SOLVATED FORMS OF A BRUTON'S TYROSINE KINASE INHIBITOR
Described herein are solvates of the Bruton's tyrosine kinase (Btk) inhibitor 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one, including crystalline forms, and pharmaceutically acceptable salts thereof. Also disclosed are pharmaceutical compositions that include the solvates, as well as methods of using the solvates, alone or in combination with other therapeutic agents, for the treatment of autoimmune diseases or conditions, heteroimmune diseases or conditions, cancer, including lymphoma, and inflammatory diseases or conditions.
1 . A solvate of 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one, wherein 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one is solvated with butyronitrile, 1,2-dimethoxyethane, hexafluorobenzene, acetophenone, chlorobenzene, dimethylacetamide, benzyl acetate, or 1,1,2-trichloroethane, or a mixture thereof.
2 . The solvate of claim 1 , which is in a crystalline form.
3 . A crystalline form (Form 1) of a butyronitrile solvate of 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one that has at least one of the following properties:
(a) an X-ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 1 ;
(b) an X-ray powder diffraction (XRPD) pattern with at least two, four, six, or all of the characteristic peaks at 5.5±0.1° 2-Theta, 10.9±0.1° 2-Theta, 13.6±0.1° 2-Theta, 14.8±0.1° 2-Theta, 17.3±0.1° 2-Theta, 18.7±0.1° 2-Theta, 20.0±0.1° 2-Theta, and 21.8±0.1° 2-Theta;
(c) a DSC thermogram substantially the same as the one set forth in FIG. 2 ;
(d) a DSC thermogram with an endotherm event at between about 100-125° C.;
(e) a thermo-gravimetric analysis (TGA) thermogram substantially the same as the one set forth in FIG. 2 ;
or
(f) combinations thereof.
4 . The crystalline form of claim 3 , wherein the crystalline form has an X-Ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 1 .
5 . The crystalline form of claim 3 , wherein the crystalline form has an X-ray powder diffraction (XRPD) pattern with characteristic peaks at 5.5±0.1° 2-Theta, 10.9±0.1° 2-Theta, 13.6±0.1° 2-Theta, 14.8±0.1° 2-Theta, 17.3±0.1° 2-Theta, 18.7±0.1° 2-Theta, 20.0±0.1° 2-Theta, and 21.8±0.1° 2-Theta.
6 . The crystalline form of claim 3 , wherein the DSC thermogram has an endotherm event at between about 100-125° C.
7 . The crystalline form of claim 3 , wherein the crystalline form has a DSC thermogram substantially the same as the one set forth in FIG. 2 .
8 . The crystalline form of claim 3 , wherein the crystalline form has a TGA thermogram substantially the same as the one set forth in FIG. 2 .
9 . The crystalline form of claim 3 , wherein the crystalline form that is characterized as having properties (a), (b), (c), (d), and (e).
10 . A crystalline form (Form 2) of a 1,2-dimethoxyethane solvate of 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one that has at least one of the following properties:
(a) an X-ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 3 ;
(b) an X-ray powder diffraction (XRPD) pattern with at least two, four, six, or all of the characteristic peaks at 6.8±0.1° 2-Theta, 13.4±0.1° 2-Theta, 17.6±0.1° 2-Theta, 18.2±0.1° 2-Theta, 20.2±0.1° 2-Theta, 21.2±0.1° 2-Theta, and 22.2±0.1° 2-Theta;
(c) substantially the same X-ray powder diffraction (XRPD) pattern post storage at 40° C. and 75% RH for 7 days;
(d) a DSC thermogram substantially the same as the one set forth in FIG. 4 ;
(e) a DSC thermogram with an endotherm having an onset at about 89° C. and a peak at about 101° C.;
(f) thermo-gravimetric analysis (TGA) thermogram substantially the same as the one set forth in FIG. 4 ;
or
(g) combinations thereof.
11 . The crystalline form of claim 10 , wherein the crystalline form has an X-Ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 3 .
