Classifications

• • 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
  • 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
  • A61K31/4965—Non-condensed pyrazines
  • A61K31/497—Non-condensed pyrazines containing further heterocyclic rings
• • 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
  • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
  • A61K31/5355—Non-condensed oxazines and containing further heterocyclic rings
• • 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
  • A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
  • A61K31/5375—1,4-Oxazines, e.g. morpholine
  • A61K31/5377—1,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
• • 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
  • A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
  • A61K31/541—Non-condensed thiazines containing further heterocyclic rings
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
  • A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
  • A61P35/00—Antineoplastic agents
  • A61P35/02—Antineoplastic agents specific for leukemia
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Definitions

• the present invention relates to combination therapies useful for treating cancer.
• the present invention relates to therapeutically effective combinations of a Src homology 2 (SH2) domain-containing phosphatase 2 (SHP-2) inhibitor and a KRas G12C inhibitor, pharmaceutical compositions comprising the inhibitors, kits comprising the compositions and methods of use therefor.
• SH2 Src homology 2
• SHP-2 Src domain-containing phosphatase 2
• KRas G12C inhibitor KRas G12C inhibitor
• pharmaceutical compositions comprising the inhibitors
• kits comprising the compositions and methods of use therefor.
• KRas Kirsten Rat Sarcoma 2 Viral Oncogene Homolog
• GDP-bound inactive
• GTP-bound active
• cellular proliferation e.g., see Alamgeer et ah, (2013) Current Opin Pharmcol. 13:394-401.
• Single nucleotide substitutions that result in missense mutations at codons 12 and 13 of the KRas primary amino acid sequence comprise approximately 40% of these KRas driver mutations in lung adenocarcinoma, with a G12C transversion being the most common activating mutation (e.g., see Dogan et al., (2012) Clin Cancer Res. 18(22):6169-6177, published online 2012 Sep 26. doi: 10.1158/1078-0432. CCR- 1 1-3265).
• KRas inhibitor has demonstrated sufficient safety and/or efficacy to obtain regulatory approval (e.g., see McCormick (2015) Clin Cancer Res. 21 (8): 1797-1801 ).
• KRas G12C inhibitors disclosed herein are potent inhibitors of KRas G12C enzymatic activity and exhibit single agent activity inhibiting the in vitro proliferation of cell lines harboring a KRas G12C mutation
• the relative potency and/or observed maximal effect of any given KRas G12C inhibitor can vary between KRAS mutant cell lines.
• the reason or reasons for the range of potencies and observed maximal effect is not fully understood but certain cell lines appear to possess differing intrinsic resistance.
• the combination therapy of the present invention in one aspect, synergistically increases the potency of KRas G12C inhibitors resulting in improved efficacy of KRas G12C inhibitors disclosed herein.
• the combination therapy of the present invention in another aspect, provides improved clinical benefit to patients compared to treatment with KRas G12C inhibitors disclosed herein as a single agent.
• kits for treating cancer in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a combination of a SHP-2 inhibitor and a KRAS G12C inhibitor of formula (I):
• X is a 4-12 membered saturated or partially saturated monocyclic, bridged or spirocyclic ring, wherein the saturated or partially saturated monocyclic ring is optionally substituted with one or more R 8 ;
• Y is a bond, ⁇ , S or NR 5 ;
• R 2 is hydrogen, alkyl, hydroxyalkyl, dihydroxy alkyl, alkylaminylalkyl, dialkylaminylalkyl, -Z-NR 5 R 10 , heterocyclyl, heterocyclylalkyl, aryl, heteroaryl, or heteroarylalkyl, wherein each of the Z, heterocyclyl, heterocyclylalkyl, aryl, heteroaryl, and heteroarylalkyl may be optionally substituted with one or more R 9 ;
• Z is Ci - C 4 alkylene
• each R 3 is independently Ci - C3 alkyl, oxo, or haloalkyl;
• L is a bond, -C(O)-, or Ci - C 3 alkylene;
• R 4 is hydrogen, cycloalkyl, heterocyclyl, aryl, aralkyl or heteroaryl, wherein each of the cycloalkyl, heterocyclyl, aryl, aralkyl and heteroaryl may be optionally substituted with one or more R 6 or R 7 ;
• each R 5 is independently hydrogen or Ci - C3 alkyl
• R 6 is cycloalkyl, heterocyclyl, heterocyclylalkyl, aryl, or heteroaryl, wherein each of the cycloalkyl, heterocyclyl, aryl, or heteroaryl may be optionally substituted with one or more R 7 ;
• each R 7 is independently halogen, hydroxyl, Ci - Ce alkyl, cycloalkyl, alkoxy, haloalkyl, amino, cyano, heteroalkyl, hydroxyalkyl or Q-haloalkyl, wherein Q is O or S;
• R 8 is oxo, Ci - C 3 alkyl, C 2 - C alkynyl, heteroalkyl, cyano, -C(0)OR 5 , -C(0)N(R 5 ) 2 , - N(R 5 ) 2 , wherein the Ci - C3 alkyl may be optionally substituted with cyano, halogen, -OR 5 , - N(R 5 ) 2 , or heteroaryl
• each R 9 is independently hydrogen, oxo, acyl, hydroxyl, hydroxyalkyl, cyano, halogen, Ci - Ce alkyl, aralkyl, haloalkyl, heteroalkyl, cycloalkyl, heterocyclylalkyl, alkoxy, dialkylaminyl, dialkylamidoalkyl, or dialkylaminylalkyl, wherein the Ci - Ce alkyl may be optionally substituted with cycloalkyl;
• each R 10 is independently hydrogen, acyl, Ci - C3 alkyl, heteroalkyl or hydroxyalkyl;
• R 11 is haloalkyl
• R A is absent, hydrogen, deuterium, cyano, halogen, Ci - C3 alkyl, haloalkyl, heteroalkyl, - C(0)N(R 5 ) 2 , or hydroxyalkyl;
• each R B is independently hydrogen, deuterium, cyano, Ci - C3 alkyl, hydroxyalkyl, heteroalkyl, Ci - C 3 alkoxy, halogen, haloalkyl, -ZNR'R 1 1 .
• heterocyclylalkyl wherein the heterocyclyl portion is substituted with one or more substituents independently selected from halogen, hydroxyl, alkoxy and Ci - C 3 alkyl, wherein the heteroaryl or the heteroaryl portion of the heteroarylalkyl is optionally substituted with one or more R 7 ;
• m is zero or an integer between 1 and 2; [0028 ] p is one or two; and wherein,
• R A is present
• R B is present and p equals two, or R A , R B and the carbon atoms to which they are attached form a 5-8 membered partially saturated cycloalkyl optionally substituted with one or more R 7 .
• KRas G12C inhibitor compounds of Formula I having the Formula I-A:
• R 1 , R 3 , R 4 , R 5 , R 10 , R 1 1 , L and m are as defined for Formula I, and the piperazinyl ring is optionally substituted with R 8 wherein R 8 is as defined for Formula I.
• KRas G12C inhibitor compounds of Formula I having the Formula I-B:
• R 1 , R 3 , R 4 , L and m are as defined for Formula I
• R 2 is heterocyclylalkyl optionally substituted with one or more R 9 where R 9 is as defined for Formula 1
• the piperazinyl ring is optionally substituted with R 8 , where R 8 is as defined for Formula I.
• compositions for use in the methods comprising a therapeutically effective amount of a combination of a SF1P-2 inhibitor and a KRas G12C inhibitor compound Formula I, Formula I-A, or Formula 1 -B, or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable excipient.
• kits for treating cancer in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a combination of a SHP-2 inhibitor or a pharmaceutically acceptable salt or a pharmaceutical composition thereof and a KRAS G12C inhibitor of Formula (I), Formula I-A or Formula I-B or a pharmaceutically acceptable salt or a pharmaceutical composition thereof.
