IP Library Granted Patent US 12,122,828
Granted Patent B2
US 12,122,828 · App. 18/460,944 · Granted Oct 22, 2024

IL-7 binding proteins and their use in medical therapy

Inventors: Gerben Bouma (Stevenage, GB); Edward Thomas Coulstock (Stevenage, GB); David Dixon (Stevenage, GB); Stephanie Hopley (Stevenage, GB); Alan Peter Lewis (Stevenage, GB); Jessica Lynn Neisen (Stevenage, GB)
Assignee: GlaxoSmithKline Intellectual Property Development Limited
C07K16/244A61K2039/505C07K2317/92C07K2317/94
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Quick Facts
Patent No.
US 12,122,828
App. No.
18/460,944
Granted
Oct 22, 2024
Kind
B2
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 (26)

1. 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:

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

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

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

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

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

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

2. The method of claim 1 , 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.

3. The method of claim 2 , 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.

4. The method of claim 1 , 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.

5. The method of claim 4 , 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.

6. The method of claim 1 , wherein the IL-7 binding protein or IL-7 binding fragment thereof is an antibody.

7. The method of claim 6 , wherein the antibody comprises an IgG1 or IgG4 Fc region.

8. The method of claim 7 , wherein the antibody comprises a human IgG1 heavy chain constant region.

9. The method of claim 8 , 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.

10. The method of claim 1 , 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.

11. The method of claim 10 , wherein the multiple sclerosis is clinically isolated syndrome, relapsed remitting, primary progressive or secondary progressive.

12. The method of claim 10 , wherein the autoimmune and/or inflammatory condition is systemic lupus erythematosus.

13. The method of claim 10 , wherein the autoimmune and/or inflammatory condition is inflammatory bowel disease.

14. The method of claim 10 , wherein the autoimmune and/or inflammatory condition is type 1 diabetes.

15. The method of claim 3 , 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.

16. The method of claim 15 , wherein the multiple sclerosis is clinically isolated syndrome, relapsed remitting, primary progressive or secondary progressive.

17. The method of claim 15 , wherein the autoimmune and/or inflammatory condition is systemic lupus erythematosus, inflammatory bowel disease, or type I diabetes.

18. The method of claim 5 , 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.

19. The method of claim 18 , wherein the multiple sclerosis is clinically isolated syndrome, relapsed remitting, primary progressive or secondary progressive.

20. The method of claim 18 , 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 Jun 10, 2024
From: BOUMA, GERBEN; COULSTOCK, EDWARD THOMAS; DIXON, DAVID; HOPLEY, STEPHANIE; LEWIS, ALAN PETER; NEISEN, JESSICA LYNN
To: GLAXOSMITHKLINE SERVICES UNLIMITED
Reel/Frame 067670/0045 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2024
From: GLAXOSMITHKLINE SERVICES UNLIMITED
To: GLAXOSMITHKLINE RESEARCH AND DEVELOPMENT LIMITED
Reel/Frame 067670/0123 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2024
From: GLAXOSMITHKLINE RESEARCH AND DEVELOPMENT LIMITED
To: GLAXOSMITHKLINE INTELLECTUAL PROPERTY DEVELOPMENT LIMITED
Reel/Frame 067670/0195 →
Continuity (3)
Continuation 17538431 · Nov 30, 2021
Provisional Application 63120564 · Dec 2, 2020
Related Publication 20240025988A1 · Jan 25, 2024