12 . The crystalline form of claim 10 , wherein the crystalline form has an X-ray powder diffraction (XRPD) pattern with at least two, four, six, or all of the characteristic peaks at 6.8±0.1° 2-Theta, 13.4±0.1° 2-Theta, 17.6±0.1° 2-Theta, 18.2±0.1° 2-Theta, 20.2±0.1° 2-Theta, 21.2±0.1° 2-Theta, and 22.2±0.1° 2-Theta.
13 . The crystalline form of claim 10 , wherein the crystalline form has substantially the same X-ray powder diffraction (XRPD) pattern post storage at 40° C. and 75% RH for 7 days.
14 . The crystalline form of claim 10 , wherein the DSC thermogram has an endotherm with an onset at about 89° C. and a peak at about 101° C.
15 . The crystalline form of claim 10 , wherein the crystalline form has a DSC thermogram substantially the same as the one set forth in FIG. 4 .
16 . The crystalline form of claim 10 , wherein the crystalline form has a TGA thermogram substantially the same as the one set forth in FIG. 4 .
17 . The crystalline form of claim 10 , wherein the crystalline form that is characterized as having properties (a), (b), (c), (d), (e), and (f).
18 . A crystalline form (Form 3) of a hexafluorobenzene solvate of 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one that has at least one of the following properties:
(a) an X-ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 5 ;
(b) an X-ray powder diffraction (XRPD) pattern with at least two, four, six, or all of the characteristic peaks at 5.4±0.1° 2-Theta, 14.0±0.1° 2-Theta, 16.1±0.1° 2-Theta, 18.6±0.1° 2-Theta, 19.3±0.1° 2-Theta, 22.4±0.1° 2-Theta, and 23.6±0.1° 2-Theta;
(c) a DSC thermogram substantially the same as the one set forth in FIG. 6 ;
(d) a DSC thermogram with an endotherm having an onset at about 51° C.;
or
(e) combinations thereof.
19 . The crystalline form of claim 18 , wherein the crystalline form has an X-Ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 5 .
20 . The crystalline form of claim 18 , wherein the crystalline form has an X-ray powder diffraction (XRPD) pattern with characteristic peaks at 5.4±0.1° 2-Theta, 14.0±0.1° 2-Theta, 16.1±0.1° 2-Theta, 18.6±0.1° 2-Theta, 19.3±0.1° 2-Theta, 22.4±0.1° 2-Theta, and 23.6±0.1° 2-Theta.
21 . The crystalline form of claim 18 , wherein the DSC thermogram has an endotherm with an onset at about 51° C.
22 . The crystalline form of claim 18 , wherein the crystalline form has a DSC thermogram substantially the same as the one set forth in FIG. 6 .
23 . The crystalline form of claim 18 , wherein the crystalline form that is characterized as having properties (a), (b), (c), and (d).
24 . A crystalline form (Form 4) of a hexafluorobenzene solvate of 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one that has at least one of the following properties:
(a) an X-ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 7 ;
(b) an X-ray powder diffraction (XRPD) pattern with at least two, four, or all of the characteristic peaks at 12.6±0.1° 2-Theta, 15.4±0.1° 2-Theta, 17.7±0.1° 2-Theta, 24.9±0.1° 2-Theta, 25.4±0.1° 2-Theta, and 26.9±0.1° 2-Theta;
(c) a DSC thermogram substantially the same as the one set forth in FIG. 8 ;
(d) a DSC thermogram with an endotherm having an onset at about 84° C. and a peak at about 100° C.;
(e) thermo-gravimetric analysis (TGA) thermogram substantially the same as the one set forth in FIG. 8 ;
or
(f) combinations thereof.
25 . The crystalline form of claim 24 , wherein the crystalline form has an X-Ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 7 .
26 . The crystalline form of claim 24 , wherein the crystalline form has an X-ray powder diffraction (XRPD) pattern with characteristic peaks at 12.6±0.1° 2-Theta, 15.4±0.1° 2-Theta, 17.7±0.1° 2-Theta, 24.9±0.1° 2-Theta, 25.4±0.1° 2-Theta, and 26.9±0.1° 2-Theta.
