IP Library Granted Patent US 12692303
Granted Patent B1
US 12692303 · App. 18/009,849 · Granted Jul 28, 2026

Anti-human interleukin 23 monoclonal antibody and application thereof

Inventors: Jiwan Qiu (Jiangsu, CN); Yong Kong (Jiangsu, CN); Wei Chen (Jiangsu, CN); Huaiyao Qiao (Jiangsu, CN); Zhihua Qiu (Jiangsu, CN); Yiliang Wu (Jiangsu, CN); Tao Chen (Jiangsu, CN); Meijuan Wu (Jiangsu, CN)
Assignee: QYUNS THERAPEUTICS CO., LTD.
C07K16/244A61P17/06C07K2317/24C07K2317/565C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 12692303
App. No.
18/009,849
Granted
Jul 28, 2026
Kind
B1
Abstract

The present invention relates to an anti-human interleukin 23 (hIL-23) monoclonal antibody and an application thereof. The anti-human interleukin 23 (hIL-23) monoclonal antibody comprises three heavy chain complementary determining regions (CDR-H1, CDR-H2 and CDR-H3) and three light chain complementary determining regions (CDR-L1, CDR-L2 and CDR-L3), wherein (a): the amino acid sequence of the CDR-H1 is as shown in SEQ ID NO: 1, (b): the amino acid sequence of the CDR-H2 is as shown in SEQ ID NO: 2, (c): the amino acid sequence of the CDR-H3 is as shown in SEQ ID NO: 3, (d): the amino acid sequence of the CDR-L1 is as shown in SEQ ID NO: 4, (e): the amino acid sequence of the CDR-L2 is as shown in SEQ ID NO: 5, and (f): the amino acid sequence of the CDR-L3 is as shown in SEQ ID NO: 6. Compared with existing anti-human interleukin 23 monoclonal antibodies (Guselkumab and Risankizumab), the hIL-23 binding affinity of the anti-human interleukin 23 (hIL-23) monoclonal antibody is equivalent, but the antagonistic activity at the cellular level is superior to Guselkumab, and equivalent to Risankizumab.

Claims (14)

1 . An isolated anti-human interleukin 23 monoclonal antibody, comprising three heavy chain complementary determining regions (CDR-H1, CDR-H2 and CDR-H3) and three light chain complementary determining regions (CDR-L1, CDR-L2 and CDR-L3), wherein:

(a) the amino acid sequence of CDR-H1 consists of SEQ ID NO: 1;

(b) the amino acid sequence of CDR-H2 consists of SEQ ID NO: 2;

(c) the amino acid sequence of CDR-H3 consists of SEQ ID NO: 3;

(d) the amino acid sequence of CDR-L1 consists of SEQ ID NO: 4;

(e) the amino acid sequence of CDR-L2 consists of SEQ ID NO: 5; and

(f) the amino acid sequence of CDR-L3 consists of SEQ ID NO: 6.

2 . The monoclonal antibody according to claim 1 , which comprises a heavy chain variable region and a light chain variable region, wherein

the amino acid sequence of the heavy chain variable region consists of SEQ ID NO: 7; and,

the amino acid sequence of the light chain variable region consists of SEQ ID NO: 8.

3 . A pharmaceutical composition, comprising the monoclonal antibody according to claim 1 , and a pharmaceutically acceptable carrier.

4 . The pharmaceutical composition according to claim 3 , which is used for treatment of a disease related to IL-23 mediated signal transduction;

wherein the disease related to IL-23 mediated signal transduction is selected from the group consisting of: psoriatic arthritis, inflammatory bowel disease, and psoriasis.

5 . The pharmaceutical composition according to claim 4 , wherein the inflammatory bowel disease is ulcerative colitis or Crohn's disease.