Fumarate salt of (R)-3-(1-(2,3-dichloro-4-(pyrazin-2-yl)phenyl)-2,2,2-trifluoroethyl)-1-methyl-1-(1-methylpiperidin-4-yl)urea, methods of preparation, and uses thereof
Provided are various embodiments relating to fumarate salt of (R)-3-(1-(2,3-dichloro-4-(pyrazin-2-yl)phenyl)-2,2,2-trifluoroethyl)-1-methyl-1-(1-methylpiperidin-4-yl) urea, and methods of producing and using the same to treat conditions and disorders associated with an increase of ghrelin level, such as food abuse, alcohol addiction, and other disorders (e.g., Prader-Willi syndrome). Also provided are various embodiments relating to crystalline HM04 free base, different crystalline forms of HM04 fumarate salt, and methods of producing the same.
1. A (R)-3-(1-(2,3-dichloro-4-(pyrazin-2-yl)phenyl)-2,2,2-trifluoroethyl)-1-methyl-1-(1-methylpiperidin-4-yl)urea fumarate salt, wherein the salt is at least 50% in crystalline form.
2. The salt of claim 1 , wherein the salt is 1:1 (R)-3-(1-(2,3-dichloro-4-(pyrazin-2-yl)phenyl)-2,2,2-trifluoroethyl)-1-methyl-1-(1-methylpiperidin-4-yl)urea: fumarate salt.
3. The salt of claim 1 , wherein the salt is at least 60%, at least 70%, at least 80%, at least 90%, at least 95%, at least 96%, at least 97%, at least 98%, at least 99%, or 100% in crystalline form.
4. The salt of claim 1 comprising Form 1 having an XRPD pattern substantially similar to the XRPD pattern of FIG. 12 as determined by XRPD using Cu K alpha radiation.
5. The salt of claim 1 comprising Form 2 characterized by an XRPD pattern substantially similar to the XRPD pattern of FIG. 3 as determined by XRPD using Cu K alpha radiation.
6. The salt of claim 1 comprising Form 3 characterized by an XRPD pattern substantially similar to the XRPD pattern of FIG. 15 as determined by XRPD using Cu K alpha radiation.
7. The salt of claim 1 comprising Form 4 characterized by an XRPD pattern substantially similar to the XRPD pattern of FIG. 16 as determined by XRPD using Cu K alpha radiation.
8. The salt of claim 1 comprising Form 1 characterized by an XRPD pattern, using Cu K alpha radiation, comprising peaks at 7.8±0.2, 9.5±0.2, 14.3±0.2, 16.7±0.2, 17.2±0.2, 18.5±0.2, 18.8±0.2, 19.3±0.2, 20.0±0.2, 20.7±0.2, 22.4±0.2, 23.2±0.2, 25.6±0.2, 27.2±0.2, 31.7±0.2, and 32.4±0.2 degrees 2 theta.
9. The salt of claim 1 comprising Form 3 characterized by an XRPD pattern, using Cu K alpha radiation, comprising peaks at 7.2±0.2, 9.4±0.2, 9.7±0.2, 10.8±0.2, 14.3±0.2, 15.1±0.2, 16.2±0.2, 17.9±0.2, 18.7±0.2, 18.9±0.2, 19.6±0.2, 21.5±0.2, 22.7±0.2, 23.7±0.2, 24.3±0.2, 25.1±0.2, 27.4±0.2, 28.7±0.2, and 34.9±0.2 degrees 2 theta.
10. The salt of claim 1 comprising Form 4 characterized by an XRPD pattern, using Cu K alpha radiation, comprising peaks at 12.2±0.2, 13.2±0.2, 15.0±0.2, 15.4±0.2, 17.6±0.2, 18.1±0.2, 19.5±0.2, 20.2±0.2, 20.9±0.2, 21.4±0.2, 23.0±0.2, 23.4±0.2, 24.4±0.2, 24.8±0.2, 25.9±0.2, 27.9±0.2, 28.9±0.2, 29.6±0.2, 30.7±0.2 degrees 2 theta.
11. (R)-3-(1-(2,3-dichloro-4-(pyrazin-2-yl)phenyl)-2,2,2-trifluoroethyl)-1-methyl-1-(1-methylpiperidin-4-yl)urea fumarate salt having an XRPD pattern substantially similar to the XRPD pattern of FIG. 11 as determined by XRPD using Cu K alpha radiation.
12. A drug product comprising the salt of claim 1 or the compound of claim 11 .
13. A composition comprising the salt of claim 1 or the compound of claim 11 and a pharmaceutically acceptable carrier.
14. A method of preparing the salt of claim 1 comprising combining (R)-3-(1-(2,3-dichloro-4-(pyrazin-2-yl)phenyl)-2,2,2-trifluoroethyl)-1-methyl-1-(1-methylpiperidin-4-yl)urea with fumaric acid.
15. The method of claim 14 , wherein the (R)-3-(1-(2,3-dichloro-4-(pyrazin-2-yl)phenyl)-2,2,2-trifluoroethyl)-1-methyl-1-(1-methylpiperidin-4-yl)urea is in solid form when combined with fumaric acid.
16. The method of claim 14 , wherein the (R)-3-(1-(2,3-dichloro-4-(pyrazin-2-yl)phenyl)-2,2,2-trifluoroethyl)-1-methyl-1-(1-methylpiperidin-4-yl)urea is in solution when combined with fumaric acid.
17. The method of claim 14 , wherein the (R)-3-(1-(2,3-dichloro-4-(pyrazin-2-yl)phenyl)-2,2,2-trifluoroethyl)-1-methyl-1-(1-methylpiperidin-4-yl)urea is subjected to acid/base extraction prior to being combined with fumaric acid.
18. The method of claim 14 , wherein the (R)-3-(1-(2,3-dichloro-4-(pyrazin-2-yl)phenyl)-2,2,2-trifluoroethyl)-1-methyl-1-(1-methylpiperidin-4-yl)urea is not subjected to an acid/base extraction prior to being combined with fumaric acid.
19. A method of reducing ghrelin signaling activity in a cell comprising exposing the cell to the salt of claim 1 .
20. The method of claim 19 , wherein the cell is exposed to the salt in vitro.
21. The method of claim 19 , wherein the ghrelin signaling activity is measured by level of intracellular calcium as detected by fluorescence imaging plate reader (FLIPR) assay.
22. The method of claim 21 , wherein the level of intracellular calcium is reduced.
23. A method of reducing ghrelin signaling activity in a subject comprising administering to the subject the salt of claim 1 .
24. A method of treating a subject having a condition or disorder associated with an increase in ghrelin level, comprising administering to the subject a therapeutically effective amount of the salt of claim 1 , wherein the condition or disorder is chosen from food abuse, alcohol addiction, and Prader-Willi syndrome.
25. The method of claim 24 , wherein the condition or disorder is chosen from binge eating, obesity, post-dieting body weight rebound, and hyperphagia.
26. The method of claim 24 , comprising orally administering the salt to the subject.
27. The method of claim 24 , wherein at least one of the following conditions apply:
i) the subject's level of circulating growth hormone is modulated;
ii) the subject's level of circulating growth hormone is reduced;
iii) the subject's food intake is reduced;
iv) the subject's body weight is reduced;
v) the subject's body weight is stabilized.