• the cancer is a KRas G12C-associated cancer.
• the KRas G12C-associated cancer is lung cancer.
• KRas G12C inhibitor compounds and SHP-2 inhibitors are the only active agents in the provided compositions and methods.
• SHP-2 inhibitors suitable for the provided compositions and methods include, but are not limited to SHP-099 (6-(4-Amino-4-methylpiperidin-l-yl)-3-(2,3- dichlorophenyl)pyrazin-2 -amine dihydrochloride); RMC-4550 (3-((3S,4S)-4-amino-3-methyl-2- oxa-8-azaspiro[4.5]decan-8-yl)-6-(2,3-dichlorophenyl)-5-methylpyrazin-2-yl)methanol), RMC- 4630 (Revolution Medicine) and TN0155 (Novartis).
• SHP-099 6-(4-Amino-4-methylpiperidin-l-yl)-3-(2,3- dichlorophenyl)pyrazin-2 -amine dihydrochloride
• RMC-4550 (3-((3S,4S)-4-amino-3-methyl-2- oxa-8-azaspiro[4.5]
• the invention provides for methods for increasing the sensitivity of a cancer cell to a KRas G12C inhibitor, comprising contacting the cancer cell with a therapeutically effective amount of a combination of a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula 1-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a SI IP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, wherein the SHP-2 inhibitor synergistically increases the sensitivity of the cancer cell to the KRas G12C inhibitor.
• the contacting is in vitro. In one embodiment, the contacting is in vivo.
• a KRas G12C mutation e.g., a KRas G12C-associated cancer
• a regulatory agency-approved e.g.
• kits comprising a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof and a KRas G12C inhibitor compound of Fonnula (1), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof.
• a kit comprising a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, for use in treating a KRas G12C cancer.
• the invention provides a kit containing a dose of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof and a KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof in an amount effective to inhibit proliferation of cancer cells in a subject.
• the kit in some cases includes an insert with instructions for administration of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof and a KRas G 12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof.
• the insert may provide a user with one set of instructions for using the a SFIP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof in combination with a KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof.
• the patient before treatment with the compositions or methods of the invention, was treated with one or more of a chemotherapy, a targeted anticancer agent, radiation therapy, and surgery, and optionally, the prior treatment was unsuccessful; and/or the patient has been administered surgery and optionally, the surgery was unsuccessful; and/or the patient has been treated with a platinum-based chemotherapeutic agent, and optionally, the patient has been previously determined to be non- responsive to treatment with the platinum- based chemotherapeutic agent; and/or the patient has been treated with a kinase inhibitor, and optionally, the prior treatment with the kinase inhibitor was unsuccessful; and/or the patient was treated with one or more other therapeutic agent(s).
• the present invention relates to combination therapies for treating KRas G12C cancers.
• the present invention relates to methods of treating cancer in a subject in need thereof, comprising administering to the subject a therapeutically effective amount of a combination of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRAS G12C inhibitor of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, pharmaceutical compositions comprising therapeutically effective amounts of the inhibitors, kits comprising the compositions and methods of use therefor.
• KRas G12C refers to a mutant form of a mammalian KRas protein that contains an amino acid substitution of a cysteine for a glycine at amino acid position 12.
• the assignment of amino acid codon and residue positions for human KRas is based on the amino acid sequence identified by UniProtKB/Swiss-Prot P01 1 16: Variant p.Glyl2Cys.
• a“KRas G12C inhibitor” refers to compounds of the present invention that are represented by Formula (I), Formula I-A and Formula I-B as described herein. These compounds are capable of negatively modulating or inhibiting all or a portion of the enzymatic activity of KRas G12C.
• the KRas G12C inhibitors of the present invention interact with and irreversibly bind to KRas G12C by forming a covalent adduct with the sulfhydryl side chain of the cysteine residue at position 12 resulting in the inhibition of tbe enzymatic activity of KRas G12C.
• the KRas G12C inhibitor is a compound selected from compound Nos 1-678 (as numbered in WO2019099524), or pharmaceutically acceptable salts thereof (e.g., Example Nos 234, 359, 478 or 507, or a pharmaceutically acceptable salt thereof).
• KRas G12C-associated disease or disorder refers to diseases or disorders associated with or mediated by or having a KRas G12C mutation.
• a non-limiting example of a KRas G12C-associated disease or disorder is a KRas G12C-associated cancer.
• “SHP-2” or“SHP2” refers to the mammalian non-receptor protein tyrosine phosphatase encoded by the PTPN 1 1 gene that is involved in signaling through the Ras-mitogen- activated protein kinase, the JAK-STAT or the phosphoinositol 3-kinase-AKT pathways.
• a“SHP-2 inhibitor” or a“SHP2 inhibitor” refers to a compound that is capable of negatively modulating or inhibiting all or a portion of the enzymatic activity of SHP- 2 phosphatase.
• the term“subject,”“individual,” or“patient,” used interchangeably, refers to any animal, including mammals such as mice, rats, other rodents, rabbits, dogs, cats, swine, cattle, sheep, horses, primates, and humans.
• the patient is a human.
• the subject has experienced and/or exhibited at least one symptom of the disease or disorder to be treated and/or prevented.
• the subject has been identified or diagnosed as having a cancer having a KRas G12C mutation (e.g., as determined using a regulatory agency-approved, e.g., FDA-approved, assay or kit).
• the subject has a tumor that is positive for a KRas G12C mutation (e.g., as determined using a regulatory agency-approved assay or kit).
• the subject can be a subject with a tumor(s) that is positive for a KRas G12C mutation (e.g., identified as positive using a regulatory agency- approved, e.g., FDA-approved, assay or kit).
• the subject can be a subject whose tumors have a KRas G12C mutation (e.g., where the tumor is identified as such using a regulatory agency- approved, e.g., FDA-approved, kit or assay).
• the subject is suspected of having a KRas G12C gene-associated cancer.
• the subject has a clinical record indicating that the subject has a tumor that has a KRas G12C mutation (and optionally the clinical record indicates that the subject should be treated with any of the compositions provided herein).
• the term“pediatric patient” as used herein refers to a patient under the age of 16 years at the time of diagnosis or treatment.
• the term“pediatric” can be further be divided into various subpopulations including: neonates (from birth through the first month of life); infants (1 month up to two years of age); children (two years of age up to 12 years of age); and adolescents (12 years of age through 21 years of age (up to, but not including, the twenty-second birthday)).
• Berhman RE Kliegman R, Arvin AM, Nelson WE. Nelson Textbook of Pediatrics, 15th Ed. Philadelphia: W.B. Saunders Company, 1996; Rudolph AM, et al. Rudolph’s Pediatrics, 21 st Ed. New York: McGraw-Hill, 2002; and Avery MD, First LR. Pediatric Medicine, 2nd Ed. Baltimore: Williams & Wilkins; 1994.
• an assay is used to determine whether the patient has KRas G12C mutation using a sample (e.g., a biological sample or a biopsy sample such as a paraffin-embedded biopsy sample) from a patient (e.g., a patient suspected of having a KRas G12C-associated cancer, a patient having one or more symptoms of a KRas G12C-associated cancer, and/or a patient that has an increased risk of developing a KRas G12C-associated cancer) can include, for example, next generation sequencing, iminunohistochemistry, fluorescence microscopy, break apart FISH analysis, Southern blotting, Western blotting, FACS analysis, Northern blotting, and PCR-based amplification (e.g., RT-PCR, quantitative real-time RT-PCR, allele-specific genotyping or ddPCR). As is well-known in the art, the assays are typically performed,
• regulatory agency is a country’s agency for the approval of the medical use of pharmaceutical agents with the country.
• a regulatory agency is the U.S. Food and Drug Administration (FDA).
• amino refers to -NH2
• acyl refers to -C(0)CH3.