27 . The crystalline form of claim 24 , wherein the DSC thermogram has an endotherm with an onset at about 84° C. and a peak at about 100° C.
28 . The crystalline form of claim 24 , wherein the crystalline form has a DSC thermogram substantially the same as the one set forth in FIG. 8 .
29 . The crystalline form of claim 24 , wherein the crystalline form has a TGA thermogram substantially the same as the one set forth in FIG. 8 .
30 . The crystalline form of claim 24 , wherein the crystalline form that is characterized as having properties (a), (b), (c), (d), and (e).
31 . A crystalline form (Form 5) of an acetophenone solvate of 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one that has at least one of the following properties:
(a) an X-ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 9 ;
(b) an X-ray powder diffraction (XRPD) pattern with at least two, four, six or all of the characteristic peaks at 7.6±0.1° 2-Theta, 8.8±0.1° 2-Theta, 15.2±0.1° 2-Theta, 17.6±0.1° 2-Theta, 18.9±0.1° 2-Theta, 19.5±0.1° 2-Theta, 20.4±0.1° 2-Theta, 21.0±0.1° 2-Theta, 21.3±0.1° 2-Theta, 21.8±0.1° 2-Theta, 24.3±0.1° 2-Theta, and 24.8±0.1° 2-Theta;
(c) a DSC thermogram substantially the same as the one set forth in FIG. 10 ;
(d) a DSC thermogram with an endotherm having an onset at about 89° C. and a peak at about 96° C.;
(e) thermo-gravimetric analysis (TGA) thermogram substantially the same as the one set forth in FIG. 10 ;
(f) unit cell parameters approximately equal to the following at a temperature of approximately 100(2) K:
Molecular formula
C 33 H 32 N 6 O 3
Molecular weight
560.64
Crystal system
Triclinic
Space group
P1
a
11.3552(5) Å
α
79.657(3)°
b
11.7741(4) Å
β
70.352(4)°
c
12.2064(4) Å
γ
67.080(4)°
V
1413.38(11) Å 3
Z
2
Density (calculated)
1.317 Mg/m 3
Absorption coefficient
0.699 mm −1
Wavelength
1.54178 Å
F(000)
592
T
100(2) K
or
(g) combinations thereof.
32 . The crystalline form of claim 31 , wherein the crystalline form has an X-Ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 9 .
33 . The crystalline form of claim 31 , wherein the crystalline form has an X-ray powder diffraction (XRPD) pattern with at least two, four, six or all of the characteristic peaks at 7.6±0.1° 2-Theta, 8.8±0.1° 2-Theta, 15.2±0.1° 2-Theta, 17.6±0.1° 2-Theta, 18.9±0.1° 2-Theta, 19.5±0.1° 2-Theta, 20.4±0.1° 2-Theta, 21.0±0.1° 2-Theta, 21.3±0.1° 2-Theta, 21.8±0.1° 2-Theta, 24.3±0.1° 2-Theta, and 24.8±0.1° 2-Theta.
34 . The crystalline form of claim 31 , wherein the DSC thermogram has an endotherm with an onset at about 89° C. and a peak at about 96° C.
35 . The crystalline form of claim 31 , wherein the crystalline form has a DSC thermogram substantially the same as the one set forth in FIG. 10 .
36 . The crystalline form of claim 31 , wherein the crystalline form has a TGA thermogram substantially the same as the one set forth in FIG. 10 .
37 . The crystalline form of claim 31 , wherein the unit cell parameters approximately equal to the following at a temperature of approximately 100(2) K:
Molecular formula
C 33 H 32 N 6 O 3
Molecular weight
560.64
Crystal system
Triclinic
Space group
P1
a
11.3552(5) Å
α
79.657(3)°
b
11.7741(4) Å
β
70.352(4)°
c
12.2064(4) Å
γ
67.080(4)°
V
1413.38(11) Å 3
Z
2
Density (calculated)
1.317 Mg/m 3
Absorption coefficient
0.699 mm −1
Wavelength
1.54178 Å
F(000)
592
T
100(2) K
38 . The crystalline form of claim 31 , wherein the crystalline form that is characterized as having properties (a), (b), (c), (d), (e), and (f).
