JP2022509724A - 組み合わせ療法 - Google Patents
組み合わせ療法 Download PDFInfo
- Publication number
- JP2022509724A JP2022509724A JP2021513314A JP2021513314A JP2022509724A JP 2022509724 A JP2022509724 A JP 2022509724A JP 2021513314 A JP2021513314 A JP 2021513314A JP 2021513314 A JP2021513314 A JP 2021513314A JP 2022509724 A JP2022509724 A JP 2022509724A
- Authority
- JP
- Japan
- Prior art keywords
- inhibitor
- kras
- formula
- alkyl
- shp
- Prior art date
- Legal status (The legal status 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 status listed.)
- Pending
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- 0 **(Cc(c(C1)n2)c(N3CCN(*)CC3)nc2O*)CN1I* Chemical compound **(Cc(c(C1)n2)c(N3CCN(*)CC3)nc2O*)CN1I* 0.000 description 2
- WPJCQLIABOVULI-UHFFFAOYSA-N C=CC(N(CC1)CCN1c1c(CCN(C2)c3cc(O)cc4c3cccc4)c2nc(NC(CC2)CCN2C2CC2)n1)=O Chemical compound C=CC(N(CC1)CCN1c1c(CCN(C2)c3cc(O)cc4c3cccc4)c2nc(NC(CC2)CCN2C2CC2)n1)=O WPJCQLIABOVULI-UHFFFAOYSA-N 0.000 description 2
- WXOSKZHOCYRUOA-UHFFFAOYSA-N C=CC(N(CC1)CCN1c1nc(OCCCN2CC(C3)C3C2)nc(C2)c1CCN2c1cc(O)cc2c1cccc2)=O Chemical compound C=CC(N(CC1)CCN1c1nc(OCCCN2CC(C3)C3C2)nc(C2)c1CCN2c1cc(O)cc2c1cccc2)=O WXOSKZHOCYRUOA-UHFFFAOYSA-N 0.000 description 2
- BOYBAZKNDIQEJS-HSZRJFAPSA-N C=CC(N(CC1)CCN1c1nc(OCCN(CCC2)C[C@@H]2F)nc(C2)c1CCN2c1cc(O)cc2ccccc12)=O Chemical compound C=CC(N(CC1)CCN1c1nc(OCCN(CCC2)C[C@@H]2F)nc(C2)c1CCN2c1cc(O)cc2ccccc12)=O BOYBAZKNDIQEJS-HSZRJFAPSA-N 0.000 description 2
- WUUYOPLSMFNPRF-ANYOKISRSA-N CN1[C@H](COc2nc(CN(CC3)c4cnccc4C(F)(F)F)c3c(N(CC3)CC(CC#N)N3C(C=C)=O)n2)CCC1 Chemical compound CN1[C@H](COc2nc(CN(CC3)c4cnccc4C(F)(F)F)c3c(N(CC3)CC(CC#N)N3C(C=C)=O)n2)CCC1 WUUYOPLSMFNPRF-ANYOKISRSA-N 0.000 description 2
- YXSCQRLUQFPPOJ-LBAQZLPGSA-N CN1[C@H](COc2nc(N(CC3)CC(CC#N)N3C(C=C)=O)c(CCN(C3)c4ccccc4C(F)(F)F)c3n2)CCC1 Chemical compound CN1[C@H](COc2nc(N(CC3)CC(CC#N)N3C(C=C)=O)c(CCN(C3)c4ccccc4C(F)(F)F)c3n2)CCC1 YXSCQRLUQFPPOJ-LBAQZLPGSA-N 0.000 description 2
- YSXBTZRNCSQYSX-UHFFFAOYSA-N Cc1ccc2[nH]ccc2c1N1Cc2nc(OCCCN3CCOCC3)nc(N(CC3)CCN3C(C=C)=O)c2CC1 Chemical compound Cc1ccc2[nH]ccc2c1N1Cc2nc(OCCCN3CCOCC3)nc(N(CC3)CCN3C(C=C)=O)c2CC1 YSXBTZRNCSQYSX-UHFFFAOYSA-N 0.000 description 2
