WO2021178296A1 - Therapeutic uses of macrocyclic compounds - Google Patents

Therapeutic uses of macrocyclic compounds Download PDF

Info

Publication number
WO2021178296A1
WO2021178296A1 PCT/US2021/020255 US2021020255W WO2021178296A1 WO 2021178296 A1 WO2021178296 A1 WO 2021178296A1 US 2021020255 W US2021020255 W US 2021020255W WO 2021178296 A1 WO2021178296 A1 WO 2021178296A1
Authority
WO
WIPO (PCT)
Prior art keywords
cancer
carcinoma
met
compound
alkyl
Prior art date
Application number
PCT/US2021/020255
Other languages
French (fr)
Inventor
Brion William MURRAY
Dayong Zhai
Jingrong J. CUI
Original Assignee
Turning Point Therapeutics, Inc.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Turning Point Therapeutics, Inc. filed Critical Turning Point Therapeutics, Inc.
Priority to CA3174455A priority Critical patent/CA3174455A1/en
Priority to EP21764224.8A priority patent/EP4114530A4/en
Priority to JP2022552626A priority patent/JP2023515687A/en
Priority to AU2021229457A priority patent/AU2021229457A1/en
Priority to MX2022010945A priority patent/MX2022010945A/en
Priority to BR112022017425A priority patent/BR112022017425A2/en
Priority to IL295938A priority patent/IL295938A/en
Priority to CN202180023879.XA priority patent/CN115397514A/en
Priority to KR1020227034099A priority patent/KR20230022151A/en
Publication of WO2021178296A1 publication Critical patent/WO2021178296A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D498/18—Bridged systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents

Definitions

  • This disclosure relates to the use of certain diaryl macrocycle compounds in the treatment of disease in mammals. This disclosure also relates to compositions including such compounds, and to methods of using such compositions in the treatment of diseases in mammals, especially in humans.
  • Protein kinases are key regulators for cell growth, proliferation and survival. Genetic and epigenetic alterations accumulate in cancer cells leading to abnormal activation of signal transduction pathways which drive malignant processes. (Manning, G. et al, The protein kinase complement of the human genome. Science 2002, 298, 1912-1934). Pharmacological inhibition of these signaling pathways presents promising intervention opportunities for targeted cancer therapies. (Sawyers, C. Targeted cancer therapy. Nature 2004, 432 , 294-297).
  • MET also called hepatocyte growth factor receptor (HGFR)
  • HGFR hepatocyte growth factor receptor
  • HGF Hepatocyte growth factor
  • SF scatter factor
  • HGF/MET signaling pathway is implicated in invasive growth during embryo development, postnatal organ regeneration, wound healing and tissue regeneration processes.
  • HGF/MET axis is frequently hijacked by cancer cells for turn ori genesis, invasive growth, and metastasis (Boccaccio, C.; Comoglio, P. M. Invasive growth: aMET-driven generic programme for cancer and stem cells. Nat. Rev. Cancer 2006, 6, 637-645).
  • Deregulations of MET and/or HGF via activating mutations, gene amplifications, overexpression, and both autocrine or paracrine loop regulation influence cell growth, proliferation, angiogenesis, invasion, survival, and metastasis, leading to tumorigenesis and tumor progression (Ma, PC et al. Expression and mutational analysis of MET in human solid cancers. Genes Chromosomes Cancer 2008, 47, 1025- 1037).
  • MET and/or HGF Over-expression of MET and/or HGF has been detected in a large variety of solid tumors such as liver, breast, pancreas, lung, kidney, bladder, ovary, brain, prostate, and many others, and is often associated with a metastatic phenotype and poor prognosis (Maulik, G., et al. Role of the hepatocyte growth factor receptor, MET, in oncogenesis and potential for therapeutic inhibition. Cytokine Growth Factor Rev. 2002, 13, 41-59). MET amplification has been reported in different human cancers including gastroesophageal carcinomas, colorectal cancers, NSCLC, medulloblastomas, and glioblastomas (Smolen, G. A., et al.
  • Amplification of MET may identify a subset of cancers with extreme sensitivity to the selective tyrosine kinase inhibitor PHA-665752. Proc. Natl. Acad. Sci. U. S. A. 2006, 103, 2316-2321).
  • a diverse set of MET mutations in the tyrosine kinase domain, juxtamembrane, and extracellular domain of both germline and somatic mutations have been described in many solid tumors, including hereditary and sporadic human papillary renal carcinomas, lung cancer, ovarian cancer, childhood hepatocellular carcinomas, squamous cell carcinoma of the head and neck, and gastric cancer (Ghiso, E.; Giordano, S.
  • MET exon 14 deletion represents a novel class of actionable oncogenic event with potential clinical impact and therapeutic applications in patients affected by different cancer types (Pilotto S, MET exon 14 juxtamembrane splicing mutations: clinical and therapeutical perspectives for cancer therapy. Ann Transl Med. 2017 5(1):2).
  • Autocrine or paracrine stimulation is one mechanism for aberrant MET activation.
  • the MET autocrine activation plays a causal role in the development of malignant melanoma and acquisition of the metastatic phenotype (Otsuka, T., et al.
  • MET autocrine activation induces development of malignant melanoma and acquisition of the metastatic phenotype. Cancer Res. 1998, 58, 5157-5167).
  • GBM glioblastoma
  • HGF autocrine expression correlated with MET phosphorylation levels in HGF autocrine cell lines, and showed high sensitivity to MET inhibition in vivo, while an HGF paracrine environment could enhance glioblastoma growth in vivo but did not demonstrated sensitivity to MET inhibition
  • HGF Hepatocyte growth factor
  • Genomic alterations to the receptor tyrosine kinase are oncogenic drivers for a range of cancers (Campbell et al 2016 Nat Genet 48, 607-16; Sadiq et al., 2013 J Clin Oncol 31, 1089-96) as well as resistance mechanisms to other molecular medicines such as osimertinib for the treatment of lung cancer patients (Ko et al., 2017 Ann TranslMed 5(1), 4; Liu et al., 2018 Molecular Cancer 17, article 53).
  • MET targeted therapies patients treated with MET targeted therapies often develop drug resistance by either bypass signaling, mutation to MET, or by unknown mechanisms as is illustrated by a recent publication (Recondo et al, 2020 Clin Cancer Res, doi 10.1158/1078- 0432.CCR-19-3608).
  • 35% of the 20 patients treated with a MET targeted therapy had MET mutations at disease progression (e.g. MET residues H1094, G1163, LI 195, D1228, Y1230, and high levels of MET amplification).
  • inhibitors that potently inhibit MET or potently inhibit mutated forms of MET are expected to have enhanced clinical benefit for patients with amplified MET or mutated forms of MET.
  • Src is a non-receptor tyrosine kinase that is deregulated in many types of cancer, and a key downstream transducer of many RTKs, including EGFR, HER2, and c-Met. Activation of Src signaling has been implicated in conferring therapeutic resistance to targeted antiendocrine therapies, receptor tyrosine kinase therapies, traditional chemotherapies, and radiation therapies. (Zhang S, et al Trends Pharmacol Sci. 2012, 33, 122). Src inhibitor may play important roles in combinatorial regimens in overcoming resistance to current anticancer therapies and in preventing metastatic recurrence.
  • Cytoplasmic tyrosine kinases also known as non-receptor tyrosine kinases
  • Src family SFKs
  • SFKs Src family
  • Elevated SFK activity is found in more than 80% of human colorectal cancer (CRC) and this has been associated with poor clinical outcome.
  • CRC colorectal cancer
  • the SFK member Yes regulates specific oncogenic signalling pathways important for colon cancer progression that is not shared with c-Src. (Scancier F. et al. PLoS One.
  • WASF2-FGR fusion genes were found in lung squamous carcinoma, ovarian serous cystadenocarcinoma, and skin cutaneous melanoma.
  • Estrogen receptor-positive (ER + ) breast cancers adapt to hormone deprivation and become resistant to antiestrogen therapy.
  • Mutations in the inhibitory SH2 domain of the SRC family kinase (SFK) LYN were related to ER + tumors that remained highly proliferative after treatment with the aromatase inhibitor letrozole.
  • LYN was upregulated in multiple ER + breast cancer lines resistant to long-term estrogen deprivation.
  • LYN was upregulated in multiple ER + breast cancer lines resistant to long-term estrogen deprivation.
  • LYN was overexpressed in castrate-resistant prostate cancer (CRPC), enhanced AR transcriptional activity, and accelerated CRPC progression, and targeting Lyn kinase induced AR dissociation from the molecular chaperone Hsp90, leading to its ubiquitination and proteasomal degradation.
  • CRPC castrate-resistant prostate cancer
  • Lyn kinase induced AR dissociation from the molecular chaperone Hsp90 leading to its ubiquitination and proteasomal degradation.
  • the Lyn tyrosine kinase is a potential therapeutic target for the treatment of CRPC.
  • the Src family kinase FYN is involved in signal transduction pathways in the nervous system, as well as the development and activation of T lymphocytes under normal physiological conditions.
  • Fyn Activation of Fyn is observed in various cancers, including melanoma, glioblastoma, squamous cell carcinoma, prostate and breast cancers.
  • Fyn was upregulated in tamoxifen-resistant breast cancer cell lines and plays a key role in the resistance mechanism.
  • Peripheral T-cell lymphomas PTCLs
  • PTCLs Peripheral T-cell lymphomas
  • FYN activating mutations were found in PTCL, and promoted the growth of cells transformed via expression of activated FYN mutant alleles.
  • SRC kinase inhibitors may play important roles in the treatment of PTCLs.
  • R 1 , R 2 , R 3 , and R 4 are defined as described herein have been shown to have activity against wild-type and mutant MET, SRC, and CSF1R.
  • One such compound is (7ri)-3-amino-14-ethyl-ll-fluoro-7-methyl-4-oxo-4,5,6,7,13,14- hexahydro-l,15-ethenopyrazolo[4,3-
  • Compound 1 has properties, including anti-tumor properties, which are pharmacologically mediated through inhibition of receptor and non-receptor tyrosine kinases.
  • Compounds of the formula I, in particular, Compound 1 are disclosed in International Patent Publication No. WO2019/023417, which is incorporated herein by reference in its entirety.
  • the present disclosure provide a method of treating disease, such as cancer, in a mammal, in particular a human patient comprising, administering to the mammal, in particular a human patient, a therapeutically effective amount of a compound that inhibits MET, SRC, and CSF1R, wherein the disease is mediated by a genetically altered MET.
  • a compound that inhibits MET, SRC, and CSF1R is of the formula I
  • the compound that inhibits MET, SRC, and CSF1R is of the formula or a pharmaceutically acceptable salt thereof.
  • the mammal in particular a human patient, has received prior treatment with one or more therapeutic agents.
  • the present disclosure provides a method of treating cancer in a patient previously shown to express a genetically altered MET comprising, administering to the patient a therapeutically effective amount of a compound that inhibits MET, SRC, and CSF1R.
  • a compound that inhibits MET, SRC, and CSF1R is of the formula I
  • the compound that inhibits MET, SRC, and CSF1R is of the formula or a pharmaceutically acceptable salt thereof.
  • the patient has received prior treatment with one or more therapeutic agents.
  • the present disclosure provides a method of treating cancer in a patient comprising; i. identifying a genetically altered MET in the patient, and ii. administering to the patient a therapeutically effective amount of a compound that inhibits MET, SRC, and CSF1R.
  • a compound that inhibits MET, SRC, and CSF1R is of the formula I
  • the compound that inhibits MET, SRC, and CSF1R is of the formula or a pharmaceutically acceptable salt thereof.
  • the patient has received prior treatment with one or more therapeutic agents.
  • the present disclosure provides a method of identifying a patient for treatment with a compound that inhibits MET, SRC, and CSF1R. comprising diagnosing the patient with a cancer mediated by a genetically altered MET.
  • the compound that inhibits MET, SRC, and CSF1R is of the formula I
  • the compound that inhibits MET, SRC, and CSF1R is of the formula or a pharmaceutically acceptable salt thereof.
  • the patient has received prior treatment with one or more therapeutic agents.
  • the present disclosure provides a use of compound that inhibits MET, SRC, and CSF1R in the preparation of a medicament for the treatment of a disease in a patient.
  • the compound that inhibits MET, SRC, and CSF1R is of the formula I
  • the compound that inhibits MET, SRC, and CSF1R is of the formula or a pharmaceutically acceptable salt thereof.
  • the patient has received prior treatment with one or more therapeutic agents.
  • the present disclosure provides a compound inhibits MET, SRC, and CSF1R for treating cancer in a patient.
  • the compound that inhibits MET, SRC, and CSF1R is of the formula I
  • the compound that inhibits MET, SRC, and CSF1R is of the formula or a pharmaceutically acceptable salt thereof.
  • the patient has received prior treatment with one or more therapeutic agents.
  • the present disclosure provides use of a compound that inhibits MET, SRC, and CSF1R for treating cancer in a patient previously shown to express a genetically altered tyrosine or serine/threonine kinase.
  • the compound that inhibits MET, SRC, and CSF1R is of the formula I
  • the compound that inhibits MET, SRC, and CSF1R is of the formula or a pharmaceutically acceptable salt thereof.
  • the patient has received prior treatment with one or more therapeutic agents.
  • the present disclosure provide a use a compound inhibits MET, SRC, and CSF1R for treating cancer in a patient, wherein the patient has been previously treated with a cancer therapeutic, and the cancer has developed resistance to the cancer therapeutic.
  • the compound that inhibits MET, SRC, and CSF1R is of the formula I or a pharmaceutically acceptable salt thereof, wherein R 1 , R 2 , R 3 , and R 4 are defined as described herein.
  • the compound that inhibits MET, SRC, and CSF1R is of the formula or a pharmaceutically acceptable salt thereof.
  • the patient has received prior treatment with one or more therapeutic agents.
  • the present disclosure provides the use of a compound that inhibits MET, SRC, and CSF1R for treating cancer in a patient previously shown to express a genetically altered tyrosine or serine/threonine kinase, wherein the patient has been previously treated with a cancer therapeutic, and the cancer has developed resistance to the cancer therapeutic.
  • the compound that inhibits MET, SRC, and CSF1R is of the formula I
  • the compound that inhibits MET, SRC, and CSF1R is of the formula or a pharmaceutically acceptable salt thereof.
  • the patient has received prior treatment with one or more therapeutic agents.
  • the genetically altered MET gene comprising a point mutation that is expressed in the c-Met protein.
  • the genetically altered MET comprises a point mutation expressed in the c-Met protein at one or more of positions P991, T992, D1010,
  • the genetically altered MET comprises a point mutation expressed in the c-Met protein that is selected from the group consisting of P991S, T992I, D1010H, D1010Y, VI 0921, H1094N, H1094R, H1094Y, N1100K, N1100S, Y1003C, Y1003F, Y1003H, H1106D,
  • the genetically altered MET comprises a point mutation expressed in the c-Met protein that is selected from the group consisting of T1173I, P991S, M1250T, T992I, V1092I,
  • the cancer is exhibiting bypass resistance.
  • the bypass resistance is mediated by a SRC/CSF1R.
  • the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitt’s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
  • the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER + breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid
  • the patient has been previously treated with a cancer therapeutic. In some embodiments, the patient has been previously treated with a cancer therapeutic, and the cancer has developed resistance to the cancer therapeutic. In some embodiments, the resistance is a primary intrinsic resistance. In some embodiments, the resistance is an acquired resistance from mutation(s). In some embodiments, the resistance is a bypass resistance. In some embodiments, the resistance is an EMT-based resistance.
  • a method of treating cancer in a patient comprising, administering to the patient a therapeutically effective amount of a compound that inhibits MET, SRC and CSF1R, wherein the cancer is mediated by a genetically altered MET.
  • R 1 is H, deuterium, or C1-C6 alkyl
  • R 2 is chloro or -CN
  • R 3 is H, deuterium, or fluoro
  • R 4 is H or Ci-C 6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
  • the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
  • a method of treating cancer in a patient previously shown to have a cancer mediated by a genetically altered MET comprising, administering to the patient a therapeutically effective amount of a compound that inhibits MET, SRC and CSF1R.
  • R 1 is H, deuterium, or C1-C6 alkyl
  • R 2 is chloro or -CN
  • R 3 is H, deuterium, or fluoro
  • R 4 is H or C 1 -C 6 alkyl, wherein each hydrogen atom in C 1 -C 6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC 1 -C 6 alkyl, -NH 2 ,
  • [051] 29 A compound that inhibits MET, SRC and CSF1R for treating cancer in a patient comprising, wherein the cancer is mediated by a genetically altered MET.
  • R 1 is H, deuterium, or C1-C6 alkyl
  • R 2 is chloro or -CN
  • R 3 is H, deuterium, or fluoro
  • R 4 is H or C 1 -C 6 alkyl, wherein each hydrogen atom in C 1 -C 6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC 1 -C 6 alkyl, -NH 2 ,
  • cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
  • the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepato
  • R 1 is H, deuterium, or C1-C6 alkyl
  • R 2 is chloro or -CN
  • R 3 is H, deuterium, or fluoro
  • R 4 is H or Ci-C 6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -ME,
  • cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
  • the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepato
  • a medicament comprising a compound that inhibits MET, SRC and CSF1R for use in a method of treating cancer in a patient comprising, wherein the cancer is mediated by a genetically altered MET.
  • R 1 is H, deuterium, or C1-C6 alkyl
  • R 2 is chloro or -CN
  • R 3 is H, deuterium, or fluoro
  • R 4 is H or Ci-C 6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -ME,
  • the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitt’s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
  • the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitt’s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepat
  • R 1 is H, deuterium, or C1-C6 alkyl
  • R 2 is chloro or -CN
  • R 3 is H, deuterium, or fluoro
  • R 4 is H or C 1 -C 6 alkyl, wherein each hydrogen atom in C 1 -C 6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC 1 -C 6 alkyl, -NH 2 ,
  • cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitt’s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
  • a method of treating cancer in a patient comprising; i. identifying a genetically altered MET in the patient, and ii. administering to the patient a therapeutically effective amount of a compound that inhibits MET, SRC and CSF1R.
  • R 1 is H, deuterium, or C1-C6 alkyl
  • R 2 is chloro or -CN
  • R 3 is H, deuterium, or fluoro
  • R 4 is H or Ci-C 6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
  • any one of clauses 86 to 96 wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER + breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid pa
  • step of identifying comprises subjecting a patient sample to a test selected from the group consisting of FISH, IHC, PCR and gene sequencing.
  • a method of identifying a patient for treatment with a compound that inhibits MET, SRC and CSF1R comprising diagnosing the patient with a cancer mediated by a genetically altered MET.
  • R 1 is H, deuterium, or C1-C6 alkyl
  • R 2 is chloro or -CN
  • R 3 is H, deuterium, or fluoro
  • R 4 is H or C1-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
  • the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
  • diagnosing comprises obtaining a sample from a patient, and modifying the sample using a biological test or biological assay selected from the group consisting of FISH, IHC, PCR and gene sequencing, to provide a measured result showing a genetically altered MET in the sample.
  • a biological test or biological assay selected from the group consisting of FISH, IHC, PCR and gene sequencing
  • alkyl includes a chain of carbon atoms, which is optionally branched and contains from 1 to 20 carbon atoms. It is to be further understood that in certain embodiments, alkyl may be advantageously of limited length, including C1-C12, C1-C1 0 , C1-C 9 , Ci- Cs, C 1 -C 7 , C 1 -C 6 , and C 1 -C 4 , Illustratively, such particularly limited length alkyl groups, including Ci-Ce, C1-C7, C1-C 6 , and C1-C4, and the like may be referred to as “lower alkyl.” Illustrative alkyl groups include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec- butyl, tert-butyl, pentyl, 2-pentyl, 3 -p
  • Alkyl may be substituted or unsubstituted.
  • alkyl may be combined with other groups, such as those provided above, to form a functionalized alkyl.
  • the combination of an “alkyl” group, as described herein, with a “carboxy” group may be referred to as a “carboxyalkyl” group.
  • Other non-limiting examples include hydroxyalkyl, aminoalkyl, and the like.
  • cycloalkyl refers to a 3 to 15 member all-carbon monocyclic ring, including an all-carbon 5-member/6-member or 6-member/6-member fused bicyclic ring, or a multi cyclic fused ring (a “fused” ring system means that each ring in the system shares an adjacent pair of carbon atoms with each other ring in the system) group, where one or more of the rings may contain one or more double bonds but the cycloalkyl does not contain a completely conjugated pi- electron system. It will be understood that in certain embodiments, cycloalkyl may be advantageously of limited size such as C3-C13, C3-C9, C3-C6 and C4-C6.
  • Cycloalkyl may be unsubstituted, or substituted as described for alkyl or as described in the various embodiments provided herein.
  • Illustrative cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclopentadienyl, cyclohexyl, cyclohexenyl, cycloheptyl, adamantyl, norbornyl, norbomenyl, 9//-fluoren-9-yl, and the like.
  • Illustrative examples of cycloalkyl groups shown in graphical representations include the following entities, in the form of properly bonded moieties:
  • hydroxy or ““hydroxyl” refers to an -OH group.
  • halo or halogen refers to fluorine, chlorine, bromine or iodine.
  • cyano refers to a -CN group.
  • substituted means that the specified group or moiety bears one or more substituents.
  • unsubstituted means that the specified group bears no substituents.
  • substituted means that the specified group or moiety bears one, two, or three substituents. In other embodiments, “substituted” means that the specified group or moiety bears one or two substituents. In still other embodiments, “substituted” means the specified group or moiety bears one substituent.
  • each hydrogen atom in C1-C6 alkyl means that a substituent may be but need not be present on the C1-C6 alkyl by replacement of a hydrogen atom for each substituent group, and the description includes situations where the C1-C6 alkyl is substituted and situations where the C1-C6 alkyl is not substituted.
  • pharmaceutically acceptable salt refers to those salts which counter ions which may be used in pharmaceuticals. See, generally, S.M.
  • Preferred pharmaceutically acceptable salts are those that are pharmacologically effective and suitable for contact with the tissues of subjects without undue toxicity, irritation, or allergic response.
  • a compound described herein may possess a sufficiently acidic group, a sufficiently basic group, both types of functional groups, or more than one of each type, and accordingly react with a number of inorganic or organic bases, and inorganic and organic acids, to form a pharmaceutically acceptable salt.
  • Such salts include:
  • acid addition salts which can be obtained by reaction of the free base of the parent compound with inorganic acids such as hydrochloric acid, hydrobromic acid, nitric acid, phosphoric acid, sulfuric acid, and perchloric acid and the like, or with organic acids such as acetic acid, oxalic acid, (D) or (L) malic acid, maleic acid, methane sulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, tartaric acid, citric acid, succinic acid or malonic acid and the like; or
  • a metal ion e.g., an alkali metal ion, an alkaline earth ion, or an aluminum ion
  • organic base such as ethanolamine, diethanolamine, triethanolamine, trimethamine, N- methylglucamine, and the like.
  • compositions are well known to those skilled in the art, and any such pharmaceutically acceptable salt may be contemplated in connection with the embodiments described herein.
  • pharmaceutically acceptable salts include sulfates, pyrosulfates, bi sulfates, sulfites, bi sulfites, phosphates, monohydrogen-phosphates, dihydrogenphosphates, metaphosphates, pyrophosphates, chlorides, bromides, iodides, acetates, propionates, decanoates, caprylates, acrylates, formates, isobutyrates, caproates, heptanoates, propiolates, oxalates, malonates, succinates, suberates, sebacates, fumarates, maleates, butyne-l,4-dioates, hexyne-1,6- dioates, benzoates, chlorobenzoates, methylbenzoates, dinitrobenzoates
  • a pharmaceutically acceptable salt may be prepared by any suitable method available in the art, for example, treatment of the free base with an inorganic acid, such as hydrochloric acid, hydrobromic acid, sulfuric acid, sulfamic acid, nitric acid, boric acid, phosphoric acid, and the like, or with an organic acid, such as acetic acid, phenylacetic acid, propionic acid, stearic acid, lactic acid, ascorbic acid, maleic acid, hydroxymaleic acid, isethionic acid, succinic acid, valeric acid, fumaric acid, malonic acid, pyruvic acid, oxalic acid, glycolic acid, salicylic acid, oleic acid, palmitic acid, lauric acid, a pyranosidyl acid
  • an inorganic acid such as hydrochloric acid, hydrobromic acid, sulfuric acid, sulfamic acid, nitric acid, boric acid, phosphoric acid, and the like
  • the disclosure also relates to pharmaceutically acceptable prodrugs of the compounds of Formula I, and treatment methods employing such pharmaceutically acceptable prodrugs.
  • prodrug means a precursor of a designated compound that, following administration to a subject, yields the compound in vivo via a chemical or physiological process such as solvolysis or enzymatic cleavage, or under physiological conditions (e.g., a prodrug on being brought to physiological pH is converted to the compound of Formula I).
  • a "pharmaceutically acceptable prodrug” is a prodrug that is non-toxic, biologically tolerable, and otherwise biologically suitable for administration to the subject. Illustrative procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in “Design of Prodrugs”, ed. H.
  • the present disclosure also relates to pharmaceutically active metabolites of compounds of Formula I, and uses of such metabolites in the methods of the disclosure.
  • a “pharmaceutically active metabolite” means a pharmacologically active product of metabolism in the body of a compound of Formula I or salt thereof.
  • Prodrugs and active metabolites of a compound may be determined using routine techniques known or available in the art. See, e.g., Bertolini et ak, ./.
  • Any formula depicted herein is intended to represent a compound of that structural formula as well as certain variations or forms.
  • a formula given herein is intended to include a racemic form, or one or more enantiomeric, diastereomeric, or geometric isomers, or a mixture thereof.
  • any formula given herein is intended to refer also to a hydrate, solvate, or polymorph of such a compound, or a mixture thereof.
  • any formula given herein is intended to refer also to a hydrate, solvate, or polymorph of such a compound, or a mixture thereof.
  • the term “genetically altered” refers to a permanent alteration in the DNA sequence that makes up a gene that can result in a change in the protein sequence encoded by the gene.
  • a gene that is “genetically altered” as described herein can possess changes in DNA sequence, and/or protein sequence encoded by the DNA sequence, that range in size; for example, a single nucleotide (a.k.a. a single nucleotide polymorphism, SNP or point mutation), a multiple nucleotide polymorphism (MNPs), a large segment of a chromosome that includes multiple genes, such as a gene fusion, and the like.
  • gene fusions include, but are not limited to, those which are the result of a chromosomal inversion in which a portion of a chromosomal DNA encoding one or more genes rearranges to provide a fusion of two genes not ordinarily in communication in the DNA sequence, chromosomal deletion in which part of a DNA sequence of a chromosome is deleted to provide a fusion of two genes not ordinarily in communication in the DNA sequence, or those which are the result of a translocation in which a portion of chromosomal DNA is spliced and inserted into the same or a different chromosome to provide a fusion of two genes not ordinarily in communication in the DNA sequence.
  • gene fusions can be found in multiple variants depending on the individual in which the gene fusion has occurred, and each of such variants is contemplated by the methods described herein.
  • a “genetically altered” gene, or the protein encoded by such gene can occur as hereditary mutations which can be inherited from a parent and are sometimes referred to as germline mutations, or a “genetically altered” gene, or the protein encoded by such gene, can occur as an acquired (or somatic) mutation that occurs at some point during a person’s life.
  • a “genetically altered” gene can be described as a de novo (new) mutation, and can be either hereditary or somatic. It will be further understood that “genetically altered” can refer to a situation in which more than one of the changes in DNA sequence described herein can occur in a patient simultaneously, such as a SNP (or point mutation) and a translocation.
  • Such situations can arise from, but are not solely the result of, so-called “acquired resistance” in which a patient having been treated with a kinase inhibitor can develop a mutation in the DNA sequence that reduces the effectiveness of the treatment.
  • acquired resistance mutations include the point mutations P991S, T992I, V1092I, T1173I, F1200I, D1228N, D1228H, Y1230A, Y1230C, Y1230D, Y1230H, Y1235D, D1246N, D1246H, Y1248D, Y1248H, Y1248C, M1250T, and M1268T in the c-Met protein that is encoded by a genetically altered MET.
  • intrinsic resistance refers to the pre-existing resistance of disease cells, especially cancer cells, to drug treatment, especially chemotherapy treatment. It will be appreciated that intrinsic resistance can result in resistance of the cells to a single drug, a small group of structurally related drugs, or a several drugs of differing chemical structure (so-called “multidrug resistance” or “MDR”). (Monti, E. 2007. Molecular Determinants of Intrinsic Multidrug Resistance in Cancer Cells and Tumors In B. Teicher (Ed.), Cancer Drug Resistance (pp. 241-260). Totowa, New Jersey: Humana Press Inc.).
  • intrinsic resistance can be the result of one or more host-related factors and/or the genetic make-up of the cells.
  • factors include but are not limited to immunomodulation; pharmacogenetic factors such as failure to achieve optimal serum drugs levels due to altered ADME or low tolerance to drug- induced side effects; restricted drug access to the tumor site; and microenvironmental cues.
  • genetic make-up factors include, but are not limited to altered expression of drug transporters; qualitative alterations of drug target(s); quantitative alterations of drug target(s); changes in intracellular drug handling/metabolism; changes in DNA repair activities, and alteration in apoptotic pathways. (Gottesman, M.M., Annu. Rev. Med., 2002, 53, 516-527).
  • the term “disease” includes, but is not limited to, cancer, pain, inflammatory diseases, such as allergy, asthma, autoimmune diseases, coeliac disease, glomerulonephritis, hepatitis, inflammatory' bowel disease (e.g. ulcerative colitis), pre-perfusion injury, transplant rejection, psoriasis, and rheumatoid arthritis; polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis.
  • cancer includes, but is not limited to, cancers such as carcinomas, sarcomas, lymphomas, Hodgekin’s disease, melanomas, mesotheliomas, Burkitf s lymphoma, nasopharyngeal carcinomas, leukemias, lung cancers, breast cancers, hereditary human papillary renal carcinomas, sporadic human papillary renal carcinomas, childhood hepatocellular carcinomas, myeloma, and the like.
  • cancers such as carcinomas, sarcomas, lymphomas, Hodgekin’s disease, melanomas, mesotheliomas, Burkitf s lymphoma, nasopharyngeal carcinomas, leukemias, lung cancers, breast cancers, hereditary human papillary renal carcinomas, sporadic human papillary renal carcinomas, childhood hepatocellular carcinomas, myeloma, and the like.
