IP Library Granted Patent US 10,105,369
Granted Patent B2
US 10,105,369 · App. 15/864,994 · Granted Oct 23, 2018

Therapeutically active compounds and their methods of use

Inventor: Samuel V. Agresta (Lexington, MA)
Assignee: Agios Pharmaceuticals, Inc.
A61K31/53A61K9/0053A61K31/185
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Quick Facts
Patent No.
US 10,105,369
App. No.
15/864,994
Granted
Oct 23, 2018
Kind
B2
Abstract

Provided are compounds useful for treating cancer and methods of treating cancer, for example an advanced solid tumor, such as a glioma, or angioimmunoblastic T-cell lymphoma (AITL).

Claims (104)

1. A method of treating a solid tumor characterized by the presence of a mutant allele of isocitrate dehydrogenase 2 (IDH2) comprising administering to a subject a therapeutically effective dose of a crystalline form of 2-methyl-1-[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl] amino}-1,3,5-triazin-2-yl)amino]propan-2-ol, wherein the crystalline form is selected from

a) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.8, 10.6, 13.6, 14.2, and 19.2°±0.2°,

b) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 8.9, 13.0, 18.9, 23.8, and 28.1°±0.2°,

c) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 12.7, 17.1, 19.2, 23.0, and 24.2°±0.2°,

d) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 7.2, 13.6, 18.5, 19.3, 21.9, and 23.5°±0.2°,

e) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.4, 8.4, 9.8, 17.8, and 19.7°±0.2°, and

f) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 8.1, 14.1, 16.4, 17.3, 20.5, and 24.1°±0.2°,

wherein the therapeutically effective dose is from about 30 mg to about 300 mg.

2. The method of claim 1 , wherein the crystalline form is selected from

a) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 1 ,

b) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 2 ,

c) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 34 ,

d) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 37 ,

e) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 38 , and

f) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 39 .

3. The method of claim 1 , wherein the solid tumor is brain tumor, melanoma, chondrosarcoma, or cholangiocarcinoma.

4. The method of claim 3 , wherein the brain tumor is glioma.

5. The method of claim 3 , wherein the brain tumor is glioblastoma multiforme.

6. The method of claim 3 , wherein the brain tumor is astrocytic tumor, oligodendroglial tumor, oligoastrocytic tumor, ependymoma, medulloblastoma; primitive neuroectodermal tumor, schwannoma, meningioma, meatypical meningioma, anaplastic meningioma; or pituitary adenoma.

7. The method of claim 1 , wherein the crystalline form of 2-methyl-1-[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl] amino}-1,3,5-triazin-2-yl)amino]propan-2-ol is administered orally.

8. The method of claim 7 , wherein the therapeutically effective dose is about 30 mg, or about 50 mg, or about 75 mg, or about 100 mg, or about 125 mg, or about 150 mg, or about 175 mg, or about 200 mg, or about 225 mg, or about 250 mg or about 275 mg, or about 300 mg.

9. A method of treating a solid tumor characterized by the presence of a mutant allele of isocitrate dehydrogenase 2 (IDH2) comprising administering to a subject a therapeutically effective dose of the crystalline form of 2-methyl-1-[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl] amino}-1,3,5-triazin-2-yl)amino]propan-2-ol methanesulfonate, wherein the crystalline form is selected from

a) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 7.5, 9.3, 14.5, 18.8, 21.3, and 24.8°±0.2°,

b) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.5, 19.0, 19.4, 19.9, and 24.7°±0.2°,

c) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 7.1, 14.5, 17.1, and 21.8°±0.2°,

d) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.3, 7.2, 8.1, 12.7, and 14.9°±0.2°,

e) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 14.1, 19.1, 21.8, 23.5, and 25.7°±0.2°,

f) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 9.0, 9.2, 21.9, 22.1, 24.2, and 24.6°±0.2°,

g) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.5, 19.6, 20.1, and 21.6°±0.2°,

h) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.7, 9.1, 10.8, 19.9, and 21.9°±0.2°,

i) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.3, 20.0, 20.2, 20.5, 21.2, and 26.5°±0.2°,

j) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 7.2, 7.4, 8.0, 8.2, 16.5, and 18.6°±0.2°,

k) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.3, 12.7, 20.3, 20.8, and 26.5°±0.2°,

l) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.6, 17.5, 20.8 and 23.3°±0.2°, and

m) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.4, 12.9, 20.2, and 26.1°±0.2°,

wherein the therapeutically effective dose is from about 30 mg to about 300 mg.

10. The method of claim 9 , wherein the crystalline form is selected from

a) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 5 ,

b) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 9 ,

c) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 11 ,

d) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 13 ,

e) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 15 ,

f) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 17 ,

g) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 19 ,

h) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 21 ,

i) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 23 ,

j) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 26 ,

k) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 28 ,

l) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 30 , and

m) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 32 .

11. The method of claim 9 , wherein the solid tumor is brain tumor, melanoma, chondrosarcoma, or cholangiocarcinoma.

12. The method of claim 11 , wherein the brain tumor is glioma.

13. The method of claim 11 , wherein the brain tumor is glioblastoma multiforme.

14. The method of claim 11 , wherein the brain tumor is astrocytic tumor, oligodendroglial tumor, oligoastrocytic tumor, ependymoma, medulloblastoma; primitive neuroectodermal tumor, schwannoma, meningioma, meatypical meningioma, anaplastic meningioma; or pituitary adenoma.

