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Last Updated: April 27, 2024

Claims for Patent: 8,536,200


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Summary for Patent: 8,536,200
Title:Pyridinone compounds
Abstract: The invention is directed to pyridinone compounds useful for modulating Met kinase, having the following structure: ##STR00001## and is further directed to pharmaceutical compositions comprising the compound; and methods for treating proliferative diseases, such as cancer by the administration of this compound.
Inventor(s): Borzilleri; Robert M. (New Hope, PA), Schroeder; Gretchen M. (Ewing, NJ), Cai; Zhen-Wei (Belle Mead, NJ)
Assignee: Bristol-Myers Squibb Company (Princeton, NJ)
Application Number:12/941,419
Patent Claims:1. A method of treating cancer in a patient in need of such treatment, comprising administering to the patient a therapeutically effective amount of Compound of Formula I: ##STR00014## or a salt thereof.

2. The method of claim 1 wherein said cancer is selected from bladder cancer, breast cancer, colorectal cancer, gastric cancer, head and neck cancer, kidney cancer, liver cancer, lung cancer, ovarian cancer, pancreas/gall bladder cancer, prostate cancer, thyroid cancer, osteosarcoma, rhabdomyosarcoma, MFH/fibrosarcoma, glioblastomas/astrocytomas, melanoma, and mesothelioma.

3. The method of claim 2 wherein said cancer is selected from bladder cancer, breast cancer, colorectal cancer, gastric cancer, head and neck cancer, kidney cancer, liver cancer, lung cancer, ovarian cancer, pancreas/gall bladder cancer, prostate cancer, and thyroid cancer.

4. The method according to claim 2 wherein said patient is a human.

5. The method according to claim 1, further comprising administering an additional anticancer agent.

6. The method according to claim 5 wherein said other anticancer agent is selected from gefitinib, erlotinib, and cetuximab.

7. The method according to claim 1, further comprising administering radiation therapy.

8. The method according to claim 1, wherein said cancer is dependent upon Met activation, wherein the Met activation is regulated by gene amplification, an activated Met mutation and/or HGF stimulation.

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