  • cancers in connection with the present disclosure include, but are not limited to, ALCL, lung cancer, such as non-small cell lung cancer (NSCLC), including adenocarcinoma, lung squamous cell carcinoma, large cell carcinoma, and large cell neuroendocrine tumors, small cell lung cancer (SCLC), neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, such as luminal A, luminal B, triple negative breast cancer, triple positive breast cancer, HER2+, and the like, mouth cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, such as anaplastic thyroid cancer, cholangiocarcinoma, ovarian cancer, gastric cancer, such as gastric adenocarcinoma, colorectal cancer (CRC), angiosarcoma, epithelioid hemangioendothelioma, intrahepatic
  • NSCLC
  • cancer includes both primary cancers or primary tumors and metastatic cancers or metastatic tumors, and includes all stages of cancer as known in the art.
  • metastatic NSCLC metastatic CRC
  • metastatic pancreatic cancer metastatic colorectal carcinoma
  • metastatic HNSCC metastatic uterine cancer
  • cancer includes cancers that involve the upregulation of certain genes or genetic mutations in certain genes that can lead to disease progression, such as small GTPases (e.g. KRAS and the like) and receptor tyrosine kinases such as MET, and the like.
  • the methods described herein relate to the treatment of disease comprising administering to a patient in need of treatment a therapeutically effective amount of a compound having activity against MET, SRC, and CSF1R.
  • the compound has activity against a genetically altered MET, SRC, and SCF1R.
  • the compound is of the formula I
  • R 1 is H, deuterium, or C 1 -C 6 alkyl
  • R 2 is chloro or -CN
  • R 3 is H, deuterium, or fluoro
  • R 4 is H or C 1 -C 6 alkyl, wherein each hydrogen atom in C 1 -C 6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC 1 -C 6 alkyl, -NH 2 ,
  • R 1 is methyl. In some embodiments, wherein R 2 is -CN. In some embodiments, R 3 is fluoro. In some embodiments, R 4 is C 1 -C 6 alkyl. In some embodiments, R 4 is ethyl. In some embodiments, the compound is of the formula or a pharmaceutically acceptable salt thereof.
  • the disease can be any of a number of diseases associated with the tyrosine kinases described herein against which the compounds of the formula I have activity.
  • the methods described herein can be used for the treatment of diseases such as cancer, pain, psoriasis, rheumatoid arthritis, polycythemia vera, essential thrombocythemia, ulcerative colitis, myeloid metaplasia with myelofibrosis, and the like.
  • the disease can be any disease associated with the activity of a genetically altered MET, a SRC, or CSF1R.
  • the disease is a cancer mediated by or associated with a genetically altered MET.
  • the disease is a cancer mediated by or associated with a genetically altered MET encoding a point mutation that is expressed in the c-Met protein. In some embodiments, the disease is a cancer mediated by or associated with a genetically altered MET encoding a point mutation expressed in the c-Met protein at one or more of positions P991, T992, VI 092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and M1268..
  • the disease is a cancer mediated by or associated with a genetically altered MET encoding a point mutation expressed in the c-Met protein that is selected from the group consisting of T11731, P991S, M1250T, T992I, V1092I, F 12001, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T.
  • the cancer can be any cancer mediated by or associated with a genetically altered MET, a SRC, or SCF1R including, but not limited to, a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
  • the cancer includes, but is not limited to, ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER + breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid
  • the present disclosure provides methods of treating disease in a patient that has received a prior treatment with one or more therapeutic agents.
  • the patient has been previously treated with one or more therapeutic agents.
  • the patent has been previously treated with one or more therapeutic agents and developed an acquired resistance to the treatment.
  • the patent has been previously treated with one or more therapeutic agents and developed an acquired resistance to the treatment in the form of a genetically altered MET.
  • the patent has been previously treated with one or more therapeutic agents and developed an acquired resistance to the treatment expressed as a mutation of the c-Met protein encoded by a genetically altered MET.
  • the patent has been previously treated with one or more therapeutic agents and developed an acquired resistance to the treatment expressed as a point mutation in the c-Met protein at one or more of positions P991, T992, V1092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and M1268.
  • the patent has been previously treated with one or more therapeutic agents and developed an acquired resistance to the treatment expressed as a point mutation selected from the group consisting of T11731,
  • the patent has been previously treated with one or more chemotherapeutic agents and developed bypass resistance to the treatment. In still other embodiments, the patent has been previously treated with one or more therapeutic agents and developed bypass resistance to the treatment regulated by SRC or SCF1R.
  • chemotherapeutic agents which the patient may be been treated with prior to treatment with one or more of the compounds described herein include but are not limited to kinase inhibitors, adrenocorticoids and corticosteroids, alkylating agents, peptide and peptidomimetic signal transduction inhibitors, antiandrogens, antiestrogens, androgens, aclamycin and aclamycin derivatives, estrogens, antimetabolites, platinum compounds, amanitins, plant alkaloids, mitomycins, discodermolides, microtubule inhibitors, epothilones, inflammatory and proinflammatory agents, purine analogs, pyrimidine analogs, camptothecins and dolastatins.
  • the chemotherapeutic agent the patient received previous to treatment with one or more compounds described herein can be one or more of afatinib, axitinib, alectinib, bosutinib, brigatini, cabozantinib, ceritinib, crizotinib, dabrefenib, dasatinib, erlotinib, everolimus, gefitinib, ibrutinib, imatinib, lapatinib, lenvatinib, nilotinib, nintedanib, palbociclib, pazopanib, ponatinib, regorafenib, ruxolitinib, sirolimus, sorafenib, sunitinib, tofacitinib, temsirolimus, trametinib, vandetanib, vemurafenib, met
  • the methods described herein provide treatment of a patient previously treated with a kinase inhibitor selected from the group consisting of afatinib, alectinib, axitinib, bosutinib, brigatini, cabozantinib, ceritinib, crizotinib, dabrefenib, dasatinib, erlotinib, everolimus, gefitinib, ibrutinib, imatinib, lapatinib, lenvatinib, nilotinib, nintedanib, palbociclib, pazopanib, ponatinib, regorafenib, ruxolitinib, sirolimus, sorafenib, sunitinib, tofacitinib, temsirolimus, trametinib, vandetanib and vemurafenib
  • compositions comprising the compounds described herein may further comprise one or more pharmaceutically-acceptable excipients.
  • a pharmaceutically-acceptable excipient is a substance that is non-toxic and otherwise biologically suitable for administration to a subject. Such excipients facilitate administration of the compounds described herein and are compatible with the active ingredient.
  • pharmaceutically- acceptable excipients include stabilizers, lubricants, surfactants, diluents, anti -oxidants, binders, coloring agents, bulking agents, emulsifiers, or taste-modifying agents.
  • pharmaceutical compositions according to the invention are sterile compositions. Pharmaceutical compositions may be prepared using compounding techniques known or that become available to those skilled in the art.
  • compositions are also contemplated by the invention, including compositions that are in accord with national and local regulations governing such compositions.
  • compositions and compounds described herein may be formulated as solutions, emulsions, suspensions, or dispersions in suitable pharmaceutical solvents or carriers, or as pills, tablets, lozenges, suppositories, sachets, dragees, granules, powders, powders for reconstitution, or capsules along with solid carriers according to conventional methods known in the art for preparation of various dosage forms.
  • Pharmaceutical compositions of the invention may be administered by a suitable route of delivery, such as oral, parenteral, rectal, nasal, topical, or ocular routes, or by inhalation.
  • the compositions are formulated for intravenous or oral administration.
  • the compounds the invention may be provided in a solid form, such as a tablet or capsule, or as a solution, emulsion, or suspension.
  • the compounds of the invention may be formulated to yield a dosage of, e.g ., from about 0.1 mg to 1 g daily, or about 1 mg to 50 mg daily, or about 50 to 250 mg daily, or about 250 mg to 1 g daily.
  • Oral tablets may include the active ingredient(s) mixed with compatible pharmaceutically acceptable excipients such as diluents, disintegrating agents, binding agents, lubricating agents, sweetening agents, flavoring agents, coloring agents and preservative agents.
  • Suitable inert fillers include sodium and calcium carbonate, sodium and calcium phosphate, lactose, starch, sugar, glucose, methyl cellulose, magnesium stearate, mannitol, sorbitol, and the like.
  • Exemplary liquid oral excipients include ethanol, glycerol, water, and the like.
  • Starch, polyvinyl-pyrrolidone (PVP), sodium starch glycolate, microcrystalline cellulose, and alginic acid are exemplary disintegrating agents.
  • Binding agents may include starch and gelatin.
  • the lubricating agent if present, may be magnesium stearate, stearic acid, or talc.
  • Capsules for oral administration include hard and soft gelatin capsules.
  • active ingredient(s) may be mixed with a solid, semi-solid, or liquid diluent.
  • Soft gelatin capsules may be prepared by mixing the active ingredient with water, an oil, such as peanut oil or olive oil, liquid paraffin, a mixture of mono and di-glycerides of short chain fatty acids, polyethylene glycol 400, or propylene glycol.
  • Liquids for oral administration may be in the form of suspensions, solutions, emulsions, or syrups, or may be lyophilized or presented as a dry product for reconstitution with water or other suitable vehicle before use.
  • Such liquid compositions may optionally contain: pharmaceutically- acceptable excipients such as suspending agents (for example, sorbitol, methyl cellulose, sodium alginate, gelatin, hydroxyethylcellulose, carboxymethylcellulose, aluminum stearate gel and the like); non-aqueous vehicles, e.g., oil (for example, almond oil or fractionated coconut oil), propylene glycol, ethyl alcohol, or water; preservatives (for example, methyl or propyl p- hydroxybenzoate or sorbic acid); wetting agents such as lecithin; and, if desired, flavoring or coloring agents.
  • suspending agents for example, sorbitol, methyl cellulose, sodium alginate, gelatin, hydroxyethylcellulose, carboxymethyl
  • the agents of the invention may be provided in sterile aqueous solutions or suspensions, buffered to an appropriate pH and isotonicity or in parenterally acceptable oil.
  • Suitable aqueous vehicles include Ringer's solution and isotonic sodium chloride.
  • Such forms may be presented in unit-dose form such as ampoules or disposable injection devices, in multi-dose forms such as vials from which the appropriate dose may be withdrawn, or in a solid form or pre concentrate that can be used to prepare an injectable formulation.
  • Illustrative infusion doses range from about 1 to 1000 pg/kg/minute of agent admixed with a pharmaceutical carrier over a period ranging from several minutes to several days.
  • inventive pharmaceutical compositions may be administered using, for example, a spray formulation also containing a suitable carrier.
  • inventive compositions may be formulated for rectal administration as a suppository.
  • the compounds of the present invention are preferably formulated as creams or ointments or a similar vehicle suitable for topical administration.
  • the inventive compounds may be mixed with a pharmaceutical carrier at a concentration of about 0.1% to about 10% of drug to vehicle.
  • Another mode of administering the agents of the invention may utilize a patch formulation to effect transdermal delivery.
  • Any formula given herein is also intended to represent unlabeled forms as well as isotopically labeled forms of the compounds. Isotopically labeled compounds have structures depicted by the formulas given herein except that one or more atoms are replaced by an atom having a selected atomic mass or mass number.
  • isotopes examples include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine, chlorine, and iodine, such as 2 H, 3 ⁇ 4, U C, 13 C, 14 C, 15 N, 18 0, 17 0, 31 P, 32 P, 35 S, 18 F, 36 C1, and 125 I, respectively.
  • isotopically labelled compounds are useful in metabolic studies (preferably with 14 C), reaction kinetic studies (with, for example 2 H or 3 ⁇ 4), detection or imaging techniques [such as positron emission tomography (PET) or single-photon emission computed tomography (SPECT)] including drug or substrate tissue distribution assays, or in radioactive treatment of patients.
  • PET positron emission tomography
  • SPECT single-photon emission computed tomography
  • isotopically labeled compounds of this disclosure and prodrugs thereof can generally be prepared by carrying out the procedures disclosed in the schemes or in the examples and preparations described below by substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent.
  • the compounds described herein may be used in pharmaceutical compositions or methods in combination with one or more additional active ingredients in the treatment of the diseases and disorders described herein.
  • Further additional active ingredients include other therapeutics or agents that mitigate adverse effects of therapies for the intended disease targets. Such combinations may serve to increase efficacy, ameliorate other disease symptoms, decrease one or more side effects, or decrease the required dose of an inventive compound.
  • the additional active ingredients may be administered in a separate pharmaceutical composition from a compound of the present invention or may be included with a compound of the present invention in a single pharmaceutical composition.
  • the additional active ingredients may be administered simultaneously with, prior to, or after administration of a compound of the present invention.
  • Combination agents include additional active ingredients are those that are known or discovered to be effective in treating the diseases and disorders described herein, including those active against another target associated with the disease.
  • compositions and formulations of the invention, as well as methods of treatment can further comprise other drugs or pharmaceuticals, e.g., other active agents useful for treating or palliative for the target diseases or related symptoms or conditions.
  • chemotherapeutic agents suitable for use in combination in the methods described herein include but are not limited to kinase inhibitors, adrenocorticoids and corticosteroids, alkylating agents, peptide and peptidomimetic signal transduction inhibitors, antiandrogens, antiestrogens, androgens, aclamycin and aclamycin derivatives, estrogens, antimetabolites, platinum compounds, amanitins, plant alkaloids, mitomycins, discodermolides, microtubule inhibitors, epothilones, inflammatory and proinflammatory agents, purine analogs, pyrimidine analogs, camptothecins and dolastatins.
  • chemotherapeutic agents suitable for combination treatments in the methods described herein include but are not limited to one or more of afatinib, alectinib, axitinib, bosutinib, brigatini, cabozantinib, ceritinib, crizotinib, dabrefenib, dasatinib, erlotinib, everolimus, gefitinib, ibrutinib, imatinib, lapatinib, lenvatinib, nilotinib, nintedanib, palbociclib, pazopanib, ponatinib, regorafenib, ruxolitinib, sirolimus, sorafenib, sunitinib, tofacitinib, temsirolimus, trametinib, vandetanib, vemurafenib, methot
  • chemotherapeutic agents suitable for combination treatments in the methods described herein include but are not limited to one or more kinase inhibitor selected from the group consisting of afatinib, alectinib, axitinib, bosutinib, brigatini, cabozantinib, ceritinib, crizotinib, dabrefenib, dasatinib, erlotinib, everolimus, gefitinib, ibrutinib, imatinib, lapatinib, lenvatinib, nilotinib, nintedanib, palbociclib, pazopanib, ponatinib, regorafenib, ruxolitinib, sirolimus, sorafenib, sunitinib, tofacitinib, temsirolimus, trametinib, vandetanib and vemur
  • the patient was previously treated with crizotinib.
  • suitable combination agents include anti-inflammatories such as NSAIDs.
  • the pharmaceutical compositions of the invention may additional comprise one or more of such active agents, and methods of treatment may additionally comprise administering an effective amount of one or more of such active agents.
  • a therapeutically effective amount of one or more compounds that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I is administered to a host animal, such as a human patient, in need of treatment for cancer.
  • a therapeutically effective amount of a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular Compound 1 is administered to a host animal, such as a human patient, in need of treatment for cancer.
  • the term “therapeutically effective amount” refers to that amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a patient, which includes alleviation of the symptoms of the disease or disorder being treated. In one aspect, the therapeutically effective amount is that which may treat or alleviate the disease or symptoms.
  • the specific therapeutically-effective dose level for any particular patient will depend upon a variety of factors, including the disorder being treated and the severity of the disorder; activity of the specific compound employed; the specific composition employed; the age, body weight, general health, gender and diet of the patient: the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidentally with the specific compound employed; and like factors.
  • an exemplary dose for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, in the various methods and compositions described herein is in the range of about from about 1 mg to about 3 g, or about 1 mg to about 500 mg, or about 50 to about 250 mg, or about 150 to about 500 mg, or about 150 to about 250 mg, or about 250 mg to about 1 g, or about 100 mg to about 2 g, or about 500 mg to about 2 g, or about 500 mg to about 1 g. It will be appreciated that all possible subranges within the dose ranges described above are contemplated and described herein.
  • a dose range of about 40 to about 500 mg for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein includes doses of about 40 mg, about 50 mg, about 60, mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 110 mg, about 120 mg, about 130 mg, about 140 mg, about 150 mg, about 160 mg, about 170 mg, about 180 mg, about 190 mg, about 200 mg, about 210 mg, about 220 mg, about 230 mg, about 240 mg, about 250 mg, about 260 mg, about 270 mg, about 280 mg, about 290 mg, about 300 mg, about 310 mg, about 320 mg, about 330 mg, about 340 mg, about 350 mg, about 360 mg, about 370 mg, about 380 mg, about 390 mg, about 400 mg, about 410 mg, about 420 mg, about 430 mg, about 440 mg, about
  • the compound that inhibits a genetically altered MET, SRC, and SCF1R in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein can be dosed at about 40 mg, about 80 mg, about 120 mg, about 160 mg, about 200 mg, about 240 mg, or about 280 mg.
  • an exemplary dose for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, in the various methods and compositions described herein is in the range of about from about 1 mg to about 3 g daily, or about 1 mg to about 500 mg daily, or about 50 to about 250 mg daily, or about 150 to about 500 mg daily, or about 150 to about 250 mg daily, or about 250 mg to about 1 g daily, or about 100 mg to about 2 g daily, or about 500 mg to about 2 g daily, or about 500 mg to about 1 g daily. It will be appreciated that all possible subranges within the daily dose ranges described above are contemplated and described herein.
  • a dose range of about 40 to about 500 mg daily for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein includes doses of about 40 mg daily, about 50 mg daily, about 60, mg daily, about 70 mg daily, about 80 mg daily, about 90 mg daily, about 100 mg daily, about 110 mg daily, about 120 mg daily, about 130 mg daily, about 140 mg daily, about 150 mg daily, about 160 mg daily, about 170 mg daily, about 180 mg daily, about 190 mg daily, about 200 mg daily, about 210 mg daily, about 220 mg daily, about 230 mg daily, about 240 mg daily, and about 250 mg daily, about 260 mg daily, about 270 mg daily, about 280 mg daily, about 290 mg daily, about 300 mg daily, about 310 mg daily, about 320 mg daily, about 330 mg daily, about 340 mg daily, about 350 mg daily, about 360 mg daily, about 370 mg daily,
  • the compound that inhibits a genetically altered MET, SRC, and SCF1R in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein can be dosed at about 40 mg daily, about 80 mg daily, about 120 mg daily, about 160 mg daily, about 200 mg, about 240 mg, or about 280 mg.
  • an alternative exemplary dose for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the various methods and compositions described herein is in the range of about from about 0.1 mg/kg to about 1 g/kg, or about 0.5 mg/kg to about 50 mg/kg, or about 0.5 mg/kg to about 25 mg/kg, or about 1.0 mg/kg to about 10 mg/kg, or about 1.0 mg/kg to about 5 mg/kg, or about 0.1 mg/kg to about 5 mg/kg, or about 0.1 mg/kg to about 1 mg/kg, or about 0.1 mg/kg to about 0.6 mg/kg.
  • a dose range of about 1.0 mg/kg to about 10 mg/kg for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein includes doses of about 1.0 mg/kg, about 2.0 mg/kg, about 3.0 mg/kg, about 4.0 mg/kg, about 5.0 mg/kg, about 6.0 mg/kg, about 7.0 mg/kg, about 8.0 mg/kg, about 9.0 mg/kg, and about 10.0 mg/kg, including all possible doses and ranges as may be required based on such factors for determining a therapeutically effective amount as described herein.
  • an alternative exemplary dose for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the various methods and compositions described herein is in the range of about from about 0.1 mg/kg to about 1 g/kg daily, or about 0.5 mg/kg to about 50 mg/kg daily, or about 0.5 mg/kg to about 25 mg/kg daily, or about 1.0 mg/kg to about 10 mg/kg daily, or about 1.0 mg/kg to about 5 mg/kg daily, or about 0.1 mg/kg to about 5 mg/kg daily, or about 0.1 mg/kg to about 1 mg/kg daily, or about 0.1 mg/kg to about 0.6 mg/kg daily.
  • a dose range of about 1.0 mg/kg to about 10 mg/kg daily for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein includes doses of about 1.0 mg/kg daily, about 2.0 mg/kg daily, about 3.0 mg/kg daily, about 4.0 mg/kg daily, about 5.0 mg/kg daily, about 6.0 mg/kg daily, about 7.0 mg/kg daily, about 8.0 mg/kg daily, about 9.0 mg/kg daily, and about 10.0 mg/kg daily, including all possible doses and ranges as may be required based on such factors for determining a therapeutically effective amount as described herein.
  • a dosing schedule for a compound administered in the various methods and compositions described herein can be defined by cycles of the dosing schedule, where such cycles are defined by the number of days of treatment, number of doses of the compound, the total dose of the compound, and the like.
  • a host animal such as a human patient in need of treatment, can be administered a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, for at least one cycle, for at least two cycles, for at least three cycles, for at least four cycles, and the like.
  • a host animal such as a human patient in need of treatment, can be administered a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, for from 1 to about 50 cycles, from 1 to about 25 cycles, from 1 to about 20 cycles, from 1 to about 10 cycles, and the like.
  • a dosing schedule for a compound administered in the various methods and compositions described herein can include a holiday period during which no compound is administered, and such holiday period can be measured in days.
  • a dosing schedule for a compound administered in the various methods and compositions described herein can be defined by a number of cycles as described herein, followed by a holiday period, followed by another number of cycles as described herein.
  • an exemplary dosing schedule for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the various methods and compositions described herein can include administration of a single daily dose (QD) or divided dosage units (e.g., BID (twice daily), TID (three times daily), QID (four times daily)).
  • a dosing schedule for a compound administered in the various methods and compositions described herein can vary within a cycle, such as a compound administered in the various methods and compositions described herein administered QD for a set number of days (e.g. QD for 1 day, 2 days, 3 days, 4 days, etc) followed by BID for a set number of days (e.g. BID for 1 day, 2 days, 3 days, 4 days, etc).
  • QD for 1 day, 2 days, 3 days, 4 days, etc
  • BID for a set number of days
  • the present disclosure provides methods for treating disease in a patient previously identified as having a genetically altered MET. In some embodiments, the present disclosure provides methods for treating cancer in a patient previously identified as having a genetically altered MET. In some embodiments, the present disclosure provides methods for treating disease in a patient comprising (i) identifying a genetically altered MET in the patient, and (ii) administering to the patient a therapeutically effective amount of a compound useful in the treatment of such disease.
  • the diagnosing or identifying a patient as having a genetically altered MET can be accomplished by any number of diagnostic tests known to one of skill in the art.
  • diagnostic tests include, but are not limited to, fluorescence in situ hybridization (FISH), polymerase chain reaction (PCR), immunohistochemistry (IHC), whole genome sequencing, next generation sequencing, circulating tumor cell, and the like.
  • any of the methods known in the art and applicable to diagnosing a patient or identifying a patient in connection with the present disclosure involve the transformation of a biological sample from one state of matter to another by direct modification, chemical synthesis, by direct non-covalent connection, or other known means, to provide a modified sample that can be used to determine whether the subject has or does not have a genetically altered MET.
  • “diagnosing” or “identifying” with respect to the disease state of a patient means applying a diagnostic test, such as FISH, PCR, IHC, or sequencing, to a biological sample obtained from the patient.
  • FISH is a test that “maps” the genetic material in a person’s cells. This test can be used to visualize specific genes or portions of genes. FISH is a cytogenetic technique that uses fluorescent probes that bind to only those parts of the chromosome with a high degree of sequence complementarity. Such FISH tests can be used to identify a patient with a genetically altered MET by any method known in the art, and such test can be used in combination with the methods described herein as either a means of prior identification of a patient for treatment, or the concomitant identification of a patient for treatment.
  • IHC refers to the process of detecting antigens (e.g., proteins) in cells of a tissue section by exploiting the principle of antibodies binding specifically to antigens in biological tissues.
  • Immunohistochemical staining is widely used in the diagnosis of abnormal cells such as those found in cancerous tumors.
  • Specific molecular markers are characteristic of particular cellular events such as proliferation or cell death (apoptosis).
  • Visualising an antibody-antigen interaction can be accomplished in a number of ways. In the most common instance, an antibody is conjugated to an enzyme, such as peroxidase, that can catalyse a color-producing reaction.
  • the antibody can also be tagged to a fluorophore, such as fluorescein or rhodamine.
  • a fluorophore such as fluorescein or rhodamine.
  • PCR refers to a technology in molecular biology used to amplify a single copy or a few copies of a piece of DNA across several orders of magnitude, generating thousands to millions of copies of a particular DNA sequence.
  • Such PCR tests can be used to identify a patient with a genetically altered MET by any method known in the art, and such test can be used in combination with the methods described herein as either a means of prior identification of a patient for treatment, or the concomitant identification of a patient for treatment.
  • whole genome sequencing or next-generation sequencing refers to a process that determines the complete DNA sequence of an organism's genome at a single time. This entails sequencing all of an organism's chromosomal DNA as well as DNA contained in the mitochondria. Such whole genome sequencing tests can be used to identify a patient with a genetically altered MET by any method known in the art, and such test can be used in combination with the methods described herein as either a means of prior identification of a patient for treatment, or the concomitant identification of a patient for treatment.
  • Compound 1 was tested toward MET and mutated MET proteins in Reaction Biology Corporation’s HotSpot kinase assays (data in Table 1).
  • the individual substrate for each kinase was prepared in freshly made Reaction Buffer with the subsequent addition of required cofactors if needed, followed by addition of the individual kinase and gentle mixing.
  • Compound 1 in DMSO was added into the kinase reaction mixture utilizing acoustic technology (Echo 550), and then g- [ 33 P]-ATP (specific activity 0.01 pCi/pL final) was delivered into the reaction mixture to initiate the reaction.
  • the kinase reaction was incubated for 120 minutes at room temperature.
  • MET(M1268T) human MET (M1268T) protein is incubated with 8 mM MOPS pH 7.0, 0.2 mM EDTA, 1 mM Na 3 V0 4 , 5 mM sodium b-glycerophosphate, 250 pM KKKGQEEEYVFIE (SEQ ID NO: 1), 10 mM MgAcetate and [g- 33 R]-ATR (specific activity and concentration as required). The reaction is initiated by the addition of the Mg/ ATP mix. After incubation for 40 minutes at room temperature, the reaction is stopped by the addition of phosphoric acid to a concentration of 0.5%. 10 pL of the reaction is then spotted onto a P30 filtermat and washed four times for 4 minutes in 0.425% phosphoric acid and once in methanol prior to drying and scintillation counting.
  • Compound 1 was evaluated in a panel of Ba/F3 engineered cell models of MET and MET harboring resistance mutations.
  • the TPR-MET fusion gene and its mutations T11731, M1250T, H1094Y, G1163R, LI 195V, D1228N and Y1230C were synthesized at GenScript and cloned into pCDH-CMV-MCS-EFl-Puro plasmid (System Biosciences, Inc), respectively.
  • Ba/F3 engineered cells were generated by infecting Ba/F3 cells with lentivirus containing the related wild type or mutant genes.
  • Ba/F3 engineered cells was selected in RPMI-1640 supplemented with 10% fetal bovine serum, 100 U/mL of penicillin, and 1 pg/mL puromycin solution, 10 ng/IL-3 (Life Technologies), followed by a further selection in the same medium without IL-3.
  • the cell potency of Compound 1 was measured using cell proliferations assay for Ba/F3 cells harboring TRP-MET constructs (Table 3).
  • cell proliferation assays stable Ba/F3 cells were seeded in 384 well white plate followed by the addition of the test compounds. After 72 hours of incubation, cell proliferation was measured using CellTiter-Glo 2.0 luciferase-based ATP detection assay (Promega) following the manufacture’s protocol.
  • ICso s were determined using GraphPad Prism software (GraphPad, Inc., San Diego, CA).
  • MET IC95 0.2 nM
  • G1163R IC90 171 nM
  • LI 195V IC90 175 nM.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Peptides Or Proteins (AREA)

