Compositions of adagrasib and mTOR inhibitors and methods of treatment therewith

Patent metadata

Field	Value
Publication number	US-12527795-B2
Application number	US-201917275180-A
Country	US
Kind code	B2
Filing date	Sep 10, 2019
Priority date	Sep 10, 2018
Publication date	Jan 20, 2026
Grant date	Jan 20, 2026

Abstract

The present invention relates to combination therapies for treating KRas G12C cancers. In particular, the present invention relates to methods of treating cancer in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a combination of a mTOR inhibitor and a KRAS G12C inhibitor of Formula (I), Formula I-A or Formula I-B, pharmaceutical compositions comprising a therapeutically effective amounts of the inhibitors, kits comprising the compositions and methods of use therefor.

First claim

We claim:

1 . A pharmaceutical composition, comprising a therapeutically effective amount of the combination of a mTOR inhibitor selected from the group consisting of everolimus, rapamycin, zoatarolimus, ridaforolimus, sapanisertib, Torin-1, dacotlisib, BEZ235, buparlisib, GDC-0941, GDC-0349, VS-5584 and vistusertib, and a KRAS G12C inhibitor of formula

or a pharmaceutically acceptable salt thereof: and a pharmaceutically acceptable excipient.

2 . A kit comprising: a) a pharmaceutical composition comprising a mTOR inhibitor selected from the group consisting of everolimus, rapamycin, zotarolimus, ridaforolimus, sapanisertib, Torin-1, dactolisib, BEZ235, buparlisib, GDC-0941, GDC-0349, VS-5584 and vistusertib; and b) a pharmaceutical composition comprising a KRAS G12C inhibitor of formula

or a pharmaceutically acceptable salt thereof for treating cancer in a subject.

3 . A kit comprising the pharmaceutical composition of claim 1 for treating KRAS G12C-associated cancer in a subject.

4 . A method for inhibiting KRAS G12C activity in a cancer cell, comprising contacting the cell in which inhibition of KRAS G12C activity is desired with an effective amount of a mTOR inhibitor selected from the group consisting of everolimus, rapamycin, zotarolimus, ridaforolimus, sapanisertib, Torin-1, dactolisib, BEZ235, buparlisib, GDC-0941, GDC-0349, VS-5584 and vistusertib, and a KRAS G12C inhibitor of formula

or a pharmaceutically acceptable salt thereof,
wherein the mTOR inhibitor synergistically increases the sensitivity of the cancer cells to the KRAS G12C inhibitor.

5 . A method of treating KRAS G12C-associated cancer in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a combination of a mTOR inhibitor selected from the group consisting of everolimus, rapamycin, zotarolimus, ridaforolimus, sapanisertib, Torin-1, dactolisib, BEZ235, buparlisib, GDC-0941, GDC-0349, VS-5584 and vistusertib, and a KRAS G12C inhibitor of formula

or a pharmaceutically acceptable salt thereof.

6 . The method according to claim 5 , wherein the therapeutically effective amount of the KRAS G12C inhibitor compound is between about 0.01 to 100 mg/kg per day.

7 . The method according to claim 5 , wherein the cancer is selected from the group consisting of
Cardiac cancer, Lung cancer, Gastrointestinal cancer, Genitourinary tract cancer, Liver cancer, Biliary tract cancer, Nervous system cancer, Gynecological cancer, Hematologic cancer and Skin cancer.

8 . The method of claim 5 , wherein the KRAS G12C-associated cancer is non-small cell lung cancer.

9 . The method according to claim 5 , wherein said cancer is a sarcoma selected from angiosarcoma, fibrosarcoma, rhabdomyosarcoma, and liposarcoma, myxoma, rhabdomyoma, fibroma, lipoma and teratoma.

10 . The method according to claim 5 , wherein said KRAS G12C-associated cancer selected from squamous cell, undifferentiated small cell, undifferentiated large cell, and adenocarcinoma, alveolar carcinoma, bronchial adenoma, sarcoma, lymphoma, chondromatous hamartoma and mesothelioma.

11 . The method according to claim 5 , wherein said cancer is a gastrointestinal cancer selected from esophagus cancer, squamous cell carcinoma, adenocarcinoma, and leiomyosarcoma.

12 . The method according to claim 5 , wherein said cancer is selected from leiomyosarcoma, pancreatic cancer, ductal adenocarcinoma, insulinoma, glucagonoma, gastrinoma, carcinoid tumors, and vipoma.

