IP Library Granted Patent US 10,323,095
Granted Patent B2
US 10,323,095 · App. 15/126,551 · Granted Jun 18, 2019

Antibody-fynomer conjugates

Inventors: Roland Newman (San Diego, CA); Steve Granger (Encinitas, CA); Michael Lyman (San Diego, CA); Dragan Grabulovski (Zurich, CH); Richard Woods (Zurich, CH); Michela Silacci (Zurich, CH); Wenjuan Zha (Zurich, CH); Isabella Attinger-Toller (Vancouver, CA)
Assignee: MITSUBISHI TANABE PHARMA CORPORATION
C07K16/2866C07K16/244C12N9/12C12N9/1205C12N9/96C12N15/62C12Y207/01112C12Y207/10A61K38/00A61K2039/505C07K2317/24C07K2317/31C07K2317/565C07K2317/76C07K2317/92C07K2317/94C07K2318/20C07K2319/00C07K2319/33C07K2319/70
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 10,323,095
App. No.
15/126,551
Granted
Jun 18, 2019
Kind
B2
Abstract

Provided is a bi-specific fusion polypeptide comprising a fynomer sequence that binds to interleukin-17a (IL-17a) and is conjugated to an antibody or subsequence thereof that binds to interleukin-6 receptor (IL-6R). The fusion polypeptide can bind to both IL-17a and IL-6R thereby suppresses, reduces, decreases, inhibits or blocks both IL-17a and IL-6R activities.

Claims (31)

1. A bi-specific fusion polypeptide comprising:

(a) a fynomer sequence comprising an amino acid sequence at least 90% identical to an amino acid sequence selected from: SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 5, SEQ ID NO: 6, SEQ ID NO: 1, SEQ ID NO: 4 and SEQ ID NO: 7, wherein the amino acid sequences at positions 12-17 and 31-36 of the selected fynomer sequence is maintained and the fynomer sequence binds to interleukin-17a (IL-17a); and

(b) an antibody or a subsequence thereof that binds to interleukin-6 receptor (IL-6R), wherein the fynomer sequence is conjugated to the antibody, or subsequence thereof, and the fusion polypeptide binds to both IL-17a and IL-6R and inhibits both IL-17a and IL-6R activities.

2. The fusion polypeptide of claim 1 , wherein the fynomer sequence is conjugated to a heavy or light chain sequence of the antibody or subsequence thereof.

3. The fusion polypeptide of claim 1 , wherein the fynomer sequence is conjugated to the amino terminus or the carboxyl terminus of a heavy chain sequence of the antibody or subsequence thereof.

4. The fusion polypeptide of claim 1 , wherein the fynomer sequence is conjugated to an amino terminus or a carboxyl terminus of a light chain sequence of the antibody or subsequence thereof.

5. The fusion polypeptide of claim 1 , wherein the fynomer sequence comprises an amino acid sequence at least 95% identical to an amino acid sequence selected from SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6 and SEQ ID NO: 7.

6. The fusion polypeptide of claim 1 , wherein the fynomer sequence comprises an amino acid sequence selected from SEQ ID NO: 1, SEQ ID NO: 2, SEQ ID NO: 3, SEQ ID NO: 4, SEQ ID NO: 5, SEQ ID NO: 6 and SEQ ID NO: 7.

7. The fusion polypeptide of claim 1 , wherein the fynomer sequence comprises the amino acid sequence of SEQ ID NO: 42.

8. The fusion polypeptide of claim 1 , wherein the fynomer sequence binds to glycosylated IL-17a and thereby inhibits IL-17 receptor function or signaling.

9. The fusion polypeptide of claim 1 , wherein the fynomer sequence has a binding affinity (K d ) for binding to glycosylated IL-17a of about 1 to about 200 nM.

10. The fusion polypeptide of claim 1 , wherein the fynomer sequence has a greater binding affinity (K d or KD) for glycosylated IL-17a than the binding affinity of the fynomer sequence as set forth in SEQ ID NO:1 for glycosylated IL-17a.

11. The fusion polypeptide of claim 1 , wherein the fusion polypeptide binds to IL-17a and binds to IL-6R simultaneously.

