US2021163618A1PendingUtilityA1
Chimeric canine anti-cd20 antibody
Est. expiryFeb 18, 2036(~9.6 yrs left)· nominal 20-yr term from priority
Inventors:James David Pancook
G01N 33/53A61K 39/00C07K 16/1271C07K 16/2887C07K 2317/24A61K 2039/505C07K 2317/31C07K 16/2809A61P 35/00C07K 2317/33A61K 39/395
72
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Claims
Abstract
The disclosure relates to caninized chimeric anti-CD20 antibodies to the canine protein CD20 and methods of use to treat certain disorders such as non-Hodgkins B-cell lymphoma in dogs.
Claims
exact text as granted — not AI-modifiedWe claim:
1 . An antibody comprising a light chain variable region (LCVR) whose amino acid sequence is that given in SEQ :ID NO: 12, and a heavy chain variable region (HCVR) whose amino acid sequence is that given in SEQ ID NO: 3.
2 . The antibody of claim 1 , wherein the antibody specifically binds to canine CD20.
3 . An antibody comprising a light chain (LC) whose amino acid sequence is that given in SEQ ID No: 10, and a heavy chain (HC) whose amino acid sequence is that given in SEQ ID NO: 1.
4 . The antibody of claim 3 , wherein the antibody specifically binds to canine CD20.
5 . An antibody comprising two light chains (LC) each having an amino acid sequence that is given in SEQ ID NO: 10, and two heavy chains (HC) each having an amino acid sequence that is given in SEQ ID NO: 1.
6 . The antibody of claim 5 , wherein the antibody specifically binds to canine CD20.
7 . A method of treating lymphoma in a canine patient, comprising administering to a lymphoma cancer canine patient in need of such treatment an effective amount of an antibody comprising a light chain variable region (LCVR) whose amino acid sequence is that given in SEQ ID NO: 12, and a heavy chain variable region (HCVR) whose amino acid sequence is that given in SEQ ID NO: 3, wherein the antibody specifically binds to canine CD20.
8 . The method according to claim 7 wherein the antibody comprises a light chain (LC) whose amino acid sequence is that given in SEQ ID NO: 10, and a heavy chain (HC) whose amino acid sequence is that given in SEQ ID NO: 1.
9 . The method according to claim 7 , wherein the antibody is K9LO-133.
10 . A kit, comprising a pharmaceutical composition, comprising K9LO-133, with one or more pharmaceutically acceptable carriers, diluents, or excipients.
11 . An antibody comprising a light chain (LC) whose amino acid sequence is that given in SEQ ID NO: 10, and a heavy chain (HC) whose amino acid sequence is that given in SEQ :11) NO: 1 and wherein the antibody specifically binds to canine CD20, and wherein the antibody binds to protein A.
12 . Use of an antibody comprising a light chain variable region (LCVR) whose amino acid sequence is that given in SEQ ID NO: 12, and a heavy chain variable region (HCVR) whose amino acid sequence is that given in SEQ ID NO: 3, wherein the antibody specifically binds to canine CD20, for treating lymphoma in a canine patient.
13 . The use according to claim 12 wherein the antibody comprises a light chain (LC) whose amino acid sequence is that given in SEQ ID NC): 10, and a heavy chain (HC) whose amino acid sequence is that given in SEQ ID NO: 1.
14 . The use according to claim 12 , wherein the antibody is K9LO-133.
15 . An antibody comprising a light chain variable region (LCVR) whose amino acid sequence is that given in SEQ ID NO: 12, and a heavy chain variable region (HCVR) whose amino acid sequence is that given in SEQ ID NO: 3, wherein the antibody specifically binds to canine CD20, for use in treating lymphoma in a canine patient.Join the waitlist — get patent alerts
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