15. The method of claim 9 , wherein the crystalline form of 2-methyl-1-[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl] amino}-1,3,5-triazin-2-yl)amino]propan-2-ol is administered orally.

16. The method of claim 15 , wherein the therapeutically effective dose is about 30 mg, or about 50 mg, or about 75 mg, or about 100 mg, or about 125 mg, or about 150 mg, or about 175 mg, or about 200 mg, or about 225 mg, or about 250 mg or about 275 mg, or about 300 mg.

17. A method of treating angioimmunoblastic T-cell lymphoma (AITL) characterized by the presence of a mutant allele of isocitrate dehydrogenase 2 (IDH2) comprising administering to a subject a therapeutically effective dose of the crystalline form of 2-methyl-1-[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl] amino}-1,3,5-triazin-2-yl)amino]propan-2-ol, wherein the crystalline form is selected from

a) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.8, 10.6, 13.6, 14.2, and 19.2°±0.2°,

b) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 8.9, 13.0, 18.9, 23.8, and 28.1°±0.2°,

c) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 12.7, 17.1, 19.2, 23.0, and 24.2°±0.2°,

d) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 7.2, 13.6, 18.5, 19.3, 21.9, and 23.5°±0.2°,

e) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.4, 8.4, 9.8, 17.8, and 19.7°±0.2°, and

f) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 8.1, 14.1, 16.4, 17.3, 20.5, and 24.1°±0.2°,

wherein the therapeutically effective dose is from about 30 mg to about 300 mg.

18. The method of claim 17 , wherein the crystalline form is selected from

a) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 1 ,

b) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 2 ,

c) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 34 ,

d) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 37 ,

e) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 38 , and

f) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 39 .

19. The method of claim 17 , wherein the crystalline form of 2-methyl-1-[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl] amino}-1,3,5-triazin-2-yl)amino]propan-2-ol is administered orally.

20. The method of claim 19 , wherein the therapeutically effective dose is about 30 mg, or about 50 mg, or about 75 mg, or about 100 mg, or about 125 mg, or about 150 mg, or about 175 mg, or about 200 mg, or about 225 mg, or about 250 mg or about 275 mg, or about 300 mg.

21. A method of treating angioimmunoblastic T-cell lymphoma (AITL) characterized by the presence of a mutant allele of isocitrate dehydrogenase 2 (IDH2) comprising administering to a subject a therapeutically effective dose of the crystalline form of 2-methyl-1-[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl] amino}-1,3,5-triazin-2-yl)amino]propan-2-ol methanesulfonate, wherein the crystalline form is selected from

a) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 7.5, 9.3, 14.5, 18.8, 21.3, and 24.8°±0.2°,

b) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.5, 19.0, 19.4, 19.9, and 24.7°±0.2°,

c) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 7.1, 14.5, 17.1, and 21.8°±0.2°,

d) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.3, 7.2, 8.1, 12.7, and 14.9°±0.2°,

e) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 14.1, 19.1, 21.8, 23.5, and 25.7°±0.2°,

f) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 9.0, 9.2, 21.9, 22.1, 24.2, and 24.6°±0.2°,

g) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.5, 19.6, 20.1, and 21.6°±0.2°,

h) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.7, 9.1, 10.8, 19.9, and 21.9°±0.2°,

i) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.3, 20.0, 20.2, 20.5, 21.2, and 26.5°±0.2°,

j) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 7.2, 7.4, 8.0, 8.2, 16.5, and 18.6°±0.2°,

k) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.3, 12.7, 20.3, 20.8, and 26.5°±0.2°,

l) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.6, 17.5, 20.8 and 23.3°±0.2°, and

m) the crystalline form characterized by an X-ray powder diffraction pattern having peaks at 2θ angles of 6.4, 12.9, 20.2, and 26.1°±0.2°,

wherein the therapeutically effective dose is from about 30 mg to about 300 mg.

22. The method of claim 21 , wherein the crystalline form is selected from

a) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 5 ,

b) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 9 ,

c) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 11 ,

d) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 13 ,

e) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 15 ,

f) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 17 ,

g) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 19 ,

h) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 21 ,

i) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 23 ,

j) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 26 ,

k) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 28 ,

l) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 30 , and

m) the crystalline form characterized by an X-ray powder diffraction pattern substantially similar to FIG. 32 .

23. The method of claim 21 , wherein the crystalline form of 2-methyl-1-[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl] amino}-1,3,5-triazin-2-yl)amino]propan-2-ol is administered orally.

24. The method of claim 23 , wherein the therapeutically effective dose is about 30 mg, or about 50 mg, or about 75 mg, or about 100 mg, or about 125 mg, or about 150 mg, or about 175 mg, or about 200 mg, or about 225 mg, or about 250 mg or about 275 mg, or about 300 mg.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE THE ASSIGNEE NAME AND THE POSTAL CODE PREVIOUSLY RECORDED AT REEL: 056756 FRAME: 0459. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Mar 16, 2022
From: AGIOS PHARMACEUTICALS, INC.
To: SERVIER PHARMACEUTICALS LLC
Reel/Frame 059907/0429 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2021
From: AGIOS PHARMACEUTICALS, INC.
To: SERVIER PHARMACEUTICALS, LLC
Reel/Frame 056756/0459 →
Continuity (4)
Continuation 15612984 · Jun 2, 2017
Continuation 14868283 · Sep 28, 2015
Provisional Application 62056996 · Sep 29, 2014
Related Publication 20180125850A1 · May 10, 2018