• alkyl refers to straight and branched chain aliphatic groups having from 1 to 12 carbon atoms, 1-8 carbon atoms 1-6 carbon atoms, or 1 -3 carbon atoms which is optionally substituted with one, two or three substituents.
• alkyl groups include, without limitation, methyl, ethyl, propyl, isopropyl, butyl, isobutyl, sec-butyl, tert-butyl, pentyl, and hexyl.
• haloalkyl refers to an alkyl chain in which one or more hydrogen has been replaced by a halogen.
• haloalkyls are trifluoromethyl, difluoromethyl and fluoromethyl.
• haloalkyloxy refers to -O-haloalkyl
• alkylene group is an alkyl group, as defined hereinabove, that is positioned between and serves to connect two other chemical groups.
• alkylene groups include, without limitation, methylene, ethylene, propylene, and butylene.
• alkoxy refers to -OCi - Ce alkyl.
• cycloalkyl as employed herein includes saturated and partially unsaturated cyclic hydrocarbon groups having 3 to 12 carbons, for example 3 to 8 carbons, and as a further example 3 to 6 carbons, wherein the cycloalkyl group additionally is optionally substituted.
• cycloalkyl groups include, without limitation, cyclopropyl, cyclobutyl, cyclopentyl, cyclopentenyl, cyclohexyl, cyclohexenyl, cycloheptyl, and cyclooctyl.
• heteroalkyl refers to an alkyl group, as defined hereinabove, wherein one or more carbon atoms in the chain are replaced by a heteroatom selected from the group consisting of O, S, and N.
• hydroxyalkyl refers to -alkyl-OH.
• dihydroxyalkyl refers to an alkyl group as defined herein wherein two carbon atoms are each substituted with a hydroxyl group.
• alkylaminyf ‘ refers to -NR x -alkyl, wherein R x is hydrogen. In one embodiment, R x is hydrogen.
• dialky laminyl refers to -N(R y )2, wherein each R y is Ci - C3 alkyl.
• alky laminyl alky P refers to -alkyl-NR x -alkyl, wherein R x is hydrogen. In one embodiment, R x is hydrogen.
• dialkylaminylalkyr refers to aIkyl-N(R y )2, wherein each R y is Ci - C4 alkyl, wherein the alkyl of the— alkyl-N(R y )2 may be optionally substituted with hydroxy or hydroxyalkyl.
• aryl is a C6-C14 aromatic moiety comprising one to three aromatic rings, which is optionally substituted.
• the aryl group is a Ce-Cw aryl group.
• aryl groups include, without limitation, phenyl, naphthyl, anthracenyl, fluorenyl, and dihy drobenzofurany 1.
• an "aralkyl” or “arylalkyl” group comprises an aryl group covalently linked to an alkyl group, either of which may independently be optionally substituted or unsubstituted.
• An example of an aralkyl group is (Ci- C 6 )alkyl(C 6 -Cio)aryl, including, without limitation, benzyl, phenethyl, and naphthylmethyl.
• An example of a substituted aralkyl is wherein the alkyl group is substituted with hydroxy alkyl.
• a “heterocyclyl” or “heterocyclic” group is a ring structure having from about 3 to about 12 atoms, for example 4 to 8 atoms, wherein one or more atoms are selected from the group consisting of N, O, and S, the remainder of the ring atoms being carbon.
• the heterocyclyl may be a monocyclic, a bicyclic, a spirocyclic or a bridged ring system.
• the heterocyclic group is optionally substituted with R 7 on carbon or nitrogen at one or more positions, wherein R 7 is as defined for Formula I.
• the heterocyclic group is also independently optionally substituted on nitrogen with alkyl, aryl, aralkyl, alkylcarbonyl, alkylsulfonyl, arylcarbonyl, arylsulfonyl, alkoxycarbonyl, aralkoxycarbonyl, or on sulfur with oxo or lower alkyl.
• heterocyclic groups include, without limitation, epoxy, azetidinyl, aziridinyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidinyl, pyrrolidinonyl, piperidinyl, piperazinyl, imidazolidinyl, thiazolidinyl, dithianyl, trithianyl, dioxolanyl, oxazolidinyl, oxazolidinonyl, decahydroquinolinyl, piperidonyl, 4-piperidinonyl, thiomorpholinyl, thiomorpholinyl 1 ,1 dioxide, morpholinyl, oxazepanyl, azabicyclohexanes, azabicycloheptanes and oxa azabiocycloheptanes. Specifically excluded from the scope of this term are compounds having adjacent annular O and/or S atoms.
• heterocyclylalkyl refers to a heterocyclyl group as defined herein linked to the remaining portion of the molecule via an alkyl linker, wherein the alkyl linker of the heterocyclylalkyl may be optionally substituted with hydroxy or hydroxyalkyl.
• heteroaryl refers to groups having 5 to 14 ring atoms, preferably 5, 6, 9, or 10 ring atoms; having 6, 10, or 14 p electrons shared in a cyclic array; and having, in addition to carbon atoms, from one to three heteroatoms per ring selected from the group consisting of N, O, and S.
• heteroaryl groups include acridinyl, azocinyl, benzimidazolyl, benzofuranyl, benzothiofuranyl, benzothiophenyl, benzoxazolyl, benzthiazolyl, benztriazolyl, benztetrazolyl, benzisoxazolyl, benzisothiazolyl, benzimidazolinyl, carbazolyl, 4aH-carbazolyl, carbolinyl, chromanyl, chromenyl, cinnolinyl, furanyl, furazanyl, imidazolinyl, imidazolyl, lH-indazolyl, indolenyl, indolinyl, indolizinyl, indolyl, 3H-indolyl, isobenzo furanyl, isochromanyl, isoindazolyl, isoindolinyl, isoindolyl
• a "heteroarylalkyl” group comprises a heteroaryl group covalently linked to an alkyl group, wherein the radical is on the alkyl group, either of which is independently optionally substituted or unsubstituted.
• heteroarylalkyl groups include a heteroaryl group having 5, 6, 9, or 10 ring atoms bonded to a C -Ce alkyl group.
• heteroaralkyl groups include pyridylmethyl, pyridylethyl, pyrrolylmethyl, pyrrolylethyl, imidazolylmethyl, imidazolylethyl, thiazolylmethyl, thiazolylethyl, benzimidazolylmethyl, benzimidazolylethyl quinazolinylmethyl, quinolinylmethyl, quinolinylethyl, benzofuranylmethyl, indolinylethyl isoquinolinylmethyl, isoinodylmethyl, cinnolinylmethyl, and benzothiophenylethyl. Specifically excluded from the scope of this term are compounds having adjacent annular O and/or S atoms.
• an effective amount of a compound is an amount that is sufficient to negatively modulate or inhibit the activity of the desired target, i.e., a SHP-2 or KRas G12C. Such amount may be administered as a single dosage or may be administered according to a regimen, whereby it is effective.
• a "therapeutically effective amount" of a compound is an amount that is sufficient to ameliorate, or in some manner reduce a symptom or stop or reverse progression of a condition, or negatively modulate or inhibit the activity of SHP-2 or KRas G12C. Such amount may be administered as a single dosage or may be administered according to a regimen, whereby it is effective.
• a "therapeutically effective amount of a combination" of two compounds is an amount that together synergistically increases the activity of the combination in comparison to the therapeutically effective amount of each compound in the combination, i.e., more than merely additive.
• the therapeutically effective amount of the combination of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof results in an increased duration of overall survival (“OS”) in subjects relative to treatment with only the KRas G12C inhibitor.
• OS overall survival
• the therapeutically effective amount of the combination of a SHP- 2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof results in an increased duration of progression-free survival (“PFS”) in subjects relative to treatment with only the KRas G12C inhibitor.
