IP Library Granted Patent US 10,322,174
Granted Patent B2
US 10,322,174 · App. 15/792,266 · Granted Jun 18, 2019

Neutralizing anti-TL1A monoclonal antibodies

Inventors: Janine Bilsborough (Simi Valley, CA); Stephan Targan (Santa Monica, CA); Bradley Henkle (West Hollywood, CA)
Assignee: Cedars-Sinai Medical Center
A61K39/39533A61K48/005A61P1/02A61P29/00A61P37/00C07K16/241C07K16/2809A61K39/3955A61K2039/505C07K2317/24C07K2317/56C07K2317/565C07K2317/76C07K2317/90
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Quick Facts
Patent No.
US 10,322,174
App. No.
15/792,266
Granted
Jun 18, 2019
Kind
B2
Abstract

Described herein are methods and pharmaceutical compositions for the treatment of inflammatory bowel disease (IBD), Crohn's Disease (CD), ulcerative colitis (UC) and medically refractive-ulcerative colitis (MR-UC). In particular, disclosed are anti-TL1A antibodies useful for the treatment of IBD.

Claims (15)

1. An antibody or antigen-binding fragment that specifically binds to a tumor necrosis factor-like protein 1A (TL1A) polypeptide, wherein said antibody or antigen-binding fragment comprises:

a) a heavy chain comprising a heavy chain complementarity determining region 1 (HCDR1), a heavy chain complementarity determining region 2 (HCDR2), and a heavy chain complementarity determining region 3 (HCDR3), wherein

i) the HCDR1 comprises a first amino acid sequence of DTYMH of SEQ ID NO: 6;

ii) the HCDR2 comprises a second amino acid sequence of PASGH of SEQ ID NO: 7; and

iii) the HCDR3 comprises a third amino acid sequence of SGGLPD of SEQ ID NO: 8; and

b) a light chain comprising a light chain complementarity determining region 1 (LCDR1), a light chain complementarity determining region 2 (LCDR2), and a light chain complementarity determining region 3 (LCDR3), wherein

i) the LCDR1 comprises a fourth amino acid sequence of ASSSVSYMY of SEQ ID NO: 14;

ii) the LCDR2 comprises a fifth amino acid sequence of ATSNLAS of SEQ ID NO: 15; and

iii) the LCDR3 comprises a sixth amino acid sequence of GNPRT of SEQ ID NO: 16.

2. The antibody or antigen-binding fragment of claim 1 , provided that the antibody or antigen-binding fragment is a chimeric antibody, a CDR-grafted antibody, a humanized antibody, a Fab, a Fab′, a F(ab′)2, a Fv, a disulfide linked Fv, a scFv, a single domain antibody, a diabody, a multispecific antibody, a dual specific antibody, an anti-idiotypic antibody, a bispecific antibody, or a combination thereof.

3. The antibody or antigen-binding fragment of claim 2 , provided that the antibody or antigen-binding fragment is a humanized antibody.

4. A composition comprising: the antibody or antigen-binding fragment of claim 1 , and a pharmaceutically acceptable carrier.

5. The antibody or antigen-binding fragment of claim 1 , provided the antibody or antigen binding fragment is an immunoglobulin G (IgG).

6. The antibody or antigen-binding fragment of claim 5 , provided the IgG comprises an IgG1.

7. The antibody or antigen-binding fragment of claim 5 , provided the IgG comprises an IgG2.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 23, 2018
From: BILSBOROUGH, JANINE; TARGAN, STEPHAN; HENKLE, BRADLEY
To: CEDARS-SINAI MEDICAL CENTER
Reel/Frame 044701/0902 →
Continuity (2)
Provisional Application 62413188 · Oct 26, 2016
Related Publication 20180110855A1 · Apr 26, 2018
Cited By (9)
US 12,215,147 US 12,269,873 US 12,305,236 US 12,391,752 US 12,466,890 US 12,473,370 US 12,509,523 US 12,540,358 US 12,618,111