IP Library › Granted Patent US 10,493,148
Granted Patent B2
US 10,493,148 · App. 16/282,609 · Granted Dec 3, 2019

PD-1 agonist antibodies and uses thereof

Inventors: Pia Pauliina Yachi (San Diego, CA); Qing Chai (San Diego, CA); Yiqing Feng (Carmel, IN); Kristin Paige Newburn (Indianapolis, IN); Stephanie Marie Truhlar (Carlsbad, CA); Petra Verdino (La Jolla, CA)
Assignee: Eli Lilly and Company
A61K39/395A61K39/00A61K39/39558C07K16/28
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Quick Facts
Patent No.
US 10,493,148
App. No.
16/282,609
Granted
Dec 3, 2019
Kind
B2
Abstract

The present invention relates to anti-human PD-1 agonist antibodies, and uses thereof for treating autoimmune disorders such as rheumatoid arthritis or for decreasing rejection of transplanted cells and/or tissues.

Claims (12)

1. An antibody that binds human PD-1, comprising: 1) a heavy chain variable region (HCVR); and 2) a light chain variable region (LCVR), wherein the HCVR comprises a HCDR1, HCDR2, and HCDR3, and the LCVR comprises a LCDR1, LCDR2, and LCDR3, wherein the amino acid sequence of the HCDR1 is SEQ ID NO:5, the amino acid sequence of the HCDR2 is SEQ ID NO:6, and the amino acid sequence of the HCDR3 is SEQ ID NO:7, the amino acid sequence of the LCDR1 is SEQ ID NO:8, the amino acid sequence of the LCDR2 is SEQ ID NO:9, and the amino acid sequence of the LCDR3 is SEQ ID NO:10, and wherein the antibody is an IgG1.

2. The antibody of claim 1 , wherein the amino acid sequence of the HCVR is SEQ ID NO:3 and the amino acid sequence of the LCVR is SEQ ID NO:4.

3. The antibody of claim 2 comprising: 1) a HC; and 2) a LC, wherein the amino acid sequence of the HC is SEQ ID NO:1, and the amino acid sequence of the LC is SEQ ID NO:2.

4. The antibody of claim 3 comprising two HCs and two LCs, wherein the amino acid sequence of each of the HCs is SEQ ID NO:1, and the amino acid sequence of each of the LCs is SEQ ID NO:2.

5. The antibody of claim 1 , wherein the antibody is an agonist of human PD-1 as determined in an in vivo model of an autoimmune disorder or transplant rejection.

6. The antibody of claim 5 wherein the in vivo model is a model for GVHD, solid organ transplantation rejection, vasculitis, SLE, T1DM, MS, GCA, PsO, PsA, RA, IBD, UC, AS, SjS, autoimmune hepatitis, or scleroderma.

7. The antibody of claim 5 wherein the in vivo model is a mouse model for GVHD and/or lupus nephritis.

8. A pharmaceutical composition comprising the antibody of claim 1 , and one or more pharmaceutically acceptable carriers, diluents, or excipients.

9. A method of treating an autoimmune disease comprising administering to a patient in need thereof, an effective amount of the antibody of claim 1 .

10. The method of claim 9 , wherein the autoimmune disease is GVHD, solid organ transplantation rejection, vasculitis, SLE, T1DM, MS, GCA, PsO, PsA, RA, IBD, UC, AS, SjS, autoimmune hepatitis, scleroderma, celiac disease, Addison's disease, Hashimoto's disease, Graves' disease, atrophic gastritis/pernicious anemia, acquired hypogonadism/infertility, hypoparathyroidism, Coombs positive-hemolytic anemia, chronic allergic diseases (such as asthma, hay fever, or allergic rhinitis), Crohn's disease, male or female infertility, Behcet's, Wegener's granulomatosis, myocarditis, myositis, PMR, spontaneous abortion, vitiligo, atherosclerosis, autoimmune pancreatitis, bullous pemphigoid, chronic viral infections, or myasthenia gravis.

11. The method of claim 10 , wherein the autoimmune disease is GVHD, solid organ transplantation rejection, vasculitis, SLE, T1DM, MS, GCA, PsO, PsA, RA, IBD, UC, AS, SjS, autoimmune hepatitis, or scleroderma.

12. The method of claim 10 , wherein the antibody is administered in combination with another therapeutic agent effective for the treatment of an autoimmune disease.

Continuity (2)
Provisional Application 62637643 · Mar 2, 2018
Related Publication 20190270818A1 · Sep 5, 2019
Cited By (1)
US 12,742,010