- QYDRRJBZNLESHH-HSNKIBKKSA-N C/C=C(\c1c(C)cccc1C)/N1Cc2nc(OC[C@@H](C3)N(C)C[C@@H]3OC)nc(N(CC3)C[C@H](CC#N)N3C3(C(F)=C)OC3)c2CC1 Chemical compound C/C=C(\c1c(C)cccc1C)/N1Cc2nc(OC[C@@H](C3)N(C)C[C@@H]3OC)nc(N(CC3)C[C@H](CC#N)N3C3(C(F)=C)OC3)c2CC1 QYDRRJBZNLESHH-HSNKIBKKSA-N 0.000 description 1
- SEUJJFVZFDHBLR-QBHOUYDASA-N C=C(C(N(CC1)[C@@H](CC#N)CN1c1c(CCN(C2)c3cccc4c3c(Cl)ccc4)c2nc(OCC(CC2)N2C2CCCC2)n1)=O)F Chemical compound C=C(C(N(CC1)[C@@H](CC#N)CN1c1c(CCN(C2)c3cccc4c3c(Cl)ccc4)c2nc(OCC(CC2)N2C2CCCC2)n1)=O)F SEUJJFVZFDHBLR-QBHOUYDASA-N 0.000 description 1
- HBLZLXQLPIHQBA-SFHVURJKSA-N C=C(C(N(CC1)[C@@H](CC#N)CN1c1n[nH]c(C2)c1CCN2c1c2c(Cl)cccc2ccc1)=O)F Chemical compound C=C(C(N(CC1)[C@@H](CC#N)CN1c1n[nH]c(C2)c1CCN2c1c2c(Cl)cccc2ccc1)=O)F HBLZLXQLPIHQBA-SFHVURJKSA-N 0.000 description 1
- OXCJEOQZAFLZFZ-UHFFFAOYSA-N C=CC(N(CC1)CCN1c1c(CCN(C2)c3c(cc(cc4)O)c4ccc3)c2ncn1)=O Chemical compound C=CC(N(CC1)CCN1c1c(CCN(C2)c3c(cc(cc4)O)c4ccc3)c2ncn1)=O OXCJEOQZAFLZFZ-UHFFFAOYSA-N 0.000 description 1
- KJGJYCRTUNZPRN-UHFFFAOYSA-N C=CC(N(CC1)CCN1c1c(CCN(C2)c3cccc4ccccc34)c2ncn1)=O Chemical compound C=CC(N(CC1)CCN1c1c(CCN(C2)c3cccc4ccccc34)c2ncn1)=O KJGJYCRTUNZPRN-UHFFFAOYSA-N 0.000 description 1
- SFWHFRMOVMVFIW-UHFFFAOYSA-N C=CC(N(CC1)CCN1c1nc(COCCCN2CCOCC2)nc(C2)c1CCN2c1cc(O)cc2cccnc12)=O Chemical compound C=CC(N(CC1)CCN1c1nc(COCCCN2CCOCC2)nc(C2)c1CCN2c1cc(O)cc2cccnc12)=O SFWHFRMOVMVFIW-UHFFFAOYSA-N 0.000 description 1
- DFOQXOCAOPDSAS-WMPKNSHKSA-N C=CC(N(CC1)CCN1c1nc(OCCCN(C[C@H]2F)C[C@@H]2F)nc(C2)c1CCN2c1cc(O)cc2ccccc12)=O Chemical compound C=CC(N(CC1)CCN1c1nc(OCCCN(C[C@H]2F)C[C@@H]2F)nc(C2)c1CCN2c1cc(O)cc2ccccc12)=O DFOQXOCAOPDSAS-WMPKNSHKSA-N 0.000 description 1
- GEBSVSDTSVCYCM-UHFFFAOYSA-N C=CC(N(CC1)CCN1c1nc(OCCCN2CCOCC2)nc(C2)c1CCN2c1cc(O)cc2cccnc12)=O Chemical compound C=CC(N(CC1)CCN1c1nc(OCCCN2CCOCC2)nc(C2)c1CCN2c1cc(O)cc2cccnc12)=O GEBSVSDTSVCYCM-UHFFFAOYSA-N 0.000 description 1
- RCJYJAPVGZQYPT-PPVAYSNCSA-N CC1(COc2nc(CN(CC3)c4cccc5cccc(Cl)c45)c3c(N(CC3)C[C@H](CC#N)N3C(C(F)=C)=O)n2)N(C)CCC1 Chemical compound CC1(COc2nc(CN(CC3)c4cccc5cccc(Cl)c45)c3c(N(CC3)C[C@H](CC#N)N3C(C(F)=C)=O)n2)N(C)CCC1 RCJYJAPVGZQYPT-PPVAYSNCSA-N 0.000 description 1
