claim 14 , wherein the therapeutically effective amount is administered at least 48 h between consecutive doses.

16. The method of claim 14 , wherein growth-hormone related condition is growth-hormone deficiency.

17. The method of claim 14 , wherein growth-hormone related condition is Turner's Syndrome.

18. The method of claim 14 , wherein growth-hormone related condition is Prader-Willi Syndrome.

19. The method of claim 14 , wherein growth-hormone related condition is idiopathic short stature.

20. The method of claim 14 , wherein the growth-hormone related condition is selected from the group consisting of AIDS wasting, multiple sclerosis, Crohn's disease, ulcerative colitis, and muscular dystrophy.

Assignments (6)
CONFIRMATORY LICENSE Recorded Feb 4, 2021
From: AMUNIX PHARMACEUTICALS INC
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 055222/0587 →
CHANGE OF NAME Recorded Feb 4, 2021
From: AMUNIX OPERATING INC.
To: AMUNIX PHARMACEUTICALS, INC.
Reel/Frame 055223/0978 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 27, 2015
From: SPINK, BENJAMIN
To: AMUNIX OPERATING INC.
Reel/Frame 036183/0200 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 24, 2015
From: SCHELLENBERGER, VOLKER; SILVERMAN, JOSHUA; STEMMER, WILLEM P.; WANG, CHIA-WEI; GEETHING, NATHAN
To: AMUNIX, INC.
Reel/Frame 036174/0323 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 24, 2015
From: AMUNIX, INC.
To: AMUNIX OPERATING INC.
Reel/Frame 036174/0451 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 24, 2015
From: CLELAND, JEFFREY L.
To: AMUNIX OPERATING INC.
Reel/Frame 036174/0670 →
Continuity (7)
Continuation 12796640 · Jun 8, 2010
Continuation 12699761 · Feb 3, 2010
Continuation PCTUS2010023106 · Feb 3, 2010
Provisional Application 61185112 · Jun 8, 2009
Provisional Application 61236836 · Aug 25, 2009
Provisional Application 61280955 · Nov 10, 2009
Related Publication 20140371136A1 · Dec 18, 2014