IP Library Granted Patent US 10,077,302
Granted Patent B2
US 10,077,302 · App. 15/202,982 · Granted Sep 18, 2018

Method of inhibiting human IL-1 beta by administering an antibody to human IL-1 beta

Inventors: Stefanie Grabulovski (Zürich, CH); Titus Kretzschmar (Steinhausen, CH); Simone Schmitt (Schlieren, CH); Abdijapar Shamshiev (Zürich, CH); Thorsten Alexander Schafer (Lörrach, DE)
Assignee: Cell Medica Switzerland AG
C07K16/245A61K39/3955G01N33/6869A61K2039/505C07K2317/24C07K2317/35C07K2317/565C07K2317/622C07K2317/76C07K2317/94G01N2333/545
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,077,302
App. No.
15/202,982
Granted
Sep 18, 2018
Kind
B2
Abstract

The present invention relates to anti-IL-1 beta binding members and in particular to monovalent high potency IL-1 beta-binding antibody fragments being highly stable and soluble. Such binding members may be used in the treatment of inflammatory and other diseases as well as in diagnostics. Also provided are related nucleic acids, vectors, cells, and compositions.

Claims (30)

1. A method for inhibiting IL-1 beta in a subject in need thereof, comprising administering a therapeutically effective amount of an antibody or a fragment thereof against IL-1 beta comprising:

a. the variable heavy chain (VH) CDR sequences CDR-H1, CDR-H2, and CDR-H3 as set forth in: SEQ ID Nos.: 1, 2 and 3, respectively, and

b. the variable light chain (VL) CDR sequences CDR-L1, CDR-L2, and CDR-L3 as set forth in: SEQ ID Nos.: 4, 5, and 6, respectively.

2. The method of claim 1 , wherein the antibody or fragment thereof has a potency (IC50) with regard to inhibiting the biological effect of human IL-1 beta of lower than 50 pM as determined by inhibiting IL-1 beta stimulated release of IL-6 from human fibroblasts.

3. The method of claim 2 , wherein said IC 50 is lower than about 30 pM.

4. The method of claim 2 , wherein said IC 50 is lower than about 1 pM.

5. The method of claim 1 , wherein the antibody or fragment thereof is a Fab, a Fab', a scFv, a Fv fragment, a nanobody, a VHH or a minimal recognition unit.

6. The method of claim 1 , wherein the antibody or fragment thereof is a full-length immunoglobulin or a bivalent antibody fragment.

7. The method of claim 1 , wherein the antibody or fragment thereof comprises the light chain variable framework region FR-L1 of SEQ ID No. 18, the light chain variable framework region FR-L2 of SEQ ID No.: 19, the light chain variable framework region FR-L3 of SEQ ID No.: 20 and/or the light chain variable framework region FR-L4 of SEQ ID No.: 21.

8. The method of claim 1 , wherein the antibody or fragment thereof comprises the heavy chain variable framework region FR-H1 of SEQ ID Nos.: 22; the heavy chain variable framework region FR-H2 of SEQ ID Nos.: 23; the heavy chain variable framework region FR-H3 of SEQ ID Nos.: 24; and/or the heavy chain variable framework region FR-H4 of SEQ ID Nos.: 25.

9. The method of claim 1 , wherein the antibody or fragment thereof comprises:

a. a VH sequence of SEQ ID No.: 7; and

b. a VL sequence of SEQ ID No.: 8.

10. The method of claim 1 , wherein the antibody or fragment thereof has the sequence of SEQ ID No.: 10.

11. The method of claim 1 , wherein the antibody or fragment thereof is humanized.

12. The method of claim 1 , wherein the antibody or fragment thereof is cross-reactive with cynomolgus IL-1 beta, rhesus monkey IL-1 beta and/or rat IL-1 beta.

13. The method of claim 1 , wherein the antibody or fragment thereof is modified to extend the half-life residence time in vivo in serum.

14. The method of claim 1 , wherein the subject has proliferative diabetic retinopathy, gouty arthritis, Schnitzler syndrome, systemic juvenile idiopathic arthritis, rheumatoid arthritis, acute gouty arthritis, chronic gouty arthritis, urticaria, vasculitis, type 1 diabetes, type 2 diabetes, ankylosing spondylitis, recurrent multifocal osteomyelitis, relapsing polychondritis, cyropyrin-associated periodic syndrome (CAPS), Behçet's disease, familial mediterranean fever, chronic obstructive pulmonary disease, polymyalgia rheumatic, NALP3-mutations, pyoderma gangrenosum, chronic idiopathic urticarial, osteoarthritis, wet age-related macular degeneration, dry eye syndrome, pustular psoriasis, synovitis-acne-pustulosis-hyperostosis-osteitis syndrome, macrophage activation syndrome, periodic fever adenitis pharyngitis aphthous ulcer syndrome, adult-onset Still's disease, mevalonate kinase deficiency, atherosclerosis, TNF-receptor associated periodic syndrome (TRAPS), acne vulgaris and/or acne inversa.

15. The method of claim 1 , wherein the subject is a human being.

16. The method of claim 1 , wherein the antibody or fragment thereof is provided in a pharmaceutical composition.

17. The method of claim 1 , wherein said antibody or fragment thereof is administered parenterally; orally; rectally; urogenitally; topically; intravitreally; intravenously; intraocularly; oticly; intranasally; by inhalation; dermally; sublingually; or buccally.

18. The method of claim 1 , wherein said antibody or fragment thereof is provided with at least one further therapeutically effective compound.

19. The method of claim 18 , wherein said compound is administered simultaneously or sequentially with said antibody or fragment thereof.

20. A method for inhibiting IL-1 beta in a subject in need thereof, comprising administering a therapeutically effective amount of a binding member against IL-1 beta comprising:

a. the variable heavy chain (VH) CDR sequences CDR-H1, CDR-H2, and CDR-H3 as set forth in SEQ ID Nos.: 1, 2 and 3, respectively; and

b. the variable light chain (VL) CDR sequences CDR-L1, CDR-L2, and CDR-L3 as set forth in SEQ ID Nos.: 4, 5, and 6, respectively.

21. The method of claim 20 , wherein the binding member is monovalent or multivalent.

22. The method of claim 21 , wherein the binding member is monovalent and is a Fab, a Fab', a scFv, or a Fv fragment.

23. The method of claim 21 , wherein the binding member is multivalent and multispecific.

24. The method of claim 21 , wherein the binding member is multivalent and is a full-length immunoglobulin, a diabody, or a bis-scFv.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 18, 2022
From: CELL MEDICA INC.
To: CELL MEDICA, INC.
Reel/Frame 060529/0195 →
SECURITY INTEREST Recorded Jul 7, 2021
From: CELL MEDICA, INC.
To: OAKTREE FUND ADMINISTRATION, LLC
Reel/Frame 056782/0954 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 21, 2021
From: CELL MEDICA SWITZERLAND AG
To: CELL MEDICA INC.
Reel/Frame 054988/0114 →
CHANGE OF NAME Recorded Aug 8, 2016
From: DELENEX THERAPEUTICS AG
To: CELL MEDICA SWITZERLAND AG
Reel/Frame 039629/0573 →
Priority Claims (1)
EP 12007503 · Nov 5, 2012 · regional
Continuity (3)
Division 14072165 · Nov 5, 2013
Provisional Application 61722532 · Nov 5, 2012
Related Publication 20170051054A1 · Feb 23, 2017
Cited By (1)
US 12,286,473