• PFS progression-free survival
• the therapeutically effective amount of the combination of a SfIP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof results in increased tumor regression in subjects relative to treatment with only the KRas G12C inhibitor.
• the therapeutically effective amount of the combination of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof results in increased tumor growth inhibition in subjects relative to treatment with only the KRas G12C inhibitor.
• the therapeutically effective amount of the combination of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof results in an improvement in the duration of stable disease in subjects compared to treatment with only the KRas G12C inhibitor.
• the amount of each compound in the combination may be the same or different than the therapeutically effective amount of each compound when administered alone as a monotherapy as long as the combination is synergistic. Such amounts may be administered as a single dosage or may be administered according to a regimen, whereby it is effective.
• treatment means any manner in which the symptoms or pathology of a condition, disorder or disease are ameliorated or otherwise beneficially altered. Treatment also encompasses any pharmaceutical use of the compositions herein. [0081] As used herein, amelioration of the symptoms of a particular disorder by administration of a particular pharmaceutical composition refers to any lessening, whether permanent or temporary, lasting or transient that can be attributed to or associated with administration of the composition.
• the term“about” when used to modify a numerically defined parameter means that the parameter may vary by as much as 10% below or above the stated numerical value for that parameter. For example, a dose of about 5 mg/kg may vary between 4.5 mg/kg and 5.5 mg/kg. “About” when used at the beginning of a listing of parameters is meant to modify each parameter. For example, about 0.5 mg, 0.75 mg or 1.0 mg means about 0.5 mg, about 0.75 mg or about 1.0 mg. Likewise, about 5% or more, 10% or more, 15% or more, 20% or more, and 25% or more means about 5% or more, about 10% or more, about 15% or more, about 20% or more, and about 25% or more.
• kits for treating cancer in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a combination of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRAS G12C inhibitor of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof.
• Src homology 2 (SH2) domain-containing phosphatase 2 (“SHP-2”) is a mammalian non receptor protein tyrosine phosphatase encoded by the PTPN1 1 gene that is involved in signaling through the Ras-mitogen-activated protein kinase, the JAK-STAT or the phosphoinositol 3-kinase (P13K)-AKT-mTOR pathways.
• SHP-2 polypeptide is comprised of two Src homology 2 (SFI2) domains (N-SH2 and C-SH2) located in the N-terminal region and two potential Grb2 SH2 domain binding sites located in the C-terminal region.
• SHP-2 has been shown to exhibit non-mutational drug resistance mechanism in response to anti-tyrosine kinase inhibitors (TKIs).
• TKIs anti-tyrosine kinase inhibitors
• an increase in SHP-2 phosphatase activity has been shown to confer resistance to the TKI inhibitor imatinib (e.g., see Li et ah, (2016) Toxicol. Lrr ⁇ . Pharmacol. 360-249-256).
• the addition of a SHP-2 inhibitor was shown to overcome resistance by blocking both the RAF/MEK/ERK pathway as well as the PI3K/ AKT/mTOR pathways.
• PI3K inhibitor e.g., see Misale et ah, Clin. Cancer Res., Online Publication doi: 10.1 158/1078-0432. CCR 18-0368.
• SHP-2 is capable of modulating the PI3K/ AKT/mTOR pathway
• dual inhibition using a SHP-2 may be able to overcome differing intrinsic cellular adaptive and/or acquired resistance mechanisms to direct KRas G12C inhibition.
• SHP-2 inhibitors include, but are not limited to, SHP-099 (6-(4-Amino-4-methylpiperidin-l-yl)- 3-(2,3-dichlorophenyl)pyrazin-2-amine dihydrochloride); RMC-4550 (3-((3S,4S)-4-amino-3- methyl-2-oxa-8-azaspiro[4.5]decan-8-yl)-6-(2,3-dichlorophenyl)-5-methylpyrazin-2- yl)methanol), RMC-4630 (Revolution Medicine) and TN0155 (Novartis). RMC-4630 and TN0155 are in Phase 1 human clinical trials for adult patients having particular advanced solid tumors.
• SHP-2 inhibitors are well known to those skilled in the art and SHP-2 inhibitors may be obtained from a wide-variety of commercial suppliers, in forms suitable for both research or human use.
• suitable SHP-2 inhibitors for use in the compositions and methods disclosed herein and methods for preparing such inhibitors are disclosed in US Patent Application Publication Nos: US20190127378; US20180251471 ; US 20180201623; US 20180186770; US20180170862; US 20180065949; US20170204080; US20170166510; US2017001 1975; US201200334186; US20120257184; IJS201 10190315; US20090042788; US20080194563; US20080058431 ; US20080058431 ; US20040121384; US20040043434; and US200401 10800.
• the KRas G12C inhibitors used in the methods are compounds of Formula (I):
• X is a 4-12 membered saturated or partially saturated monocyclic, bridged or spirocyclic ring, wherein the saturated or partially saturated monocyclic ring is optionally substituted with one or more R 8 ;
• Y is a bond, O, S or NR 5 ;
• R 2 is hydrogen, alkyl, hydroxyalkyl, dihydroxyalkyl, alkylaminylalkyl, dialkylaminylalkyl, -Z-NR 3 R 10 , heterocyclyl, heterocyclylalkyl, aryl, heteroaryl, or heteroarylalkyl, wherein each of the Z, heterocyclyl, heterocyclylalkyl, aryl, heteroaryl, and heteroarylalkyl may be optionally substituted with one or more R 9 ;
• Z is Ci - C 4 alkylenc
• each R 3 is independently Ci - C3 alkyl, oxo, or haloalkyl;
• L is a bond, -C(O)-, or Ci - C3 alkylene;
• R 4 is hydrogen, cycloalkyl, heterocyclyl, aryl, aralkyl or heteroaryl, wherein each of the cycloalkyl, heterocyclyl, aryl, aralkyl and heteroaryl may be optionally substituted with one or more R 6 or R 7 ;
• each R 5 is independently hydrogen or Ci - C3 alkyl
• R 6 is cycloalkyl, heterocyclyl, heterocyclylalkyl, aryl, or heteroaryl, wherein each of the cycloalkyl, heterocyclyl, aryl, or heteroaryl may be optionally substituted with one or more R 7 ;
• each R 7 is independently halogen, hydroxyl, Ci - C alkyl, cycloalkyl, alkoxy, haloalkyl, amino, cyano, heteroalkyl, hydroxyalkyl or Q-haloalkyl, wherein Q is O or S;
• R 8 is oxo, Ci - C3 alkyl, C2 - C4 alkynyl, heteroalkyl, cyano, -C(0)OR 5 , -C(0)N(R 5 )2, - N(R3 ⁇ 4 wherein the Ci - C3 alkyl may be optionally substituted with cyano, halogen, -OR 5 , - N(R 3 ) 2 , or heteroaryl;
• each R 9 is independently hydrogen, oxo, acyl, hydroxyl, hydroxyalkyl, cyano, halogen, Ci - Ci, alkyl, aralkyl, haloalkyl, heteroalkyl, cycloalkyl, heterocyclylalkyl, alkoxy, dialkylaminyl, dialkylamidoalkyl, or dialkylaminylalkyl, wherein the Ci - C ( , alkyl may be optionally substituted with cycloalkyl;
• each R 10 is independently hydrogen, acyl, Ci - C3 alkyl, heteroalkyl or hydroxyalkyl; [0106] R n is haloalkyl;
• R A is absent, hydrogen, deuterium, cyano, halogen, Ci - C3 alkyl, haloalkyl, heteroalkyl, - C(0)N(R 5 ) 2 , or hydroxyalkyl;
• each R B is independently hydrogen, deuterium, cyano, Ci - C3 alkyl, hydroxyalkyl, heteroalkyl, Ci - C3 alkoxy, halogen, haloalkyl, -ZNR 5 R n , -C(0)N(R 5 )2, -NHC(0)C ] - C3 alkyl, -CH 2 NHC(0)C I C3 alkyl, heteroaryl, heteroarylalkyl, dialkylaminylalkyl, or heterocyclylalkyl wherein the heterocyclyl portion is substituted with one or more substituents independently selected from halogen, hydroxyl, alkoxy and Ci - C3 alkyl, wherein the heteroaryl or the heteroaryl portion of the heteroarylalkyl is optionally substituted with one or more R 7 ;
• [0109] is zero or an integer between 1 and 2; [01 10] p is one or Iwo; and wherein,
• R B and the carbon atoms to which they are attached form a 5-8 membered partially saturated cycloalkyl optionally substituted with one or more R 7 .
