IP Library Granted Patent US 12,318,386
Granted Patent B2
US 12,318,386 · App. 17/273,884 · Granted Jun 3, 2025

Combination of XPO1 inhibitors and second agents for the treatment of prostate cancer

Inventor: Erkan Baloglu (Stoneham, MA)
Assignee: Karyopharm Therapeutics Inc.
A61K31/506A61K9/0053A61K31/433A61K31/573A61K31/58A61P35/00
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 12,318,386
App. No.
17/273,884
Granted
Jun 3, 2025
Kind
B2
Abstract

This invention relates to a method of treating prostate cancer comprising administering a compound of Formula (I) or a salt thereof in combination with either abiraterone or enzalutamide.

Claims (9)

1. A method of treating prostate cancer in an abiraterone-refractory subject in need thereof, comprising the combination administration to the subject over a 28-day treatment cycle of a first amount of abiraterone, and a second amount of a compound of Formula (I):

or a pharmaceutically acceptable salt thereof, wherein the first and second amounts together comprise an effective amount; and wherein the compound of Formula (I) is administered on days 1-5, 8-12, 15-19, and 22-26 of the 28-day treatment cycle and abiraterone is administered daily during the 28-day treatment cycle.

2. The method of claim 1 , wherein the subject was previously administered at least one treatment regimen for prostate cancer, and further wherein, for each subject who previously received two or more treatment regimens, different active ingredients were administered in each treatment regimen.

3. The method of claim 1 , wherein the compound of Formula (I) is administered at a dose of 5 mg to 40 mg per day.

4. The method of claim 1 , wherein the prostate cancer is metastatic castration-resistant prostate cancer or castration-resistant prostate cancer.

5. The method of claim 1 , wherein abiraterone is abiraterone acetate.

6. The method of claim 1 , wherein abiraterone is administered orally once daily at a dose of 200 mg to 2000 mg.

7. The method of claim 1 , wherein prednisone is administered in combination with abiraterone.

8. The method of claim 7 , wherein prednisone is administered orally at a dose of 1 mg to 20 mg.

Assignments (6)
RELEASE OF SECURITY INTEREST IN PATENTS AT REEL/FRAME NO. 67396/0532 Recorded Oct 14, 2025
From: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS AGENT
To: KARYOPHARM THERAPEUTICS INC.
Reel/Frame 073111/0142 →
PATENT SECURITY AGREEMENT Recorded Oct 10, 2025
From: KARYOPHARM THERAPEUTICS INC.
To: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS AGENT
Reel/Frame 073058/0647 →
PATENT SECURITY AGREEMENT Recorded Oct 10, 2025
From: KARYOPHARM THERAPEUTICS INC.
To: WILMINGTON SAVINGS FUND SOCIETY, FSB, AS COLLATERAL TRUSTEE
Reel/Frame 073058/0504 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2025
From: BALOGLU, ERKAN
To: KARYOPHARM THERAPEUTICS INC.
Reel/Frame 070968/0959 →
SECOND LIEN PATENT SECURITY AGREEMENT Recorded May 13, 2024
From: KARYOPHARM THERAPEUTICS INC.
To: WILMINGTON SAVINGS FUND SOCIETY, FSB
Reel/Frame 067396/0532 →
SECURITY INTEREST Recorded May 8, 2024
From: KARYOPHARM THERAPEUTICS INC.
To: WILMINGTON SAVINGS FUND SOCIETY, FSB
Reel/Frame 067345/0255 →
Continuity (3)
Provisional Application 62803136 · Feb 8, 2019
Provisional Application 62728267 · Sep 7, 2018
Related Publication 20210315897A1 · Oct 14, 2021
References Cited (14)
US 9738624B2 · Baloglu · 2017 [cited by examiner]
US 10407405B2 · Baloglu · 2019 [cited by examiner]
US 11124493B2 · Baloglu · 2021 [cited by examiner]
US 20160152596A1 · Baloglu · 2016 [cited by examiner]
WO WO2015065919A1 · 2015 [cited by applicant]
WO WO2020051294A1 · 2020 [cited by applicant]
Wei et al. The Oncologist 2018, 23, 656-e64 (Year: 2018). [cited by examiner]
Ryan et al. Lancet Oncol. 2015, 16, 152-160 (Year: 2015). [cited by examiner]
Aboukameel et al., “Down-regulation of AR splice variants through XP01 suppression contributes to the inhibition of prostate cancer progression,” Oncotarget, 9(82):35327-35342 (2018). [cited by applicant]
Argueta et al., “Disruption of niclear export with selinexor or KPT-8602 reduces androgen receptor expression and leads to potent anti-tumor activity in preclinical models of androgen-independent prostate cancer,” Cance… [cited by applicant]
International Search Report and Written Opinion for International Application No. PCT/US2019/049689 dated Jan. 13, 2020. [cited by applicant]
Irfana et al., “Down-regulation of AR splice variants through XP01 suppression contributes to the inhibition of prostate cancer progression,” Cancer Research, 78(13):2492 (2018). [cited by applicant]
Xiao et al., “A phase II trial of slinexor, an oral selective inhibitor of nuclear export compound, in abiraterone- and/or enxalutamide-refractory metastatic castration-resistant prostate cancer,” The Oncologist, 23(6):… [cited by applicant]
Zhang et al., “Eltanexor (KPT-8602), a secondgeneration selective inhibitor of nuclear export (SINE) compound, in patients with metastatic castration-resistant prostate cancer (mCRPC),” Journal of Clinical Oncology, 37:… [cited by applicant]