- HBBFXRZSZARDMI-LDNAWNGRSA-N CC12C(Cl)=CC=CC1C=CC=C2N(CC1)Cc2c1c(N(CC1)C[C@H](CC#N)N1C(/C=C/CO)=O)nc(OC[C@H]1N(C)CCC1)n2 Chemical compound CC12C(Cl)=CC=CC1C=CC=C2N(CC1)Cc2c1c(N(CC1)C[C@H](CC#N)N1C(/C=C/CO)=O)nc(OC[C@H]1N(C)CCC1)n2 HBBFXRZSZARDMI-LDNAWNGRSA-N 0.000 description 1
- SQSPHLBZAOINIK-NBZVVLFJSA-N CCC1(COc2nc(CN(CC3)c4c5c(Cl)cccc5ccc4)c3c(N(CC3)C[C@H](CC#N)N3C(/C=C/CF)=O)n2)N(C)CCC1 Chemical compound CCC1(COc2nc(CN(CC3)c4c5c(Cl)cccc5ccc4)c3c(N(CC3)C[C@H](CC#N)N3C(/C=C/CF)=O)n2)N(C)CCC1 SQSPHLBZAOINIK-NBZVVLFJSA-N 0.000 description 1
- ACHOQXUYKLAAPU-UHFFFAOYSA-N CCN(Cc1c(C)c(N(CC2)CCN2C(C=C)=O)nc(OCCCN2CCOCC2)n1)c1c(C)c(C)cc(O)c1 Chemical compound CCN(Cc1c(C)c(N(CC2)CCN2C(C=C)=O)nc(OCCCN2CCOCC2)n1)c1c(C)c(C)cc(O)c1 ACHOQXUYKLAAPU-UHFFFAOYSA-N 0.000 description 1
- XUBGTZPGSBYUOK-JEVDYFGZSA-N CN(C)C/C=C/C(N(CC1)CCN1c1nc(OC[C@H]2N(C)CCC2)nc(C2)c1CCN2c1cc(O)cc2ccccc12)=O Chemical compound CN(C)C/C=C/C(N(CC1)CCN1c1nc(OC[C@H]2N(C)CCC2)nc(C2)c1CCN2c1cc(O)cc2ccccc12)=O XUBGTZPGSBYUOK-JEVDYFGZSA-N 0.000 description 1
- WALXKNUIXQWICD-LBAQZLPGSA-N CN1[C@H](COc2nc(CN(CC3)c(cccc4)c4OC(F)(F)F)c3c(N(CC3)CC(CC#N)N3C(C=C)=O)n2)CCC1 Chemical compound CN1[C@H](COc2nc(CN(CC3)c(cccc4)c4OC(F)(F)F)c3c(N(CC3)CC(CC#N)N3C(C=C)=O)n2)CCC1 WALXKNUIXQWICD-LBAQZLPGSA-N 0.000 description 1
- XMYPBYHRAIBTEZ-QHCPKHFHSA-N CN1[C@H](COc2nc(CN(CC3)c4c(cccc5)c5ccc4)c3c(N(CC3)CCN3C(C=C)=O)n2)CCC1 Chemical compound CN1[C@H](COc2nc(CN(CC3)c4c(cccc5)c5ccc4)c3c(N(CC3)CCN3C(C=C)=O)n2)CCC1 XMYPBYHRAIBTEZ-QHCPKHFHSA-N 0.000 description 1
- DFGKZGMPZJULDC-DQEYMECFSA-N CN1[C@H](COc2nc(CN(CC3)c4cccc5cccc(Cl)c45)c3c(N(CC3)C[C@H](CC#N)N3C(C(OC)=C)=O)n2)CCC1 Chemical compound CN1[C@H](COc2nc(CN(CC3)c4cccc5cccc(Cl)c45)c3c(N(CC3)C[C@H](CC#N)N3C(C(OC)=C)=O)n2)CCC1 DFGKZGMPZJULDC-DQEYMECFSA-N 0.000 description 1
- OBKBMFMBHWUYHS-DQEYMECFSA-N CN1[C@H](COc2nc(CN(CC3)c4cccc5ccccc45)c3c(N(CC3)C[C@H](CC#N)N3C(C=C)=O)n2)CCC1 Chemical compound CN1[C@H](COc2nc(CN(CC3)c4cccc5ccccc45)c3c(N(CC3)C[C@H](CC#N)N3C(C=C)=O)n2)CCC1 OBKBMFMBHWUYHS-DQEYMECFSA-N 0.000 description 1
- WZPYXLTZCVTREL-YDBIPVDTSA-N CN1[C@H](COc2nc(N(CC3)CC(CC#N)N3C3OC3C=C)c(CCN(C3)c4ccccc4OC(F)(F)F)c3n2)CCC1 Chemical compound CN1[C@H](COc2nc(N(CC3)CC(CC#N)N3C3OC3C=C)c(CCN(C3)c4ccccc4OC(F)(F)F)c3n2)CCC1 WZPYXLTZCVTREL-YDBIPVDTSA-N 0.000 description 1
