US2020283533A1PendingUtilityA1
Antibody
Est. expiryAug 11, 2035(~9 yrs left)· nominal 20-yr term from priority
G01N 33/57557G01N 33/5758A61K 40/421A61K 40/31A61K 40/11A61K 2239/31A61K 2239/38A61K 2039/505A61P 35/02A61K 2039/5158A61K 2039/5156A61K 39/0011A61K 35/17C12N 5/0636C07K 16/2839G01N 33/577C12N 2510/00C07K 2319/33C07K 2319/03C07K 2317/92C07K 2317/73C07K 2317/622C07K 2317/565C07K 2317/56C07K 2317/34C07K 2317/31C07K 14/7051A61P 35/00C12N 5/10C07K 16/30C12N 15/09C07K 19/00A61K 39/395
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Claims
Abstract
Provided is an active ingredient of a pharmaceutical composition for treating myeloma. Specifically, provided is an antibody whose epitope is present in the region of the amino acid residue positions 20 to 109 of human integrin β7.
Claims
exact text as granted — not AI-modified1 . An anti-human integrin β 7 antibody, whose epitope is present in a region of the amino acid residue positions 20 to 109 of human integrin β 7 .
2 . An antibody according to claim 1 , whose affinity for the epitope is increased in the presence of at least part of a region of the amino acid residue positions 379 to 721 of the human integrin β 7 .
3 . An antibody according to claim 1 or 2 , whose affinity for the epitope is increased through activation of the human integrin β 7 .
4 . An antibody according to any one of claims 1 to 3 , the antibody comprising:
a heavy chain variable region including
heavy-chain CDR1 having the amino acid sequence set forth in SEQ ID NO: 1,
heavy-chain CDR2 having the amino acid sequence set forth in SEQ ID NO: 2, and/or
heavy-chain CDR3 having the amino acid sequence set forth in SEQ ID NO: 3; and/or
a light chain variable region including
light-chain CDR1 having the amino acid sequence set forth in SEQ ID NO: 6,
light-chain CDR2 having the amino acid sequence set forth in SEQ ID NO: 7, and/or
light-chain CDR3 having the amino acid sequence set forth in SEQ ID NO: 8.
5 . An antibody according to any one of claims 1 to 4 , the antibody comprising:
a heavy chain variable region having the amino acid sequence set forth in SEQ ID NO: 4; and/or
a light chain variable region having the amino acid sequence set forth in SEQ ID NO: 9.
6 . An antibody according to any one of claims 1 to 5 , which is a multispecific antibody.
7 . A polynucleotide, which has a base sequence encoding the antibody of any one of claims 1 to 6 .
8 . A host cell, which harbors the polynucleotide of claim 7 .
9 . A chimeric antigen receptor, comprising an antigen recognition site of the antibody of any one of claims 1 to 6 .
10 . A polynucleotide, which encodes the chimeric antigen receptor of claim 9 .
11 . A polynucleotide according to claim 10 , which has the base sequence set forth in SEQ ID NO: 22.
12 . A cell, which harbors the polynucleotide of claim 10 or 11 .
13 . A cell according to claim 12 , which is a chimeric antigen receptor T-cell.
14 . A pharmaceutical composition, comprising the antibody of any one of claims 1 to 6 or the cell of claim 12 .
15 . A pharmaceutical composition, comprising the antibody of any one of claims 1 to 6 or the chimeric antigen receptor T-cell of claim 13 .Join the waitlist — get patent alerts
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