Abstract

This disclosure relates to the use of certain diaryl macrocycle compounds in the treatment of disease in mammals. This disclosure also relates to compositions including such compounds, and to methods of using such compositions in the treatment of diseases in mammals, especially in humans.

Description

THERAPEUTIC USES OF MACROCYCLIC COMPOUNDS
TECHNICAL FIELD
[001] This disclosure relates to the use of certain diaryl macrocycle compounds in the treatment of disease in mammals. This disclosure also relates to compositions including such compounds, and to methods of using such compositions in the treatment of diseases in mammals, especially in humans.
BACKGROUND
[002] Protein kinases are key regulators for cell growth, proliferation and survival. Genetic and epigenetic alterations accumulate in cancer cells leading to abnormal activation of signal transduction pathways which drive malignant processes. (Manning, G. et al, The protein kinase complement of the human genome. Science 2002, 298, 1912-1934). Pharmacological inhibition of these signaling pathways presents promising intervention opportunities for targeted cancer therapies. (Sawyers, C. Targeted cancer therapy. Nature 2004, 432 , 294-297).
[003] MET, also called hepatocyte growth factor receptor (HGFR), was discovered in 1984 (Cooper, C. S., et al Molecular cloning of a new transforming gene from a chemically transformed human cell line. Nature 1984, 311 , 29-33). Hepatocyte growth factor (HGF), also known as scatter factor (SF), is the high-affinity natural ligand of MET (Bottaro DP et al. Identification of the hepatocyte growth factor receptor as the c-met proto-oncogene product. Science. 1991, 251 (4995), 802-804). The HGF/MET signaling pathway is implicated in invasive growth during embryo development, postnatal organ regeneration, wound healing and tissue regeneration processes. However, the HGF/MET axis is frequently hijacked by cancer cells for turn ori genesis, invasive growth, and metastasis (Boccaccio, C.; Comoglio, P. M. Invasive growth: aMET-driven generic programme for cancer and stem cells. Nat. Rev. Cancer 2006, 6, 637-645). Deregulations of MET and/or HGF via activating mutations, gene amplifications, overexpression, and both autocrine or paracrine loop regulation influence cell growth, proliferation, angiogenesis, invasion, survival, and metastasis, leading to tumorigenesis and tumor progression (Ma, PC et al. Expression and mutational analysis of MET in human solid cancers. Genes Chromosomes Cancer 2008, 47, 1025- 1037). Over-expression of MET and/or HGF has been detected in a large variety of solid tumors such as liver, breast, pancreas, lung, kidney, bladder, ovary, brain, prostate, and many others, and is often associated with a metastatic phenotype and poor prognosis (Maulik, G., et al. Role of the hepatocyte growth factor receptor, MET, in oncogenesis and potential for therapeutic inhibition. Cytokine Growth Factor Rev. 2002, 13, 41-59). MET amplification has been reported in different human cancers including gastroesophageal carcinomas, colorectal cancers, NSCLC, medulloblastomas, and glioblastomas (Smolen, G. A., et al. Amplification of MET may identify a subset of cancers with extreme sensitivity to the selective tyrosine kinase inhibitor PHA-665752. Proc. Natl. Acad. Sci. U. S. A. 2006, 103, 2316-2321). A diverse set of MET mutations in the tyrosine kinase domain, juxtamembrane, and extracellular domain of both germline and somatic mutations have been described in many solid tumors, including hereditary and sporadic human papillary renal carcinomas, lung cancer, ovarian cancer, childhood hepatocellular carcinomas, squamous cell carcinoma of the head and neck, and gastric cancer (Ghiso, E.; Giordano, S. Targeting MET: why, where and how? Curr. Opin. Pharmacol. 2013, 13, 511-518). MET exon 14 deletion represents a novel class of actionable oncogenic event with potential clinical impact and therapeutic applications in patients affected by different cancer types (Pilotto S, MET exon 14 juxtamembrane splicing mutations: clinical and therapeutical perspectives for cancer therapy. Ann Transl Med. 2017 5(1):2). Autocrine or paracrine stimulation is one mechanism for aberrant MET activation. The MET autocrine activation plays a causal role in the development of malignant melanoma and acquisition of the metastatic phenotype (Otsuka, T., et al. MET autocrine activation induces development of malignant melanoma and acquisition of the metastatic phenotype. Cancer Res. 1998, 58, 5157-5167). For glioblastoma (GBM), HGF autocrine expression correlated with MET phosphorylation levels in HGF autocrine cell lines, and showed high sensitivity to MET inhibition in vivo, while an HGF paracrine environment could enhance glioblastoma growth in vivo but did not demonstrated sensitivity to MET inhibition (Xie, Q., et al. Hepatocyte growth factor (HGF) autocrine activation predicts sensitivity to MET inhibition in glioblastoma. Proc. Natl.
Acad. Sci. U. S. A. 2012, 109, 570-575). The aberrant expression of HGF is a crucial element in AML pathogenesis that leads to autocrine activation of MET in nearly half of the AML cell lines and clinical samples (Kentsis, A., et al. Autocrine activation of the MET receptor tyrosine kinase in acute myeloid leukemia. Nat. Med. 2012, 18, 1118-1122).
[004] Upregulation of HGF/MET signaling has been frequently reported as compensatory signaling to confer resistance for kinase targeted therapies. MET amplification has been detected in erlotinib treatment (Sequist, L. V., et al. Analysis of tumor specimens at the time of acquired resistance to EGFR-TKI therapy in 155 patients with EGFR-mutant lung cancers. Clin. Cancer Res. 2013, 79, 2240-2247). Upregulation of ligand HGF represents another mechanism of EGFR- TKI resistance. High HGF expression was discovered among clinical specimens with acquired resistance that did not have a T790M mutation or MET amplification as well as among cases that exhibited primary resistance despite having EGFR-TKI sensitive activating EGFR gene mutations (Yano, S., et al. Hepatocyte growth factor induces gefitinib resistance of lung adenocarcinoma with epidermal growth factor receptor-activating mutations. Cancer Res. 2008, 68, 9479-9487). Amplification of MET is associated with acquired resistance to cetuximab or panitumumab in metastatic colorectal cancer patients that do not develop KRAS mutations during anti-EGFR therapy (Bardelli, A., et al. Amplification of the MET Receptor Drives Resistance to Anti-EGFR Therapies in Colorectal Cancer. Cancer Discov. 2013, 3, 658-673). Growth factor-driven resistance from tumor microenvironment represents a potential common mechanism for anticancer kinase inhibitors. The upregulation of stromal HGF confers resistance to the BRAF inhibitor ramurafenib in BRAF-mutant melanoma cells (Straussman, R., et al. Tumour micro-environment elicits innate resistance to RAF inhibitors through HGF secretion. Nature 2012, 487, 500-504). It was reported that ligand-mediated activation of alternative receptor tyrosine kinases was observed in cancer cells originally dependent on either MET, FGFR2, or FGFR3, and RTKs from the HER and EGFR families as well as MET compensated for loss of each other (Harbinski, F., et al. Rescue screens with secreted proteins reveal compensatory potential of receptor tyrosine kinases in driving cancer growth. Cancer Discov. 2012, 2, 948-959). Therefore, blocking adaptive cellular responses that drive compensatory ligand expression is necessary for achieving optimal and sustained antitumor effects.
[005] Genomic alterations to the receptor tyrosine kinase are oncogenic drivers for a range of cancers (Campbell et al 2016 Nat Genet 48, 607-16; Sadiq et al., 2013 J Clin Oncol 31, 1089-96) as well as resistance mechanisms to other molecular medicines such as osimertinib for the treatment of lung cancer patients (Ko et al., 2017 Ann TranslMed 5(1), 4; Liu et al., 2018 Molecular Cancer 17, article 53). Patients treated with MET targeted therapies often develop drug resistance by either bypass signaling, mutation to MET, or by unknown mechanisms as is illustrated by a recent publication (Recondo et al, 2020 Clin Cancer Res, doi 10.1158/1078- 0432.CCR-19-3608). In the Recondo study, 35% of the 20 patients treated with a MET targeted therapy had MET mutations at disease progression (e.g. MET residues H1094, G1163, LI 195, D1228, Y1230, and high levels of MET amplification). As such, inhibitors that potently inhibit MET or potently inhibit mutated forms of MET are expected to have enhanced clinical benefit for patients with amplified MET or mutated forms of MET.
[006] Src is a non-receptor tyrosine kinase that is deregulated in many types of cancer, and a key downstream transducer of many RTKs, including EGFR, HER2, and c-Met. Activation of Src signaling has been implicated in conferring therapeutic resistance to targeted antiendocrine therapies, receptor tyrosine kinase therapies, traditional chemotherapies, and radiation therapies. (Zhang S, et al Trends Pharmacol Sci. 2012, 33, 122). Src inhibitor may play important roles in combinatorial regimens in overcoming resistance to current anticancer therapies and in preventing metastatic recurrence. Cytoplasmic tyrosine kinases (also known as non-receptor tyrosine kinases) of the Src family (SFKs) play important roles in signal transduction induced by a large number of extracellular stimuli including growth factors and integrins. Elevated SFK activity is found in more than 80% of human colorectal cancer (CRC) and this has been associated with poor clinical outcome. (Summy JM, et al. Cancer Metastasis Rev. 2003, 22, 337-358) The SFK member Yes regulates specific oncogenic signalling pathways important for colon cancer progression that is not shared with c-Src. (Scancier F. et al. PLoS One. 2011, 6(2): el7237) WASF2-FGR fusion genes were found in lung squamous carcinoma, ovarian serous cystadenocarcinoma, and skin cutaneous melanoma. (Stransky N, et al. Nature Communications 2014, 5, 4846) Estrogen receptor-positive (ER+) breast cancers adapt to hormone deprivation and become resistant to antiestrogen therapy. Mutations in the inhibitory SH2 domain of the SRC family kinase (SFK) LYN were related to ER+ tumors that remained highly proliferative after treatment with the aromatase inhibitor letrozole. LYN was upregulated in multiple ER+ breast cancer lines resistant to long-term estrogen deprivation. (Schwarz LJ, et al. J Clin Invest. 2014, 124, 5490-5502) Therefore, targeting LYN will be a rational strategy overcoming the escape from antiestrogens in a subset of ER+ breast cancers.
It was reported that LYN was overexpressed in castrate-resistant prostate cancer (CRPC), enhanced AR transcriptional activity, and accelerated CRPC progression, and targeting Lyn kinase induced AR dissociation from the molecular chaperone Hsp90, leading to its ubiquitination and proteasomal degradation. (Zardan A., et al. Oncogenesis 2014, 3, el 15) The Lyn tyrosine kinase is a potential therapeutic target for the treatment of CRPC. The Src family kinase FYN is involved in signal transduction pathways in the nervous system, as well as the development and activation of T lymphocytes under normal physiological conditions. Activation of Fyn is observed in various cancers, including melanoma, glioblastoma, squamous cell carcinoma, prostate and breast cancers. (Elias D., et al. Pharmacological Research 2015, 100, 250-254) Fyn was upregulated in tamoxifen-resistant breast cancer cell lines and plays a key role in the resistance mechanism. Peripheral T-cell lymphomas (PTCLs) are a heterogeneous group of aggressive non Hodgkin lymphomas with poor prognosis. FYN activating mutations were found in PTCL, and promoted the growth of cells transformed via expression of activated FYN mutant alleles. SRC kinase inhibitors may play important roles in the treatment of PTCLs. (Couronne L, et al. Blood 2013, 122, 811). [007] It is desirable to prepare compounds that have activity against disease-driving kinase inhibitors, especially compounds that have activity against genetically altered MET, SCR and CSF1R. New compounds with polypharmacology profiles are also desired for targeting the primary oncogene drivers and their acquired resistance mechanisms including secondary mutations, bypass signaling, EMT, cancer sternness, and metastasis.
SUMMARY
[008] Compounds that inhibit MET, SRC, and CSF1R gene products have been discovered. Compounds of the formula I
Figure imgf000006_0001
I wherein R1, R2, R3, and R4 are defined as described herein have been shown to have activity against wild-type and mutant MET, SRC, and CSF1R. [009] One such compound is (7ri)-3-amino-14-ethyl-ll-fluoro-7-methyl-4-oxo-4,5,6,7,13,14- hexahydro-l,15-ethenopyrazolo[4,3- |[l,4,8,10]benzoxatriazacyclotridecine-12-carbonitrile (also herein referred to as “Compound 1”), represented by the formula
Figure imgf000007_0001
has been shown to be a potent small-molecule kinase inhibitor showing activity against wild-type and mutant wild-type and mutant MET, SRC, and CSF1R. Compound 1 has properties, including anti-tumor properties, which are pharmacologically mediated through inhibition of receptor and non-receptor tyrosine kinases. Compounds of the formula I, in particular, Compound 1, are disclosed in International Patent Publication No. WO2019/023417, which is incorporated herein by reference in its entirety.
[010] In one aspect, the present disclosure provide a method of treating disease, such as cancer, in a mammal, in particular a human patient comprising, administering to the mammal, in particular a human patient, a therapeutically effective amount of a compound that inhibits MET, SRC, and CSF1R, wherein the disease is mediated by a genetically altered MET. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula I
Figure imgf000007_0002
I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, and R4 are defined as described herein. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula
Figure imgf000008_0001
or a pharmaceutically acceptable salt thereof. In some embodiments, the mammal, in particular a human patient, has received prior treatment with one or more therapeutic agents.
[Oil] In another aspect, the present disclosure provides a method of treating cancer in a patient previously shown to express a genetically altered MET comprising, administering to the patient a therapeutically effective amount of a compound that inhibits MET, SRC, and CSF1R. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula I
Figure imgf000008_0002
I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, and R4 are defined as described herein. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula
Figure imgf000008_0003
or a pharmaceutically acceptable salt thereof. In some embodiments, the patient, has received prior treatment with one or more therapeutic agents.
[012] In another aspect, the present disclosure provides a method of treating cancer in a patient comprising; i. identifying a genetically altered MET in the patient, and ii. administering to the patient a therapeutically effective amount of a compound that inhibits MET, SRC, and CSF1R. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula I
Figure imgf000009_0001
I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, and R4 are defined as described herein. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula
Figure imgf000009_0002
or a pharmaceutically acceptable salt thereof. In some embodiments, the patient, has received prior treatment with one or more therapeutic agents.
[013] In another aspect, the present disclosure provides a method of identifying a patient for treatment with a compound that inhibits MET, SRC, and CSF1R. comprising diagnosing the patient with a cancer mediated by a genetically altered MET. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula I
Figure imgf000010_0001
I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, and R4 are defined as described herein. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula
Figure imgf000010_0002
or a pharmaceutically acceptable salt thereof. In some embodiments, the patient, has received prior treatment with one or more therapeutic agents.
[014] In another aspect, the present disclosure provides a use of compound that inhibits MET, SRC, and CSF1R in the preparation of a medicament for the treatment of a disease in a patient. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula I
Figure imgf000010_0003
I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, and R4 are defined as described herein. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula
Figure imgf000011_0001
or a pharmaceutically acceptable salt thereof. In some embodiments, the patient, has received prior treatment with one or more therapeutic agents.
[015] In another aspect, the present disclosure provides a compound inhibits MET, SRC, and CSF1R for treating cancer in a patient. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula I
Figure imgf000011_0002
I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, and R4 are defined as described herein. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula
Figure imgf000011_0003
or a pharmaceutically acceptable salt thereof. In some embodiments, the patient, has received prior treatment with one or more therapeutic agents.
[016] In another aspect, the present disclosure provides use of a compound that inhibits MET, SRC, and CSF1R for treating cancer in a patient previously shown to express a genetically altered tyrosine or serine/threonine kinase. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula I
Figure imgf000012_0001
or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, and R4 are defined as described herein. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula
Figure imgf000012_0002
or a pharmaceutically acceptable salt thereof. In some embodiments, the patient, has received prior treatment with one or more therapeutic agents.
[017] In another aspect, the present disclosure provide a use a compound inhibits MET, SRC, and CSF1R for treating cancer in a patient, wherein the patient has been previously treated with a cancer therapeutic, and the cancer has developed resistance to the cancer therapeutic. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula I
Figure imgf000012_0003
or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, and R4 are defined as described herein. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula
Figure imgf000013_0001
or a pharmaceutically acceptable salt thereof. In some embodiments, the patient, has received prior treatment with one or more therapeutic agents.
[018] In another aspect, the present disclosure provides the use of a compound that inhibits MET, SRC, and CSF1R for treating cancer in a patient previously shown to express a genetically altered tyrosine or serine/threonine kinase, wherein the patient has been previously treated with a cancer therapeutic, and the cancer has developed resistance to the cancer therapeutic. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula I
Figure imgf000013_0002
I or a pharmaceutically acceptable salt thereof, wherein R1, R2, R3, and R4 are defined as described herein. In some embodiments, the compound that inhibits MET, SRC, and CSF1R is of the formula
Figure imgf000013_0003
or a pharmaceutically acceptable salt thereof. In some embodiments, the patient, has received prior treatment with one or more therapeutic agents. [019] In some embodiments, the genetically altered MET gene comprising a point mutation that is expressed in the c-Met protein. In some embodiments, the genetically altered MET comprises a point mutation expressed in the c-Met protein at one or more of positions P991, T992, D1010,
VI 092, H1094, G1163, T1173, H1094, N1100, Y1003, H1106, V1070, V1188, V1092, H1094,
Gil 62, LI 195, F1200, V1220, D1228, Y1230, D1231, Y1235, D1246, Y1248, M1250, and M1268. In some embodiments, the genetically altered MET comprises a point mutation expressed in the c-Met protein that is selected from the group consisting of P991S, T992I, D1010H, D1010Y, VI 0921, H1094N, H1094R, H1094Y, N1100K, N1100S, Y1003C, Y1003F, Y1003H, H1106D,
VI 070 A, VI 0921, V1188I, T1173I, H1094Y, G1163R, L1195F, F1195I, L1195V, F1200I, V1220I, D1228N, D1228H, D1228V, Y1230A, Y1230C, Y1230D, Y1230H, Y1230H, Y1230S, D1231Y, Y1235D, D1246N, D1246H, Y1248D, Y1248H, Y1248C, M1250T, and M1268T. In some embodiments, the genetically altered MET comprises a point mutation expressed in the c-Met protein that is selected from the group consisting of T1173I, P991S, M1250T, T992I, V1092I,
FI 2001, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T. In some embodiments, the cancer is exhibiting bypass resistance. In some embodiments, the bypass resistance is mediated by a SRC/CSF1R.
[020] In some embodiments, the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitt’s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma. In some embodiments, the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, serous and clear cell endometrial cancer.
[021] In some embodiments, the patient has been previously treated with a cancer therapeutic. In some embodiments, the patient has been previously treated with a cancer therapeutic, and the cancer has developed resistance to the cancer therapeutic. In some embodiments, the resistance is a primary intrinsic resistance. In some embodiments, the resistance is an acquired resistance from mutation(s). In some embodiments, the resistance is a bypass resistance. In some embodiments, the resistance is an EMT-based resistance.
[022] Additional embodiments, features, and advantages of the disclosure will be apparent from the following detailed description and through practice of the disclosure. The compounds of the present disclosure can be described as embodiments in any of the following enumerated clauses. It will be understood that any of the embodiments described herein can be used in connection with any other embodiments described herein to the extent that the embodiments do not contradict one another.
[023] 1. A method of treating cancer in a patient comprising, administering to the patient a therapeutically effective amount of a compound that inhibits MET, SRC and CSF1R, wherein the cancer is mediated by a genetically altered MET.
[024] 2. The method of clause 1, wherein the compound of the formula
Figure imgf000015_0001
wherein
R1 is H, deuterium, or C1-C6 alkyl; R2 is chloro or -CN; R3 is H, deuterium, or fluoro;
R4 is H or Ci-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof, wherein the cancer is mediated by a genetically altered MET.
[025] 3. The method of clause 1 or 2, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein.
[026] 4. The method of any one of clauses 1 to 3, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein at one or more of positions P991, T992, VI 092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and M1268.
[027] 5. The method of any one of the preceding clauses, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein that is selected from the group consisting of T1173I, P991S, M1250T, T992I, V1092I, F1200I, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T.
[028] 6. The method of any one of the preceding clauses, wherein the cancer is exhibiting bypass resistance mediated by a SRC/C SF1R.
[029] 7. The method of any one of the preceding clauses, wherein R1 is methyl.
[030] 8. The method of any one of the preceding clauses, wherein R2 is -CN.
[031] 9. The method of any one of the preceding clauses, wherein R3 is fluoro.
[032] 10. The method of any one of the preceding clauses, wherein R4 is C1-C6 alkyl.
[033] 11. The method of any one of the preceding clauses, wherein the compound is of the formula
Figure imgf000016_0001
or a pharmaceutically acceptable salt thereof.
[034] 12. The method of any one of the preceding clauses, wherein the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
[035] 13. The method of any one of clauses 1 to 12, wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, and serous and clear cell endometrial cancer.
[036] 14. The method of any one of the preceding clauses, wherein the patient has received prior treatment with one or more therapeutic agents.
[037] 15. A method of treating cancer in a patient previously shown to have a cancer mediated by a genetically altered MET comprising, administering to the patient a therapeutically effective amount of a compound that inhibits MET, SRC and CSF1R.
[038] 16. The method of clause 15, wherein the compound of the formula
Figure imgf000017_0001
wherein
R1 is H, deuterium, or C1-C6 alkyl;
R2 is chloro or -CN;
R3 is H, deuterium, or fluoro;
R4 is H or C1-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof.
