US2021000812A1PendingUtilityA1
Anti-Androgens For The Treatment Of Non-Metastatic Castrate-Resistant Prostate Cancer
Est. expirySep 26, 2032(~6.2 yrs left)· nominal 20-yr term from priority
Inventors:Isan Chen
A61P 5/28A61P 5/02A61K 38/09A61K 2300/00A61K 31/4439A61P 35/00A61K 31/4166A61P 37/00A61P 13/08A61K 31/00A61P 43/00H05K 999/99
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Claims
Abstract
Described herein are methods of treating non-metastatic castrate-resistant prostate cancer with anti-androgens.
Claims
exact text as granted — not AI-modified1 - 20 . (canceled)
21 . A method of treating non-metastatic castration-resistant prostate cancer in a male human comprising administering a second-generation anti-androgen to a male human in need of such treatment, wherein the second-generation anti-androgen is administered in combination with a gonadotropin-releasing hormone (GnRH) agonist or antagonist or orchiectomy.
22 . The method of claim 21 , wherein the non-metastatic castration-resistant prostate cancer is a high risk non-metastatic castration-resistant prostate cancer.
23 . The method of claim 21 , wherein the second-generation anti-androgen is administered in combination with the GnRH agonist or antagonist.
24 . The method of claim 21 , wherein the second-generation anti-androgen is administered in combination with the GnRH agonist and the GnRH agonist is leuprolide, buserelin, nafarelin, histrelin, goserelin, or deslorelin.
25 . The method of claim 21 , wherein the second-generation anti-androgen is administered post-orchiectomy.
26 . The method of claim 21 , wherein the male human previously received a first-generation anti-androgen, and wherein the first-generation anti-androgen is bicalutamide, flutamide or nilutamide.
27 . The method of claim 21 , wherein the second-generation anti-androgen is administered daily to the male human.
28 . The method of claim 21 , wherein the second-generation anti-androgen is administered orally to the male human.
29 . The method of claim 21 , wherein the second-generation anti-androgen is administered orally to the male human on a continuous daily dosing schedule.
30 . The method of claim 21 , wherein the second-generation anti-androgen is administered orally to the male human at a dose of about 600 mg.
31 . The method of claim 21 , wherein the second-generation anti-androgen is administered orally to the male human at a dose of about 600 mg twice a day.
32 . The method of claim 21 , wherein the second-generation anti-androgen is in a unit dosage form, and wherein the unit dosage form is in the form of a tablet.
33 . A method of treating non-metastatic castration-resistant prostate cancer in a male human consisting essentially of administering a second-generation anti-androgen to a male human in need of such treatment, wherein the second-generation anti-androgen is administered in combination with a gonadotropin-releasing hormone (GnRH) agonist or antagonist or orchiectomy.
34 . The method of claim 33 , wherein the non-metastatic castration-resistant prostate cancer is a high risk non-metastatic castration-resistant prostate cancer.
35 . The method of claim 33 , wherein the second-generation anti-androgen is administered in combination with the GnRH agonist or antagonist.
36 . The method of claim 33 , wherein the second-generation anti-androgen is administered in combination with the GnRH agonist and the GnRH agonist is leuprolide, buserelin, nafarelin, histrelin, goserelin, or deslorelin.
37 . The method of claim 33 , wherein the second-generation anti-androgen is administered post-orchiectomy.
38 . The method of claim 33 , wherein the second-generation anti-androgen is administered orally to the male human at a dose of about 600 mg.
39 . The method of claim 33 , wherein the second-generation anti-androgen is administered orally to the male human at a dose of about 600 mg twice a day.Join the waitlist — get patent alerts
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