SALT AND CRYSTAL FORMS OF AN ACTIVIN RECEPTOR-LIKE KINASE INHIBITOR
Various salt forms of Compound (I) represented by the following structural formula, and their corresponding pharmaceutical compositions, are disclosed. Particular single crystalline forms of 1:1.5 Compound (I) succinate, 1:1 Compound (I) hydrochloride salt, and 1:1 Compound (I) fumarate salt are characterized by a variety of properties and physical measurements. Methods of preparing specific crystalline forms are also disclosed. The present disclosure also provides methods of treating or ameliorating fibrodysplasia ossificans progressive in a subject.
1 . A succinate salt of Compound (I) represented by the following structural formula:
wherein the molar ratio between Compound (I) and succinic acid is 1:1.5.
2 . The succinate salt of claim 1 , wherein the succinate salt is crystalline.
3 . The succinate salt of claim 1 , wherein the succinate salt is in a single crystalline form.
4 . The succinate salt of claim 1 , wherein the succinate salt is unsolvated.
5 . The succinate salt of claim 1 , wherein the succinate salt is in a single crystalline form, Form A, characterized by an X-ray powder diffraction pattern which comprises peaks at 8.5°, 15.4°, and 21.3°±0.2 in 2θ.
6 . The succinate salt of claim 1 , wherein the succinate salt is in a single crystalline form, Form A, characterized by an X-ray powder diffraction pattern which comprises at least three peaks chosen from 4.3°, 8.5°, 14.0°, 15.4°, and 21.3°±0.2 in 2θ.
7 . The succinate salt of claim 1 , wherein the succinate salt is in a single crystalline form, Form A, characterized by an X-ray powder diffraction pattern which comprises peaks at 4.3°, 8.5°, 14.0°, 15.4°, and 21.3°±0.2 in 2θ.
8 . The succinate salt of claim 1 , wherein the succinate salt is in a single crystalline form, Form A, characterized by an X-ray powder diffraction pattern which comprises peaks at 4.3°, 6.7°, 8.5°, 12.8°, 14.0°, 15.4°, 17.0°, and 21.3°±0.2 in 2θ.
9 . The succinate salt of claim 1 , wherein the succinate salt is in a single crystalline form, Form A, characterized by an X-ray powder diffraction pattern which comprises peaks at 4.3°, 6.7°, 8.5°, 12.8°, 14.0°, 15.4°, 15.7°, 16.6°, 17.0°, 18.1°, 19.4°, 19.8°, 20.1°, 20.7°, 21.3°, 22.3°, 25.0°, 29.1°, and 34.4°±0.2 in 2θ.
10 - 11 . (canceled)
12 . A hydrochloride salt of Compound (I) represented by the following structural formula:
wherein the molar ratio between Compound (I) and hydrochloric acid is 1:1.
13 - 16 . (canceled)
17 . The hydrochloride salt of claim 12 , wherein the hydrochloride salt is in a single crystalline form, Form A, characterized by an X-ray powder diffraction pattern which comprises at least three peaks chosen from 12.9°, 17.0°, 19.0°, 21.1°, and 22.8°±0.2 in 2θ.
18 - 21 . (canceled)
22 . The hydrochloride salt of claim 12 , wherein the hydrochloride salt is in a single crystalline form, Form I, characterized by an X-ray powder diffraction pattern which comprises at least three peaks chosen from 5.4°, 8.2°, 16.3°, 16.5°, 18.4°, and 21.5°±0.2 in 2θ.
23 - 27 . (canceled)
28 . A fumarate salt of Compound (I) represented by the following structural formula:
wherein the molar ratio between Compound (I) and fumaric acid is 1:1.
29 - 30 . (canceled)
31 . The fumarate salt of claim 28 , wherein the fumarate salt is in a single crystalline form, Form A, characterized by an X-ray powder diffraction pattern which comprises at least three peaks chosen from 5.7°, 15.3°, 16.9°, 22.4°, and 23.0°±0.2 in 2θ.
32 - 35 . (canceled)
36 . The fumarate salt of claim 28 , wherein the fumarate salt is in a single crystalline form, Form C, characterized by an X-ray powder diffraction pattern which comprises at least three peaks chosen from 6.3°, 9.0°, 13.5°, 18.9°, and 22.5°±0.2 in 2θ.
37 - 39 . (canceled)
40 . The fumarate salt of claim 28 , wherein the fumarate salt is in a single crystalline form, Form D, characterized by an X-ray powder diffraction pattern which comprises at least three peaks chosen from 4.6°, 11.0°, 18.5°, 20.5°, and 21.0°±0.2 in 2θ.
41 - 48 . (canceled)
49 . A pharmaceutical composition comprising the salt of claim 1 , and a pharmaceutically acceptable carrier or diluent.
50 . A method of treating or ameliorating fibrodysplasia ossificans progressiva in a subject, comprising administering to the subject in need thereof a pharmaceutically effective amount of the salt of claim 1 .
51 - 52 . (canceled)
53 . A method of treating or ameliorating diffuse intrinsic pontine glioma in a subject, comprising administering to the subject in need thereof a pharmaceutically effective amount of at least one compound of claim 1 .
54 - 55 . (canceled)
56 . A method of inhibiting aberrant ALK2 activity in a subject comprising the step of administering to the subject in need thereof a pharmaceutically effective amount of at least one compound of claim 1 .
57 - 59 . (canceled)