39 . A crystalline form (Form 6) of a chlorobenzene solvate of 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one that has at least one of the following properties:
(a) an X-ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 11 ;
(b) an X-ray powder diffraction (XRPD) pattern with at least two, four, or all of the characteristic peaks at 18.4±0.1° 2-Theta, 19.4±0.1° 2-Theta, 20.2±0.1° 2-Theta, 20.9±0.1° 2-Theta, 21.2±0.1° 2-Theta, 21.9±0.1° 2-Theta, and 25.0±0.1° 2-Theta;
(c) substantially the same X-ray powder diffraction (XRPD) pattern post storage at 40° C. and 75% RH for 7 days;
(d) a DSC thermogram substantially the same as the one set forth in FIG. 12 ;
(e) a DSC thermogram with an endotherm having an onset at about 92° C. and a peak at about 95° C.;
(f) thermo-gravimetric analysis (TGA) thermogram substantially the same as the one set forth in FIG. 12 ;
or
(g) combinations thereof.
40 . The crystalline form of claim 39 , wherein the crystalline form has an X-Ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 11 .
41 . The crystalline form of claim 39 , wherein the crystalline form has an X-ray powder diffraction (XRPD) pattern with characteristic peaks at 18.4±0.1° 2-Theta, 19.4±0.1° 2-Theta, 20.2±0.1° 2-Theta, 20.9±0.1° 2-Theta, 21.2±0.1° 2-Theta, 21.9±0.1° 2-Theta, and 25.0±0.1° 2-Theta.
42 . The crystalline form of claim 39 , wherein the crystalline form has substantially the same X-ray powder diffraction (XRPD) pattern post storage at 40° C. and 75% RH for 7 days.
43 . The crystalline form of claim 39 , wherein the DSC thermogram has an endotherm with an onset at about 92° C. and a peak at about 95° C.
44 . The crystalline form of claim 39 , wherein the crystalline form has a DSC thermogram substantially the same as the one set forth in FIG. 12 .
45 . The crystalline form of claim 39 , wherein the crystalline form has a TGA thermogram substantially the same as the one set forth in FIG. 12 .
46 . The crystalline form of claim 39 , wherein the crystalline form that is characterized as having properties (a), (b), (c), (d), (e), and (f).
47 . A crystalline form (Form 7) of an acetophenone solvate of 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one that has at least one of the following properties:
(a) an X-ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 13 ;
(b) an X-ray powder diffraction (XRPD) pattern with at least two, four, six, or all of the characteristic peaks at 6.5±0.1° 2-Theta, 13.0±0.1° 2-Theta, 17.6±0.1° 2-Theta, 18.4±0.1° 2-Theta, 19.9±0.1° 2-Theta, 21.0±0.1° 2-Theta, 21.5±0.1° 2-Theta, 22.1±0.1° 2-Theta, and 23.9±0.1° 2-Theta;
(c) a DSC thermogram substantially the same as the one set forth in FIG. 14 ;
(d) a DSC thermogram with an endotherm having an onset at about 124° C. and a peak at about 127° C.;
(e) thermo-gravimetric analysis (TGA) thermogram substantially the same as the one set forth in FIG. 14 ;
or
(f) combinations thereof.
48 . The crystalline form of claim 47 , wherein the crystalline form has an X-Ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 13 .
49 . The crystalline form of claim 47 , wherein the crystalline form has an X-ray powder diffraction (XRPD) pattern with characteristic peaks at 6.5±0.1° 2-Theta, 13.0±0.1° 2-Theta, 17.6±0.1° 2-Theta, 18.4±0.1° 2-Theta, 19.9±0.1° 2-Theta, 21.0±0.1° 2-Theta, 21.5±0.1° 2-Theta, 22.1±0.1° 2-Theta, and 23.9±0.1° 2-Theta.
