IP Library Granted Patent US 11,168,061
Granted Patent B2
US 11,168,061 · App. 16/331,728 · Granted Nov 9, 2021

Small molecule prolactin receptor inhibitors, pharmaceutical compositions and treatment methods using such inhibitors

Inventors: Nira Ben-Jonathan (Cincinnati, OH); Eric R. Hugo (Cincinnati, OH); Edward J. Merino (Cincinnati, OH); Abraham J. Domb (Jerusalem, IL); Armen N. Akopian (Austin, TX)
Assignees: University of Cincinnati; University of Texas System; The Hebrew University of Jerusalem
C07D253/075A61K9/0019A61K9/0053A61K31/135A61K31/415A61K31/475A61K31/53A61K45/06A61P35/00A61K31/122A61K31/337A61K31/4184A61K31/437A61K33/243
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 11,168,061
App. No.
16/331,728
Granted
Nov 9, 2021
Kind
B2
Abstract

Small molecule inhibitors (SMIs) of the Prolactin receptor, pharmaceutical compositions of the SMIs, and methods for treating patients suffering from disorders characterized increased expression or excitation of the Prolactin receptor, including breast cancer, prostate cancer and nociceptive pain disorders such as migraine headache, by administering pharmaceutical compositions of SMIs are provided.

Claims (19)

1. A pharmaceutical composition comprising:

a small molecule prolactin receptor (PRLR) inhibitor according to Formula I or a pharmaceutically acceptable salt thereof; and

at least one pharmaceutically acceptable carrier,

wherein Formula I is structurally depicted as:

and wherein:

R 1 and R 2 are independently selected from —CY 3 , linear or cyclic alkyl, halogen, cycloalkyl, heterocycloalkyl, alkenyl, alkynyl, aryl, heteroaryl, and H;

a, b, and c are independently 0, 1, 2, or 3; and

each Y is independently H or halogen selected from Cl, Br, F, and I.

2. The pharmaceutical composition according to claim 1 , wherein R 1 is selected from —CY 3 , halogen and H; R 2 is selected from CY 3 , halogen, and linear C2-C3 alkyl; a, b, and c are independently 0, 1, or 2; and each Y is independently F or H.

3. The pharmaceutical composition according to claim 1 wherein the small molecule PRLR inhibitor is a compound according to Formula I and structurally depicted as:

4. The pharmaceutical composition according to claim 1 , formulated as an injectable solution or as an oral dosing form.

5. The pharmaceutical composition according to claim 4 , wherein the molar concentration of inhibitor is up to 10 μM, up to 5 μM, between 1 μM and 10 μM, between 5 μM and 10 μM, or between 1 μM and 5 μM.

6. A method of treating breast cancer or prostate cancer in a subject in need thereof, the method comprising: administering to the subject an effective amount of a pharmaceutical composition according to claim 1 .

7. The method according to claim 6 , wherein administration of the pharmaceutical composition is by a parenteral route or an oral route.

8. The method according to claim 6 wherein the pharmaceutical composition is administered in conjunction with one or more chemotherapeutic agents that affect cellular microtubules.

9. The method according to claim 8 , wherein the one or more chemotherapeutic agents are selected from the group consisting of cisplatin, demecolcine, nocodazole, vinblastine, and paclitaxel.

10. A method of reducing or substantially eliminating acquired resistance to chemotherapeutic drugs in a patient undergoing or about to undergo treatment for breast cancer or prostate cancer comprising a regimen of one or more chemotherapeutic drugs, the method comprising administering to the patient an effective amount of a pharmaceutical composition according to claim 1 .

11. The method according to claim 10 , wherein administering the pharmaceutical composition is before, during, and/or after initiation of the regimen of one or more chemotherapeutic drugs.

12. The method according to claim 10 , wherein the one or more chemotherapeutic drugs are selected from the group consisting of cisplatin, demecolcine, nocodazole, vinblastine, and paclitaxel.

Assignments (4)
CONFIRMATORY LICENSE Recorded Feb 15, 2023
From: UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANTONIO
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 062760/0261 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 7, 2019
From: AKOPIAN, ARMEN N.
To: UNIVERSITY OF TEXAS SYSTEM
Reel/Frame 049095/0970 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 7, 2019
From: DOMB, ABRAHAM J.
To: THE HEBREW UNIVERSITY OF JERUSALEM
Reel/Frame 049096/0052 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 11, 2019
From: BEN-JOHNSON, NIRA; HUGO, ERIC; MERINO, EDWARD J.
To: UNIVERSITY OF CINCINNATI
Reel/Frame 048861/0395 →
Continuity (3)
Provisional Application 62385948 · Sep 9, 2016
Provisional Application 62410907 · Oct 21, 2016
Related Publication 20190202794A1 · Jul 4, 2019