12. The fusion polypeptide of claim 1 , wherein the fusion polypeptide binds to human IL-17a or IL-6R.

13. The fusion polypeptide of claim 1 , wherein the fynomer sequence is conjugated to a heavy or light chain sequence of the antibody or subsequence thereof via a linker.

14. The fusion polypeptide of claim 1 , wherein the polypeptide is isolated or purified.

15. A pharmaceutical composition comprising the fusion polypeptide of claim 1 .

16. The fusion polypeptide of claim 1 , wherein the antibody or subsequence thereof comprises a heavy chain having the following CDR1-3: SEQ ID NO: 47, SEQ ID NO: 48, and SEQ ID NO: 49, and a light chain having the following CDR1-3: SEQ ID NO: 50, SEQ ID NO: 51, and SEQ ID NO: 52.

17. The fusion polypeptide of claim 16 , wherein the antibody or subsequence thereof comprises a sequence at least 90% identical to the following heavy chain (HC) and light chain (LC) sequences: (HC) SEQ ID NO: 12 and (LC) SEQ ID NO: 13.

18. The fusion polypeptide of claim 17 , wherein the antibody or subsequence thereof comprises the following heavy chain (HC) and light chain (LC) sequences:

(HC) SEQ ID NO: 12 and (LC) SEQ ID NO: 13.

19. The fusion polypeptide of claim 16 , wherein the antibody or subsequence thereof comprises a pair of heavy chain (HC) and light chain (LC) sequences selected from the following:

(HC) a heavy chain sequence at least 90% identical to SEQ ID NO: 14 and (LC) a light chain sequence at least 90% identical to SEQ ID NO: 15;

(HC) a heavy chain sequence at least 90% identical to SEQ ID NO: 16 and (LC) a light chain sequence at least 90% identical to SEQ ID NO: 17;

(HC) a heavy chain sequence at least 90% identical to SEQ ID NO: 18 and (LC) a light chain sequence at least 90% identical to SEQ ID NO: 19;

(HC) a heavy chain sequence at least 90% identical to SEQ ID NO: 20 and (LC) a light chain sequence at least 90% identical to SEQ ID NO: 21;

(HC) a heavy chain sequence at least 90% identical to SEQ ID NO: 22 and (LC) a light chain sequence at least 90% identical to SEQ ID NO: 23;

(HC) a heavy chain sequence at least 90% identical to SEQ ID NO: 24 and (LC) a light chain sequence at least 90% identical to SEQ ID NO: 25;

(HC) a heavy chain sequence at least 90% identical to SEQ ID NO: 26 and (LC) a light chain sequence at least 90% identical to SEQ ID NO: 27; and

(HC) a heavy chain sequence at least 90% identical to SEQ ID NO: 28 and (LC) a light chain sequence at least 90% identical to SEQ ID NO: 29.

20. The fusion polypeptide of claim 19 , wherein the antibody or subsequence thereof comprises a pair of heavy chain (HC) and light chain (LC) sequences selected from the following: SEQ ID NO: 14 and 15; SEQ ID NO: 16 and 17; SEQ ID NO: 18 and 19; SEQ ID NO: 20 and 21; SEQ ID NO: 22 and 23; SEQ ID NO: 24 and 25; SEQ ID NO: 26 and 27; and SEQ ID NO: 28 and 29.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2016
From: GRANGER, STEVE; NEWMAN, ROLAND; LYMAN, MICHAEL
To: TANABE RESEARCH LABORATORIES U.S.A., INC.
Reel/Frame 039760/0359 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2016
From: GRABULOVSKI, DRAGAN; WOODS, RICHARD; SILACCI, MICHELA; ZHA, WENJUAN; ATTINGER-TOLLER, ISABELLA
To: COVAGEN AG
Reel/Frame 039760/0470 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2016
From: TANABE RESEARCH LABORATORIES U.S.A., INC.; COVAGEN AG
To: MITSUBISHI TANABE PHARMA CORPORATION
Reel/Frame 039760/0636 →
Continuity (2)
Provisional Application 61954437 · Mar 17, 2014
Related Publication 20170081412A1 · Mar 23, 2017
Cited By (1)
US 12,247,071