US2020222463A1PendingUtilityA1
Pharmaceutical Composition for Cancer Treatment
Est. expiryMar 29, 2037(~10.7 yrs left)· nominal 20-yr term from priority
Inventors:Tetsuya YoshidaYujiro KidaniMitsunobu MatsumotoTakayuki KanazawaSatomi ShinonomeKanji HojoNaganari OhkuraShimon SakaguchiAtsushi TanakaHisashi WadaAtsunari KawashimaNorio Nonomura
A61K 35/17C07K 2317/76C07K 2317/732C07K 16/2866C07K 16/2827C07K 16/2818A61K 2039/507A61P 35/00A61K 2039/505A61K 47/6435A61K 47/6883A61K 9/0019G01N 33/5011A61K 47/60A61K 2039/572A61K 39/39533
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Claims
Abstract
The disclosure provides a pharmaceutical composition with a polypeptide that binds to a peptide produced by cDNA of GenBank ACC No. NM_005201.3 or NM_007720.2, and methods of use thereof.
Claims
exact text as granted — not AI-modified1 . A method of treating cancer in a subject in need thereof, comprising
administering to the subject a therapeutically effective amount of a pharmaceutical composition comprising an antibody against CCR8.
2 . (canceled)
3 . The method according to claim 1 , wherein the cancer is breast cancer.
4 . The method according to claim 1 , wherein the cancer is colorectal cancer.
5 . The method according to claim 1 , wherein the cancer is kidney cancer.
6 . The method according claim 1 , wherein the cancer is sarcoma.
7 . The method according to claim 1 , wherein the cancer is lung cancer.
8 - 10 . (canceled)
11 . The method according to claim 1 , wherein the antibody is an IgG antibody.
12 . The method according to claim 1 , wherein the antibody against CCR8 is a CCR8-neutralizing antibody.
13 . The method according to claim 1 , wherein the therapeutically effective amount is at a dose of 5 mg to 5000 mg.
14 . The method according to claim 1 , wherein the therapeutically effective amount is at a dose of 10 mg to 500 mg.
15 . The method according to claim 1 , wherein the antibody is administered intravenously.
16 . The method according to claim 1 , wherein the antibody is administered intraperitoneally.
17 . The method according to claim 1 , wherein the antibody has antibody-dependent cell-mediated cytotoxicity (ADCC) activity against cells expressing CCR8.
18 . The method according to claim 1 , wherein in the administering step, the only antibody administered is the antibody against CCR8.
19 . The method according to claim 1 , wherein an Fc region of the antibody against CCR8 is free from a fucose bond with N-acetylglucosamine.
20 . The method according to claim 1 , further comprising administering an anti-PD-1 antibody or an anti-PD-L1 antibody.
21 . The method according to claim 1 , wherein the method further comprises administering at least one antibody selected from the group consisting of nivolumab, pembrolizumab, atezolizumab, avelumab, and durvalumab.Join the waitlist — get patent alerts
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