50 . The crystalline form of claim 47 , wherein the DSC thermogram has an endotherm with an onset at about 124° C. and a peak at about 127° C.
51 . The crystalline form of claim 47 , wherein the crystalline form has a DSC thermogram substantially the same as the one set forth in FIG. 14 .
52 . The crystalline form of claim 47 , wherein the crystalline form has a TGA thermogram substantially the same as the one set forth in FIG. 14 .
53 . The crystalline form of claim 47 , wherein the crystalline form that is characterized as having properties (a), (b), (c), (d), and (e).
54 . A crystalline form (Form 8) of a dimethylacetamide solvate of 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one that has at least one of the following properties:
(a) an X-ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 15 ;
(b) an X-ray powder diffraction (XRPD) pattern with at least two, four, or all of the characteristic peaks at 8.8±0.1° 2-Theta, 19.2±0.1° 2-Theta, 19.9±0.1° 2-Theta, 22.5±0.1° 2-Theta, 24.5±0.1° 2-Theta, and 25.3±0.1° 2-Theta;
(c) a DSC thermogram substantially the same as the one set forth in FIG. 16 ;
(d) a DSC thermogram with an endotherm having an onset at about 82° C. and a peak at about 85° C.;
(e) a thermo-gravimetric analysis (TGA) thermogram substantially the same as the one set forth in FIG. 16 ;
(f) unit cell parameters approximately equal to the following at a temperature of approximately 100(2) K:
Molecular formula
C 29 H 33 N 7 O 3
Molecular weight
527.62
Crystal system
Triclinic
Space group
P1
a
9.3627(3) Å
α
70.831(3)°
b
10.9543(4) Å
β
76.034(3)°
c
14.7742(5) Å
γ
70.721(3)°
V
1335.88(9) Å 3
Z
2
Density (calculated)
1.312 Mg/m 3
Absorption coefficient
0.711 mm −1
Wavelength
1.54178 Å
F(000)
560
T
100(2) K
or
(g) combinations thereof.
55 . The crystalline form of claim 54 , wherein the crystalline form has an X-Ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 15 .
56 . The crystalline form of claim 54 , wherein the crystalline form has an X-ray powder diffraction (XRPD) pattern with characteristic peaks at 8.8±0.1° 2-Theta, 19.2±0.1° 2-Theta, 19.9±0.1° 2-Theta, 22.5±0.1° 2-Theta, 24.5±0.1° 2-Theta, and 25.3±0.1° 2-Theta.
57 . The crystalline form of claim 54 , wherein the DSC thermogram has an endotherm with an onset at about 82° C. and a peak at about 85° C.
58 . The crystalline form of claim 54 , wherein the crystalline form has a DSC thermogram substantially the same as the one set forth in FIG. 16 .
59 . The crystalline form of claim 54 , wherein the crystalline form has a TGA thermogram substantially the same as the one set forth in FIG. 16 .
60 . The crystalline form of claim 54 , wherein the unit cell parameters approximately equal to the following at a temperature of approximately 100(2) K:
Molecular formula
C 29 H 33 N 7 O 3
Molecular weight
527.62
Crystal system
Triclinic
Space group
P1
a
9.3627(3) Å
α
70.831(3)°
b
10.9543(4) Å
β
76.034(3)°
c
14.7742(5) Å
γ
70.721(3)°
V
1335.88(9) Å 3
Z
2
Density (calculated)
1.312 Mg/m 3
Absorption coefficient
0.711 mm −1
Wavelength
1.54178 Å
F(000)
560
T
100(2) K
61 . The crystalline form of claim 54 , wherein the crystalline form that is characterized as having properties (a), (b), (c), (d), (e), and (f).
