US2014037632A1PendingUtilityA1
Multi-specific antigen-binding molecules and uses thereof
Assignee: CHUGAI PHARMACEUTICAL CO LTDPriority: Nov 17, 2010Filed: Sep 6, 2013Published: Feb 6, 2014
Est. expiryNov 17, 2030(~4.3 yrs left)· nominal 20-yr term from priority
Inventors:Tomoyuki IgawaZenjiro SampeiTetsuo KojimaTetsuhiro SoedaAtsushi MutoTakehisa KitazawaYukiko NishidaChifumi ImaiTsukasa SuzukiKazutaka Yoshihashi
A61P 7/00A61P 43/00A61P 7/04C07K 2317/31C07K 16/18C07K 2317/51C07K 2317/94C07K 2317/75C07K 2317/565A61K 2039/505C07K 16/40C07K 16/468C07K 2317/56C07K 2317/76C07K 16/36C07K 2317/52A61K 2039/54
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Claims
Abstract
Various bispecific antibodies that specifically bind to both blood coagulation factor IX/activated blood coagulation factor IX and blood coagulation factor X and functionally substitute for the cofactor function of blood coagulation factor VIII, that is, the function to promote activation of blood coagulation factor X by activated blood coagulation factor IX, were produced. From these antibodies, multispecific antigen-binding molecules having a high activity of functionally substituting for blood coagulation factor VIII were successfully discovered.
Claims
exact text as granted — not AI-modified1 .- 29 . (canceled)
30 . A bispecific antibody that recognizes blood coagulation factor IX and/or activated blood coagulation factor IX, and recognizes blood coagulation factor X, wherein the bispecific antibody comprises:
a first antibody H chain comprising CDRs 1, 2, and 3 that comprise SEQ ID NOs: 102-104, respectively; a second antibody H chain comprising CDRs 1, 2, and 3 that comprise SEQ ID NOs: 126-128, respectively; a first antibody L chain comprising CDRs 1, 2, and 3 that comprise SEQ ID NOs: 150-152, respectively; and a second antibody L chain comprising CDRs 1, 2, and 3 that comprise SEQ ID NOs: 150-152, respectively.
31 . The bispecific antibody of claim 30 , wherein:
the first antibody H chain comprises a variable region comprising SEQ ID NO: 44; the second antibody H chain comprises a variable region comprising SEQ ID NO: 52; and each of the first and second antibody L chains comprises a variable region comprising SEQ ID NO: 60.
32 . The bispecific antibody of claim 31 , wherein:
the first antibody H chain comprises an antibody H chain constant region consisting of SEQ ID NO: 70 or 73; the second antibody H chain comprises an antibody H chain constant region of: SEQ ID NO: 70, when the first antibody H chain comprises an H chain constant region of SEQ ID NO: 73, or SEQ ID NO: 73, when the first antibody H chain comprises an H chain constant region of SEQ ID NO: 70; and each of the first and second antibody L chains comprises an antibody L chain constant region of SEQ ID NO: 74.
33 . The bispecific antibody of claim 32 , wherein:
the first antibody H chain comprises SEQ ID NO: 18; the second antibody H chain comprises SEQ ID NO: 25; and each of the first and second antibody L chains comprises SEQ ID NO: 30.
34 . A bispecific antibody that recognizes blood coagulation factor IX and/or activated blood coagulation factor IX, and recognizes blood coagulation factor X, wherein the bispecific antibody comprises:
a first antibody H chain that is an H chain of an antibody that binds to an epitope overlapping with an epitope bound by an antibody that consists of an antibody H chain consisting of SEQ ID NO: 18 and an antibody L chain consisting of SEQ ID NO: 30; a second antibody H chain that is an H chain of an antibody that binds to an epitope overlapping with an epitope bound by an antibody that consists of an antibody H chain consisting of SEQ ID NO: 25 and an antibody L chain consisting of SEQ ID NO: 30; and a first antibody L chain and a second antibody L chain, each of which is independently selected from (a) and (b): (a) an L chain of an antibody that binds to an epitope overlapping with an epitope bound by an antibody that consists of an antibody H chain consisting of SEQ ID NO: 18 and an antibody L chain consisting of SEQ ID NO: 30; and (b) an L chain of an antibody that binds to an epitope overlapping with an epitope bound by an antibody that consists of an antibody H chain consisting of SEQ ID NO: 25 and an antibody L chain consisting of SEQ ID NO: 30.
