Crystalline forms of 5-chloro-N4-[-2-(dimethylphosphoryl) phenyl]-N2-{2-methoxy-4-[4-(4-methylpiperazin-1-yl) piperidin-1-yl] phenyl} pyrimidine-2,4-diamine
Crystalline forms of brigatinib, pharmaceutical compositions comprising the same, and methods of their preparation and use of the same are disclosed herein.
1. Crystalline Form B of brigatinib having the structure:
wherein the crystalline form has an x-ray powder diffraction pattern with peaks at 11.5, 14.5, 16.9, 19.2, and 23.2° 2θ, with a variance of ±0.2° 2θ.
2. The crystalline form of claim 1 , having an x-ray powder diffraction pattern as shown in FIG. 14 .
3. The crystalline form of claim 1 , having an x-ray powder diffraction pattern with peaks at 5.7, 9.2, 11.5, 12.8, 14.5, 15.5, 16.9, 17.7, 19.2, 20.4, 21.8, 23.2, and 29.5° 2θ, with a variance of 0.2° 2θ.
4. Crystalline Form C of brigatinib having the structure:
wherein the crystalline form has an x-ray powder diffraction pattern with peaks at 5.4, 14.9, 15.9, 17.3, 19.2, and 23.9° 2θ, with a variance of 0.2° 2θ.
5. Crystalline Form D of brigatinib having the structure:
wherein the crystalline form has an x-ray powder diffraction pattern with peaks at 9.7, 11.1, 17.4, 18.9, and 23.7° 2θ, with a variance of 0.2° 2θ.
6. Crystalline Form E of brigatinib having the structure:
which is a chloroform solvate,
wherein the crystalline form has an x-ray powder diffraction pattern with peaks at 9.1, 10.2, 15.8, 19.2, and 23.9° 2θ, with a variance of 0.2° 2θ.
7. Crystalline Form F of brigatinib having the structure:
which is a TFE solvate,
wherein the crystalline form has an x-ray powder diffraction pattern with peaks at 9.8, 17.0, 19.4, 20.3, and 27.1° 2θ, with a variance of 0.2° 2θ.
8. Crystalline Form G of brigatinib having the structure:
which is a chloroform solvate,
wherein the crystalline form has an x-ray powder diffraction pattern with peaks at 8.3, 9.7, 12.9, 15.8, 18.1, 20.7, 22.8, and 26.8° 2θ, with a variance of 0.2° 2θ.
9. A pharmaceutical composition comprising the Crystalline Form B of brigatinib of claim 1 and at least one component chosen from pharmaceutically acceptable carriers, pharmaceutically acceptable vehicles, and pharmaceutically acceptable excipients.
10. A method for treating non-small cell lung cancer in a subject in need thereof comprising administering to the subject the Crystalline Form B of brigatinib of claim 1 .
11. The method of claim 10 , wherein the non-small cell lung cancer is ALK-positive non-small cell lung cancer.
12. The method of claim 11 , wherein the non-small cell lung cancer is ALK-positive metastatic non-small cell lung cancer.
13. The method of claim 12 , wherein the subject has been previously treated with crizotinib.