US2017157148A1PendingUtilityA1
Treatment of prostate cancer
Est. expiryAug 7, 2029(~3.1 yrs left)· nominal 20-yr term from priority
A61P 43/00A61P 35/00A61P 15/08A61P 17/14A61P 13/08A61P 17/00A61P 1/14A61K 9/0053A61K 9/20A61K 31/58A61K 31/4184A61K 2121/00A61K 31/56A61K 9/0019C07J 43/003A61K 9/48A61K 9/2095
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Claims
Abstract
Described herein are compounds, methods of making such compounds, pharmaceutical compositions, and medicaments comprising such compounds, and methods of using such compounds to treat androgen receptor mediated diseases or conditions. The present invention provides therapies and therapeutic regimens for the treatment of prostate cancer.
Claims
exact text as granted — not AI-modified1 - 52 . (canceled)
53 . A method of manufacturing a pharmaceutical composition, the method comprising steps of:
preparing the pharmaceutical composition comprising an effective amount of Compound (1):
or a pharmaceutically acceptable salt thereof,
from a crystalline form of Compound (1), wherein the crystalline form of Compound (1) is characterized by a powder X-ray diffraction pattern having characteristic peaks expressed in angle 2-theta at about 13.1° and about 14.1°.
54 . The method of claim 53 , wherein some or all of the Compound (1) in the pharmaceutical composition is in the crystalline form.
55 . The method of claim 54 , wherein some or all of the Compound (1) in the pharmaceutical composition is in amorphous form.
56 . The method of claim 53 , wherein some or all of the Compound (1) in the pharmaceutical composition is in amorphous form.
57 . The method of claim 53 , wherein the step of preparing comprises formulating for oral delivery.
58 . The method of claim 57 , wherein the formulating for oral delivery comprises formulating as a tablet
59 . The method of claim 58 , wherein the formulating as a tablet comprises
combining the crystalline form of Compound (1) with a pharmaceutically acceptable carrier or excipient; and compressing the combination.
60 . The method of claim 53 , wherein the step of preparing comprises formulating for local administration.
61 . The method of claim 60 , wherein the formulating for local administration comprises formulating for injection.
62 . The method of claim 53 , wherein the step of preparing comprises formulating for rapid release.
63 . The method of claim 53 , wherein the step of preparing comprises formulating for extended release.
64 . The method of claim 53 , wherein the step of preparing comprises formulating for intermediate release.
65 . The method of claim 53 , wherein the step of preparing comprises combining with at least one pharmaceutically acceptable chemical component selected from: a carrier, a stabilizer, a diluent, a dispersing agent, a suspending agent, a thickening agent, and/or an excipient.
66 . The method of claim 65 , wherein the at least one pharmaceutically acceptable chemical component is a carrier and/or an excipient.
67 . The method of claim 66 wherein the step of preparing comprises formulating into a solid, a semi-solid, or a liquid.
68 . The method of claim 67 , wherein the step of preparing comprises formulating into a solid.
69 . The method of claim 68 , wherein the formulating comprises formulating the solid into a solution, a suspension, or an emulsion.
70 . The method of claim 53 , wherein the step of preparing comprises mixing, dissolving, granulating, dragee-making, levigating, emulsifying, encapsulating, entrapping, or compressing the Compound (1).Cited by (0)
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