US2012039885A1PendingUtilityA1
Composition and method for cancer treatment
Est. expiryMar 27, 2024(expired)· nominal 20-yr term from priority
Inventors:Daruka Mahadevan
A61K 2039/505C07K 2317/56C07K 2317/565C07K 2317/622C07K 2317/24G01N 2333/70596C07K 16/2803A61P 43/00A61P 35/00G01N 33/57565
52
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Claims
Abstract
Anti-CEACAM6 antibodies and antibody fragments, nucleic acids encoding them, methods of their manufacture, and methods to treat cancer using these compounds are provided.
Claims
exact text as granted — not AI-modified1 - 54 . (canceled)
55 . A method of treating brain cancer, prostate cancer, liver cancer, and/or kidney cancer, comprising administering an effective amount of an anti-CEACAM6 antibody or antibody fragment thereof comprising all six of the CDRs of monoclonal antibody 13.1 to a patient with brain cancer, prostate cancer, liver cancer, and/or kidney cancer, wherein the antibody or antibody fragment induces apoptosis in cancer cells.
56 . The method of claim 55 , wherein the antibody or antibody fragment thereof induces apoptosis against cancer cells in the Cellular Cytotoxicity Assay described herein.
57 . The method of claim 55 , which is a method of treating brain cancer.
58 . The method of claim 55 , which is a method of treating prostate cancer.
59 . The method of claim 55 , which is a method of treating liver cancer.
60 . The method of claim 55 , which is a method of treating lung cancer.
61 . The method of claim 55 , wherein the antibody or antibody fragment thereof is humanized.
62 . The method of claim 55 , wherein the antibody or antibody fragment thereof is chimeric.
63 . The method of claim 55 , wherein said antibody or antibody fragment thereof is an antibody fragment, and the antibody fragment is an ScFv.
64 . The method of claim 63 , wherein the ScFv is murine or humanized.
65 . The method of claim 55 , wherein the patient is a human or a non-human animal.
66 . The method of claim 55 , wherein the patient is a human.
67 . The method of claim 66 , wherein the antibody or antibody fragment thereof is administered parenterally, intraperitoneally, intravenously, subcutaneously, orally, nasally, via inhalation or rectally.
68 . The method of claim 55 , wherein the antibody or antibody fragment thereof is administered intravenously at a dosage of from 5 mg/m 2 to 2000 mg/m 2 .
69 . The method of claim 55 , wherein the antibody or antibody fragment thereof is monoclonal antibody 13.1.Cited by (0)
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