- PEMUGDMSUDYLHU-ZEQRLZLVSA-N CN1[C@H](COc2nc(N(CC3)C[C@H](CC#N)N3C(C(F)=C)=O)c(CCN(C3)c4cccc5c4c(Cl)ccc5)c3n2)CCC1 Chemical compound CN1[C@H](COc2nc(N(CC3)C[C@H](CC#N)N3C(C(F)=C)=O)c(CCN(C3)c4cccc5c4c(Cl)ccc5)c3n2)CCC1 PEMUGDMSUDYLHU-ZEQRLZLVSA-N 0.000 description 1
- LTVKHYYCQYQXDM-JTHBVZDNSA-N C[C@@H](CN(CC1)C(C=C)=O)N1c1nc(OC[C@@H]2N(C)CCC2)nc(C2)c1CCN2c1cc(O)cc2ccccc12 Chemical compound C[C@@H](CN(CC1)C(C=C)=O)N1c1nc(OC[C@@H]2N(C)CCC2)nc(C2)c1CCN2c1cc(O)cc2ccccc12 LTVKHYYCQYQXDM-JTHBVZDNSA-N 0.000 description 1
- LTVKHYYCQYQXDM-GMAHTHKFSA-N C[C@@H](CN(CC1)C(C=C)=O)N1c1nc(OC[C@H]2N(C)CCC2)nc(C2)c1CCN2c1cc(O)cc2ccccc12 Chemical compound C[C@@H](CN(CC1)C(C=C)=O)N1c1nc(OC[C@H]2N(C)CCC2)nc(C2)c1CCN2c1cc(O)cc2ccccc12 LTVKHYYCQYQXDM-GMAHTHKFSA-N 0.000 description 1
- LGWLXNOJQYLNDP-VWNXMTODSA-N C[C@H](CN(CC1)c2nc(OC[C@H]3N(C)CCC3)nc(C3)c2CCN3c2cccc3ccccc23)N1C(C=C)=O Chemical compound C[C@H](CN(CC1)c2nc(OC[C@H]3N(C)CCC3)nc(C3)c2CCN3c2cccc3ccccc23)N1C(C=C)=O LGWLXNOJQYLNDP-VWNXMTODSA-N 0.000 description 1
- ZQKKPIWKNOKJMG-NZHJDXKMSA-N Cc1c2c(N(CC3)Cc4c3c(N(CC3)C=C(CC#N)N3C(/C=C/CO)=O)nc(OC[C@@H]3N(C)CCC3)n4)cccc2ccc1 Chemical compound Cc1c2c(N(CC3)Cc4c3c(N(CC3)C=C(CC#N)N3C(/C=C/CO)=O)nc(OC[C@@H]3N(C)CCC3)n4)cccc2ccc1 ZQKKPIWKNOKJMG-NZHJDXKMSA-N 0.000 description 1
- PTKJWNJYHGWQSD-PFDXZPFDSA-N Cc1c2c(N(CC3)Cc4c3c(N(CC3)C[C@H](CC#N)N3C(/C=C/CN(C3)CC3F)=O)nc(OC[C@H]3N(C)CCC3)n4)cccc2ccc1 Chemical compound Cc1c2c(N(CC3)Cc4c3c(N(CC3)C[C@H](CC#N)N3C(/C=C/CN(C3)CC3F)=O)nc(OC[C@H]3N(C)CCC3)n4)cccc2ccc1 PTKJWNJYHGWQSD-PFDXZPFDSA-N 0.000 description 1
- GCIBCXNMHYTFJB-UHFFFAOYSA-N Cc1cc(O)cc(N(CC2)Cc3c2c(N(CC2)CCN2C(C=C)=O)nc(OCCCN2CCOCC2)n3)c1C Chemical compound Cc1cc(O)cc(N(CC2)Cc3c2c(N(CC2)CCN2C(C=C)=O)nc(OCCCN2CCOCC2)n3)c1C GCIBCXNMHYTFJB-UHFFFAOYSA-N 0.000 description 1
- YPUTZWWHKAMVGK-UHFFFAOYSA-N Cc1ccc2[nH]ncc2c1N1Cc2ncnc(N(CC3)CCN3C(C=C)=O)c2CC1 Chemical compound Cc1ccc2[nH]ncc2c1N1Cc2ncnc(N(CC3)CCN3C(C=C)=O)c2CC1 YPUTZWWHKAMVGK-UHFFFAOYSA-N 0.000 description 1
- BWZAAMUSWRMXGW-IZZNHLLZSA-N Cc1cccc2c1c(N1Cc3nc(OC[C@@H]4N(C)CCC4)nc(N(CC4)C[C@H](CC#N)N4C(C(F)=C)=O)c3CC1)ccc2 Chemical compound Cc1cccc2c1c(N1Cc3nc(OC[C@@H]4N(C)CCC4)nc(N(CC4)C[C@H](CC#N)N4C(C(F)=C)=O)c3CC1)ccc2 BWZAAMUSWRMXGW-IZZNHLLZSA-N 0.000 description 1