• KRas G12C inhibitors used in the methods herein includes compounds having the Formula I-A:
• R 1 , R 3 , R 4 , R 5 , R 10 , L and m are as defined for Formula I, R 1 1 is hydrogen, methyl or hydroxyalkyl, and the piperidinyl ring is optionally substituted with R 8 wherein R 8 is as defined for Formula I.
• KRas G12C inhibitors used in the methods herein include compounds having the Formula I-B:
• KRas G12C inhibitor compounds of Formula (I), Formula I-A and Formula I-B useful in the methods disclosed herein are selected from the group consisting of Example Nos 1-678 (as numbered in WO 2019099524) including the following structures:
• the KRas G12C inhibitor is selected from:
• the KRas G12C inhibitor is:
• the KRas G12C inhibitor is:
• Example 359 (also referred to as Example 359) or a pharmaceutically acceptable salt thereof.
• the KRas G12C inhibitor is:
• Example 4708 (also referred to as Example 478) or a pharmaceutically acceptable salt thereof.
• the KRas G12C inhibitor is:
• Example 507 (also referred to as Example 507) or a pharmaceutically acceptable salt thereof.
• the KRas G12C inhibitors used in the methods of the present invention may have one or more chiral center and may be synthesized as stereoisomeric mixtures, isomers of identical constitution that differ in the arrangement of their atoms in space.
• the compounds may be used as mixtures or the individual components/isomers may be separated using commercially available reagents and conventional methods for isolation of stereoisomers and enantiomers well-known to those skilled in the art, e.g., using CHIRALPAK® (Sigma-Aldrich) or CHIRALCEL® (Diacel Corp) chiral chromatographic HPLC columns according to the manufacturer’s instructions.
• compounds of the present invention may be synthesized using optically pure, chiral reagents and intermediates to prepare individual isomers or enantiomers. Unless otherwise indicated, all chiral (enantiomeric and diastereomeric) and racemic forms are within the scope of the invention. Unless otherwise indicated, whenever the specification, including the claims, refers to compounds of the invention, the term“compound” is to be understood to encompass all chiral (enantiomeric and diastereomeric) and racemic forms.
• the KRas G12C inhibitor compounds of Formula I, Formula I-A, or Formula I-B used in the methods include trifluoroacetic acid salts of the above compounds
• the invention provides pharmaceutical compositions comprising a SHP- 2 inhibitor, or a pharmaceutically acceptable salt thereof, and KRas G 12C inhibitor, or a pharmaceutically acceptable salt thereof according to the invention and a pharmaceutically acceptable carrier, excipient, or diluent that may be used in the methods disclosed herein.
• the SHP-2 inhibitor, or a pharmaceutically acceptable salt thereof, and KRas G12C inhibitor, or a pharmaceutically acceptable salt thereof may be independently formulated by any method well known in the art and may be prepared for administration by any route, including, without limitation, parenteral, oral, sublingual, transdermal, topical, intranasal, intratracheal, or intrarectal.
• SHP-2 inhibitor, or a pharmaceutically acceptable salt thereof, and KRas G 12C inhibitor, or a pharmaceutically acceptable salt thereof are administered intravenously in a hospital setting. In one embodiment, administration may be by the oral route.
• compositions may contain, in addition to the inhibitor, diluents, fillers, salts, buffers, stabilizers, solubilizers, and other materials well known in the art.
• diluents fillers, salts, buffers, stabilizers, solubilizers, and other materials well known in the art.
• the preparation of pharmaceutically acceptable formulations is described in, e.g., Remington's Pharmaceutical Sciences, 1 8th Edition, ed. A. Gennaro, Mack Publishing Co., Easton, Pa., 1990.
• the term pharmaceutically acceptable salt refers to salts that retain the desired biological activity of the above-identified compounds and exhibit minimal or no undesired toxicological effects.
• examples of such salts include, but are not limited to acid addition salts formed with inorganic acids (for example, hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid, and the like), and salts formed with organic acids such as acetic acid, oxalic acid, tartaric acid, succinic acid, malic acid, ascorbic acid, benzoic acid, tannic acid, pamoic acid, alginic acid, polyglutamic acid, naphthalenesulfonic acid, naphthalenedisulfonic acid, and polygalacturonic acid.
• inorganic acids for example, hydrochloric acid, hydrobromic acid, sulfuric acid, phosphoric acid, nitric acid, and the like
• organic acids such as acetic acid, oxalic acid, tartaric acid
• the compounds can also be administered as pharmaceutically acceptable quaternary salts known by those skilled in the art, which specifically include the quaternary ammonium salt of the formula— NR+Z-, wherein R is hydrogen, alkyl, or benzyl, and Z is a counterion, including chloride, bromide, iodide, -O-alkyl, toluenesulfonate, methylsulfonate, sulfonate, phosphate, or carboxylate (such as benzoate, succinate, acetate, glycolate, maleate, malate, citrate, tartrate, ascorbate, benzoate, cinnamoate, mandeloate, benzyloate, and diphenylacetate).
• R is hydrogen, alkyl, or benzyl
• Z is a counterion, including chloride, bromide, iodide, -O-alkyl, toluenesulfonate, methylsulf
• the active compound is included in the pharmaceutically acceptable carrier or diluent in an amount sufficient to deliver to a patient a therapeutically effective amount without causing serious toxic effects in the patient treated.
• a dose of the active compound for all of the above-mentioned conditions is in the range from about 0.01 to 300 mg/kg, for example 0.1 to 100 mg/kg per day, and as a further example 0.5 to about 25 mg per kilogram body weight of the recipient per day.
• a typical topical dosage will range from 0.01-3% wt/wt in a suitable carrier.
• the effective dosage range of the pharmaceutically acceptable derivatives can be calculated based on the weight of the parent compound to be delivered. If the derivative exhibits activity in itself, the effective dosage can be estimated as above using the weight of the derivative, or by other means known to those skilled in the art.
• compositions comprising a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof and a KRas G12C inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, may be used in the methods of use described herein.
• the SHP-2 inhibitor, or a pharmaceutically acceptable salt thereof, and the KRas G12C inhibitor, or a pharmaceutically acceptable salt thereof can be formulated into separate or individual dosage forms which can be co-administered one after the other. Another option is that if the route of administration is the same (e.g. oral) two active compounds can be formulated into a single form for co-administration, both methods of co-administration, however, being part of the same therapeutic treatment or regimen.
• the pharmaceutical compositions comprising a SHP-2 inhibitor, or a pharmaceutically acceptable salt thereof, and/or a KRas G12C inhibitor, or a pharmaceutically acceptable salt thereof, for use in the methods may be for simultaneous, separate or sequential use.
• the SHP-2 inhibitor, or a pharmaceutically acceptable salt thereof is administered prior to administration of the KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt thereof.
• the SHP-2 inhibitor, or a pharmaceutically acceptable salt thereof is administered after administration of the KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt thereof.
• the SHP-2 inhibitor, or a pharmaceutically acceptable salt thereof is administered at about the same time as administration of the KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt thereof.
• each inhibitor at different times and by different routes, in some cases would be advantageous.