13 . The method according to claim 5 , wherein said cancer is small bowel cancer selected from adenocarcinoma, lymphoma, carcinoid tumors, Kaposi's sarcoma, leiomyoma, hemangioma, lipoma, neurofibroma, and fibroma.

14 . The method according to claim 5 , wherein said cancer is large bowel cancer selected from adenocarcinoma, tubular adenoma, villous adenoma, hamartoma, and leiomyoma.

15 . The method according to claim 5 , wherein said cancer is genitourinary tract cancer, kidney cancer, adenocarcinoma or nephroblastoma.

16 . The method according to claim 5 , wherein said cancer is genitourinary tract bladder or urethra cancer selected from squamous cell carcinoma, transitional cell carcinoma, and adenocarcinoma.

17 . The method according to claim 5 , wherein said cancer is prostate cancer selected from adenocarcinoma and sarcoma.

18 . The method according to claim 5 , wherein said cancer is testicular cancer selected from seminoma, teratoma, embryonal carcinoma, teratocarcinoma, choriocarcinoma, sarcoma, interstitial cell carcinoma, fibroma, fibroadenoma, adenomatoid tumors and lipoma.

19 . The method according to claim 5 , wherein said cancer is liver cancer.

20 . The method according to claim 19 , wherein said liver cancer is selected from hepatocellular carcinoma, cholangiocarcinoma, hepatoblastoma, angiosarcoma, hepatocellular adenoma, and hemangioma.

21 . The method according to claim 5 , wherein said cancer is selected from gallbladder carcinoma, ampullary carcinoma, cholangiocarcinoma, osteosarcoma, fibrosarcoma, malignant fibrous histiocytoma, chondrosarcoma, Ewing's sarcoma, malignant lymphoma, reticulum cell sarcoma, multiple myeloma, malignant giant cell tumor chordoma, osteochronfroma, osteocartilaginous exostoses, benign chondroma, chondroblastoma, chondromyxofibroma, osteoid osteoma and giant cell tumors.

22 . The method according to claim 5 , wherein said cancer is selected from meningioma, meningiosarcoma, gliomatosis, astrocytoma, medulloblastoma, glioma, ependymoma, germinoma, pinealoma, glioblastoma multiform, oligodendroglioma, schwannoma, retinoblastoma, and congenital tumors, spinal cord neurofibroma, meningioma, glioma, and sarcoma.

23 . The method according to claim 5 , wherein said cancer is selected from uterine cancer, endometrial carcinoma, serous cystadenocarcinoma, mucinous cystadenocarcinoma, and unclassified carcinoma, granulosa-thecal cell tumors, Sertoli-Leydig cell tumors, dysgerminoma, and malignant teratoma, vulva cancer, squamous cell carcinoma, intraepithelial carcinoma, adenocarcinoma, fibrosarcoma, melanoma, vagina cancer, squamous cell carcinoma, botryoid sarcoma, embryonal rhabdomyosarcoma, and fallopian tube cancer.

24 . The method according to claim 5 , wherein said cancer is selected from myeloid leukemia, acute lymphoblastic leukemia, chronic lymphocytic leukemia, myeloproliferative diseases, multiple myeloma, and myelodysplastic syndrome, Hodgkin's disease, non-Hodgkin's lymphoma.

25 . The method according to claim 5 , wherein said cancer is selected from malignant melanoma, basal cell carcinoma, squamous cell carcinoma, Kaposi's sarcoma, adrenal gland cancer and neuroblastoma.

26 . A method of treating KRAS G12C-associated cancer in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a mTOR inhibitor selected from the group consisting of everolimus, rapamycin, zotarolimus, ridaforolimus, sapanisertib

Assignees

• Mirati Therapeutics Inc

Inventors

• Olson Peter
• Aranda Ruth Wei
• Christensen James Gail
• Engstrom Lars Daniel
• Hallin Jill

Classifications

• A61K31/5377

  not condensed and containing further heterocyclic rings, e.g. timolol · CPC title

• A61K31/4745

  condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines (yohimbine derivatives, vinblastine A61K31/475; ergoline derivatives A61K31/48) · CPC title

• A61K31/436

  the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin · CPC title

• A61P35/00

  Antineoplastic agents · CPC title

• A61K31/506

  not condensed and containing further heterocyclic rings · CPC title