62 . A crystalline form (Form 9) of a benzyl acetate solvate of 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one that has at least one of the following properties:
(a) an X-ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 17 ;
(b) an X-ray powder diffraction (XRPD) pattern with at least two, four, or all of the characteristic peaks at 12.8±0.1° 2-Theta, 17.8±0.1° 2-Theta, 18.7±0.1° 2-Theta, 19.2±0.1° 2-Theta, 20.1±0.1° 2-Theta, 20.7±0.1° 2-Theta, 22.1±0.1° 2-Theta and 22.9±0.1° 2-Theta;
(c) a DSC thermogram substantially the same as the one set forth in FIG. 18 ;
(d) a DSC thermogram with an endotherm having an onset at about 106° C. and a peak at about 108° C. and an endotherm having an onset at about 155° C. and a peak at about 158° C.;
(e) a thermo-gravimetric analysis (TGA) thermogram substantially the same as the one set forth in FIG. 18 ;
or
(f) combinations thereof.
63 . The crystalline form of claim 62 , wherein the crystalline form has an X-Ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 17 .
64 . The crystalline form of claim 62 , wherein the crystalline form has an X-ray powder diffraction (XRPD) pattern with characteristic peaks at 12.8±0.1° 2-Theta, 17.8±0.1° 2-Theta, 18.7±0.1° 2-Theta, 19.2±0.1° 2-Theta, 20.1±0.1° 2-Theta, 20.7±0.1° 2-Theta, 22.1±0.1° 2-Theta and 22.9±0.1° 2-Theta.
65 . A crystalline form (Form 10) of a 1,1,2-trichloroethane solvate of 1-((R)-3-(4-amino-3-(4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)prop-2-en-1-one that has at least one of the following properties:
(a) an X-ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 19 ;
(b) an X-ray powder diffraction (XRPD) pattern with at least two, four, or all of the characteristic peaks at 5.4±0.1° 2-Theta, 18.6±0.1° 2-Theta, 20.1±0.1° 2-Theta, 20.8±0.1° 2-Theta, 21.3±0.1° 2-Theta, 21.7±0.1° 2-Theta, and 22.6±0.1° 2-Theta;
(c) a DSC thermogram substantially the same as the one set forth in FIG. 20 ;
(d) a DSC thermogram with an endotherm having an onset at about 150° C. and a peak at about 154° C.;
(e) a thermo-gravimetric analysis (TGA) thermogram substantially the same as the one set forth in FIG. 20 ;
or
(f) combinations thereof.
66 . The crystalline form of claim 65 , wherein the crystalline form has an X-Ray powder diffraction (XRPD) pattern substantially the same as shown in FIG. 19 .
67 . The crystalline form of claim 65 , wherein the crystalline form has an X-ray powder diffraction (XRPD) pattern with characteristic peaks at 5.4±0.1° 2-Theta, 18.6±0.1° 2-Theta, 20.1±0.1° 2-Theta, 20.8±0.1° 2-Theta, 21.3±0.1° 2-Theta, 21.7±0.1° 2-Theta, and 22.6±0.1° 2-Theta.
68 . A pharmaceutical composition comprising a crystalline form of any one of claims 1 - 67 , and a pharmaceutically acceptable excipient.
69 . A method of treating cancer in a mammal in need thereof comprising administering to the mammal a pharmaceutical composition according to claim 68 .
70 . The method of claim 69 , wherein the cancer is a B cell malignancy.
71 . The method of claim 69 , wherein the cancer is a B cell malignancy selected from chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), mantle cell lymphoma (MCL), diffuse large B Cell lymphoma (DLBCL), and multiple myeloma.
72 . The method of claim 69 , wherein the cancer is a lymphoma, leukemia or a solid tumor.
73 . The method of claim 69 , wherein the cancer is diffuse large B cell lymphoma, follicular lymphoma, chronic lymphocytic lymphoma, chronic lymphocytic leukemia, B-cell prolymphocytic leukemia, lymphoplasmacytic lymphoma/Waldenström macroglobulinemia, splenic marginal zone lymphoma, plasma cell myeloma, plasmacytoma, extranodal marginal zone B cell lymphoma, nodal marginal zone B cell lymphoma, mantle cell lymphoma, mediastinal (thymic) large B cell lymphoma, intravascular large B cell lymphoma, primary effusion lymphoma, burkitt lymphoma/leukemia, or lymphomatoid granulomatosis.