• the components in the combination i.e. the KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt thereof and the SHP-2 inhibitor, or a pharmaceutically acceptable salt thereof, need not be necessarily administered at essentially the same time or in any order.
• Oncology drugs are typically administered at the maximum tolerated dose (“MTD”), which is the highest dose of drug that does not cause unacceptable side effects.
• MTD maximum tolerated dose
• the KRas G12C inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof and the SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof are each dosed at their respective MTDs.
• the KRas G12C inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof is dosed at its MTD and the SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, is dosed in an amount less than its MTD.
• the KRas G12C inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof is dosed at an amount less than its MTD and the SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, is dosed at its MTD.
• the KRas G12C inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof and the SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof are each dosed at less than their respective MTDs.
• the administration can be so timed that the peak pharmacokinetic effect of one compound coincides with the peak pharmacokinetic effect of the other.
• a single dose of KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula 1-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof is administered per day (i.e., in about 24 hour intervals) (i.e., QD).
• two doses of the KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof are administered per day (i.e., BID).
• three doses of the KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof are administered per day (i.e., TID).
• the SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof is administered QD.
• the SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof are administered BID.
• the SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, of the invention are administered TID.
• a single dose of KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof are each administered once daily.
• SHP-2 inhibitors suitable for the provided compositions and methods include, but are not limited to SHP-099 (6-(4-Amino-4-methylpiperidin-l-yl)-3-(2,3- dichlorophenyl)pyrazin-2-amine dihydrochloride); RMC-4550 (3-((3S,4S)-4-amino-3-methyl-2- oxa-8-azaspiro[4.5]decan-8-yl)-6-(2,3-dichlorophenyl)-5-methylpyrazin-2-yl)methanol) RMC- 4360 and TO0155 (Novartis).
• kits for treating cancer in a subject in need thereof comprising administering to the subject a therapeutically effective amount of a combination of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRAS G12C inhibitor of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof.
• the cancer is a KRas G12C-associated cancer.
• the KRas G12C-associated cancer is lung cancer.
• the invention provides for methods for increasing the sensitivity of a cancer cell to a KRas G12C inhibitor, comprising contacting the cancer cell with an effective amount of a combination of a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, wherein the SHP-2 inhibitor synergistically increases the sensitivity of the cancer cell to the KRas G12C inhibitor.
• the contacting is in vitro. In one embodiment, the contacting is in vivo.
• the combination therapy comprises a combination of a compound having the formula:
• the SHP-2 inhibitor is SIIP-099. In one embodiment, the SHP-2 inhibitor is RMC-4550. In one embodiment, the SHP-2 inhibitor is RMC-4360. In one embodiment, the SHP-2 inhibitor is TN0155.
• the combination therapy comprises a combination of a compound having the formula:
• the SHP-2 inhibitor is SHP-099. In one embodiment, the SHP-2 inhibitor is RMC-4550. In one embodiment, the SHP-2 inhibitor is RMC-4360. In one embodiment, the SHP-2 inhibitor is TN0155.
• the combination therapy comprises a combination of a compound having the formula:
• the SHP-2 inhibitor is SHP-099. In one embodiment, the SHP-2 inhibitor is RMC-4550. In one embodiment, the SHP-2 inhibitor is RMC-4360. In one embodiment, the SHP-2 inhibitor is TN0155.
• the combination therapy comprises a combination of a compound having the formula: or a pharmaceutically acceptable salt thereof, and a SHP-2 inhibitor.
• the SHP-2 inhibitor is SPIP-099.
• the SHP-2 inhibitor is RMC-4550.
• the SHP-2 inhibitor is RMC-4360.
• the SHP-2 inhibitor is TN0155.
• contacting refers to the bringing together of indicated moieties in an in vitro system or an in vivo system.
• "contacting" a cancer cell includes the administration of a combination provided herein to an individual or subject, such as a human, having KRas G12C, as well as, for example, introducing a combination provided herein into a sample containing a cellular or purified preparation containing KRas G12C.
• the methods described herein are designed to inhibit undesired cellular proliferation resulting from enhanced KRas G12C activity within the cell.
• the degree of covalent modification of KRas G12C may be monitored in vitro using well known methods, including those described in published international PCT application numbers WO2017201161 and WO2019099524.
• the inhibitory activity of combination in cells may be monitored, for example, by measuring the inhibition of KRas G12C activity of the amount of phosphorylated ERK to assess the effectiveness of treatment and dosages may be adjusted accordingly by the attending medical practitioner.
• compositions and methods provided herein may be used for the treatment of a KRas G12C-associated cancer in a subject in need thereof, comprising administering to said subject a therapeutically effective amount of a combination of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G 12C inhibitor compound of Formula (I), Formula i-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, wherein the SHP-2 inhibitor synergistically increases the sensitivity of the KRas G12C-associated cancer to the KRas G12C inhibitor.
• the KRas G12C-associated cancer is lung cancer.
• the therapeutically effective amount of the combination of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof results in an increased duration of overall survival (“OS”) in subjects relative to treatment with only the KRas G12C inhibitor.
• OS overall survival
• the therapeutically effective amount of the combination of a SHP- 2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof results in an increased duration of progression-free survival (“PFS”) in subjects relative to treatment with only the KRas G12C inhibitor.
• PFS progression-free survival
• the therapeutically effective amount of the combination of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof results in increased tumor regression in subjects relative to treatment with only the KRas G12C inhibitor.
• the therapeutically effective amount of the combination of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof results in increased tumor growth inhibition in subjects relative to treatment with only the KRas G12C inhibitor.
• the therapeutically effective amount of the combination of a SFIP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A, or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof results in an improvement in the duration of stable disease in subjects compared to treatment with only the KRas G12C inhibitor.
• the KRas G12C inhibitor is a compound selected from compound Nos. 1 -678 (as numbered in WO2019099524), or a pharmaceutically acceptable salt thereof (e.g., Example No. 234, 359, 478 or 507 or a pharmaceutically acceptable salt thereof).
• the SHP- 2 inhibitor is selected from SHP-099, RMC-4550, RMC-4360 and TN0155.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and SHP-099.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and RMC-4550.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and RMC-4360.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and TN0155.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and SHP-099.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and RMC-4550.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and RMC-4360. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and TN0155. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and SHP-099. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and RMC-4550. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and RMC-4360. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and TN0155. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and SHP-099. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and RMC-4550. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and RMC-4360. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and TN0155.
• the SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof is administered in combination with the KRas G12C inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, once disease progression has been observed for KRas G12C monotherapy, in which the combination therapy results in enhanced clinical benefit for the patient by increasing OS, PFS, tumor regression, tumor growth inhibition or the duration of stable disease in the patient.
• the KRas G12C inhibitor is a compound selected from compound Nos. 1 -678 (as numbered in WO2019099524), or a pharmaceutically acceptable salt thereof (e.g., Example No. 234, 359, 478 or 507 or a pharmaceutically acceptable salt thereof).
• the SHP- 2 inhibitor is selected from SHP-099, RMC-4550, RMC-4360 and TN0155.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and SHP-099.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and RMC-4550.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and RMC-4360.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and TN0155.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and SHP-099.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and RMC-4550.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and RMC-4360. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and TN0155. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and SHP-099. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and RMC-4550. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and RMC-4360. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and TN0155. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and SHP-099. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and RMC-4550. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and RMC-4360. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and TN0155.
• compositions and methods provided herein may be used for the treatment of a wide variety of cancers including tumors such as lung, colorectal, pancreas, prostate, breast, brain, skin, cervical carcinomas, testicular carcinomas, etc. More particularly, cancers that may be treated by the compositions and methods of the invention include, but are not limited to, tumor types such as astrocytic, breast, cervical, colorectal, endometrial, esophageal, gastric, head and neck, hepatocellular, laryngeal, lung, oral, ovarian, prostate and thyroid carcinomas and sarcomas.
