Formulation of Syk inhibitors
Disclosed are pharmaceutical compositions comprising a compound having the formula: or a pharmaceutically acceptable salt thereof, or a hydrate of thereof, and at least one pharmaceutically acceptable polymer. The pharmaceutically acceptable salt of the compound of Formula I, or a hydrate thereof, can be a mesylate salt, including, for example, a mono-mesylate or a bis-mesylate salt, or a hydrate thereof. Also disclosed are methods of use for the pharmaceutical composition.
1. A method of treating a hematologic cancer in a human in need thereof, comprising administering to the human a therapeutically effective amount of a composition comprising:
(i) a bis-mesylate salt of a compound of Formula I:
or a hydrate thereof, and
(ii) at least one pharmaceutically acceptable carrier; and
one or more additional agents selected from the group consisting of fludarabine, rituximab, alemtuzumab and obinutuzumab.
2. The method of claim 1 , wherein the hematologic cancer is selected from the group consisting of acute lymphocytic leukemia (ALL), acute myeloid leukemia (AML), chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), myelodysplastic syndrome (MDS), myeloproliferative disease (MPD), chronic myeloid leukemia (CML), multiple myeloma (MM), non-Hodgkin's lymphoma (NHL), mantle cell lymphoma (MCL), follicular lymphoma (FL), Waldenstrom's macroglobulinemia (WM), T-cell lymphoma, B-cell lymphoma, diffuse large B-cell lymphoma (DLBCL), lymphoplasmacytic lymphoma (LPL), and marginal zone lymphoma (MZL).
3. The method of claim 2 , wherein the hematologic cancer is non-Hodgkin's lymphoma (NHL).
4. The method of claim 3 , wherein the NHL is indolent non-Hodgkin's lymphoma (iNHL).
5. The method of claim 4 , wherein the iNHL is refractory iNHL.
6. The method of claim 4 , wherein the iNHL is non-FL iNHL.
7. The method according to claim 2 , wherein the hematologic cancer is acute lymphocytic leukemia (ALL).
8. The method according to claim 2 , wherein the hematologic cancer is acute myeloid leukemia (AML).
9. The method according to claim 2 , wherein the hematologic cancer is chronic lymphocytic leukemia (CLL).
10. The method according to claim 2 , wherein the hematologic cancer is small lymphocytic lymphoma (SLL).
11. The method according to claim 2 , wherein the hematologic cancer is myelodysplastic syndrome (MDS).
12. The method according to claim 2 , wherein the hematologic cancer is chronic myeloid leukemia (CML).
13. The method according to claim 2 , wherein the hematologic cancer is Waldenstrom's macroglobulinemia (WM).
14. The method according to claim 2 , wherein the hematologic cancer is T-cell lymphoma.
15. The method according to claim 2 , wherein the hematologic cancer is B-cell lymphoma.
16. The method according to claim 2 , wherein the hematologic cancer is diffuse large B-cell lymphoma (DLBCL).
17. The method according to claim 1 , wherein said additional agent is selected from alemtuzumab and obinutuzumab.
18. The method according to claim 1 , wherein said additional agent is obinutuzumab.
19. The method according to claim 9 , wherein said additional agent is selected from alemtuzumab and obinutuzumab.
20. The method according to claim 9 , wherein said additional agent is obinutuzumab.
21. The method according to claim 1 , wherein the bis-mesylate salt is a monohydrate, bis-mesylate salt of the compound of Formula I.
22. The method according to claim 1 , wherein the bis-mesylate salt is a polymorph having an X-ray diffraction pattern comprising 2θ-reflections, plus or minus 0.2 degrees 2θ, at 7.7, 12.9, 17.7, and 18.1.
23. The method according to claim 1 , wherein the bis-mesylate salt is a polymorph having an X-ray diffraction pattern further comprising 2θ-reflections, plus or minus 0.2 degrees 2θ, at 13.8, 16.9, 22.9 and 26.1.