[039] 17. The method of clause 15 or 16, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein.
[040] 18. The method of any one of clauses 15 to 17, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein at one or more of positions P991, T992,
VI 092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and M1268.
[041] 19. The method of any one of clauses 15 to 18, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein that is selected from the group consisting of T1173I, P991S, M1250T, T992I, V1092I, F 12001, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T.
[042] 20. The method of any one of clauses 15 to 19, wherein the cancer is exhibiting bypass resistance mediated by a SRC/C SF1R.
[043] 21. The method of any one of clauses 15 to 20, wherein R1 is methyl.
[044] 22. The method of any one of clauses 15 to 21, wherein R2 is -CN.
[045] 23. The method of any one of clauses 15 to 22, wherein R3 is fluoro.
[046] 24. The method of any one of clauses 15 to 23, wherein R4 is C1-C6 alkyl.
[047] 25. The method of any one of clauses 15 to 24, wherein the compound is of the formula
Figure imgf000018_0001
or a pharmaceutically acceptable salt thereof. [048] 26. The method of any one of clauses 15 to 25, wherein the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitt’s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
[049] 27. The method of any one of clauses 15 to 25, wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, and serous and clear cell endometrial cancer.
[050] 28. The method of any one of clauses 15 to 27, wherein the patient has received prior treatment with one or more therapeutic agents.
[051] 29. A compound that inhibits MET, SRC and CSF1R for treating cancer in a patient comprising, wherein the cancer is mediated by a genetically altered MET.
[052] 30. The compound of clause 29 having of the formula
Figure imgf000020_0001
wherein
R1 is H, deuterium, or C1-C6 alkyl;
R2 is chloro or -CN;
R3 is H, deuterium, or fluoro;
R4 is H or C1-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof, for treating cancer in a patient comprising, wherein the cancer is mediated by a genetically altered MET.
[053] 31. The compound of clause 29 or 30, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein.
[054] 32. The compound of any one of clauses 29 to 31, wherein the genetically altered MET encodes comprises a point mutation expressed in the c-Met protein at one or more of positions P991, T992, VI 092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and Ml 268.
[055] 33. The compound of any one of clauses 29 to 32, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein that is selected from the group consisting of T1173I, P991S, M1250T, T992I, V1092I, F 12001, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T.
[056] 34. The compound of any one of clauses 29 to 33, wherein the cancer is exhibiting bypass resistance mediated by a SRC/C SF1R.
[057] 35. The compound of any one of clauses 29 to 34, wherein R1 is methyl.
[058] 36. The compound of any one of clauses 29 to 35, wherein R2 is -CN.
[059] 37. The compound of any one of clauses 29 to 36, wherein R3 is fluoro. [060] 38. The compound of any one of clauses 29 to 37, wherein R4 is C1-C6 alkyl.
[061] 39. The compound of any one of clauses 29 to 38, wherein the compound is of the formula
Figure imgf000021_0001
or a pharmaceutically acceptable salt thereof.
[062] 40. The compound of any one of clauses 29 to 39, wherein the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
[063] 41. The compound of any one of clauses 29 to 39, wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, and serous and clear cell endometrial cancer.
[064] 42. The compound of any one of clauses 29 to 41, wherein the patient has received prior treatment with one or more therapeutic agents. [065] 43. Use of a compound that inhibits MET, SRC and CSF1R in the preparation of a medicament for treating cancer in a patient, wherein the cancer is mediated by a genetically altered
MET.
[066] 44. The use of clause 43, wherein the compound is of the formula
Figure imgf000022_0001
wherein
R1 is H, deuterium, or C1-C6 alkyl;
R2 is chloro or -CN;
R3 is H, deuterium, or fluoro;
R4 is H or Ci-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -ME,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof, in the preparation of a medicament for treating cancer in a patient comprising, wherein the cancer is mediated by a genetically altered MET.
[067] 45. The use of clause 43 or 44, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein.
[068] 46. The use of any one of clauses 43 to 45, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein at one or more of positions P991, T992, VI 092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and M1268.
[069] 47. The use of any one of clauses 43 to 46, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein that is selected from the group consisting of T11731, P991S, M1250T, T992I, VI 0921, F 12001, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T. [070] 48. The use of any one of clauses 43 to 47, wherein the cancer is exhibiting bypass resistance mediated by a SRC/C SF1R.
[071] 49. The use of any one of clauses 43 to 48, wherein R1 is methyl.
[072] 50. The use of any one of clauses 43 to 49, wherein R2 is -CN.
[073] 51. The use of any one of clauses 43 to 50, wherein R3 is fluoro.
[074] 52. The use of any one of clauses 43 to 51, wherein R4 is C1-C6 alkyl.
[075] 53. The use of any one of clauses 43 to 52, wherein the compound is of the formula
Figure imgf000023_0001
or a pharmaceutically acceptable salt thereof.
[076] 54. The use of any one of clauses 43 to 53, wherein the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
[077] 55. The use of any one of clauses 43 to 53, wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, and serous and clear cell endometrial cancer.
[078] 56. The method of any one of clauses 43 to 55, wherein the patient has received prior treatment with one or more therapeutic agents.
[079] 57. A medicament comprising a compound that inhibits MET, SRC and CSF1R for use in a method of treating cancer in a patient comprising, wherein the cancer is mediated by a genetically altered MET.
[080] 58. The medicament of clause 57, wherein the compound is of the formula
Figure imgf000024_0001
wherein
R1 is H, deuterium, or C1-C6 alkyl;
R2 is chloro or -CN;
R3 is H, deuterium, or fluoro;
R4 is H or Ci-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -ME,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof, for use in a method of treating cancer in a patient comprising, wherein the cancer is mediated by a genetically altered MET.
[081] 59. The medicament of clause 57 or 58, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein.
[082] 60. The medicament of any one of clauses 57 to 59, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein at one or more of positions P991, T992,
VI 092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and
M1268. [083] 61. The medicament of any one of clauses 57 to 60, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein that is selected from the group consisting of T1173I, P991S, M1250T, T992I, V1092I, F1200I, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T.
[084] 62. The medicament of any one of clauses 57 to 61, wherein the cancer is exhibiting bypass resistance mediated by a SRC/C SF1R.
[085] 63. The medicament of any one of clauses 57 to 62, wherein R1 is methyl.
[086] 64. The medicament of any one of clauses 57 to 63, wherein R2 is -CN.
[087] 65. The medicament of any one of clauses 57 to 64, wherein R3 is fluoro.
[088] 66. The medicament of any one of clauses 57 to 65, wherein R4 is C1-C6 alkyl.
[089] 67. The medicament of any one of clauses 57 to 66, wherein the compound is of the formula
Figure imgf000025_0001
or a pharmaceutically acceptable salt thereof.
[090] 68. The medicament of any one of clauses 57 to 67, wherein the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitt’s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
[091] 69. The medicament of any one of clauses 57 to 68, wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, and serous and clear cell endometrial cancer.
[092] 70. The medicament of any one of clauses 57 to 69, wherein the patient has received prior treatment with one or more therapeutic agents.
[093] 71. Use of a compound that inhibits MET, SRC and CSF1R in a method of treating cancer in a patient comprising, wherein the cancer is mediated by a genetically altered MET.
[094] 72. The use of clause 71, wherein the compound is of the formula
Figure imgf000026_0001
wherein
R1 is H, deuterium, or C1-C6 alkyl;
R2 is chloro or -CN;
R3 is H, deuterium, or fluoro;
R4 is H or C1-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof, in a method of treating cancer in a patient comprising, wherein the cancer is mediated by a genetically altered MET.
[095] 73. The use of clause 71 or 72, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein. [096] 74. The use of any one of clauses 71 to 73, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein at one or more of positions P991, T992, VI 092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and M1268.
[097] 75. The use of any one of clauses 71 to 74, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein that is selected from the group consisting of T11731, P991S, M1250T, T992I, VI 0921, F 12001, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T.
[098] 76. The use of any one of clauses 71 to 75, wherein the cancer is exhibiting bypass resistance mediated by a SRC/C SF1R.
[099] 77. The use of any one of clauses 71 to 76, wherein R1 is methyl.
[0100] 78. The use of any one of clauses 71 to 77, wherein R2 is -CN.
[0101] 79. The use of any one of clauses 71 to 78, wherein R3 is fluoro.
[0102] 80. The use of any one of clauses 71 to 79, wherein R4 is C1-C6 alkyl.
[0103] 81. The use of any one of clauses 71 to 80, wherein the compound is of the formula
Figure imgf000027_0001
or a pharmaceutically acceptable salt thereof.
[0104] 82. The use of any one of clauses 71 to 81, wherein the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitt’s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
[0105] 83. The use of any one of clauses 71 to 81, wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, and serous and clear cell endometrial cancer.
[0106] 84. The use of any one of clauses 71 to 83, wherein the patient was previously shown to express a c-Met comprising a mutation encoded by a genetically altered MET.
[0107] 85. The use of any one of clauses 71 to 84, wherein the patient has received prior treatment with one or more therapeutic agents.
[0108] 86. A method of treating cancer in a patient comprising; i. identifying a genetically altered MET in the patient, and ii. administering to the patient a therapeutically effective amount of a compound that inhibits MET, SRC and CSF1R.
[0109] 87. The method of clause 86, wherein the compound is of the formula
Figure imgf000028_0001
wherein
R1 is H, deuterium, or C1-C6 alkyl; R2 is chloro or -CN;
R3 is H, deuterium, or fluoro; R4 is H or Ci-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof.
[0110] 88. The method of clause 86 or 87, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein.
[0111] 89. The method of any one of clauses 86 to 88, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein at one or more of positions P991, T992,
VI 092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and M1268.
[0112] 90. The method of any one of clauses 86 to 89, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein that is selected from the group consisting of T1173I, P991S, M1250T, T992I, V1092I, F1200I, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T.
[0113] 91. The method of any one of clauses 86 to 90, wherein the cancer is exhibiting bypass resistance mediated by a SRC/C SF1R.
[0114] 92. The method of any one of clauses 86 to 91, wherein R1 is methyl.
[0115] 93. The method of any one of clauses 86 to 92, wherein R2 is -CN.
[0116] 94. The method of any one of clauses 86 to 93, wherein R3 is fluoro.
[0117] 95. The method of any one of clauses 86 to 94, wherein R4 is C1-C6 alkyl.
[0118] 96. The method of any one of clauses 86 to 95, wherein the compound is of the formula
Figure imgf000029_0001
or a pharmaceutically acceptable salt thereof.
[0119] 97. The method of any one of clauses 86 to 96, wherein the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma. [0120] 98. The method of any one of clauses 86 to 96, wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, and serous and clear cell endometrial cancer.
[0121] 99. The method of any one of clauses 86 to 98, wherein the patient has received prior treatment with one or more therapeutic agents.
[0122] 100. The method of any one of clauses 86 to 99, wherein the step of identifying comprises subjecting a patient sample to a test selected from the group consisting of FISH, IHC, PCR and gene sequencing.
[0123] 101. A method of identifying a patient for treatment with a compound that inhibits MET, SRC and CSF1R comprising diagnosing the patient with a cancer mediated by a genetically altered MET.
[0124] 102. The method of clause 101, wherein the compound is of the formula
Figure imgf000031_0001
wherein
R1 is H, deuterium, or C1-C6 alkyl;
R2 is chloro or -CN;
R3 is H, deuterium, or fluoro;
R4 is H or C1-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof.
[0125] 103. The method of clause 101 or 102, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein.
[0126] 104. The method of any one of clauses 101 to 103, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein at one or more of positions P991, T992,
VI 092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and M1268.
[0127] 105. The method of any one of clauses 101 to 104, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein that is selected from the group consisting of T1173I, P991S, M1250T, T992I, V1092I, F 12001, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T.
[0128] 106. The method of any one of clauses 101 to 105, wherein the cancer is exhibiting bypass resistance mediated by a SRC/C SF1R.
[0129] 107. The method of any one of clauses 101 to 106, wherein R1 is methyl.
[0130] 108. The method of any one of clauses 101 to 107, wherein R2 is -CN.
[0131] 109. The method of any one of clauses 101 to 108, wherein R3 is fluoro.
[0132] 110. The method of any one of clauses 101 to 109, wherein R4 is C1-C6 alkyl. [0133] 111. The method of any one of clauses 101 to 110, wherein the compound is of the formula
Figure imgf000032_0001
or a pharmaceutically acceptable salt thereof.
[0134] 112. The method of any one of clauses 101 to 111, wherein the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
[0135] 113. The method of any one of clauses 101 to 111, wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, and serous and clear cell endometrial cancer.
[0136] 114. The method of any one of clauses 101 to 113, wherein the patient has received prior treatment with one or more therapeutic agents. [0137] 115. The method of any one of clauses 101 to 114, wherein the patient is identified by subjecting a patient sample to a test selected from the group consisting of FISH, IHC, PCR and gene sequencing.
[0138] 116. The method of any one of clauses 101 to 114, wherein the diagnosing comprises obtaining a sample from a patient, and modifying the sample using a biological test or biological assay selected from the group consisting of FISH, IHC, PCR and gene sequencing, to provide a measured result showing a genetically altered MET in the sample.
DETAILED DESCRIPTION
[0139] Before the present disclosure is further described, it is to be understood that this disclosure is not limited to particular embodiments described, as such may, of course, vary. It is also to be understood that the terminology used herein is for the purpose of describing particular embodiments only, and is not intended to be limiting, since the scope of the present disclosure will be limited only by the appended claims.
[0140] Unless defined otherwise, all technical and scientific terms used herein have the same meaning as is commonly understood by one of ordinary skill in the art to which this disclosure belongs. All patents, applications, published applications and other publications referred to herein are incorporated by reference in their entireties. If a definition set forth in this section is contrary to or otherwise inconsistent with a definition set forth in a patent, application, or other publication that is herein incorporated by reference, the definition set forth in this section prevails over the definition incorporated herein by reference.
[0141] As used herein and in the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the context clearly dictates otherwise. It is further noted that the claims may be drafted to exclude any optional element. As such, this statement is intended to serve as antecedent basis for use of such exclusive terminology as “solely,” “only” and the like in connection with the recitation of claim elements, or use of a “negative” limitation.
[0142] As used herein, the terms “including,” “containing,” and “comprising” are used in their open, non-limiting sense.
[0143] To provide a more concise description, some of the quantitative expressions given herein are not qualified with the term “about”. It is understood that, whether the term “about” is used explicitly or not, every quantity given herein is meant to refer to the actual given value, and it is also meant to refer to the approximation to such given value that would reasonably be inferred based on the ordinary skill in the art, including equivalents and approximations due to the experimental and/or measurement conditions for such given value. Concentrations that are given as percentages refer to mass ratios, unless indicated differently.
[0144] Except as otherwise noted, the methods and techniques of the present embodiments are generally performed according to conventional methods well known in the art and as described in various general and more specific references that are cited and discussed throughout the present disclosure.
Definitions
[0145] As used herein, the term “alkyl” includes a chain of carbon atoms, which is optionally branched and contains from 1 to 20 carbon atoms. It is to be further understood that in certain embodiments, alkyl may be advantageously of limited length, including C1-C12, C1-C10, C1-C9, Ci- Cs, C1-C7, C1-C6, and C1-C4, Illustratively, such particularly limited length alkyl groups, including Ci-Ce, C1-C7, C1-C6, and C1-C4, and the like may be referred to as “lower alkyl.” Illustrative alkyl groups include, but are not limited to, methyl, ethyl, n-propyl, isopropyl, n-butyl, isobutyl, sec- butyl, tert-butyl, pentyl, 2-pentyl, 3 -pentyl, neopentyl, hexyl, heptyl, octyl, and the like. Alkyl may be substituted or unsubstituted. Typical substituent groups include cycloalkyl, aryl, heteroaryl, heteroalicyclic, hydroxy, alkoxy, aryloxy, mercapto, alkylthio, arylthio, cyano, halo, carbonyl, oxo, (=0), thiocarbonyl, O-carbamyl, N-carbamyl, O-thiocarbamyl, N-thiocarbamyl, C-amido, N- amido, C-carboxy, O-carboxy, nitro, and amino, or as described in the various embodiments provided herein. It will be understood that “alkyl” may be combined with other groups, such as those provided above, to form a functionalized alkyl. By way of example, the combination of an “alkyl” group, as described herein, with a “carboxy” group may be referred to as a “carboxyalkyl” group. Other non-limiting examples include hydroxyalkyl, aminoalkyl, and the like.
[0146] As used herein, the term “cycloalkyl” refers to a 3 to 15 member all-carbon monocyclic ring, including an all-carbon 5-member/6-member or 6-member/6-member fused bicyclic ring, or a multi cyclic fused ring (a “fused” ring system means that each ring in the system shares an adjacent pair of carbon atoms with each other ring in the system) group, where one or more of the rings may contain one or more double bonds but the cycloalkyl does not contain a completely conjugated pi- electron system. It will be understood that in certain embodiments, cycloalkyl may be advantageously of limited size such as C3-C13, C3-C9, C3-C6 and C4-C6. Cycloalkyl may be unsubstituted, or substituted as described for alkyl or as described in the various embodiments provided herein. Illustrative cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclopentadienyl, cyclohexyl, cyclohexenyl, cycloheptyl, adamantyl, norbornyl, norbomenyl, 9//-fluoren-9-yl, and the like. Illustrative examples of cycloalkyl groups shown in graphical representations include the following entities, in the form of properly bonded moieties:
Figure imgf000035_0001
[0147] As used herein, “hydroxy” or ““hydroxyl” refers to an -OH group.
[0148] As used herein, “halo” or “halogen” refers to fluorine, chlorine, bromine or iodine.
[0149] As used herein, “cyano” refers to a -CN group.
[0150] The term “substituted” means that the specified group or moiety bears one or more substituents. The term “unsubstituted” means that the specified group bears no substituents.
Where the term “substituted” is used to describe a structural system, the substitution is meant to occur at any valency-allowed position on the system. In some embodiments, “substituted” means that the specified group or moiety bears one, two, or three substituents. In other embodiments, “substituted” means that the specified group or moiety bears one or two substituents. In still other embodiments, “substituted” means the specified group or moiety bears one substituent.
[0151] As used herein, “optional” or “optionally” means that the subsequently described event or circumstance may but need not occur, and that the description includes instances where the event or circumstance occurs and instances in which it does not. For example, “wherein each hydrogen atom in C1-C6 alkyl” means that a substituent may be but need not be present on the C1-C6 alkyl by replacement of a hydrogen atom for each substituent group, and the description includes situations where the C1-C6 alkyl is substituted and situations where the C1-C6 alkyl is not substituted. [0152] As used herein, the term “pharmaceutically acceptable salt” refers to those salts which counter ions which may be used in pharmaceuticals. See, generally, S.M. Berge, et al., “Pharmaceutical Salts,” J. Pharm. Sci., 1977, 66, 1-19. Preferred pharmaceutically acceptable salts are those that are pharmacologically effective and suitable for contact with the tissues of subjects without undue toxicity, irritation, or allergic response. A compound described herein may possess a sufficiently acidic group, a sufficiently basic group, both types of functional groups, or more than one of each type, and accordingly react with a number of inorganic or organic bases, and inorganic and organic acids, to form a pharmaceutically acceptable salt. Such salts include:
(1) acid addition salts, which can be obtained by reaction of the free base of the parent compound with inorganic acids such as hydrochloric acid, hydrobromic acid, nitric acid, phosphoric acid, sulfuric acid, and perchloric acid and the like, or with organic acids such as acetic acid, oxalic acid, (D) or (L) malic acid, maleic acid, methane sulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid, salicylic acid, tartaric acid, citric acid, succinic acid or malonic acid and the like; or
(2) salts formed when an acidic proton present in the parent compound either is replaced by a metal ion, e.g., an alkali metal ion, an alkaline earth ion, or an aluminum ion; or coordinates with an organic base such as ethanolamine, diethanolamine, triethanolamine, trimethamine, N- methylglucamine, and the like.