• tumor types such as astrocytic, breast, cervical, colorectal, endometrial, esophageal, gastric, head and neck, hepatocellular, laryngeal, lung, oral, ovarian, prostate and thyroid carcinomas and sarcomas.
• these compounds can be used to treat: Cardiac: sarcoma (angiosarcoma, fibrosarcoma, rhabdomyosarcoma, liposarcoma), myxoma, rhabdomyoma, fibroma, lipoma and teratoma; Lung: bronchogenic carcinoma (squamous cell, undifferentiated small cell, undifferentiated large cell, adenocarcinoma), alveolar (bronchiolar) carcinoma, bronchial adenoma, sarcoma, lymphoma, chondromatous hamartoma, mesothelioma; Gastrointestinal: esophagus (squamous cell carcinoma, adenocarcinoma, leiomyosarcoma, lymphoma), stomach (carcinoma, lymphoma, leiomyosarcoma), pancreas (ductal adenocarcinoma, insulinom
• Also provided herein is a method for treating cancer in a subject in need thereof, the method comprising (a) determining that cancer is associated with a KRas G12C mutation (e.g., a KRas G12C-associated cancer) (e.g., as determined using a regulatory agency-approved, e.g., FDA- approved, assay or kit); and (b) administering to the patient a therapeutically effective amount of a combination of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula I, Formula I-A, Formula 1 -B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, wherein the SHP-2 inhibitor synergistically increases the sensitivity of the KRas G12C-associated cancer to the KRas G12C inhibitor.
• a KRas G12C mutation e.g., a KRas G12C-associated cancer
• a regulatory agency-approved e
• the KRas G12C inhibitor is a compound selected from compound Nos. 1-678 (as numbered in WO2019099524), or a pharmaceutically acceptable salt thereof (e.g., Example No. 234, 359, 478 or 507 or a pharmaceutically acceptable salt thereof).
• the SHP-2 inhibitor is selected from SHP-099, RMC-4550, RMC-4360 and TN0155.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and SHP-099.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and RMC-4550.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and RMC-4360.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and TN0155. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and SHP-099. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and RMC-4550. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and RMC-4360. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and TN0155. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and SHP-099. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and RMC-4550. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and RMC-4360.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and TN0155. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and SHP-099. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and RMC-4550. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and RMC-4360. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and TNOl 55.
• a compound of Formula I is administered as a capsule during the period of time.
• a tablet or capsule formulation of a compound of Fonnula I comprises about 10 mg to about 100 mg (e.g., about 10 mg to about 95 mg, about 10 mg to about 90 mg, about 10 mg to about 85 mg, about 10 mg to about 80 mg, about 10 mg to about 75 mg, about 10 mg to about 70 mg, about 10 mg to about 65 mg, about 10 mg to about 60 mg, about 10 mg to about 55 mg, about 10 mg to about 50 mg, about 10 mg to about 45 mg, about 10 mg to about 40 mg, about 10 mg to about 35 mg, about 10 mg to about 30 mg, about 10 mg to about 25 mg, about 10 mg to about 20 mg, about 10 mg to about 15 mg, about 15 mg to about 100 mg, about 15 mg to about 95 mg, about 15 mg to about 90 mg, about 15 mg to about 85 mg, about 15 mg to about 80 mg, about 15 mg to about 75 mg, about 15 mg to about 70 mg, about 15
• a compound of Formula I is orally administered once a day (QD) on a daily basis during a period of time. In one embodiment, a compound of Formula I is orally administered twice a day (BID) on a daily basis during a period of time.
• QD once a day
• BID twice a day
• a compound of Formula I is orally administered in the amount of about 20 mg to about 500 mg (e.g., about 20 mg to about 480 mg, about 20 mg to about 460 mg, about 20 mg to about 440 mg, about 20 mg to about 420 mg, about 20 mg to about 400 mg, about 20 mg to about 380 mg, about 20 mg to about 360 mg, about 20 mg to about 340 mg, about 20 mg to about 320 mg, about 20 mg to about 300 mg, about 20 mg to about 280 mg, about 20 mg to about 260 mg, about 20 mg to about 240 mg, about 20 mg to about 220 mg, about 20 mg to about 200 mg, about 20 mg to about 180 mg, about 20 mg to about 160 mg, about 20 mg to about 140 mg, about 20 mg to about 120 mg, about 20 mg to about 100 mg, about 20 mg to about 80 mg, about 20 mg to about 60 mg, about 20 mg to about 40 mg, about 40 mg to about 500 mg, about 40 mg to about 480 mg, about 40 mg to about 460 mg, about 40 mg
• the combination therapy comprises oral administration of a compound of Formula I once or twice a day on a daily basis (during a period of time), e.g., in an amount of about 10 mg to about 400 mg (e.g., about 10 mg to about 380 mg, about 10 mg to about 360 mg, about 10 mg to about 340 mg, about 10 g to about 320 mg, about 10 mg to about 300 mg, about 10 mg to about 280 mg, about 10 mg to about 260 mg, about 10 mg to about 240 mg, about 10 g to about 220 mg, about 10 mg to about 200 mg, about 10 mg to about 180 mg, about 10 mg to about 160 mg, about 10 mg to about 140 mg, about 10 mg to about 120 mg, about 10 mg to about 100 mg, about 10 mg to about 80 mg, about 10 mg to about 60 mg, about 10 mg to about 40 mg, about 10 g to about 20 mg, about 20 mg to about 400 mg, about 20 g to about 380 mg, about 20 mg to about 360 g, about 20 mg to about 400 mg, about
• the KRAS G12C inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof is orally administered once daily. In one embodiment, the KRAS G12C inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, is orally administered twice daily.
• the addition of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof synergistically increases the activity of KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof against cancer or cancer cell lines expressing KRas G 12C. Any method for determining whether two compounds exhibit synergy may be used for determining the synergistic effect of the combination.
• #7568331) are well known models in the pharmaceutical industry and may be used to calculate a“synergy score” that indicates whether synergy was detected and the magnitude of such synergy. Combining these synergy scores produces a composite synergy score which may be used to evaluate and characterize the KRas G12C inhibitor compounds of Formula (1), Formula I-A or Formula I-B in combination with a SHP-2 inhibitor.
• the mathematical models use data obtained from single agent values to determine the predicted additive effect of the combination which is compared to the observed effect for the combination. If the observed effect is greater than the predicted effect, the combination is deemed to be synergistic.
• the Bliss independence model compares the observed combination response (To) with the predicted combination response ( Yp). which was obtained based on the assumption that there is no effect from drug-drug interactions.
• the combination effect is declared synergistic if Yo is greater than Yp.
• “synergistic effect” as used herein refers to combination of a KRAS inhibitor or a pharmaceutically acceptable salt thereof, and a SHP-2 inhibitor or a pharmaceutically acceptable salt thereof producing an effect, for example, any of the beneficial or desired results including clinical results or endpoints as described herein, which is greater than the sum of the effect observed when a compound of Formula I or a pharmaceutically acceptable salt thereof (e.g., a compound selected from compound Nos. 1-678 as numbered in WO2019099524) and a SHP-2 inhibitor or a pharmaceutically acceptable salt thereof are administered alone.
• the KRas G12C inhibitor is a compound selected from compound Nos.
• the SHP-2 inhibitor is selected from SHP-099, RMC-4550 and TN0155.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and SHP-099.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and RMC-4550.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 234 and TN0155.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and SHP-099.
• the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and RMC-4550. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 359 and TN0155. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and SHP-099. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and RMC-4550. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 478 and TN0155. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and SHP-099. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and RMC-4550. In one embodiment, the therapeutic combination comprises therapeutically effective amounts of Example No. 507 and TN0155.
