Claims for Patent: 11,452,725

Summary for Patent: 11,452,725

Title:	Chiral diaryl macrocycles and uses thereof
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.
Inventor(s):	Jingrong J. CUI, Yishan LI, Evan W. ROGERS, Dayong Zhai, Wei Deng, Zhongdong HUANG
Assignee:	Turning Point Therapeutics Inc
Application Number:	US16/998,763
Patent Claims:	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: or a pharmaceutically acceptable salt thereof, wherein the cancer is mediated by a kinase selected from the group consisting of ALK, ROS1, TRKA, TRKB, TRKC, JAK1, JAK2, JAK3, SRC, FYN, LYN, YES, FGR, FAK, and ARK5. 2. The method of claim 1, wherein the cancer is mediated by a genetically altered ALK. 3. The method of claim 1, wherein the cancer is mediated by a fusion protein comprising a fragment of a protein encoded by an ALK gene and a fragment of a protein encoded by a gene selected from the group consisting of NPM, EML4, TPR, TFG, ATIC, CLTC1, TPM4, MSN ALO17 and MYH9. 4. The method of claim 3, wherein the fusion protein is one or more of an EML4-ALK fusion protein, an NPM-ALK fusion protein, or a TPR-ALK fusion protein. 5. The method of claim 1, wherein the cancer is mediated by a genetically altered ROS1. 6. 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. 7. The method of claim 6, wherein the fusion protein is one or more of a CD74-ROS1 fusion protein, a SDC4-ROS1 fusion protein, or a SLC34A2-ROS1 fusion protein. 8. The method of claim 1, wherein the cancer is mediated by a genetically altered TRKA, TRKB or TRKC. 9. The method of claim 8, wherein the genetically altered TRKA is a TPM3-TRKA or LMNA-TRKA fusion protein. 10. The method of claim 1, wherein the cancer is mediated by JAK1, JAK2, or JAK3. 11. The method of claim 10, wherein the JAK2 is a TEL-JAK2 fusion protein or a PCM1-JAK2 fusion protein. 12. The method of claim 1, wherein the cancer is mediated by SRC. 13. A method of treating a cancer in a patient, comprising: (i) identifying a genetically altered kinase selected from the group consisting of ALK, ROS1, TRKA, TRKB, TRKC, JAK1, JAK2, JAK3, SRC, FYN, LYN, YES, FGR, FAK, and ARK5, in the patient, and (ii) administering to the patient a therapeutically effective amount of Compound 1: or a pharmaceutically acceptable salt thereof. 14. The method of claim 13, wherein the cancer is mediated by a genetically altered ALK. 15. The method of claim 13, wherein the cancer is mediated by a fusion protein comprising a fragment of a protein encoded by an ALK gene and a fragment of a protein encoded by a gene selected from the group consisting of NPM, EML4, TPR, TFG, ATIC, CLTC1, TPM4, MSN ALO17 and MYH9. 16. The method of claim 15, wherein the fusion protein is one or more of an EML4-ALK fusion protein, an NPM-ALK fusion protein, or a TPR-ALK fusion protein. 17. The method of claim 13, wherein the cancer is mediated by a genetically altered ROS1. 18. The method of claim 13, 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. 19. The method of claim 18, wherein the fusion protein is one or more of a CD74-ROS1 fusion protein, a SDC4-ROS1 fusion protein, or a SLC34A2-ROS1 fusion protein. 20. The method of claim 13, wherein the cancer is mediated by a genetically altered TRKA, TRKB or TRKC.