Hydrochloride salt of((1S,2S,4R)-4-{4-[(1S)-2,3-dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-D]pyrimidin-7-YL}-2-hydroxycyclopentyl) methyl sulfamate
View Patent ↗Disclosed is a compound of formula (I): crystalline forms thereof, and solvates thereof; pharmaceutical compositions comprising a pharmaceutically effective amount of the compound of formula (I), or a crystalline form thereof, or a solvate thereof, and a pharmaceutically acceptable carrier or diluent; and the use of a compound of formula (I), or a crystalline form thereof, or a solvate thereof, for treating a patient suffering from, or subject to, a pathological condition capable of being ameliorated by inhibiting an E1 activating enzyme, particularly NAE, including, e.g., cancer.
1. A method for treating cancer, comprising:
administering, to a patient having cancer or experiencing a recurrence of a cancer, a therapeutically effective amount of a liquid suspension or solution formed by mixing the compound ((1S,2S,4R)-4-{4-[(1S)-2,3-dihydro-1H-inden-1-ylamino]-7H-pyrrolo[2,3-d]pyrimidin-7-yl}-2-hydroxycyclopentyl) methyl sulfamate hydrochloride in at least one crystalline form chosen from Form 1, Form 2, Form 3A, Form 3B, Form 3C, Form 5, and Form 7, a cyclodextrin, and a liquid,
wherein the cancer is selected from acute myeloid leukemia (AML); myelodysplastic syndromes (MDS); chronic myelogenous leukemia (CML); acute lymphoblastic leukemia (ALL); chronic lymphocytic leukemia (CLL); Hodgkin's disease (HD); non-Hodgkin's lymphoma (NHL); B-cell lymphoma; T-cell lymphoma; multiple myeloma (MM); Waldenstrom's macroglobulinemia; myeloproliferative syndrome; colorectal cancer; ovarian cancer; lung cancer; pancreatic cancer; bladder cancer; breast cancer, prostate cancer; renal cancer; hepatocellular cancer; cervical cancer; gastric cancer; esophageal cancer; head and neck cancer; melanoma, neuroendocrine cancer, a brain tumor; bone cancer; and soft tissue sarcoma.
2. The method of claim 1 , wherein the cancer is selected from acute myeloid leukemia (AML); myelodysplastic syndromes (MDS); chronic myelogenous leukemia (CML); acute lymphoblastic leukemia (ALL); chronic lymphocytic leukemia (CLL); Hodgkin's disease (HD); non-Hodgkin's lymphoma (NHL); B-cell lymphoma; T-cell lymphoma; multiple myeloma (MM); Waldenstrom's macroglobulinemia; and myeloproliferative syndrome.
3. The method of claim 2 , wherein the cancer is acute myeloid leukemia (AML).
4. The method of claim 2 , wherein the cancer is a myelodysplastic syndrome (MDS).
5. The method of claim 2 , wherein the cancer is acute lymphoblastic leukemia (ALL).
6. The method of claim 1 , wherein the cancer is selected from colorectal cancer; ovarian cancer; lung cancer; pancreatic cancer; bladder cancer; breast cancer; prostate cancer; renal cancer; hepatocellular cancer; cervical cancer; gastric cancer; esophageal cancer; head and neck cancer; melanoma; neuroendocrine cancer; a brain tumor; bone cancer; and soft tissue sarcoma.
7. The method of claim 6 , wherein the cancer is selected from colorectal cancer, ovarian cancer, lung cancer, pancreatic cancer, breast cancer, and prostate cancer.
8. The method of claim 1 , wherein the compound is substantially Form 1.
9. The method of claim 8 , wherein Form 1 is characterized by an XRPD pattern having peaks at 2θ angles of 9.6°, 13.6° and 19.1°, wherein each 2θ angle value is ±0.2°.
10. The method of claim 8 , wherein Form 1 is characterized by an XRPD pattern having peaks at 2θ angles of 9.6°, 13.6°, 14.5°, 19.1° and 23.7°, wherein each 2θ angle value is ±0.2°.
11. The method of claim 8 , wherein Form 1 is characterized by at least two of (I-i)-(I-iv):
(I-i) an XRPD pattern having peaks at 2θ angles of 9.6°, 13.6° and 19.1°, wherein each 2θ angle value is ±0.2°;
(I-ii) a DSC profile substantially as shown in FIG. 2 ;
(I-iii) a TGA profile substantially as shown in FIG. 3 ; or
(I-iv) a solubility of about 7.8 mg/mL in water.
12. The method of claim 1 , wherein the compound is substantially Form 2 characterized by an XRPD pattern having peaks at 2θ angles of 8.7°, 18.2° and 23.8°, wherein each 2θ angle value is ±0.2°.
13. The method of claim 1 , wherein the compound is substantially Form 3A characterized by an XRPD pattern having peaks at 2θ angles of 10.9°, 14.6°, 19.5° and 24.0°, wherein each 2θ angle value is ±0.2°.
14. The method of claim 1 , wherein the compound is substantially Form 3B characterized by an XRPD pattern having peaks at 2θ angles of 10.8°, 16.9°, 23.7° and 24.0°, wherein each 2θ angle value is ±0.2°.
15. The method of claim 1 , wherein the compound is substantially Form 3C characterized by an XRPD pattern having peaks at 2θ angles of 11.0°, 12.2° and 24.4°, wherein each 2θ angle value is ±0.2°.
16. The method of claim 1 , wherein the compound is substantially Form 5 characterized by an XRPD pattern having peaks at 2θ angles of 16.7° and 22.9°, wherein each 2θ angle value is ±0.2°.
17. The method of claim 1 , wherein the compound is substantially Form 7 characterized by an XRPD pattern having peaks at 2θ angles of 15.4°, 17.3°, 19.6° and 22.5°, wherein each 2θ angle value is ±0.2°.
18. The method of claim 1 , wherein the cyclodextrin is hydroxypropyl beta-cyclodextrin.
19. The method of claim 1 , wherein the cyclodextrin is beta-cyclodextrin sulfobutylether.
20. The method of claim 1 , wherein the liquid is water.
21. The method of claim 1 , wherein the liquid suspension or solution further comprises one or more pharmaceutically acceptable excipients.
22. The method of claim 21 , wherein the pharmaceutically acceptable excipient is citric acid.
23. The method of claim 1 , wherein the liquid suspension or solution is administered by injection.