IP Library Granted Patent US 10,604,578
Granted Patent B2
US 10,604,578 · App. 15/207,188 · Granted Mar 31, 2020

PDGF receptor beta binding polypeptides

Inventors: Yan Chen (Lexington, MA); Richard W. Wagner (Cambridge, MA); Csaba Pazmany (Cambridge, MA)
Assignee: X-BODY, INC.
C07K16/2863C07K14/49C07K14/71C07K16/22C12N15/1093C12P21/005A61K39/00C07K16/28C07K2317/565C07K2317/622C07K2317/76C07K2317/92C07K2317/94
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,604,578
App. No.
15/207,188
Granted
Mar 31, 2020
Kind
B2
Abstract

The present invention provides binding polypeptides (e.g., antibodies or fragments thereof) that specifically bind to a target antigen (e.g., a human antigen, e.g., human PDGFRβ) with high affinity. The invention also provides, libraries of binding polypeptides, pharmaceutical compositions, as well as nucleic acids encoding binding polypeptides, recombinant expression vectors and host cells for making such binding polypeptides. Methods of using binding polypeptide of the invention to diagnose and treat disease are also encompassed by the invention.

Claims (11)

1. A method for treating a platelet derived growth factor receptor beta (PDGFRβ)-associated disease or disorder, the method comprising administering to a subject in need thereof an effective amount of an isolated binding polypeptide that specifically binds to human PDGFRβ, said binding polypeptide comprising a heavy chain variable (VH) domain comprising a HCDR1, HCDR2, and HCDR3, and a light chain variable (VL) domain comprising a LCDR1, LCDR2, and LCDR3,

wherein the HCDR1, HCDR2, and HCDR3 comprise the amino acid sequences set forth in SEQ ID NOs: 33, 2, and 1, respectively, and the LCDR1, LCDR2, and LCDR3 comprise the amino acid sequences set forth in SEQ ID NOs: 268, 183, and 98, respectively, or

wherein the HCDR1, HCDR2, and HCDR3 comprise the amino acid sequences set forth in SEQ ID NOs: 35, 3, and 1, respectively, and the LCDR1, LCDR2, and LCDR3 comprise the amino acid sequences set forth in SEQ ID NOs: 289, 204, and 119, respectively,

wherein the binding polypeptide binds to human PDGFRβ with a K D less than or equal to 5 nM, and

wherein the PDGFRβ-associated disease or disorder is age-related macular degeneration (AMD).

2. The method of claim 1 , wherein the VH domain comprises the amino acid sequence set forth in SEQ ID NO: 318, and the VL domain comprises the amino acid sequence set forth in SEQ ID NO: 404.

3. The method of claim 1 , wherein the VH domain comprises the amino acid sequence set forth in SEQ ID NO: 321, and the VL domain comprises the amino acid sequence set forth in SEQ ID NO: 425.

4. The method of claim 1 , wherein the binding polypeptide inhibits PDGFRβ-induced vascularization of the eye.

5. The method of claim 1 , wherein the binding polypeptide binds specifically to mouse and human PDGFRβ.

6. The method of claim 1 , wherein the binding polypeptide is an antibody.

7. The method of claim 1 , wherein the binding polypeptide is an scFv.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 7, 2016
From: CHEN, YAN; WAGNER, RICHARD W.; PAZMANY, CSABA
To: X-BODY, INC.
Reel/Frame 039659/0883 →
Continuity (4)
Continuation 13705978 · Dec 5, 2012
Provisional Application 61610905 · Mar 14, 2012
Provisional Application 61566778 · Dec 5, 2011
Related Publication 20170029510A1 · Feb 2, 2017