35 . The bispecific antibody of claim 34 , wherein:
the first antibody H chain comprises, by Kabat numbering, any one or more of an isoleucine at amino acid position 34; an asparagine, glutamine, or serine at amino acid position 35; a serine at amino acid position 49; an arginine at amino acid position 61; a glutamic acid at amino acid position 62; a serine or threonine at amino acid position 96; a lysine or arginine at amino acid position 98; a phenylalanine or tyrosine at amino acid position 100; a glycine at amino acid position 100b; and a tyrosine at amino acid position 102; the second antibody H chain comprises, by Kabat numbering, any one or more of an aspartic acid at amino acid position 35; an arginine at amino acid position 53; a lysine at amino acid position 73; a glycine at amino acid position 76; a lysine or arginine at amino acid position 96; a tyrosine at amino acid position 98; a tyrosine at amino acid position 100; and a histidine at amino acid position 100a; and the first antibody L chain and the second antibody L chain each independently comprises, by Kabat numbering, any one or more of a lysine or arginine at amino acid position 27; a glutamic acid at amino acid position 30; an arginine at amino acid position 31; a glutamine at amino acid position 32; an arginine or glutamine at amino acid position 50; a serine at amino acid position 52; an arginine at amino acid position 53; a lysine at amino acid position 54; a glutamic acid at amino acid position 55; a serine at amino acid position 92; a serine at amino acid position 93; a proline at amino acid position 94; and a proline at amino acid position 95.
36 . The bispecific antibody of claim 34 , wherein the first and second antibody L chains are identical.
37 . The bispecific antibody of claim 35 , wherein the first and second antibody L chains are identical.
38 . A bispecific antibody comprising a first polypeptide, a second polypeptide, a third polypeptide, and a fourth polypeptide, wherein:
the first polypeptide is an antibody H chain consisting of SEQ ID NO: 18, the second polypeptide is an antibody H chain consisting of SEQ ID NO: 25, and the third and fourth polypeptides are antibody L chains, each consisting of SEQ ID NO: 30.
39 . A pharmaceutical composition comprising the bispecific antibody of claim 30 and a pharmaceutically acceptable carrier.
40 . A pharmaceutical composition comprising the bispecific antibody of claim 31 and a pharmaceutically acceptable carrier.
41 . A pharmaceutical composition comprising the bispecific antibody of claim 32 and a pharmaceutically acceptable carrier.
42 . A pharmaceutical composition comprising the bispecific antibody of claim 33 and a pharmaceutically acceptable carrier.
43 . A pharmaceutical composition comprising the bispecific antibody of claim 34 and a pharmaceutically acceptable carrier.
44 . A pharmaceutical composition comprising the bispecific antibody of claim 35 and a pharmaceutically acceptable carrier.
45 . A pharmaceutical composition comprising the bispecific antibody of claim 36 and a pharmaceutically acceptable carrier.
46 . A pharmaceutical composition comprising the bispecific antibody of claim 38 and a pharmaceutically acceptable carrier.
47 . A kit comprising the bispecific antibody of claim 30 .
48 . A kit comprising the bispecific antibody of claim 31 .
49 . A kit comprising the bispecific antibody of claim 32 .
50 . A kit comprising the bispecific antibody of claim 33 .
51 . A kit comprising the bispecific antibody of claim 34 .
52 . A kit comprising the bispecific antibody of claim 36 .
53 . A kit comprising the bispecific antibody of claim 38 .
54 . A method for treating or reducing the incidence of bleeding, a disease accompanying bleeding, or a disease caused by bleeding in a subject in need thereof, the method comprising administering a therapeutically effective amount of a pharmaceutical composition of claim 39 to the subject.
55 . A method for treating or reducing the incidence of bleeding, a disease accompanying bleeding, or a disease caused by bleeding in a subject in need thereof, the method comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 40 to the subject.
56 . A method for treating or reducing the incidence of bleeding, a disease accompanying bleeding, or a disease caused by bleeding in a subject in need thereof, the method comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 43 to the subject.
57 . A method for treating or reducing the incidence of bleeding, a disease accompanying bleeding, or a disease caused by bleeding in a subject in need thereof, the method comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 44 to the subject.
58 . A method for treating or reducing the incidence of bleeding, a disease accompanying bleeding, or a disease caused by bleeding in a subject in need thereof, the method comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 45 to the subject.
59 . A method for treating or reducing the incidence of bleeding, a disease accompanying bleeding, or a disease caused by bleeding in a subject in need thereof, the method comprising administering a therapeutically effective amount of the pharmaceutical composition of claim 46 to the subject.Join the waitlist — get patent alerts
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