- NTXRHPWWLPFAAB-JUSIKRICSA-N Cc1cccc2cccc(N3Cc4nc(OC[C@H](C5)N(C)CC5(F)F)nc(N(CC5)C[C@H](CC#N)N5C(/C=C/CN(C5)CC5F)=O)c4CC3)c12 Chemical compound Cc1cccc2cccc(N3Cc4nc(OC[C@H](C5)N(C)CC5(F)F)nc(N(CC5)C[C@H](CC#N)N5C(/C=C/CN(C5)CC5F)=O)c4CC3)c12 NTXRHPWWLPFAAB-JUSIKRICSA-N 0.000 description 1
- OMDVESRMCYZTTR-UHFFFAOYSA-N OCC(CC1)N1C1CCOCC1 Chemical compound OCC(CC1)N1C1CCOCC1 OMDVESRMCYZTTR-UHFFFAOYSA-N 0.000 description 1
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
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Oncology (AREA)
- Hematology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2025051088A JP2025098159A (ja) | 2018-12-05 | 2025-03-26 | 組み合わせ療法 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201862775628P | 2018-12-05 | 2018-12-05 | |
| US62/775,628 | 2018-12-05 | ||
| PCT/US2019/064707 WO2020118066A1 (en) | 2018-12-05 | 2019-12-05 | Combination therapies |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2025051088A Division JP2025098159A (ja) | 2018-12-05 | 2025-03-26 | 組み合わせ療法 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2022509724A true JP2022509724A (ja) | 2022-01-24 |
| JP2022509724A5 JP2022509724A5 (https=) | 2022-10-12 |
| JPWO2020118066A5 JPWO2020118066A5 (https=) | 2022-10-12 |
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2019
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| JP2025509202A (ja) * | 2022-03-04 | 2025-04-11 | イーライ リリー アンド カンパニー | Kras g12c阻害剤及びshp2阻害剤を含む治療方法 |
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| EA202190630A1 (ru) | 2021-10-11 |
| IL281348A (en) | 2021-04-29 |
| CA3112129A1 (en) | 2020-06-11 |
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| EP3890716A1 (en) | 2021-10-13 |
| US20220079947A1 (en) | 2022-03-17 |
| AU2019392683A1 (en) | 2021-04-01 |
| AU2019392683B2 (en) | 2025-08-14 |
| KR20210113587A (ko) | 2021-09-16 |
| MX2024009727A (es) | 2024-08-19 |
| JP2025098159A (ja) | 2025-07-01 |
| ZA202102016B (en) | 2022-06-29 |
| MX2021002804A (es) | 2021-07-15 |
| EP3890716A4 (en) | 2022-12-21 |
| US12377101B2 (en) | 2025-08-05 |
| CN113164418A (zh) | 2021-07-23 |
| SG11202102357RA (en) | 2021-04-29 |
| WO2020118066A1 (en) | 2020-06-11 |
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