[0153] Pharmaceutically acceptable salts are well known to those skilled in the art, and any such pharmaceutically acceptable salt may be contemplated in connection with the embodiments described herein. Examples of pharmaceutically acceptable salts include sulfates, pyrosulfates, bi sulfates, sulfites, bi sulfites, phosphates, monohydrogen-phosphates, dihydrogenphosphates, metaphosphates, pyrophosphates, chlorides, bromides, iodides, acetates, propionates, decanoates, caprylates, acrylates, formates, isobutyrates, caproates, heptanoates, propiolates, oxalates, malonates, succinates, suberates, sebacates, fumarates, maleates, butyne-l,4-dioates, hexyne-1,6- dioates, benzoates, chlorobenzoates, methylbenzoates, dinitrobenzoates, hydroxybenzoates, methoxybenzoates, phthalates, sulfonates, methyl sulfonates, propyl sulfonates, besylates, xylenesulfonates, naphthalene- 1 -sulfonates, naphthalene-2-sulfonates, phenylacetates, phenylpropionates, phenylbutyrates, citrates, lactates, g-hydroxybutyrates, glycolates, tartrates, and mandelates. Lists of other suitable pharmaceutically acceptable salts are found in Remington's Pharmaceutical Sciences, 17th Edition, Mack Publishing Company, Easton, Pa., 1985. [0154] For a compound of Formula I that contains a basic nitrogen, a pharmaceutically acceptable salt may be prepared by any suitable method available in the art, for example, treatment of the free base with an inorganic acid, such as hydrochloric acid, hydrobromic acid, sulfuric acid, sulfamic acid, nitric acid, boric acid, phosphoric acid, and the like, or with an organic acid, such as acetic acid, phenylacetic acid, propionic acid, stearic acid, lactic acid, ascorbic acid, maleic acid, hydroxymaleic acid, isethionic acid, succinic acid, valeric acid, fumaric acid, malonic acid, pyruvic acid, oxalic acid, glycolic acid, salicylic acid, oleic acid, palmitic acid, lauric acid, a pyranosidyl acid, such as glucuronic acid or galacturonic acid, an alpha-hydroxy acid, such as mandelic acid, citric acid, or tartaric acid, an amino acid, such as aspartic acid or glutamic acid, an aromatic acid, such as benzoic acid, 2-acetoxybenzoic acid, naphthoic acid, or cinnamic acid, a sulfonic acid, such as laurylsulfonic acid, p-toluenesulfonic acid, methanesulfonic acid, or ethanesulfonic acid, or any compatible mixture of acids such as those given as examples herein, and any other acid and mixture thereof that are regarded as equivalents or acceptable substitutes in light of the ordinary level of skill in this technology.
[0155] The disclosure also relates to pharmaceutically acceptable prodrugs of the compounds of Formula I, and treatment methods employing such pharmaceutically acceptable prodrugs. The term “prodrug” means a precursor of a designated compound that, following administration to a subject, yields the compound in vivo via a chemical or physiological process such as solvolysis or enzymatic cleavage, or under physiological conditions (e.g., a prodrug on being brought to physiological pH is converted to the compound of Formula I). A "pharmaceutically acceptable prodrug” is a prodrug that is non-toxic, biologically tolerable, and otherwise biologically suitable for administration to the subject. Illustrative procedures for the selection and preparation of suitable prodrug derivatives are described, for example, in “Design of Prodrugs”, ed. H.
Bundgaard, Elsevier, 1985.
[0156] The present disclosure also relates to pharmaceutically active metabolites of compounds of Formula I, and uses of such metabolites in the methods of the disclosure. A “pharmaceutically active metabolite” means a pharmacologically active product of metabolism in the body of a compound of Formula I or salt thereof. Prodrugs and active metabolites of a compound may be determined using routine techniques known or available in the art. See, e.g., Bertolini et ak, ./.
Med. Chem. 1997, 40, 2011-2016; Shan et ak, J Pharm. Sci. 1997, 86 (7), 765-767; Bagshawe, Drug Dev. Res. 1995, 34, 220-230; Bodor, Adv. Drug Res. 1984, 13, 255-331; Bundgaard, Design of Prodrugs (Elsevier Press, 1985); and Larsen, Design and Application of Prodrugs, Drug Design and Development (Krogsgaard-Larsen et al., eds., Harwood Academic Publishers, 1991).
[0157] Any formula depicted herein is intended to represent a compound of that structural formula as well as certain variations or forms. For example, a formula given herein is intended to include a racemic form, or one or more enantiomeric, diastereomeric, or geometric isomers, or a mixture thereof. Additionally, any formula given herein is intended to refer also to a hydrate, solvate, or polymorph of such a compound, or a mixture thereof. Additionally, any formula given herein is intended to refer also to a hydrate, solvate, or polymorph of such a compound, or a mixture thereof. For example, it will be appreciated that compounds depicted by a structural formula containing the symbol “ Ά/W ” include both stereoisomers for the carbon atom to which the symbol “ ΆLL, ” is attached, specifically both the bonds
Figure imgf000038_0001
and .. mil” are encompassed by the meaning of “ nLLL,”
[0158] As used herein, the term “genetically altered” refers to a permanent alteration in the DNA sequence that makes up a gene that can result in a change in the protein sequence encoded by the gene. A gene that is “genetically altered” as described herein, can possess changes in DNA sequence, and/or protein sequence encoded by the DNA sequence, that range in size; for example, a single nucleotide (a.k.a. a single nucleotide polymorphism, SNP or point mutation), a multiple nucleotide polymorphism (MNPs), a large segment of a chromosome that includes multiple genes, such as a gene fusion, and the like. Examples of gene fusions include, but are not limited to, those which are the result of a chromosomal inversion in which a portion of a chromosomal DNA encoding one or more genes rearranges to provide a fusion of two genes not ordinarily in communication in the DNA sequence, chromosomal deletion in which part of a DNA sequence of a chromosome is deleted to provide a fusion of two genes not ordinarily in communication in the DNA sequence, or those which are the result of a translocation in which a portion of chromosomal DNA is spliced and inserted into the same or a different chromosome to provide a fusion of two genes not ordinarily in communication in the DNA sequence. One of skill in the art will readily appreciate that such gene fusions can be found in multiple variants depending on the individual in which the gene fusion has occurred, and each of such variants is contemplated by the methods described herein.
[0159] A “genetically altered” gene, or the protein encoded by such gene, can occur as hereditary mutations which can be inherited from a parent and are sometimes referred to as germline mutations, or a “genetically altered” gene, or the protein encoded by such gene, can occur as an acquired (or somatic) mutation that occurs at some point during a person’s life. In some instances, a “genetically altered” gene can be described as a de novo (new) mutation, and can be either hereditary or somatic. It will be further understood that “genetically altered” can refer to a situation in which more than one of the changes in DNA sequence described herein can occur in a patient simultaneously, such as a SNP (or point mutation) and a translocation. Such situations can arise from, but are not solely the result of, so-called “acquired resistance” in which a patient having been treated with a kinase inhibitor can develop a mutation in the DNA sequence that reduces the effectiveness of the treatment. Non-limiting examples of such acquired resistance mutations include the point mutations P991S, T992I, V1092I, T1173I, F1200I, D1228N, D1228H, Y1230A, Y1230C, Y1230D, Y1230H, Y1235D, D1246N, D1246H, Y1248D, Y1248H, Y1248C, M1250T, and M1268T in the c-Met protein that is encoded by a genetically altered MET.
[0160] As used herein, the term “intrinsic resistance” refers to the pre-existing resistance of disease cells, especially cancer cells, to drug treatment, especially chemotherapy treatment. It will be appreciated that intrinsic resistance can result in resistance of the cells to a single drug, a small group of structurally related drugs, or a several drugs of differing chemical structure (so-called “multidrug resistance” or “MDR”). (Monti, E. 2007. Molecular Determinants of Intrinsic Multidrug Resistance in Cancer Cells and Tumors In B. Teicher (Ed.), Cancer Drug Resistance (pp. 241-260). Totowa, New Jersey: Humana Press Inc.). It will be appreciated that intrinsic resistance can be the result of one or more host-related factors and/or the genetic make-up of the cells. Such factors include but are not limited to immunomodulation; pharmacogenetic factors such as failure to achieve optimal serum drugs levels due to altered ADME or low tolerance to drug- induced side effects; restricted drug access to the tumor site; and microenvironmental cues. Such genetic make-up factors include, but are not limited to altered expression of drug transporters; qualitative alterations of drug target(s); quantitative alterations of drug target(s); changes in intracellular drug handling/metabolism; changes in DNA repair activities, and alteration in apoptotic pathways. (Gottesman, M.M., Annu. Rev. Med., 2002, 53, 516-527).
[0161] As used herein, the term “disease” includes, but is not limited to, cancer, pain, inflammatory diseases, such as allergy, asthma, autoimmune diseases, coeliac disease, glomerulonephritis, hepatitis, inflammatory' bowel disease (e.g. ulcerative colitis), pre-perfusion injury, transplant rejection, psoriasis, and rheumatoid arthritis; polycythemia vera, essential thrombocythemia, and myeloid metaplasia with myelofibrosis.
[0162] As used herein, the term “cancer” includes, but is not limited to, cancers such as carcinomas, sarcomas, lymphomas, Hodgekin’s disease, melanomas, mesotheliomas, Burkitf s lymphoma, nasopharyngeal carcinomas, leukemias, lung cancers, breast cancers, hereditary human papillary renal carcinomas, sporadic human papillary renal carcinomas, childhood hepatocellular carcinomas, myeloma, and the like. Examples of “cancers” in connection with the present disclosure include, but are not limited to, ALCL, lung cancer, such as non-small cell lung cancer (NSCLC), including adenocarcinoma, lung squamous cell carcinoma, large cell carcinoma, and large cell neuroendocrine tumors, small cell lung cancer (SCLC), neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, such as luminal A, luminal B, triple negative breast cancer, triple positive breast cancer, HER2+, and the like, mouth cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, such as anaplastic thyroid cancer, cholangiocarcinoma, ovarian cancer, gastric cancer, such as gastric adenocarcinoma, colorectal cancer (CRC), angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, such as skin cutaneous melanoma, head and neck squamous cell carcinoma (HNSCC), pediatric glioma CML, prostate cancer, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, castrate-resistant prostate cancer, Hodgkin lymphoma, uterine cancer, such as serous and clear cell endometrial cancer, endometrial cancer, and the like, oral cancer, endocrine cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, colon cancer, bladder cancer, bone cancer, cervical cancer, testicular cancer, rectal cancer, kidney cancer, liver cancer, neuroendocrine tumors, and stomach cancer. It will be appreciated that the term “cancer” includes both primary cancers or primary tumors and metastatic cancers or metastatic tumors, and includes all stages of cancer as known in the art. For example, metastatic NSCLC, metastatic CRC, metastatic pancreatic cancer, metastatic colorectal carcinoma, metastatic HNSCC, metastatic uterine cancer, and the like. It will be appreciated that the term “cancer” includes cancers that involve the upregulation of certain genes or genetic mutations in certain genes that can lead to disease progression, such as small GTPases (e.g. KRAS and the like) and receptor tyrosine kinases such as MET, and the like..
Representative Embodiments
[0163] In some embodiments, the methods described herein relate to the treatment of disease comprising administering to a patient in need of treatment a therapeutically effective amount of a compound having activity against MET, SRC, and CSF1R. In some embodiments, the compound has activity against a genetically altered MET, SRC, and SCF1R. In some embodiments, the compound is of the formula I
Figure imgf000041_0001
I wherein
R1 is H, deuterium, or C1-C6 alkyl;
R2 is chloro or -CN;
R3 is H, deuterium, or fluoro;
R4 is H or C1-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof.
[0164] In some embodiments, wherein R1 is methyl. In some embodiments, wherein R2 is -CN. In some embodiments, R3 is fluoro. In some embodiments, R4 is C1-C6 alkyl. In some embodiments, R4 is ethyl. In some embodiments, the compound is of the formula
Figure imgf000042_0001
or a pharmaceutically acceptable salt thereof.
[0165] It will be appreciated that the disease can be any of a number of diseases associated with the tyrosine kinases described herein against which the compounds of the formula I have activity. For example, the methods described herein can be used for the treatment of diseases such as cancer, pain, psoriasis, rheumatoid arthritis, polycythemia vera, essential thrombocythemia, ulcerative colitis, myeloid metaplasia with myelofibrosis, and the like. It will be appreciated that the disease can be any disease associated with the activity of a genetically altered MET, a SRC, or CSF1R. In some embodiments, the disease is a cancer mediated by or associated with a genetically altered MET. In some embodiments, the disease is a cancer mediated by or associated with a genetically altered MET encoding a point mutation that is expressed in the c-Met protein. In some embodiments, the disease is a cancer mediated by or associated with a genetically altered MET encoding a point mutation expressed in the c-Met protein at one or more of positions P991, T992, VI 092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and M1268.. In some embodiments, the disease is a cancer mediated by or associated with a genetically altered MET encoding a point mutation expressed in the c-Met protein that is selected from the group consisting of T11731, P991S, M1250T, T992I, V1092I, F 12001, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T.
[0166] It will be appreciated that the cancer can be any cancer mediated by or associated with a genetically altered MET, a SRC, or SCF1R including, but not limited to, a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma. In some embodiments, the cancer includes, but is not limited to, ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, serous and clear cell endometrial cancer
[0167] In some embodiments, the present disclosure provides methods of treating disease in a patient that has received a prior treatment with one or more therapeutic agents. In some embodiments, the patient has been previously treated with one or more therapeutic agents. In some embodiments, the patent has been previously treated with one or more therapeutic agents and developed an acquired resistance to the treatment. In some embodiments, the patent has been previously treated with one or more therapeutic agents and developed an acquired resistance to the treatment in the form of a genetically altered MET. In some embodiments, the patent has been previously treated with one or more therapeutic agents and developed an acquired resistance to the treatment expressed as a mutation of the c-Met protein encoded by a genetically altered MET. In some embodiments, the patent has been previously treated with one or more therapeutic agents and developed an acquired resistance to the treatment expressed as a point mutation in the c-Met protein at one or more of positions P991, T992, V1092, H1094, G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and M1268. In some embodiments, the patent has been previously treated with one or more therapeutic agents and developed an acquired resistance to the treatment expressed as a point mutation selected from the group consisting of T11731,
P991S, M1250T, T992I, VI 0921, F 12001, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T in the c-Met protein that is encoded by a genetically altered MET. In some embodiments, the patent has been previously treated with one or more chemotherapeutic agents and developed bypass resistance to the treatment. In still other embodiments, the patent has been previously treated with one or more therapeutic agents and developed bypass resistance to the treatment regulated by SRC or SCF1R.
[0168] Other chemotherapeutic agents which the patient may be been treated with prior to treatment with one or more of the compounds described herein include but are not limited to kinase inhibitors, adrenocorticoids and corticosteroids, alkylating agents, peptide and peptidomimetic signal transduction inhibitors, antiandrogens, antiestrogens, androgens, aclamycin and aclamycin derivatives, estrogens, antimetabolites, platinum compounds, amanitins, plant alkaloids, mitomycins, discodermolides, microtubule inhibitors, epothilones, inflammatory and proinflammatory agents, purine analogs, pyrimidine analogs, camptothecins and dolastatins. In some embodiments, the chemotherapeutic agent the patient received previous to treatment with one or more compounds described herein can be one or more of afatinib, axitinib, alectinib, bosutinib, brigatini, cabozantinib, ceritinib, crizotinib, dabrefenib, dasatinib, erlotinib, everolimus, gefitinib, ibrutinib, imatinib, lapatinib, lenvatinib, nilotinib, nintedanib, palbociclib, pazopanib, ponatinib, regorafenib, ruxolitinib, sirolimus, sorafenib, sunitinib, tofacitinib, temsirolimus, trametinib, vandetanib, vemurafenib, methotrexate, busulfan, carboplatin, chlorambucil, cisplatin, tamoxiphen, taxol, paclitaxel, docetaxel, cytosine arabinoside, cyclophosphamide, daunomycin, rhizoxin, prednisone, hydroxyurea, teniposide, vincristine, vinblastine, eribulin, camptothecin, irinotecan, geldanamycin, estramustine and nocodazole. In some embodiments, the methods described herein provide treatment of a patient previously treated with a kinase inhibitor selected from the group consisting of afatinib, alectinib, axitinib, bosutinib, brigatini, cabozantinib, ceritinib, crizotinib, dabrefenib, dasatinib, erlotinib, everolimus, gefitinib, ibrutinib, imatinib, lapatinib, lenvatinib, nilotinib, nintedanib, palbociclib, pazopanib, ponatinib, regorafenib, ruxolitinib, sirolimus, sorafenib, sunitinib, tofacitinib, temsirolimus, trametinib, vandetanib and vemurafenib. In some embodiments, the patient was previously treated with crizotinib.
Pharmaceutical Compositions
[0169] For treatment purposes, pharmaceutical compositions comprising the compounds described herein may further comprise one or more pharmaceutically-acceptable excipients. A pharmaceutically-acceptable excipient is a substance that is non-toxic and otherwise biologically suitable for administration to a subject. Such excipients facilitate administration of the compounds described herein and are compatible with the active ingredient. Examples of pharmaceutically- acceptable excipients include stabilizers, lubricants, surfactants, diluents, anti -oxidants, binders, coloring agents, bulking agents, emulsifiers, or taste-modifying agents. In preferred embodiments, pharmaceutical compositions according to the invention are sterile compositions. Pharmaceutical compositions may be prepared using compounding techniques known or that become available to those skilled in the art.
[0170] Sterile compositions are also contemplated by the invention, including compositions that are in accord with national and local regulations governing such compositions.
[0171] The pharmaceutical compositions and compounds described herein may be formulated as solutions, emulsions, suspensions, or dispersions in suitable pharmaceutical solvents or carriers, or as pills, tablets, lozenges, suppositories, sachets, dragees, granules, powders, powders for reconstitution, or capsules along with solid carriers according to conventional methods known in the art for preparation of various dosage forms. Pharmaceutical compositions of the invention may be administered by a suitable route of delivery, such as oral, parenteral, rectal, nasal, topical, or ocular routes, or by inhalation. Preferably, the compositions are formulated for intravenous or oral administration.
[0172] For oral administration, the compounds the invention may be provided in a solid form, such as a tablet or capsule, or as a solution, emulsion, or suspension. To prepare the oral compositions, the compounds of the invention may be formulated to yield a dosage of, e.g ., from about 0.1 mg to 1 g daily, or about 1 mg to 50 mg daily, or about 50 to 250 mg daily, or about 250 mg to 1 g daily. Oral tablets may include the active ingredient(s) mixed with compatible pharmaceutically acceptable excipients such as diluents, disintegrating agents, binding agents, lubricating agents, sweetening agents, flavoring agents, coloring agents and preservative agents. Suitable inert fillers include sodium and calcium carbonate, sodium and calcium phosphate, lactose, starch, sugar, glucose, methyl cellulose, magnesium stearate, mannitol, sorbitol, and the like. Exemplary liquid oral excipients include ethanol, glycerol, water, and the like. Starch, polyvinyl-pyrrolidone (PVP), sodium starch glycolate, microcrystalline cellulose, and alginic acid are exemplary disintegrating agents. Binding agents may include starch and gelatin. The lubricating agent, if present, may be magnesium stearate, stearic acid, or talc. If desired, the tablets may be coated with a material such as glyceryl monostearate or glyceryl distearate to delay absorption in the gastrointestinal tract, or may be coated with an enteric coating. [0173] Capsules for oral administration include hard and soft gelatin capsules. To prepare hard gelatin capsules, active ingredient(s) may be mixed with a solid, semi-solid, or liquid diluent. Soft gelatin capsules may be prepared by mixing the active ingredient with water, an oil, such as peanut oil or olive oil, liquid paraffin, a mixture of mono and di-glycerides of short chain fatty acids, polyethylene glycol 400, or propylene glycol.
[0174] Liquids for oral administration may be in the form of suspensions, solutions, emulsions, or syrups, or may be lyophilized or presented as a dry product for reconstitution with water or other suitable vehicle before use. Such liquid compositions may optionally contain: pharmaceutically- acceptable excipients such as suspending agents (for example, sorbitol, methyl cellulose, sodium alginate, gelatin, hydroxyethylcellulose, carboxymethylcellulose, aluminum stearate gel and the like); non-aqueous vehicles, e.g., oil (for example, almond oil or fractionated coconut oil), propylene glycol, ethyl alcohol, or water; preservatives (for example, methyl or propyl p- hydroxybenzoate or sorbic acid); wetting agents such as lecithin; and, if desired, flavoring or coloring agents.
[0175] For parenteral use, including intravenous, intramuscular, intraperitoneal, intranasal, or subcutaneous routes, the agents of the invention may be provided in sterile aqueous solutions or suspensions, buffered to an appropriate pH and isotonicity or in parenterally acceptable oil.
Suitable aqueous vehicles include Ringer's solution and isotonic sodium chloride. Such forms may be presented in unit-dose form such as ampoules or disposable injection devices, in multi-dose forms such as vials from which the appropriate dose may be withdrawn, or in a solid form or pre concentrate that can be used to prepare an injectable formulation. Illustrative infusion doses range from about 1 to 1000 pg/kg/minute of agent admixed with a pharmaceutical carrier over a period ranging from several minutes to several days.
[0176] For nasal, inhaled, or oral administration, the inventive pharmaceutical compositions may be administered using, for example, a spray formulation also containing a suitable carrier. The inventive compositions may be formulated for rectal administration as a suppository.
[0177] For topical applications, the compounds of the present invention are preferably formulated as creams or ointments or a similar vehicle suitable for topical administration. For topical administration, the inventive compounds may be mixed with a pharmaceutical carrier at a concentration of about 0.1% to about 10% of drug to vehicle. Another mode of administering the agents of the invention may utilize a patch formulation to effect transdermal delivery. [0178] Any formula given herein is also intended to represent unlabeled forms as well as isotopically labeled forms of the compounds. Isotopically labeled compounds have structures depicted by the formulas given herein except that one or more atoms are replaced by an atom having a selected atomic mass or mass number. Examples of isotopes that can be incorporated into compounds of the disclosure include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, fluorine, chlorine, and iodine, such as 2H, ¾, UC, 13C, 14C, 15N, 180, 170, 31P, 32P, 35S, 18F, 36C1, and 125I, respectively. Such isotopically labelled compounds are useful in metabolic studies (preferably with 14C), reaction kinetic studies (with, for example 2H or ¾), detection or imaging techniques [such as positron emission tomography (PET) or single-photon emission computed tomography (SPECT)] including drug or substrate tissue distribution assays, or in radioactive treatment of patients. Further, substitution with heavier isotopes such as deuterium (i.e., 2H) may afford certain therapeutic advantages resulting from greater metabolic stability, for example increased in vivo half-life or reduced dosage requirements. Isotopically labeled compounds of this disclosure and prodrugs thereof can generally be prepared by carrying out the procedures disclosed in the schemes or in the examples and preparations described below by substituting a readily available isotopically labeled reagent for a non-isotopically labeled reagent.
