IP Library › Granted Patent US 10,774,140
Granted Patent B2
US 10,774,140 · App. 16/085,567 · Granted Sep 15, 2020

Anti-TNFα-antibodies and functional fragments thereof

Inventors: Tea Gunde (Zürich, CH); Sebastian Meyer (Eggenwil, CH)
Assignee: Numab Therapeutics AG
C07K16/241C12N15/85C07K2317/24C07K2317/33C07K2317/622C07K2317/626C07K2317/76C07K2317/92C07K2317/94
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Quick Facts
Patent No.
US 10,774,140
App. No.
16/085,567
Granted
Sep 15, 2020
Kind
B2
Abstract

The present invention relates to antibody molecules and functional fragments thereof, capable of binding to tumor necrosis factor alpha (TNFα), to processes for their production, and to their therapeutic uses.

Claims (21)

1. An antibody or a functional fragment thereof capable of binding to human tumor necrosis factor alpha (TNFα), wherein said antibody or functional fragment comprises (i) a V L domain comprising a CDR1 region having an amino acid sequence in accordance with the amino acid sequence as shown in SEQ ID NO:1, a CDR2 region having an amino acid sequence in accordance with the amino acid sequence as shown in SEQ ID NO:2, and a CDR3 region having an amino acid sequence in accordance with the amino acid sequence as shown in SEQ ID NO:3, and (ii) a V H domain comprising a CDR1 region having an amino acid sequence in accordance with the amino acid sequence as shown in SEQ ID NO:4, a CDR2 region having an amino acid sequence in accordance with the amino acid sequence as shown in SEQ ID NO:5, and a CDR3 region having an amino acid sequence in accordance with the amino acid sequence as shown in SEQ ID NO:6.

2. The antibody or functional fragment thereof of claim 1 , wherein said antibody or functional fragment comprises (i) a V L domain comprising a CDR1 region having the amino acid sequence as shown in SEQ ID NO:7, a CDR2 region having the amino acid sequence as shown in SEQ ID NO:2, and a CDR3 region having the amino acid sequence as shown in SEQ ID NO:8, and (ii) a V H domain comprising a CDR1 region having the amino acid sequence as shown in SEQ ID NO:9, a CDR2 region having the amino acid sequence as shown in SEQ ID NO:10, and a CDR3 region having the amino acid sequence as shown in SEQ ID NO:11.

3. The antibody or functional fragment thereof of claim 2 , wherein said antibody or functional fragment

(i) binds to human TNFα with a dissociation constant (K D ) of less than 1 nM, particularly less than 750 pM, more particularly less than 100 pM;

(ii) is cross-reactive with Macaca mulatta (Rhesus) TNFα and with Macaca fascicularis (Cynomolgus) TNFα;

(iii) has a potency to inhibit TNFα-induced apoptosis that is greater than the potency of infliximab;

(iv) comprises a variable domain having a melting temperature, determined by differential scanning fluorimetry, of at least 60° C., particularly at least 63° C., more particularly at least 66° C.; and/or

(v) is capable of binding to human TNFα Trimer in a stoichiometry (antibody: TNFα Trimer ) of at least 2.

4. The antibody or functional fragment thereof of claim 2 , which binds to human TNFα with a K D of less than 75 pM.

5. The antibody or functional fragment thereof of claim 2 , wherein said antibody or functional fragment comprises a V H domain having the amino acid sequence as shown in SEQ ID NO:14.

6. The antibody or functional fragment thereof of claim 2 , wherein said antibody or functional fragment comprises a V L domain having the amino acid sequence as shown in SEQ ID NO:17.

7. The antibody or functional fragment thereof of claim 2 , which is a single-chain variable fragment (scFv).

8. The antibody or functional fragment thereof of claim 7 , wherein said scFv has the amino acid sequence as shown in SEQ ID NO:20.

9. The antibody or functional fragment thereof of claim 2 , which is an immunoglobulin G (IgG).

10. An antibody or functional fragment thereof binding to the same epitope as the functional fragment of claim 8 .

11. A nucleic acid encoding the antibody or functional fragment thereof of claim 1 .

12. A vector or plasmid comprising the nucleic acid of claim 11 .

13. A cell comprising the nucleic acid of claim 11 .

14. A method of preparing an antibody or functional fragment thereof capable of binding to human TNFα, comprising culturing the cell of claim 13 in a medium under conditions that allow expression of the nucleic acid encoding the antibody or functional fragment thereof, and recovering the antibody or functional fragment thereof from the cells or from the medium.

15. A pharmaceutical composition comprising the antibody or functional fragment thereof of claim 2 , and optionally a pharmaceutically acceptable carrier and/or excipient.

16. The antibody or functional fragment thereof as defined in claim 2 for use in a method of treating a TNFα-related disorder or disease.

Assignments (3)
CORRECTIVE ASSIGNMENT TO CORRECT THE CITY OF THE ASSIGNEE FROM WADENSWIL TO WÄDENSWIL PREVIOUSLY RECORDED ON REEL 049922 FRAME 0697. ASSIGNOR(S) HEREBY CONFIRMS THE MERGER. Recorded Aug 20, 2019
From: NUMAB INNOVATION AG
To: NUMAB THERAPEUTICS AG
Reel/Frame 050111/0212 →
MERGER Recorded Jul 31, 2019
From: NUMAB INNOVATION AG
To: NUMAB THERAPEUTICS AG
Reel/Frame 049922/0697 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 16, 2018
From: GUNDE, TEA; MEYER, SEBASTIAN
To: NUMAB INNOVATION AG
Reel/Frame 047175/0642 →
Priority Claims (1)
EP 16000653 · Mar 17, 2016 · regional
Continuity (1)
Related Publication 20190092850A1 · Mar 28, 2019