• the methods provided herein can result in a 1% to 99% (e.g., 1% to 98%, 1% to 95%, 1% to 90%, 1 to 85%, 1 to 80%, 1% to 75%, 1% to 70%, 1% to 65%, 1% to 60%, 1% to 55%, 1 % to 50%, 1% to 45%, 1% to 40%, 1% to 35%, 1% to 30%, 1% to 25%, 1 % to 20%, 1 % to 15%, 1% to 10%, 1% to 5%, 2% to 99%, 2% to 90%, 2% to 85%, 2% to 80%, 2% to 75%, 2% to 70%, 2% to 65%, 2% to 60%, 2% to 55%, 2% to 50%, 2% to 45%, 2% to 40%, 2% to 35%, 2% to 30%, 2% to 25%, 2% to 20%, 2% to 15%, 2% to 10%, 2% to 5%, 4% to 99%, 4% to 98%, 1% to 95%,
• time of survival means the length of time between the identification or diagnosis of cancer (e.g., any of the cancers described herein) in a mammal by a medical professional and the time of death of the mammal (caused by the cancer). Methods of increasing the time of survival in a mammal having a cancer are described herein.
• any of the methods described herein can result in an increase (e.g., a 1% to 400%, 1 % to 380%, 1% to 360%, 1 % to 340%, 1 % to 320%, 1% to 300%, 1% to 280%, 1% to 260%, 1% to 240%, 1% to 220%, 1% to 200%, 1 % to 180%, 1% to 160%, 1% to 140%, 1% to 120%, 1% to 100%, 1% to 95%, 1 % to 90%, 1% to 85%, 1% to 80%, 1% to 75%, 1% to 70%, 1% to 65%, 1% to 60%, 1 % to 55%, 1 % to 50%, 1% to 45%, 1% to 40%, 1 % to 35%, 1 % 30%, 1% to 25%, 1% to 20%, 1% to 15%, 1% to 10%, 1% to 5%, 5% to 400%, 5% to 380%,% to 360%, 5%
• the patient before treatment with the compositions or methods of the invention, was treated with one or more of a chemotherapy, a targeted anticancer agent, radiation therapy, and surgery, and optionally, the prior treatment was unsuccessful; and/or the patient has been administered surgery and optionally, the surgery was unsuccessful; and/or the patient has been treated with a platinum-based chemotherapeutic agent, and optionally, the patient has been previously determined to be non- responsive to treatment with the platinum-based chemotherapeutic agent; and/or the patient has been treated with a kinase inhibitor, and optionally, the prior treatment with the kinase inhibitor was unsuccessful; and/or the patient was treated with one or more other therapeutic agent(s).
• KITS potassium-based chemotherapeutic agent
• the present invention also relates to a kit comprising a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof,. Also provided is a kit comprising a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, for use in treating a hematological cancer.
• the invention provides a kit containing a dose of a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and dose of a KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, in an amount effective to inhibit proliferation of cancer cells, particularly KRas G12C-expressing cancer cells, in a subject.
• the kit in some cases includes an insert with instructions for administration of the a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, and a KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a phannaceutical composition thereof,.
• the insert may provide a user with one set of instructions for using the a SHP-2 inhibitor, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof, in combination with a KRas G12C inhibitor compound of Formula (I), Formula I-A or Formula I-B, or a pharmaceutically acceptable salt or a pharmaceutical composition thereof.
• This Example illustrates that the combination of exemplary KRas G12C inhibitor compounds of Formula I, Formula I-A and Formula 1-B and a SHP-2 inhibitor synergistically inhibits the growth of tumor cell lines that express KRas G12C.
• a panel of 8 lung cancer and 1 colorectal cell lines harboring KRas G12C mutations was assembled to determine whether combining SHP-2 inhibitors with exemplary KRas G12C inhibitors disclosed herein results in synergistic activity.
• the collection included NCI-Ill 373 (ATCC CRL-5866); NCI-H1792 (ATCC CRL-5895); NCI-H2030 (ATCC CRL-5985); NCI- H2122 (ATCC CRT-5985); HCC1 171 (KCLB 71 171); HCC44 (DSMZ ACC-534); LU99 (RGB 1900); SW1573 (ATCC CRL-2170) and SW837 (ATCC CCL-235).
• Assays for determining the synergy score for the pairwise combinations for each cell line were performed in triplicate. Three 96-well plates plus an additional 4 wells of a separate 96- well control plate for determining baseline luminescence were seeded with 2000 cells/well of a particular cell line in a total volume of 90m1 of a suitable growth medium for that cell line, e.g., RPMI 1640 medium supplemented with 10% FBS and any cell line specific reagents need for growth. The plates were incubated overnight at 37°C in a 5% CO2 atmosphere.
• a suitable growth medium for that cell line e.g., RPMI 1640 medium supplemented with 10% FBS and any cell line specific reagents need for growth.
• a series of working stock 1000X drug dilutions in 100% DMSO was prepared that includes an 8 point single agent dilution of the exemplary KRas G12C inhibitor of Formula (I), Formula I-A and Formula I-B and a 5-point single agent dilution of the SFIP-2 inhibitor.
• the dilutions used for the KRas G12C inhibitor and the SFIP-2 inhibitor varied for each individual compound but were in the range of 3- to 6-fold/serial dilution.
• Example Number refers to the example number for each compound as disclosed in published international PCT application No. WO2019099524.
• a 10X intermediate dosing plate was prepared in scrum free RPMI medium that contains arrayed single agent dilutions of exemplary KRas G12C inhibitor of Formula (I) or the SHP-2 inhibitor.
• a matrix of 40 dilution combinations of exemplary KRas G12C inhibitor of Formula (I), Formula 1-A or Formula I-B and the SHP-2 inhibitor was prepared as test samples.
• 10m1 of each 10X single agent and the 40 combinations of the dose matrix was added and the plates were incubated for 72 hours at 37C in 5% CO2 atmosphere.
• CCG Cell- Titer Glo reagent
• the output of the data from each mathematical model is the assignment of a relative synergy score.
• the data reported in fable 1 are the aggregate sum of the Loewe additivity, Bliss independence, Highest Single Agent and ZIP scores (“Composite Synergy Score”).
• Immunocompromised nude/nude mice are inoculated in the right hind flank with cells or patient derived tumor samples harboring a KRas G12C mutation. When tumor volumes reach between 200 - 400 mm 3 in size, the mice are divided into four groups of 5-12 mice each. The first group is administered vehicle only. The second group is administered a single agent dose of the KRas G12C inhibitor at a concentration that yields a maximal biological effect or a less than maximal biological effect, depending on the cell line and the single agent activity, that does not result in complete tumor regression.
• the third group is administered a single agent dose of the SHP-2 inhibitor at a concentration that yields a maximal biological effect or a less than maximal biological effect, depending on the cell line and the single agent activity, that also does not result in complete tumor regression.
• the fourth group is administered the single agent dose of the KRas G12C inhibitor in combination with the single agent dose of the SHP-2 inhibitor.
• the treatment period varies from cell line to cell line but typically is between 21 -35 days. Tumor volumes are measured using a caliper every two - three days and tumor volumes are calculated by the formula: 0.5 x (Length x Width) 2 .
• a greater degree of tumor growth inhibition for the combination in this model demonstrates that the combination therapy is likely to have a clinically meaningful benefit to treated subjects relative to treatment with only a KRas G12C inhibitor.
• mice 20 nude/nude mice per study were inoculated in the right hind limb with 5 x 10 6 SW1573 cells, KYSE410 cells or H358 cells. When tumor volume reached ⁇ 300 - 350 mm 3 (Study Day 0), 5 mice in each of the four groups were administered p.o.
• mice 25 nude/nude mice were inoculated in the right hind limb with 5 x 10 6 112122 cells.
• tumor volume reached -350 mm 3 (Study Day 0)
• 5 mice in each of the five groups were administered p.o.

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