AR070861A1 - Uso de terapia de combinacion con antagonistas de c-met y egfr - Google Patents

Uso de terapia de combinacion con antagonistas de c-met y egfr

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Publication number
AR070861A1
AR070861A1 ARP090100815A ARP090100815A AR070861A1 AR 070861 A1 AR070861 A1 AR 070861A1 AR P090100815 A ARP090100815 A AR P090100815A AR P090100815 A ARP090100815 A AR P090100815A AR 070861 A1 AR070861 A1 AR 070861A1
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AR
Argentina
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nr6r6
alkyl
halo
optionally substituted
independently selected
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ARP090100815A
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English (en)
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Genentech Inc
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Publication of AR070861A1 publication Critical patent/AR070861A1/es

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    • 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
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • 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
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    • A61K39/00—Medicinal preparations containing antigens or antibodies
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    • A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/39558—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
    • 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
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
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    • C12N15/113—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing
    • C12N15/1135—Non-coding nucleic acids modulating the expression of genes, e.g. antisense oligonucleotides; Antisense DNA or RNA; Triplex- forming oligonucleotides; Catalytic nucleic acids, e.g. ribozymes; Nucleic acids used in co-suppression or gene silencing against oncogenes or tumor suppressor genes
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

Para el tratamiento de afecciones patologicas, como el cáncer. Reivindicacion 1: Uso de una cantidad terapéuticamente efectiva de un antagonista de c-met y un antagonista de EGFR, para la manufactura de un medicamento para el tratamiento de cáncer en un sujeto. Reivindicacion 2: El uso de la reivindicacion 1, en donde el antagonista de EGFR tiene una formula general (1) de acuerdo con US 5.757.498, se incorpora a la presente a modo de referencia, en donde: m es 1, 2 o 3; cada R1 es independientemente seleccionado de un grupo que consiste de hidrogeno, halo, hidroxi, hidroxiamino, carboxi, nitro, guanidino, ureido, ciano, trifluorometil, y -(alquileno C1-4)-W-(fenilo) en donde W es un enlace simple, O, S o NH; o cada R1 es independientemente seleccionado de R9 y alquilo C1-4 sustituido con ciano, en donde R9 se selecciona de un grupo que consiste de R5, -OR6, -NR6R6, -C(O)R7, -NHOR5, -OC(O)R6, ciano, A y -YR5; R5 es alquilo C1-4; R6 es independientemente hidrogeno o R5; R7 es R5, -OR6 o -NR6R6; A se selecciona de piperidino, morfolino, pirrolidino, 4-R6-piperazin-1-ilo, imidazol-1-ilo, 4-piridon-1-ilo, -(alquileno C1-4)(CO2H), fenoxi, fenilo, fenilsulfanilo, alquenilo C2-4, y -(alquileno C1-4)C(O)NR6R6; e Y es S, SO, o SO2; en donde las porciones de alquilo en R5, -OR6 y -NR6R6 están opcionalmente sustituidas con uno a tres sustituyentes halo y las porciones de alquilo en R5, -OR6 y -NR6R6 están opcionalmente sustituidas con 1 o 2 grupos R9, y en donde las porciones de alquilo de dichos sustituyentes opcionales están opcionalmente sustituidas con halo o R9, con la condicion de que dos heteroátomos no estén unidos al mismo átomo de carbono; o cada R1 es independientemente seleccionado de -NHSO2R5, ftalimido-alquil C1-4sulfonilamino, benzamido, bencensulfonilamino, 3-fenilureido, 2-oxopirrolidin-1-ilo, 2,5-dioxopirrolidin-1-ilo, y R10-alcanoilamino C2-4 en donde R10 se selecciona de halo, -OR6, alcanoiloxi C2-4, -C(O)R7, y -NR6R6; y en donde dicho -NHSO2R5, ftalimido-alquil C1-4sulfonilamino, benzamido, bencensulfonilamino, 3-fenilureido, 2-oxopirrolidin-1ilo, 2,5-dioxopirrolidin-1-ilo, y R10-alcanoilamino C2-4 están opcionalmente sustituidos con 1 o 2 sustituyentes independientemente seleccionados de halo, alquilo C1-4, ciano, metansulfonilo y alcoxi C1-4; o dos grupos R1 se toman junto con los carbonos a los que están unidos para formar un anillo de 5 a 8 miembros que incluye 1 o 2 heteroátomos seleccionados de O, S y N; R2 es hidrogeno o alquilo C1-6 opcionalmente sustituido con 1 a 3 sustituyentes independientemente seleccionados de halo, alcoxi C1-4, -NR6R6, y -SO2R5; n es 1 o 2 y cada R3 es independientemente seleccionado de hidrogeno, halo, hidroxi, alquilo C1-6, -NR6R6, y alcoxi C1-4, en donde las porciones de alquilo de dichos grupos R3 están opcionalmente sustituidas con 1 a 3 sustituyentes independientemente seleccionados de halo, alcoxi C1-4, -NR6R6, y -SO2R; y R4 es azido o -(etinilo)-R11 en donde R11 es hidrogeno o alquilo C1-6 opcionalmente sustituido con hidroxi, -OR6, o -NR6R6. Reivindicacion 7: El uso de la reivindicacion 1, en donde el antagonista de c-met es un anticuerpo. Reivindicacion 9: El uso de la reivindicacion 7, en donde el anticuerpo es monovalente y comprende una region Fc, en donde la region Fc comprende un primer y un segundo polipéptido, en donde el primer polipéptido comprende la secuencia de Fc que se muestra en la figura (SEC ID Ns 17) y el segundo polipéptido comprende la secuencia que se muestra en la figura (SEC ID Ns 18).
ARP090100815A 2008-03-06 2009-03-06 Uso de terapia de combinacion con antagonistas de c-met y egfr AR070861A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US3444608P 2008-03-06 2008-03-06
US4443808P 2008-04-11 2008-04-11

Publications (1)

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AR070861A1 true AR070861A1 (es) 2010-05-12

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ARP090100815A AR070861A1 (es) 2008-03-06 2009-03-06 Uso de terapia de combinacion con antagonistas de c-met y egfr

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Country Link
US (3) US20090226443A1 (es)
EP (1) EP2257293A2 (es)
JP (1) JP2011513427A (es)
KR (2) KR20160095186A (es)
CN (1) CN102014913A (es)
AR (1) AR070861A1 (es)
AU (1) AU2009221808A1 (es)
BR (1) BRPI0906099A2 (es)
CA (1) CA2716851A1 (es)
CL (1) CL2009000542A1 (es)
CR (1) CR11717A (es)
EC (1) ECSP10010527A (es)
IL (1) IL207777A0 (es)
MA (1) MA32177B1 (es)
MX (1) MX2010009669A (es)
RU (1) RU2601892C2 (es)
SG (1) SG188802A1 (es)
TW (1) TW200940064A (es)
WO (1) WO2009111691A2 (es)
ZA (1) ZA201006028B (es)

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