US2020232973A1PendingUtilityA1
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 9/0019A61K 2039/572A61K 47/60A61K 47/6435A61K 47/6883G01N 33/5011A61K 39/39533
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Claims
Abstract
The disclosure provides a method of measuring an efficacy of a drug composition for cancer and a method for treating a cancer by administering to a subject an effective amount of a pharmaceutical composition having a polypeptide that binds to a peptide produced by cDNA of GenBank ACC No. NM_005201.3 or NM_007720.2.
Claims
exact text as granted — not AI-modified1 . A method of measuring an efficacy of a drug composition for cancer in a subject in need thereof, comprising
administering the pharmaceutical composition to the subject; and measuring an ability to stimulate Fc gamma receptors (FcgR) on effector cells in the subject.
2 . The method according to claim 1 , wherein the method treats cancer in the subject.
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 to claim 1 , wherein the cancer is sarcoma.
7 . The method according to claim 1 , wherein the cancer is lung cancer.
8 . A method for treating a cancer in a subject indeed thereof, comprising:
administering to the subject an effective amount of a pharmaceutical composition comprising a polypeptide that binds to a peptide produced by cDNA of GenBank ACC No. NM_005201.3 or NM 007720.2.
9 . The method according to claim 8 , wherein the pharmaceutical composition is administered at a dose of 5 mg to 5000 mg.
10 . The method according to claim 8 , wherein the pharmaceutical composition is administered at a dose of 10 mg to 500 mg.
11 . The method according to claim 8 , wherein the pharmaceutical composition is administered intravenously.Join the waitlist — get patent alerts
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