IP Library Patent Application 18823000
Patent Application
App. No. 18/823,000

IL-7 Binding Proteins and Their Use in Medical Therapy

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Patent No.
US None
App. No.
18/823,000
Abstract

Provided herein are interleukin 7 (IL-7) binding proteins, pharmaceutical compositions and their use in the treatment or prevention of a disease or condition.

Claims (27)

1 - 35 . (canceled)

36 . A method for the treatment of an autoimmune and/or inflammatory condition in a subject in need thereof, the method comprising administering to the subject a therapeutically effective amount of an interleukin 7 (IL-7) binding protein or IL-7 binding fragment thereof comprising:

(1) a heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 6;

(2) a heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 7;

(3) a heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 8;

(4) a light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO: 9;

(5) a light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO: 10; and

(6) a light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO: 11.

37 . The method of claim 36 , wherein the IL-7 binding protein or IL-7 binding fragment thereof comprises a heavy chain variable region having a sequence at least 90% identical to the amino acid sequence of SEQ ID NO: 4 and a light chain variable region having a sequence at least 90% identical to the amino acid sequence of SEQ ID NO: 5.

38 . The method of claim 37 , wherein the IL-7 binding protein or IL-7 binding fragment thereof comprises a heavy chain variable region comprising the amino acid sequence of SEQ ID NO: 4 and a light chain variable region comprising the amino acid sequence of SEQ ID NO: 5.

39 . The method of claim 36 , wherein the IL-7 binding protein or IL-7 binding fragment thereof comprises a heavy chain having a sequence at least 80% identical to the amino acid sequence of SEQ ID NO: 2 and a light chain having a sequence at least 80% identical to the amino acid sequence of SEQ ID NO: 3.

40 . The method of claim 39 , wherein the IL-7 binding protein or IL-7 binding fragment thereof comprises a heavy chain comprising the amino acid sequence of SEQ ID NO: 2 and a light chain comprising the amino acid sequence of SEQ ID NO: 3.

41 . The method of claim 36 , wherein the IL-7 binding protein or IL-7 binding fragment thereof is an antibody.

42 . The method of claim 41 , wherein the antibody comprises an IgG1 or IgG4 Fc region.

43 . The method of claim 42 , wherein the antibody comprises a human IgG1 heavy chain constant region.

44 . The method of claim 43 , wherein the antibody comprises a human IgG1 heavy chain constant region having an alanine residue at position 235 and position 237 according to EU numbering.

45 . The method of claim 36 , wherein the autoimmune and/or inflammatory condition is multiple sclerosis, Sjögren's syndrome, rheumatoid arthritis, inflammatory bowel disease, Crohn's disease, ulcerative colitis, systemic lupus erythematosus, or type I diabetes.

46 . The method of claim 45 , wherein the multiple sclerosis is clinically isolated syndrome, relapsed remitting, primary progressive or secondary progressive.

47 . The method of claim 45 , wherein the autoimmune and/or inflammatory condition is systemic lupus erythematosus.

48 . The method of claim 45 , wherein the autoimmune and/or inflammatory condition is inflammatory bowel disease.

49 . The method of claim 45 , wherein the autoimmune and/or inflammatory condition is type 1 diabetes.

50 . The method of claim 38 , wherein the autoimmune and/or inflammatory condition is multiple sclerosis, Sjögren's syndrome, rheumatoid arthritis, inflammatory bowel disease, Crohn's disease, ulcerative colitis, systemic lupus erythematosus, or type I diabetes.

51 . The method of claim 50 , wherein the multiple sclerosis is clinically isolated syndrome, relapsed remitting, primary progressive or secondary progressive.

52 . The method of claim 50 , wherein the autoimmune and/or inflammatory condition is systemic lupus erythematosus, inflammatory bowel disease, or type I diabetes.

53 . The method of claim 50 , wherein the autoimmune and/or inflammatory condition is multiple sclerosis, Sjögren's syndrome, rheumatoid arthritis, inflammatory bowel disease, Crohn's disease, ulcerative colitis, systemic lupus erythematosus, or type I diabetes.

54 . The method of claim 53 , wherein the multiple sclerosis is clinically isolated syndrome, relapsed remitting, primary progressive or secondary progressive.

55 . The method of claim 53 , wherein the autoimmune and/or inflammatory condition is systemic lupus erythematosus, inflammatory bowel disease, or type I diabetes.

Assignments (4)
CHANGE OF ADDRESS Recorded Oct 8, 2025
From: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 073032/0390 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2024
From: BOUMA, GERBEN; COULSTOCK, EDWARD THOMAS; DIXON, DAVID; HOPLEY, STEPHANIE; LEWIS, ALAN PETER; NEISEN, JESSICA LYNN
To: GLAXOSMITHKLINE SERVICES UNLIMITED
Reel/Frame 068826/0429 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2024
From: GLAXOSMITHKLINE SERVICES UNLIMITED
To: GLAXOSMITHKLINE RESEARCH AND DEVELOPMENT LIMITED
Reel/Frame 068826/0624 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2024
From: GLAXOSMITHKLINE RESEARCH AND DEVELOPMENT LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 068826/0676 →