Drug Combinations
[0179] The compounds described herein may be used in pharmaceutical compositions or methods in combination with one or more additional active ingredients in the treatment of the diseases and disorders described herein. Further additional active ingredients include other therapeutics or agents that mitigate adverse effects of therapies for the intended disease targets. Such combinations may serve to increase efficacy, ameliorate other disease symptoms, decrease one or more side effects, or decrease the required dose of an inventive compound. The additional active ingredients may be administered in a separate pharmaceutical composition from a compound of the present invention or may be included with a compound of the present invention in a single pharmaceutical composition. The additional active ingredients may be administered simultaneously with, prior to, or after administration of a compound of the present invention.
[0180] Combination agents include additional active ingredients are those that are known or discovered to be effective in treating the diseases and disorders described herein, including those active against another target associated with the disease. For example, compositions and formulations of the invention, as well as methods of treatment, can further comprise other drugs or pharmaceuticals, e.g., other active agents useful for treating or palliative for the target diseases or related symptoms or conditions.
[0181] Other chemotherapeutic agents suitable for use in combination in the methods described herein include but are not limited to kinase inhibitors, adrenocorticoids and corticosteroids, alkylating agents, peptide and peptidomimetic signal transduction inhibitors, antiandrogens, antiestrogens, androgens, aclamycin and aclamycin derivatives, estrogens, antimetabolites, platinum compounds, amanitins, plant alkaloids, mitomycins, discodermolides, microtubule inhibitors, epothilones, inflammatory and proinflammatory agents, purine analogs, pyrimidine analogs, camptothecins and dolastatins. In some embodiments, chemotherapeutic agents suitable for combination treatments in the methods described herein include but are not limited to one or more of afatinib, alectinib, axitinib, bosutinib, brigatini, cabozantinib, ceritinib, crizotinib, dabrefenib, dasatinib, erlotinib, everolimus, gefitinib, ibrutinib, imatinib, lapatinib, lenvatinib, nilotinib, nintedanib, palbociclib, pazopanib, ponatinib, regorafenib, ruxolitinib, sirolimus, sorafenib, sunitinib, tofacitinib, temsirolimus, trametinib, vandetanib, vemurafenib, methotrexate, busulfan, carboplatin, chlorambucil, cisplatin, tamoxiphen, taxol, paclitaxel, docetaxel, cytosine arabinoside, cyclophosphamide, daunomycin, rhizoxin, prednisone, hydroxyurea, teniposide, vincristine, vinblastine, eribulin, camptothecin, irinotecan, geldanamycin, estramustine and nocodazole. chemotherapeutic agents suitable for combination treatments in the methods described herein include but are not limited to one or more kinase inhibitor selected from the group consisting of afatinib, alectinib, axitinib, bosutinib, brigatini, cabozantinib, ceritinib, crizotinib, dabrefenib, dasatinib, erlotinib, everolimus, gefitinib, ibrutinib, imatinib, lapatinib, lenvatinib, nilotinib, nintedanib, palbociclib, pazopanib, ponatinib, regorafenib, ruxolitinib, sirolimus, sorafenib, sunitinib, tofacitinib, temsirolimus, trametinib, vandetanib and vemurafenib. In some embodiments, the patient was previously treated with crizotinib. For pain indications, suitable combination agents include anti-inflammatories such as NSAIDs. The pharmaceutical compositions of the invention may additional comprise one or more of such active agents, and methods of treatment may additionally comprise administering an effective amount of one or more of such active agents.
Dosing and Administration [0182] In some embodiments of the methods and compositions described herein, a therapeutically effective amount of one or more compounds that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, is administered to a host animal, such as a human patient, in need of treatment for cancer. In some embodiments of the methods and compositions described herein, a therapeutically effective amount of a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular Compound 1, is administered to a host animal, such as a human patient, in need of treatment for cancer.
[0183] As used herein, the term “therapeutically effective amount” refers to that amount of active compound or pharmaceutical agent that elicits the biological or medicinal response in a patient, which includes alleviation of the symptoms of the disease or disorder being treated. In one aspect, the therapeutically effective amount is that which may treat or alleviate the disease or symptoms. The specific therapeutically-effective dose level for any particular patient will depend upon a variety of factors, including the disorder being treated and the severity of the disorder; activity of the specific compound employed; the specific composition employed; the age, body weight, general health, gender and diet of the patient: the time of administration, route of administration, and rate of excretion of the specific compound employed; the duration of the treatment; drugs used in combination or coincidentally with the specific compound employed; and like factors.
[0184] In some embodiments, an exemplary dose for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, in the various methods and compositions described herein is in the range of about from about 1 mg to about 3 g, or about 1 mg to about 500 mg, or about 50 to about 250 mg, or about 150 to about 500 mg, or about 150 to about 250 mg, or about 250 mg to about 1 g, or about 100 mg to about 2 g, or about 500 mg to about 2 g, or about 500 mg to about 1 g. It will be appreciated that all possible subranges within the dose ranges described above are contemplated and described herein. For example, a dose range of about 40 to about 500 mg for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein includes doses of about 40 mg, about 50 mg, about 60, mg, about 70 mg, about 80 mg, about 90 mg, about 100 mg, about 110 mg, about 120 mg, about 130 mg, about 140 mg, about 150 mg, about 160 mg, about 170 mg, about 180 mg, about 190 mg, about 200 mg, about 210 mg, about 220 mg, about 230 mg, about 240 mg, about 250 mg, about 260 mg, about 270 mg, about 280 mg, about 290 mg, about 300 mg, about 310 mg, about 320 mg, about 330 mg, about 340 mg, about 350 mg, about 360 mg, about 370 mg, about 380 mg, about 390 mg, about 400 mg, about 410 mg, about 420 mg, about 430 mg, about 440 mg, about 450 mg, about 460 mg, about 470 mg, about 480 mg, about 490 mg, about 500 mg, including all possible doses and ranges as may be required based on such factors for determining a therapeutically effective amount as described herein. In some embodiments, the compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein can be dosed at about 40 mg, about 80 mg, about 120 mg, about 160 mg, about 200 mg, about 240 mg, or about 280 mg.
[0185] In some embodiments, an exemplary dose for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, in the various methods and compositions described herein is in the range of about from about 1 mg to about 3 g daily, or about 1 mg to about 500 mg daily, or about 50 to about 250 mg daily, or about 150 to about 500 mg daily, or about 150 to about 250 mg daily, or about 250 mg to about 1 g daily, or about 100 mg to about 2 g daily, or about 500 mg to about 2 g daily, or about 500 mg to about 1 g daily. It will be appreciated that all possible subranges within the daily dose ranges described above are contemplated and described herein. For example, a dose range of about 40 to about 500 mg daily for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein includes doses of about 40 mg daily, about 50 mg daily, about 60, mg daily, about 70 mg daily, about 80 mg daily, about 90 mg daily, about 100 mg daily, about 110 mg daily, about 120 mg daily, about 130 mg daily, about 140 mg daily, about 150 mg daily, about 160 mg daily, about 170 mg daily, about 180 mg daily, about 190 mg daily, about 200 mg daily, about 210 mg daily, about 220 mg daily, about 230 mg daily, about 240 mg daily, and about 250 mg daily, about 260 mg daily, about 270 mg daily, about 280 mg daily, about 290 mg daily, about 300 mg daily, about 310 mg daily, about 320 mg daily, about 330 mg daily, about 340 mg daily, about 350 mg daily, about 360 mg daily, about 370 mg daily, about 380 mg daily, about 390 mg daily, about 400 mg daily, about 410 mg daily, about 420 mg daily, about 430 mg daily, about 440 mg daily, about 450 mg daily, about 460 mg daily, about 470 mg daily, about 480 mg daily, about 490 mg daily, about 500 mg daily, including all possible doses and ranges as may be required based on such factors for determining a therapeutically effective amount as described herein. In some embodiments, the compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein can be dosed at about 40 mg daily, about 80 mg daily, about 120 mg daily, about 160 mg daily, about 200 mg, about 240 mg, or about 280 mg.
[0186] In some embodiments, an alternative exemplary dose for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the various methods and compositions described herein is in the range of about from about 0.1 mg/kg to about 1 g/kg, or about 0.5 mg/kg to about 50 mg/kg, or about 0.5 mg/kg to about 25 mg/kg, or about 1.0 mg/kg to about 10 mg/kg, or about 1.0 mg/kg to about 5 mg/kg, or about 0.1 mg/kg to about 5 mg/kg, or about 0.1 mg/kg to about 1 mg/kg, or about 0.1 mg/kg to about 0.6 mg/kg. It will be appreciated that all possible subranges within the dose ranges described above are contemplated and described herein. For example, a dose range of about 1.0 mg/kg to about 10 mg/kg for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein includes doses of about 1.0 mg/kg, about 2.0 mg/kg, about 3.0 mg/kg, about 4.0 mg/kg, about 5.0 mg/kg, about 6.0 mg/kg, about 7.0 mg/kg, about 8.0 mg/kg, about 9.0 mg/kg, and about 10.0 mg/kg, including all possible doses and ranges as may be required based on such factors for determining a therapeutically effective amount as described herein.
[0187] In some embodiments, an alternative exemplary dose for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the various methods and compositions described herein is in the range of about from about 0.1 mg/kg to about 1 g/kg daily, or about 0.5 mg/kg to about 50 mg/kg daily, or about 0.5 mg/kg to about 25 mg/kg daily, or about 1.0 mg/kg to about 10 mg/kg daily, or about 1.0 mg/kg to about 5 mg/kg daily, or about 0.1 mg/kg to about 5 mg/kg daily, or about 0.1 mg/kg to about 1 mg/kg daily, or about 0.1 mg/kg to about 0.6 mg/kg daily. It will be appreciated that all possible subranges within the dose ranges described above are contemplated and described herein. For example, a dose range of about 1.0 mg/kg to about 10 mg/kg daily for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the methods and compositions described herein includes doses of about 1.0 mg/kg daily, about 2.0 mg/kg daily, about 3.0 mg/kg daily, about 4.0 mg/kg daily, about 5.0 mg/kg daily, about 6.0 mg/kg daily, about 7.0 mg/kg daily, about 8.0 mg/kg daily, about 9.0 mg/kg daily, and about 10.0 mg/kg daily, including all possible doses and ranges as may be required based on such factors for determining a therapeutically effective amount as described herein.
[0188] It will be appreciated that various dosing schedules for administration of a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, can be applied to the methods and compositions described herein.
It will be further appreciated that a dosing schedule for a compound administered in the various methods and compositions described herein can be defined by cycles of the dosing schedule, where such cycles are defined by the number of days of treatment, number of doses of the compound, the total dose of the compound, and the like. In some embodiments, a host animal, such as a human patient in need of treatment, can be administered a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, for at least one cycle, for at least two cycles, for at least three cycles, for at least four cycles, and the like. Alternatively, in some embodiments, a host animal, such as a human patient in need of treatment, can be administered a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, for from 1 to about 50 cycles, from 1 to about 25 cycles, from 1 to about 20 cycles, from 1 to about 10 cycles, and the like. It will be appreciate that, in some embodiments, a dosing schedule for a compound administered in the various methods and compositions described herein can include a holiday period during which no compound is administered, and such holiday period can be measured in days. In some embodiments, a dosing schedule for a compound administered in the various methods and compositions described herein can be defined by a number of cycles as described herein, followed by a holiday period, followed by another number of cycles as described herein. [0189] In some embodiments, an exemplary dosing schedule for a compound that inhibits a genetically altered MET, SRC, and SCF1R, in particular a compound of the formula I, more particularly Compound 1, provided in the various methods and compositions described herein can include administration of a single daily dose (QD) or divided dosage units (e.g., BID (twice daily), TID (three times daily), QID (four times daily)). In some embodiments, a dosing schedule for a compound administered in the various methods and compositions described herein can vary within a cycle, such as a compound administered in the various methods and compositions described herein administered QD for a set number of days (e.g. QD for 1 day, 2 days, 3 days, 4 days, etc) followed by BID for a set number of days (e.g. BID for 1 day, 2 days, 3 days, 4 days, etc).
Diagnostic Tests
[0190] In some embodiments, the present disclosure provides methods for treating disease in a patient previously identified as having a genetically altered MET. In some embodiments, the present disclosure provides methods for treating cancer in a patient previously identified as having a genetically altered MET. In some embodiments, the present disclosure provides methods for treating disease in a patient comprising (i) identifying a genetically altered MET in the patient, and (ii) administering to the patient a therapeutically effective amount of a compound useful in the treatment of such disease.
[0191] It will be appreciated that the diagnosing or identifying a patient as having a genetically altered MET can be accomplished by any number of diagnostic tests known to one of skill in the art. For example, such diagnostic tests include, but are not limited to, fluorescence in situ hybridization (FISH), polymerase chain reaction (PCR), immunohistochemistry (IHC), whole genome sequencing, next generation sequencing, circulating tumor cell, and the like. It will also be appreciated that any of the methods known in the art and applicable to diagnosing a patient or identifying a patient in connection with the present disclosure involve the transformation of a biological sample from one state of matter to another by direct modification, chemical synthesis, by direct non-covalent connection, or other known means, to provide a modified sample that can be used to determine whether the subject has or does not have a genetically altered MET. In some embodiments, “diagnosing” or “identifying” with respect to the disease state of a patient means applying a diagnostic test, such as FISH, PCR, IHC, or sequencing, to a biological sample obtained from the patient.
[0192] It will be appreciated that FISH is a test that “maps” the genetic material in a person’s cells. This test can be used to visualize specific genes or portions of genes. FISH is a cytogenetic technique that uses fluorescent probes that bind to only those parts of the chromosome with a high degree of sequence complementarity. Such FISH tests can be used to identify a patient with a genetically altered MET by any method known in the art, and such test can be used in combination with the methods described herein as either a means of prior identification of a patient for treatment, or the concomitant identification of a patient for treatment. [0193] It will be appreciated that IHC refers to the process of detecting antigens (e.g., proteins) in cells of a tissue section by exploiting the principle of antibodies binding specifically to antigens in biological tissues. Immunohistochemical staining is widely used in the diagnosis of abnormal cells such as those found in cancerous tumors. Specific molecular markers are characteristic of particular cellular events such as proliferation or cell death (apoptosis). Visualising an antibody-antigen interaction can be accomplished in a number of ways. In the most common instance, an antibody is conjugated to an enzyme, such as peroxidase, that can catalyse a color-producing reaction. Alternatively, the antibody can also be tagged to a fluorophore, such as fluorescein or rhodamine. Such IHC tests can be used to identify a patient with a genetically altered MET by any method known in the art, and such test can be used in combination with the methods described herein as either a means of prior identification of a patient for treatment, or the concomitant identification of a patient for treatment.
[0194] It will be appreciated that PCR refers to a technology in molecular biology used to amplify a single copy or a few copies of a piece of DNA across several orders of magnitude, generating thousands to millions of copies of a particular DNA sequence. Such PCR tests can be used to identify a patient with a genetically altered MET by any method known in the art, and such test can be used in combination with the methods described herein as either a means of prior identification of a patient for treatment, or the concomitant identification of a patient for treatment.
[0195] It will be appreciated that whole genome sequencing or next-generation sequencing refers to a process that determines the complete DNA sequence of an organism's genome at a single time. This entails sequencing all of an organism's chromosomal DNA as well as DNA contained in the mitochondria. Such whole genome sequencing tests can be used to identify a patient with a genetically altered MET by any method known in the art, and such test can be used in combination with the methods described herein as either a means of prior identification of a patient for treatment, or the concomitant identification of a patient for treatment.
EXAMPLES
[0196] The examples and preparations provided below further illustrate and exemplify particular aspects of embodiments of the disclosure. It is to be understood that the scope of the present disclosure is not limited in any way by the scope of the following examples. Compounds of the formula I, in particular Compound 1, are disclosed in International Patent Publication No. WO20 19/023417, and were prepared according to the methods described therein, and which is incorporated herein by reference in its entirety, in particular with respect to the preparation of compounds of the formula I, and specifically the preparation of Compound 1.
In- Vitro Assays
[0197] Materials and Methods
[0198] Compound 1 was tested toward MET and mutated MET proteins in Reaction Biology Corporation’s HotSpot kinase assays (data in Table 1). The individual substrate for each kinase was prepared in freshly made Reaction Buffer with the subsequent addition of required cofactors if needed, followed by addition of the individual kinase and gentle mixing. Compound 1 in DMSO was added into the kinase reaction mixture utilizing acoustic technology (Echo 550), and then g- [33P]-ATP (specific activity 0.01 pCi/pL final) was delivered into the reaction mixture to initiate the reaction. The kinase reaction was incubated for 120 minutes at room temperature. Reactions were then spotted onto P81 ion exchange paper (Whatman # 3698-915), which was washed extensively in 0.75% Phosphoric acid. The radioactive phosphorylated substrate remaining on the filter paper was measured. Compound 1 was tested in a 10-dose IC50 mode with 3 -fold serial dilution starting at 1 mM, and the control compound, staurosporine, was tested in both a 10-dose IC50 mode with 4-fold serial dilution starting at 20 pM, and a 10-dose IC50 mode with 3 -fold serial dilution starting at 0.1 pM. All the reactions were carried out in the presence of 10 pM ATP concentration. Kinase activity data were expressed as the percent remaining kinase activity in test samples compared to vehicle (dimethyl sulfoxide) reactions. IC50 values and curve fits were obtained using Prism4 Software (GraphPad).
[0199] The enzymatic kinase inhibitory activities of Compound 1 were evaluated in the radiolabeled kinase KinaseProfiler assays performed by Eurofms Pharma Discovery Services (data in Table 2). Full details of the assay for each kinase are available on the Eurofms website, or in the accompanying protocol document. An example of the assay is for MET(M1268T): human MET (M1268T) protein is incubated with 8 mM MOPS pH 7.0, 0.2 mM EDTA, 1 mM Na3V04, 5 mM sodium b-glycerophosphate, 250 pM KKKGQEEEYVFIE (SEQ ID NO: 1), 10 mM MgAcetate and [g-33R]-ATR (specific activity and concentration as required). The reaction is initiated by the addition of the Mg/ ATP mix. After incubation for 40 minutes at room temperature, the reaction is stopped by the addition of phosphoric acid to a concentration of 0.5%. 10 pL of the reaction is then spotted onto a P30 filtermat and washed four times for 4 minutes in 0.425% phosphoric acid and once in methanol prior to drying and scintillation counting.
[0200] The enzymatic inhibitory activities of Compound 1 against MET and 12 mutated MET proteins at Reaction Biology Corporation using the radiolabeled HotSpot kinase assay platform (Table 1). Compound 1 had potent inhibition to MET proteins with a range of different mutations (Table 1). A small subset of the mutations tested (i.e. positions D1228X and Y1230) displayed the least potency of those tested. In the Eurofms KinaseProfder biochemical assays, Compound 1 had potent inhibitory activities toward a range of mutant forms of MET (Table 2). Taken together, Compound 1 has potent inhibitory activities toward a range of mutated MET proteins.
Table 1
Figure imgf000056_0001
Table 2
Figure imgf000056_0002
Figure imgf000057_0001
[0201] Compound 1 was evaluated in a panel of Ba/F3 engineered cell models of MET and MET harboring resistance mutations. For creation of engineered cell lines, the TPR-MET fusion gene and its mutations T11731, M1250T, H1094Y, G1163R, LI 195V, D1228N and Y1230C were synthesized at GenScript and cloned into pCDH-CMV-MCS-EFl-Puro plasmid (System Biosciences, Inc), respectively. Ba/F3 engineered cells were generated by infecting Ba/F3 cells with lentivirus containing the related wild type or mutant genes. Ba/F3 engineered cells was selected in RPMI-1640 supplemented with 10% fetal bovine serum, 100 U/mL of penicillin, and 1 pg/mL puromycin solution, 10 ng/IL-3 (Life Technologies), followed by a further selection in the same medium without IL-3.
[0202] The cell potency of Compound 1 was measured using cell proliferations assay for Ba/F3 cells harboring TRP-MET constructs (Table 3). For cell proliferation assays, stable Ba/F3 cells were seeded in 384 well white plate followed by the addition of the test compounds. After 72 hours of incubation, cell proliferation was measured using CellTiter-Glo 2.0 luciferase-based ATP detection assay (Promega) following the manufacture’s protocol. ICsos were determined using GraphPad Prism software (GraphPad, Inc., San Diego, CA).
Table 3
Figure imgf000057_0002
Figure imgf000058_0001
[0203] Based on the dose-response analysis, the following values were also calculated: MET IC95 = 0.2 nM, G1163R IC90 = 171 nM, and LI 195V IC90 = 175 nM.

