Substituted tricyclic compounds as FGFR inhibitors

US10131667B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-10131667-B2
Application numberUS-201715408768-A
CountryUS
Kind codeB2
Filing dateJan 18, 2017
Priority dateJun 13, 2012
Publication dateNov 20, 2018
Grant dateNov 20, 2018

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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Abstract

Official abstract text for this publication.

The present invention relates to tricyclic compounds, and pharmaceutical compositions of the same, that are inhibitors of one or more FGFR enzymes and are useful in the treatment of FGFR-associated diseases such as cancer.

First claim

Opening claim text (preview).

What is claimed is: 1. A method of treating cancer in a patient comprising administering to said patient a therapeutically effective amount of 3-(2,6-difluoro-3,5-dimethoxyphenyl)-1-ethyl-8-(morpholin-4-ylmethyl)-1,3,4,7-tetrahydro-2H-pyrrolo[3′,2′:5,6]pyrido[4,3-d]pyrimidin-2-one, or a pharmaceutically acceptable salt thereof, wherein said cancer is selected from bladder cancer, breast cancer, endometrial cancer, gastric cancer, lung cancer, non-small cell lung cancer, adenocarcinoma, multiple myeloma, myeloproliferative neoplasms (MPN), esophageal cancer, head and neck cancer, glioblastoma, ovarian cancer, cervical cancer and liver cancer. 2. The method of claim 1 , wherein the cancer is bladder cancer. 3. The method of claim 1 , wherein the cancer is breast cancer. 4. The method of claim 1 , wherein the cancer is endometrial cancer. 5. The method of claim 1 , wherein the cancer is gastric cancer. 6. The method of claim 1 , wherein the cancer is lung cancer. 7. The method of claim 1 , wherein the cancer is non-small cell lung cancer. 8. The method of claim 1 , wherein the cancer is adenocarcinoma. 9. The method of claim 1 , wherein the cancer is myeloproliferative neoplasms (MPN). 10. The method of claim 1 , wherein the cancer is multiple myeloma. 11. The method of claim 1 , wherein the cancer is esophageal cancer. 12. The method of claim 1 , wherein the cancer is head and neck cancer. 13. The method of claim 1 , wherein the cancer is glioblastoma. 14. The method of claim 1 , wherein the cancer is ovarian cancer. 15. The method of claim 1 , wherein the cancer is cervical cancer. 16. The method of claim 1 , wherein the cancer is liver cancer.

Assignees

Inventors

Classifications

  • Spiro-condensed systems · CPC title

  • C07D471/14Primary

    Ortho-condensed systems · CPC title

  • Ortho-condensed systems · CPC title

  • in which the condensed systems contains four or more hetero rings · CPC title

  • in which the condensed system contains four or more hetero rings · CPC title

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Frequently asked questions

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What does patent US10131667B2 cover?
The present invention relates to tricyclic compounds, and pharmaceutical compositions of the same, that are inhibitors of one or more FGFR enzymes and are useful in the treatment of FGFR-associated diseases such as cancer.
Who is the assignee on this patent?
Incyte Corp, Incyte Holdings Corp
What technology area does this patent fall under?
Primary CPC classification C07D471/14. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Tue Nov 20 2018 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 12 related publications on this page (citations in our corpus or others sharing the same primary CPC).