US2010256340A1PendingUtilityA1
Trivalent, bispecific antibodies
Est. expiryApr 7, 2029(~2.7 yrs left)· nominal 20-yr term from priority
Inventors:Ulrich BrinkmannRebecca CroasdaleEike HoffmannChristian KleinEkkehard MoessnerJuergen Michael SchanzerClaudio SustmannPablo Umana
A61P 35/00C07K 16/00C07K 2317/73C07K 16/32C07K 2317/622C07K 16/2863C07K 2317/31C07K 2317/24C07K 2317/76C07K 2319/00C07K 2317/565C07K 16/46A61K 39/395C07K 16/28
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Claims
Abstract
The present invention relates to trivalent, bispecific antibodies, methods for their production, pharmaceutical compositions containing the antibodies, and uses thereof.
Claims
exact text as granted — not AI-modified1 . A trivalent, bispecific antibody comprising
a) a full length antibody that specifically binds to a first antigen wherein the full length antibody consists of two antibody heavy chains and two antibody light chains; b) a polypeptide consisting of ba) an antibody heavy chain variable domain (VH); or bb) an antibody heavy chain variable domain (VH) and an antibody constant domain 1 (CH1), wherein the N-terminus of the VH domain of the polypeptide is fused via a peptide connector to the C-terminus of one of the two heavy chains of the full length antibody; c) a polypeptide consisting of ca) an antibody light chain variable domain (VL), or cb) an antibody light chain variable domain (VL) and an antibody light chain constant domain (CL); wherein N-terminus of the VL domain of the polypeptide is fused via a peptide connector to the C-terminus of the other of the two heavy chains of the full length antibody; and wherein the antibody heavy chain variable domain (VH) of the polypeptide under b) and the antibody light chain variable domain (VL) of the polypeptide under c) together form an antigen-binding site specifically binding to a second antigen.
2 . The trivalent, bispecific antibody according to claim 1 , wherein
the CH3 domain of one heavy chain and the CH3 domain of the other heavy chain each meet at an interface which comprises an alteration in the original interface between the antibody CH3 domains; wherein i) in the CH3 domain of one heavy chain an amino acid residue is replaced with an amino acid residue having a larger side chain volume, thereby generating a protuberance within the interface of the CH3 domain of one heavy chain which is positionable in a cavity within the interface of the CH3 domain of the other heavy chain and wherein ii) in the CH3 domain of the other heavy chain an amino acid residue is replaced with an amino acid residue having a smaller side chain volume, thereby generating a cavity within the interface of the second CH3 domain within which a protuberance within the interface of the first CH3 domain is positionable.
3 . The trivalent, bispecific antibody according to claim 2 , wherein
i) the amino acid residue having a larger side chain volume is selected from the group consisting of arginine (R), phenylalanine (F), tyrosine (Y), tryptophan (W); and ii) the amino acid residue having a smaller side chain volume is selected from the group consisting of alanine (A), serine (S), threonine (T), valine (V).
4 . The trivalent, bispecific antibody according to claim 3 , wherein
both CH3 domains are further altered by the introduction of cysteine as an amino acid in each CH3 domain such that a disulfide bridge between both CH3 domains can be formed.
5 . The trivalent, bispecific antibody according to claim 4 , wherein
the CH3 domain under i) comprises a T366W mutation; and the CH3 domain under ii) comprises T366S, L368A, and Y407V mutations.
6 . The trivalent, bispecific antibody according to claim 5 , wherein
the CH3 domain under i) comprises Y349C and T366W mutations; and the CH3 domain under ii) comprises S354C, T366S, L368A, and Y407V mutations.
7 . The trivalent, bispecific antibody according to claim 4 , wherein
the antibody heavy chain variable domain (VH) of the polypeptide under b) and the antibody light chain variable domain (VL) of the polypeptide under c) are linked and stabilized via a interchain disulfide bridge by introduction of a disulfide bond between the following positions: i) heavy chain variable domain position 44 to light chain variable domain position 100, ii) heavy chain variable domain position 105 to light chain variable domain position 43, or iii) heavy chain variable domain position 101 to light chain variable domain position 100.
8 . The trivalent, bispecific antibody according to claim 7 , wherein
the antibody heavy chain variable domain (VH) of the polypeptide under b) and the antibody light chain variable domain (VL) of the polypeptide under c) are linked and stabilized via a interchain disulfide bridge by introduction of a disulfide bond between the following positions: i) heavy chain variable domain position 44 to light chain variable domain position 100.
9 . The trivalent, bispecific antibody according to claim 6 , wherein the peptide connectors under b) and c) are identical peptides with a length between 25 and 50 amino acids.
10 . A pharmaceutical composition comprising a trivalent, bispecific antibody according to claim 1 .
11 . A nucleic acid encoding a trivalent, bispecific antibody according to claim 2 .
12 . A nucleic acid encoding a trivalent, bispecific antibody according to claim 3 .
13 . A nucleic acid encoding a trivalent, bispecific antibody according to claim 4 .
14 . A nucleic acid encoding a trivalent, bispecific antibody according to claim 5 .
15 . A nucleic acid encoding a trivalent, bispecific antibody according to claim 6 .
16 . A nucleic acid encoding a trivalent, bispecific antibody according to claim 7 .
17 . A nucleic acid encoding a trivalent, bispecific antibody according to claim 8 .
18 . A method for treating a human suffering from cancer by administering an effective amount of the trivalent, bispecific antibody according to claim 8 to a human in need of such treatment.Cited by (0)
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