Combination of immunotherapies with MDM2 inhibitors

Patent metadata

Field	Value
Publication number	US-12268665-B2
Application number	US-201916618794-A
Country	US
Kind code	B2
Filing date	Aug 7, 2019
Priority date	Aug 8, 2018
Publication date	Apr 8, 2025
Grant date	Apr 8, 2025

Abstract

Disclosed herein are combination therapies comprising an effective amount of a modulator of the immune checkpoint molecule; and an effective amount of a MDM2 inhibitor.

First claim

What is claimed is:

1. A method of treating liver cancer- or colon cancer, comprising administering to a subject in need thereof:
a) an effective amount of a modulator of an immune checkpoint molecule; wherein the modulator of the immune checkpoint molecule is an anti-PD-1 antibody; and
b) an effective amount of a MDM2 inhibitor, wherein the MDM2 inhibitor is represented by the following formula:

or a pharmaceutically acceptable salt thereof, wherein

is selected from the group consisting of

B is a C 4-7 carbocyclic ring;
R 1 is H, substituted or unsubstituted C 1-4 alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted heterocycloalkyl, OR a , or NR a R b ;
n is 0, 1, or 2;
R 2 , R 3 , R 4 , R 5 , R 7 , R 8 , R 9 , and R 10 , independently, are selected from the group consisting of H, F, Cl, CH 3 , and CF 3 ;
R 6 is

R a is hydrogen or substituted or unsubstituted C 1-4 alkyl;
R b is hydrogen or substituted or unsubstituted C 1-4 alkyl;
R c and R d are substituents on one carbon atom of ring B, wherein
R e is H, C 1-3 alkyl, C 1-3 alkylene-OR a , OR a , or halo;
R d is H, C 1-3 alkyl, C 1-3 alkylene-OR a , OR a , or halo; or
R c and R d are taken together with the carbon to which they are attached to form a 4 to 6-membered Spiro substituent, optionally containing an oxygen atom; and
R e is —C(═O) OR a , —C(═O) NR a R b , or —C(═O) NHSO 2 CH 3 .

2. The method of claim 1 , wherein the MDM2 inhibitor is selected from:

3. The method of claim 1 , wherein the MDM2 inhibitor is

or a pharmaceutically acceptable salt thereof.

4. The method of claim 1 , wherein the anti-PD-1 antibody is pembrolizumab, ipilimumab, nivolumab, atezolizumab, avelumab or durvalumab.

5. The method of claim 1 , wherein the effective amount of a MDM2 inhibitor is from about 1 mg to about 300 mg.

6. The method of claim 1 , wherein the MDM2 inhibitor is administered orally in an amount from about 30 mg to about 250 mg every other day, or about 50 mg to about 200 mg every other day.

7. The method of claim 1 , wherein the anti-PD-1 antibody is administered via intravenous infusion in an amount of 200 mg on day 1 of a 21-day or 28-day treatment cycle.

8. The method of claim 1 , wherein the method comprises at least one 21-day or 28-day treatment cycle, wherein the MDM2 inhibitor, or pharmaceutically acceptable salt thereof, is administered orally every other day in a patient in need thereof for the first two consecutive weeks of a 21-day or 28-day treatment cycle and is not administered during the third week of the treatment cycle; or the method comprises at least one 28-day treatment cycle, wherein the MDM2 inhibitor, or pharmaceutically acceptable salt thereof, is administered orally every other day in a patient in need thereof for the first three consecutive weeks of a 28-day treatment cycle and is not administered during the fourth week of the treatment cycle.

9. The method of claim 8 , wherein the MDM2 inhibitor is administered orally in the patient in an amount from about 50 mg to about 200 mg on day 1, 3, 5, 7, 9, 11, and 13 of the 21-day treatment cycle; or wherein the MDM2 inhibitor is administered orally in the patient in an amount from about 50 mg to about 200 mg on day 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, and 21 of the 28-day treatment cycle.

10. The method of claim 9 , wherein the MDM2 inhibitor is administered orally in the patient in an amount of about 50 mg, about 100 mg, about 150 mg, or about 200 mg on day 1, 3, 5, 7, 9, 11, and 13 of the 21-day treatment cycle, or wherein the MDM2 inhibitor is administered orally in the patient in an amount of about 50 mg, about 100 mg, about 150 mg, or about 200 mg on day 1, 3, 5, 7, 9, 11, 13, 15, 17, 19, and 21 of the 28-day treatment cycle.

11. The method of claim 8 , wherein the patient is refractory or relapse of or resistant to anti-PD-1 therapy.

12. The method of claim 8 , wherein the patient is suffering from advanced solid tumors.

13. A method for treating hyper-progression in a patient receiving anti-PD-1/PD-L1 therapy for the treatment of liver cancer, wherein the method comprises administering to the patient in need thereof a therapeutically effective amount of a MDM2 inhibitor, wherein the MDM2 inhibitor is

or a pharmaceutically acceptable salt thereof.

Assignees

• Ascentage Pharma Suzhou Co Ltd

Inventors

• Yang Dajun
• Zhai Yifan
• Fang Douglas Dong
• Tang Qiuqiong

Classifications

• A61K39/3955

  against proteinaceous materials, e.g. enzymes, hormones, lymphokines · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• A61K2039/55

  characterised by the host/recipient, e.g. newborn with maternal antibodies · CPC title

• A61K2039/507

  Comprising a combination of two or more separate antibodies · CPC title

• A61K2039/505

  comprising antibodies · CPC title