Granted Patent
B2
US 12,310,968 · App. 17/819,858 · Granted May 27, 2025
Chiral diaryl macrocycles and uses thereof
Inventors:
Jingrong J. Cui (Princeton, NJ); Yishan Li (Princeton, NJ); Evan W. Rogers (Princeton, NJ); Dayong Zhai (Princeton, NJ); Wei Deng (Princeton, NJ); Zhongdong Huang (Princeton, NJ)
Assignee:
Turning Point Therapeutics, Inc.
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Abstract
This disclosure relates to the use of certain diaryl macrocycle compounds, specifically (7S13R)-11-fluoro-7,13-di-methyl-6,7,13,14-tetrahydro-1,15-ethenopyrazolo[4,3-f][1,4,8,10]benzoxatriazacyclotridecin-4(5H)-one in the treatment of disease in mammals. This disclosure also relates to compositions including such compounds, and to methods of using such compositions in the treatment of diseases in mammals, especially in humans.
Claims (29)
1. A method of treating a cancer in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of Compound 1:
wherein the cancer is mediated by a ROS1 kinase.
2. The method of claim 1 , wherein the cancer is mediated by a genetically altered ROS1 kinase.
3. The method of claim 1 wherein the cancer is mediated by a fusion protein comprising a fragment of a protein encoded by an ROS1 gene and a fragment of a protein encoded by a gene selected from the group consisting of FIG, TPM3, SDC4, SLC34A2, CD74, EZR, and LRIG3.
4. The method of claim 3 , wherein the fusion protein comprises a fragment of a protein encoded by an ROS1 gene and a fragment of a protein encoded by a CD74 gene.
5. The method of claim 2 , wherein the genetically altered ROS1 kinase is a CD74-ROS1 fusion protein.
6. The method of claim 5 , wherein the CD74-ROS1 fusion protein is a wild-type protein.
7. The method of claim 5 , wherein the CD74-ROS1 fusion protein comprises at least one resistance mutation.
8. The method of claim 5 , wherein the CD74-ROS1 fusion protein comprises a G2032R, L2026M or D2033N point mutation.
9. The method of claim 2 , wherein the genetically altered ROS1 kinase is a SDC4-ROS1 fusion protein.
10. The method of claim 9 , wherein the SDC4-ROS1 fusion protein is a wild-type protein.
11. The method of claim 9 , wherein the SDC4-ROS1 fusion protein comprises at least one resistance mutation.
12. The method of claim 9 , wherein the SDC4-ROS1 fusion protein comprises a G2032R point mutation.
13. The method of claim 2 , wherein the genetically altered ROS1 kinase is a SLC34A2-ROS1 fusion protein.
14. The method of claim 13 , wherein the SLC34A2-ROS1 fusion protein is a wild-type protein.
15. The method of claim 13 , wherein the SLC34A2-ROS1 fusion protein comprises at least one resistance mutation.
16. The method of claim 13 , wherein the SLC34A2-ROS1 fusion protein comprises a G2032R point mutation.
17. The method of claim 1 , wherein the cancer is selected from the group consisting of glioblastoma, glioblastoma multiforme, non-small cell lung cancer (NSCLC), cholangiocarcinoma, ovarian cancer, gastric adenocarcinoma, colorectal cancer, inflammatory myofibroblastic tumor, angiosarcoma, and epithelioid hemangioendothelioma.
18. The method of claim 1 , wherein the cancer is non-small cell lung cancer (NSCLC).
19. The method of claim 1 , wherein the patient has been previously treated with a cancer therapeutic.
20. The method of claim 19 , wherein the cancer has developed resistance to the cancer therapeutic.
21. The method of claim 1 , wherein the therapeutically effective amount of Compound 1 comprises about 250 mg to 1 g daily.
22. The method of claim 1 , wherein the therapeutically effective amount of Compound 1 comprises about 50 to 250 mg daily.
23. The method of claim 1 , wherein the patient was previously identified as having a cancer mediated by a ROS1 kinase through fluorescence in situ hybridization (FISH), polymerase chain reaction (PCR), or next generation sequencing.
24. The method of claim 1 , wherein the administering comprises oral administration.
25. The method of claim 1 , comprising administering the therapeutically effective amount of Compound 1 once daily.
26. The method of claim 1 , comprising administering the therapeutically effective amount of Compound 1 twice daily.
27. A method of treating a non-small cell lung cancer (NSCLC) in a patient in need thereof, comprising orally administering to the patient a therapeutically effective amount of Compound 1:
wherein the NSCLC is mediated by a ROS1 kinase.
Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST
Recorded Aug 10, 2023
From: CUI, JINGRONG JEAN; LI, YISHAN; ROGERS, EVAN W.; ZHAI, DAYONG; DENG, WEI; HUANG, ZHONGDONG
To: TP THERAPEUTICS, INC.
Reel/Frame 064549/0748 →
CHANGE OF NAME
Recorded Aug 10, 2023
From: TP THERAPEUTICS, INC.
To: TURNING POINT THERAPEUTICS, INC.
Reel/Frame 064557/0657 →
Continuity (5)
Continuation
15745915
Provisional Application
62302231
· Mar 2, 2016
Provisional Application
62195081
· Jul 21, 2015
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