IP Library Granted Patent US 9,175,065
Granted Patent B2
US 9,175,065 · App. 13/612,044 · Granted Nov 3, 2015

FGFR extracellular domain acidic region muteins

Inventors: Shannon Marshall (Baltimore, MD); Deborah H. Charych (Albany, CA); Ali Sadra (San Mateo, CA)
Assignee: Five Prime Therapeutics, Inc.
C07K14/71A61K38/177A61K38/179C07K14/705C07K2319/30C07K2319/31
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Quick Facts
Patent No.
US 9,175,065
App. No.
13/612,044
Granted
Nov 3, 2015
Kind
B2
Abstract

Fibroblast growth factor receptor (FGFR) extracellular domain (ECD) acidic region muteins that have been engineered to exhibit decreased tissue binding by increasing the number of acidic amino acid residues within the D1-D2 linker region are provided. Polynucleotides encoding FGFR ECD acidic region muteins are also provided. Methods of making FGFR ECD acidic region muteins, and methods of using such molecules to treat proliferative disorders, including cancers, disorders of angiogenesis, and macular degeneration, are also provided.

Claims (9)

1. A polypeptide comprising a fibroblast growth factor receptor 4 extracellular domain (FGFR4 ECD) D1-D2 linker chimera comprising a D1-D2 linker selected from an FGFR1 D1-D2 linker, an FGFR2 D1-D2 linker, and an FGFR3 D1-D2 linker, in place of the FGFR4 D1-D2 linker.

2. The polypeptide of claim 1 , wherein the D1-D2 linker comprises an amino acid sequence selected from SEQ ID NOs: 22, 26, 28, and 32, in place of an FGFR4 D1-D2 linker selected from SEQ ID NOs: 16 and 17.

3. An FGFR4 ECD fusion molecule comprising a polypeptide of claim 1 and a fusion partner.

4. The FGFR4 ECD fusion molecule of claim 3 , wherein the fusion partner is selected from Fe, albumin, and polyethylene glycol.

5. A method of treating cancer in a patient comprising administering to the patient an effective amount of (i) a polypeptide comprising an FGFR4 ECD D1-D2 linker chimera, or (ii) an FGFR4 ECD fusion molecule comprising an FGFR4 ECD D1-D2 linker chimera and a fusion partner.

6. The method of claim 5 , wherein the D1-D2 linker comprises an amino acid sequence selected from SEQ ID NOs: 22, 26, 28, and 32, in place of an FGFR4 D1-D2 linker selected from SEQ ID NOs: 16 and 17.

7. The method of claim 5 , wherein the fusion partner is selected from Fe, albumin, and polyethylene glycol.

8. The method of claim 7 , wherein the fusion partner is Fe.

9. The method of claim 5 , wherein the cancer is selected from colon cancer, liver cancer, lung cancer, breast cancer, ovarian cancer, and prostate cancer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 26, 2013
From: MARSHALL, SHANNON; CHARYCH, DEBORAH H.; SADRA, ALI
To: FIVE PRIME THERAPEUTICS
Reel/Frame 029873/0383 →
Continuity (3)
Continuation 12535479 · Aug 4, 2009
Provisional Application 61086121 · Aug 4, 2008
Related Publication 20130004492A1 · Jan 3, 2013