Claims

WHAT IS CLAIMED IS:
1. A method of treating cancer in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of a compound that inhibits MET, SRC and CSF1R, wherein the cancer is mediated by a genetically altered MET, wherein the compound is of formula
Figure imgf000059_0001
wherein
R1 is H, deuterium, or C1-C6 alkyl;
R2 is chloro or -CN;
R3 is H, deuterium, or fluoro;
R4 is H or C1-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -ME,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof.
2. The method of claim 1, wherein the compound is of the formula
Figure imgf000059_0002
or a pharmaceutically acceptable salt thereof.
3. The method of claim 1 or 2, wherein the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitt’s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
4. The method of any one of claims 1 to 3, wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, and serous and clear cell endometrial cancer.
5. The method of any one of the preceding claims, wherein the patient has received prior treatment with one or more therapeutic agents.
6. The method of any one of the preceding claims, wherein the cancer is mediated by a genetically altered MET.
7. The method of claim 5, wherein the genetically altered MET encodes a point mutation that is expressed in the c-Met protein.
8. The method of any one of claims 6 to 7, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein at one or more of positions P991, T992, VI 092, HI 094,
G1163, T1173, LI 195, F1200, D1228, Y1230, Y1235, D1246, Y1248, M1250, and M1268.
9. The method of any one of claims 6 to 8, wherein the genetically altered MET encodes a point mutation expressed in the c-Met protein that is selected from the group consisting of T11731, P991S, M1250T, T992I, VI 0921, F 12001, Y1235D, Y1230H, D1246N, D1246H, Y1248D, Y1248H, Y1248C, and M1268T.
10. The method of any one of claims 6 to 9, wherein the cancer is exhibiting bypass resistance mediated by a SRC/CSF1R.
11. A compound that inhibits MET, SRC and CSF1R for use in treating cancer in a patient, wherein the cancer is mediated by a genetically altered MET, the compound having formula
Figure imgf000061_0001
wherein
R1 is H, deuterium, or C1-C6 alkyl;
R2 is chloro or -CN;
R3 is H, deuterium, or fluoro;
R4 is H or Ci-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof.
12. The compound of claim 11, wherein the compound is of formula
Figure imgf000061_0002
or a pharmaceutically acceptable salt thereof.
13. The compound for use of claim 11 or 12, wherein the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitt’s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
14. The compound for use of claim 11 or 12, wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, and serous and clear cell endometrial cancer.
15. The compound of any one of claims 11 to 14, wherein the patient has received prior treatment with one or more therapeutic agents.
16. Use of a compound that inhibits MET, SRC and CSF1R in the preparation of a medicament for treating cancer in a patient, wherein the cancer is mediated by a genetically altered MET, and wherein the compound is of formula
Figure imgf000063_0001
wherein
R1 is H, deuterium, or C1-C6 alkyl;
R2 is chloro or -CN;
R3 is H, deuterium, or fluoro;
R4 is H or Ci-C6 alkyl, wherein each hydrogen atom in C1-C6 alkyl is independently optionally substituted by deuterium, fluoro, chloro, bromo, -OH, -CN, -OC1-C6 alkyl, -NH2,
-NH(CI-C6 alkyl), -N(CI-C6 alkyl)2, or C3-C7 cycloalkyl, or a pharmaceutically acceptable salt thereof.
17. The use of claim 16, wherein the compound is of formula
Figure imgf000063_0002
or a pharmaceutically acceptable salt thereof.
18. The use of claim 16 or 17, wherein the cancer is a carcinoma, a sarcoma, a lymphoma, Hodgekin’s disease, a melanoma, a mesothelioma, Burkitf s lymphoma, a nasopharyngeal carcinoma, a leukemia, a lung cancer, a breast cancer, a hereditary human papillary renal carcinoma, a sporadic human papillary renal carcinoma, a childhood hepatocellular carcinoma, or a myeloma.
19. The use of claim 16 or 17, wherein the cancer is selected from the group consisting of ALCL, NSCLC, neuroblastoma, inflammatory myofibroblastic tumor, renal cancer, adult renal cell carcinoma, pediatric renal cell carcinoma, breast cancer, triple negative breast cancer, triple positive breast cancer, HER+ breast cancer, mouth cancer, esophageal cancer, laryngeal cancer, pancreatic cancer, bladder cancer, colon cancer, colonic adenocarcinoma, glioblastoma, glioblastoma multiforme, thyroid cancer, anaplastic thyroid cancer, endocrine cancer, bone cancer, cholangiocarcinoma, ovarian cancer, cervical cancer, uterine cancer, testicular cancer, gastric cancer, gastric adenocarcinoma, colorectal cancer, rectal cancer, liver cancer, kidney cancer, angiosarcoma, epithelioid hemangioendothelioma, intrahepatic cholangiocarcinoma, thyroid papillary cancer, spitzoid neoplasms, sarcoma, astrocytoma, brain lower grade glioma, secretory breast carcinoma, mammary analogue carcinoma, acute myeloid leukemia, congenital mesoblastic nephroma, congenital fibrosarcomas, Ph-like acute lymphoblastic leukemia, thyroid carcinoma, skin cancer, head and neck squamous cell carcinoma, pediatric glioma CML, prostate cancer, lung squamous carcinoma, ovarian serous cystadenocarcinoma, skin cutaneous melanoma, metastatic castration-resistant prostate cancer, Hodgkin lymphoma, neuroendocrine tumors, and serous and clear cell endometrial cancer.
20. The use of any one of claims 16 to 19, wherein the patient has received prior treatment with one or more therapeutic agents.
PCT/US2021/020255 2020-03-02 2021-03-01 Therapeutic uses of macrocyclic compounds WO2021178296A1 (en)

Priority Applications (9)

Application Number Priority Date Filing Date Title
CA3174455A CA3174455A1 (en) 2020-03-02 2021-03-01 Therapeutic uses of macrocyclic compounds
EP21764224.8A EP4114530A4 (en) 2020-03-02 2021-03-01 Therapeutic uses of macrocyclic compounds
JP2022552626A JP2023515687A (en) 2020-03-02 2021-03-01 Therapeutic use of macrocycles
AU2021229457A AU2021229457A1 (en) 2020-03-02 2021-03-01 Therapeutic uses of macrocyclic compounds
MX2022010945A MX2022010945A (en) 2020-03-02 2021-03-01 Therapeutic uses of macrocyclic compounds.
BR112022017425A BR112022017425A2 (en) 2020-03-02 2021-03-01 THERAPEUTIC USES OF MACROCYCLIC COMPOUNDS
IL295938A IL295938A (en) 2020-03-02 2021-03-01 Therapeutic uses of macrocyclic compounds
CN202180023879.XA CN115397514A (en) 2020-03-02 2021-03-01 Therapeutic uses of macrocyclic compounds
KR1020227034099A KR20230022151A (en) 2020-03-02 2021-03-01 Therapeutic Uses of Macrocyclic Compounds

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US202062984159P 2020-03-02 2020-03-02
US62/984,159 2020-03-02

Publications (1)

Publication Number Publication Date
WO2021178296A1 true WO2021178296A1 (en) 2021-09-10

Family

ID=77613771

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2021/020255 WO2021178296A1 (en) 2020-03-02 2021-03-01 Therapeutic uses of macrocyclic compounds

Country Status (10)

Country Link
EP (1) EP4114530A4 (en)
JP (1) JP2023515687A (en)
KR (1) KR20230022151A (en)
CN (1) CN115397514A (en)
AU (1) AU2021229457A1 (en)
BR (1) BR112022017425A2 (en)
CA (1) CA3174455A1 (en)
IL (1) IL295938A (en)
MX (1) MX2022010945A (en)
WO (1) WO2021178296A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022171139A1 (en) * 2021-02-10 2022-08-18 北京国鸿生物医药科技有限公司 Macrocyclic compound, pharmaceutical composition, and use thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20160339027A1 (en) * 1998-01-12 2016-11-24 Novartis Ag Bicyclic heteroaromatic compounds as protein tyrosine kinase inhibitors
US20170002023A1 (en) * 2014-01-24 2017-01-05 Tp Therapeutics, Inc. Diaryl macrocycles as modulators of protein kinases
WO2018022911A1 (en) * 2016-07-28 2018-02-01 Tp Therapeutics, Inc. Macrocycle kinase inhibitors
WO2019023417A1 (en) * 2017-07-28 2019-01-31 Tp Therapeutics, Inc. Macrocyclic compounds and uses thereof
US20190233437A1 (en) * 2015-07-06 2019-08-01 Tp Therapeutics, Inc. Diaryl macrocycle polymorph

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2021063276A1 (en) * 2019-09-30 2021-04-08 浙江海正药业股份有限公司 Macrocyclic derivative, preparation method therefor and use thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20160339027A1 (en) * 1998-01-12 2016-11-24 Novartis Ag Bicyclic heteroaromatic compounds as protein tyrosine kinase inhibitors
US20170002023A1 (en) * 2014-01-24 2017-01-05 Tp Therapeutics, Inc. Diaryl macrocycles as modulators of protein kinases
US20190233437A1 (en) * 2015-07-06 2019-08-01 Tp Therapeutics, Inc. Diaryl macrocycle polymorph
WO2018022911A1 (en) * 2016-07-28 2018-02-01 Tp Therapeutics, Inc. Macrocycle kinase inhibitors
WO2019023417A1 (en) * 2017-07-28 2019-01-31 Tp Therapeutics, Inc. Macrocyclic compounds and uses thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See also references of EP4114530A4 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022171139A1 (en) * 2021-02-10 2022-08-18 北京国鸿生物医药科技有限公司 Macrocyclic compound, pharmaceutical composition, and use thereof

Also Published As

Publication number Publication date
IL295938A (en) 2022-10-01
CN115397514A (en) 2022-11-25
JP2023515687A (en) 2023-04-13
EP4114530A1 (en) 2023-01-11
BR112022017425A2 (en) 2022-11-29
EP4114530A4 (en) 2024-04-17
MX2022010945A (en) 2022-10-07
KR20230022151A (en) 2023-02-14
AU2021229457A1 (en) 2022-10-20
CA3174455A1 (en) 2021-09-10

Similar Documents

Publication Publication Date Title
US11452725B2 (en) Chiral diaryl macrocycles and uses thereof
US9657008B2 (en) Chemical compounds
WO2018156812A1 (en) Treatment of egfr-driven cancer with fewer side effects
US20130004481A1 (en) Anticancer therapy
US8937095B2 (en) Anticancer compounds
US20140018372A1 (en) Crystalline form of a indolinone derivative and its use
US10835525B2 (en) Method of inhibiting mutant C-KIT
AU2021229457A1 (en) Therapeutic uses of macrocyclic compounds
US11642340B2 (en) Method of inhibiting mutant C-KIT

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 21764224

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2022552626

Country of ref document: JP

Kind code of ref document: A

Ref document number: 3174455

Country of ref document: CA

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112022017425

Country of ref document: BR

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2021764224

Country of ref document: EP

Effective date: 20221004

ENP Entry into the national phase

Ref document number: 2021229457

Country of ref document: AU

Date of ref document: 20210301

Kind code of ref document: A

ENP Entry into the national phase

Ref document number: 112022017425

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20220831