Claims for Patent: 11,091,469

Summary for Patent: 11,091,469

Title:	Crystalline form of N-[5-(3,5-difluoro-benzyl)-1H-indazol-3-yl]-4-(4-methyl-piperazin-1-yl)-2-(tetrahydro-pyran-4-ylamino)-benzamide
Abstract:	The present invention relates to a new crystalline form of N-[5-(3,5-difluoro-benzyl)-1H-indazol-3-yl]-4-(4-methyl-piperazin-1-yl)-2-(tetrahydro-pyran-4-ylamino)-benzamide, process for its preparation, its utility in treating diseases caused by deregulated protein kinase activity and pharmaceutical compositions containing it.
Inventor(s):	Ilaria Candiani, Giovanni OTTAIANO, Attilio Tomasi
Assignee:	Nerviano Medical Sciences SRL
Application Number:	US16/912,965
Patent Claims:	1. A method of treating cancer in a mammal comprising: administering to said mammal a therapeutically effective amount of crystalline Form 4 of N-[5-(3,5-difluoro-benzyl)-1H-indazol-3-yl]-4-(4-methyl-piperazin-1-yl)-2-(tetrahydro-pyran-4-ylamino)-benzamide of the following formula (I) wherein said crystalline form is characterized by an X-ray powder diffraction pattern comprising peaks at 2-theta values of about 8.6, 15.6, 17.9, and 21.3±0.2 degrees, wherein the cancer is selected from the group consisting of a sarcoma, lung cancer, salivary gland cancer, breast cancer, thyroid cancer, pancreatic cancer, ovarian cancer, endometrial cancer, cholangiocarcinoma, and neuroblastoma. 2. The method of claim 1, wherein the mammal is a human being. 3. The method of claim 1, wherein said X-ray powder diffraction pattern further comprises the peaks at 2-theta values of about 19.7, 22.1, and 24.3±0.2 degrees. 4. The method of claim 1, wherein said crystalline form is further characterized by exhibiting a peak in a differential scanning calorimetry scan of from about 200° C. to about 205° C. 5. The method of claim 1, wherein said crystalline form is further characterized by a Delta H in the range 70-82 J/g. 6. The method of claim 1, wherein said X-ray powder diffraction pattern further comprises the peaks at 2-theta values of about 19.6 and 22.7±0.2 degrees. 7. The method of claim 6, wherein said X-ray powder diffraction pattern further comprises the peaks at a reflection angle 2-theta of about 10.3, 11.0, 11.9, 14.3, 14.6, 15.1, 15.3, 16.1, 17.1, 19.0, 19.2, 20.1, 20.7, 24.6, 25.3, 25.5, 25.9, 26.7, 26.9, 27.3, 27.7, 28.1, 28.6, 29.0, 29.5, 29.9, 30.5, 31.0, 31.6, 32.2, 33.3, 34.0, 35.4, 36.4, 36.8, and 39.0±0.2 degrees. 8. A method of treating cancer in a mammal having at least one genetic alteration in at least one target gene selected from the group consisting of ROS1, NTRK1, NTRK2 and NTRK3, comprising: administering to said mammal a therapeutically effective amount of crystalline Form 4 of N-[5-(3,5-difluoro-benzyl)-1H-indazol-3-yl]-4-(4-methyl-piperazin-1-yl)-2-(tetrahydro-pyran-4-ylamino)-benzamide of the following formula (I) wherein said crystalline form is characterized by an X-ray powder diffraction pattern comprising peaks at 2-theta values of about 8.6, 15.6, 17.9, and 21.3±0.2 degrees. 9. The method of claim 8, wherein the mammal is a human being. 10. The method of claim 8, wherein said X-ray powder diffraction pattern further comprises the peaks at 2-theta values of about 19.7, 22.1, and 24.3±0.2 degrees. 11. The method of claim 8, wherein said crystalline form is further characterized by exhibiting a peak in a differential scanning calorimetry scan of from about 200° C. to about 205° C. 12. The method of claim 8, wherein said crystalline form is further characterized by a Delta H in the range 70-82 J/g. 13. The method of claim 8, wherein said X-ray powder diffraction pattern further comprises the peaks at 2-theta values of about 19.6 and 22.7±0.2 degrees. 14. The method of claim 13, wherein said X-ray powder diffraction pattern further comprises the peaks at a reflection angle 2-theta of about 10.3, 11.0, 11.9, 14.3, 14.6, 15.1, 15.3, 16.1, 17.1, 19.0, 19.2, 20.1, 20.7, 24.6, 25.3, 25.5, 25.9, 26.7, 26.9, 27.3, 27.7, 28.1, 28.6, 29.0, 29.5, 29.9, 30.5, 31.0, 31.6, 32.2, 33.3, 34.0, 35.4, 36.4, 36.8, and 39.0±0.2 degrees. 15. The method of claim 1, wherein the cancer is selected from the group consisting of a sarcoma, lung cancer, salivary gland cancer, breast cancer, thyroid cancer, and pancreatic cancer. 16. The method of claim 1, wherein the cancer is selected from the group consisting of non-small cell lung cancer, a sarcoma, mammary analog secretory carcinoma (MASC), breast cancer, and thyroid cancer. 17. The method of claim 1, wherein the cancer is selected from the group consisting of non-small cell lung cancer, a sarcoma, and mammary analog secretory carcinoma (MASC). 18. The method of claim 8, wherein said cancer is a non-small cell lung cancer and said at least one target gene is ROS1. 19. The method of claim 8, wherein said cancer is a solid tumor and said at least one target gene is selected from at least one of NTRK1, NTRK2, and NTRK3. 20. The method of claim 8, wherein said cancer is selected from non-small cell lung cancer, papillary thyroid cancer, neuroblastoma, pancreatic cancer and colorectal cancer. 21. The method of claim 20, wherein said cancer is selected from non-small cell lung cancer, neuroblastoma, and colorectal cancer. 22. The method of claim 8, wherein the cancer is selected from the group consisting of a sarcoma, lung cancer, salivary gland cancer, breast cancer, thyroid cancer, colorectal cancer, and pancreatic cancer. 23. The method of claim 8, wherein the cancer is selected from the group consisting of non-small cell lung cancer, a sarcoma, mammary analog secretory carcinoma (MASC), breast cancer, and thyroid cancer. 24. The method of claim 8, wherein the cancer is selected from the group consisting of non-small cell lung cancer, a sarcoma, and mammary analog secretory carcinoma (MASC).