US2023242542A1PendingUtilityA1
COMPOSITIONS COMPRISING (S)-7-(1-ACRYLOYLPIPERIDIN-4-YL)-2-(4-PHENOXYPHENYL)-4,5,6,7-TETRA-HYDROPYRAZOLO[1,5-a]PYRIMIDINE-3-CARBOXAMIDE
Est. expiryAug 16, 2036(~10.1 yrs left)· nominal 20-yr term from priority
A61P 35/00Y02P20/55C07D 487/04C07B 2200/13C07B 2200/07A61K 31/519A61P 37/00A61P 29/00A61P 35/02A61P 37/02A61P 37/08C07B 2200/05A61P 35/04
85
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The present invention relates to pharmaceutical compositions comprising (S)-7-(1-acryloylpiperidin-4-yl)-2-(4-phenoxyphenyl)-4,5,6,7-tetra-hydropyrazolo[1,5-a]pyrimidine-3-carboxamide for the treatment of B-cell malignancies.
Claims
exact text as granted — not AI-modified1 - 42 . (canceled)
43 . A pharmaceutical composition comprising:
a) at least one pharmaceutically acceptable excipient, and b) a means for treating a B-cell malignancy, wherein the pharmaceutical composition comprises said means in an amount effective to treat the B-cell malignancy.
44 . The pharmaceutical composition according to claim 43 , wherein the B-cell malignancy is mantle cell lymphoma (MCL), Waldenstrom macroglobulinemia (WM), or marginal zone lymphoma (MZL).
45 . The pharmaceutical composition according to claim 43 , wherein the B-cell malignancy is diffuse large B cell lymphoma (DLBCL), mantle cell lymphoma (MCL), follicular lymphoma (FL), chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), Waldenstrom macroglobulinemia (WM), or marginal zone lymphoma (MZL).
46 . The pharmaceutical composition according to claim 43 , wherein the B-cell malignancy is a relapsed/refractory B-cell malignancy.
47 . The pharmaceutical composition according to claim 43 , wherein the B-cell malignancy is relapsed/refractory mantle cell lymphoma (R/R MCL), relapsed/refractory chronic lymphocytic leukemia (R/R CLL), relapsed/refractory small lymphocytic lymphoma (R/R SLL), or relapsed/refractory Waldenstrom macroglobulinemia (R/R WM).
48 . The pharmaceutical composition according to claim 43 , comprising from 40 mg to 320 mg of said means.
49 . The pharmaceutical composition according to claim 43 , comprising 160 mg of said means.
50 . The pharmaceutical composition according to claim 43 , comprising 320 mg of said means.
51 . The pharmaceutical composition according to claim 43 , wherein the effective amount is an amount sufficient to provide a total daily dose of 320 mg of said means in one or more doses.
52 . The pharmaceutical composition according to claim 43 , wherein the effective amount is an amount sufficient to provide a twice-daily dose of 160 mg of said means.
53 . The pharmaceutical composition according to claim 43 , comprising from 1 wt % to 99 wt % of said means, relative to the total weight of the composition.
54 . The pharmaceutical composition according to claim 43 , comprising from 1 wt % to 70 wt % of said means, relative to the total weight of the composition.
55 . The pharmaceutical composition according to claim 43 , comprising from 10 wt % to 30 wt % of said means, relative to the total weight of the composition.
56 . A pharmaceutical composition comprising:
a) at least one pharmaceutically acceptable excipient, and b) an amount of a means for treating a B-cell malignancy sufficient to provide a total daily dose of 320 mg of said means, wherein the B-cell malignancy is diffuse large B cell lymphoma (DLBCL), mantle cell lymphoma (MCL), follicular lymphoma (FL), chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), Waldenstrom macroglobulinemia (WM), marginal zone lymphoma (MZL), relapsed/refractory mantle cell lymphoma (R/R MCL), relapsed/refractory chronic lymphocytic leukemia (R/R CLL), relapsed/refractory small lymphocytic lymphoma (R/R SLL), or relapsed/refractory Waldenstrom macroglobulinemia (R/R WM).
57 . A pharmaceutical composition comprising:
a) at least one pharmaceutically acceptable excipient, and b) a means for treating a B-cell malignancy in a patient, wherein the pharmaceutical composition comprises from 40 mg to 320 mg of said means.
58 . The pharmaceutical composition according to claim 57 , comprising:
a) at least one pharmaceutically acceptable excipient, and b) a means for treating diffuse large B cell lymphoma (DLBCL), mantle cell lymphoma (MCL), follicular lymphoma (FL), chronic lymphocytic leukemia (CLL), small lymphocytic lymphoma (SLL), Waldenstrom macroglobulinemia (WM), or marginal zone lymphoma (MZL).
59 . The pharmaceutical composition according to claim 57 , comprising:
a) at least one pharmaceutically acceptable excipient, and b) a means for treating mantle cell lymphoma (MCL), Waldenstrom macroglobulinemia (WM), or marginal zone lymphoma (MZL).
60 . The pharmaceutical composition according to claim 57 , comprising:
a) at least one pharmaceutically acceptable excipient, and b) a means for treating a relapsed/refractory B-cell malignancy in a patient.
61 . The pharmaceutical composition according to claim 58 , comprising 160 mg of said means.
62 . The pharmaceutical composition according to claim 58 , comprising 320 mg of said means.Cited by (0)
No later patents cite this yet.
References (0)
No backward citations on record.