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AR097685A1 - Métodos de uso de anticuerpos anti-lgr5 - Google Patents

Métodos de uso de anticuerpos anti-lgr5

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Publication number
AR097685A1
AR097685A1 ARP140103456A ARP140103456A AR097685A1 AR 097685 A1 AR097685 A1 AR 097685A1 AR P140103456 A ARP140103456 A AR P140103456A AR P140103456 A ARP140103456 A AR P140103456A AR 097685 A1 AR097685 A1 AR 097685A1
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AR
Argentina
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independently selected
halo
nrr
formula
optionally substituted
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ARP140103456A
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Genentech Inc
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Publication of AR097685A1 publication Critical patent/AR097685A1/es

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    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4402Non condensed pyridines; Hydrogenated derivatives thereof only substituted in position 2, e.g. pheniramine, bisacodyl
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • A61K31/55171,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
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    • A61K31/704Compounds having saccharide radicals attached to non-saccharide compounds by glycosidic linkages attached to a carbocyclic compound, e.g. phloridzin attached to a condensed carbocyclic ring system, e.g. sennosides, thiocolchicosides, escin, daunorubicin
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    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
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    • A61K47/68Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment
    • A61K47/6835Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site
    • A61K47/6851Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an antibody, an immunoglobulin or a fragment thereof, e.g. an Fc-fragment the modifying agent being an antibody or an immunoglobulin bearing at least one antigen-binding site the antibody targeting a determinant of a tumour cell
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    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/30Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
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    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/30Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants from tumour cells
    • C07K16/3053Skin, nerves, brain
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    • C07K14/705Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/72Receptors; Cell surface antigens; Cell surface determinants for hormones
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    • C07K16/28Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2869Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against hormone receptors
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Abstract

Se proporcionan en la presente métodos de uso de anticuerpos anti-LGR5, por ejemplo, para tratar una enfermedad relacionada con hedgehog que incluye carcinoma de células basales. Reivindicación 1: Un método de tratamiento de una enfermedad relacionada con hedgehog en un individuo que comprende la administración al individuo de una cantidad efectiva de un anticuerpo anti-LGR5. Reivindicación 18: El método de acuerdo con cualquiera de las reivindicaciones 1 - 17, en donde el anticuerpo anti-LGR5 tiene la fórmula Ab-(L-D)ₚ, en donde: (a) Ab es el anticuerpo anti-LGR5; (b) L es un ligador; (c) D es un fármaco seleccionado de un maitansinoide, una auristatina, una calicheamicina, una pirrolobenzodiazepina y un derivado de nemorrubicina; y (d) p varía de 1 - 8. Reivindicación 20: El método de acuerdo con la reivindicación 18, en donde D tiene la fórmula (1) y en donde R² y R⁶ son cada uno metilo, R³ y R⁴ son cada uno isopropilo, R⁵ es H, R⁷ es sec-butilo, cada R⁸ se selecciona, de modo independiente, de CH₃, O-CH₃, OH y H; R⁹ es H; y R¹⁸ es -C(R⁸)₂-C(R⁸)₂-arilo. Reivindicación 22: El método de acuerdo con la reivindicación 18, en donde D es una pirrolobenzodiazepina de la fórmula (2) en donde las líneas de puntos indican la presencia opcional de un enlace doble entre C¹ y C² ó C² y C³; R² se selecciona, de modo independiente, de H, OH, =O, =CH₂, CN, R, OR, =CH-RD, =C(RD)₂, O-SO₂-R, y COR y opcionalmente también está seleccionado de halo o dihalo, en donde RD se selecciona, de modo independiente, de R, CO₂R, COR, CHO, CO₂H y halo; R⁶ y R⁹ se seleccionan, de modo independiente, de H, R, OH, OR, SH, SR, NH₂, NHR, NRR, NO₂, Me₃Sn y halo; R⁷ se selecciona, de modo independiente, de H, R, OH, OR, SH, SR, NH₂, NHR, NRR, NO₂, Me₃Sn y halo; Q se selecciona, de modo independiente, de O, S y NH; R¹¹ es H o R o, cuando Q es O, SO₃M, donde M es un catión metálico; R y R se seleccionan cada uno, de modo independiente, de grupos alquilo C₁₋₈ opcionalmente sustituido, heterociclilo C₃₋₈ y arilo C₅₋₂₀ y opcionalmente en relación con el grupo NRR, R y R junto con el átomo de nitrógeno al que están unidos forman un anillo heterocíclico opcionalmente sustituido de 4, 5, 6 ó 7 miembros; R¹², R¹⁶, R¹⁹ y R¹⁷ son como se definen para R², R⁶, R⁹ y R⁷, respectivamente; R es un grupo alquileno C₃₋₁₂, cuya cadena puede estar interrumpida por uno o varios heteroátomos y/o anillos aromáticos que están opcionalmente sustituidos; y X y X se seleccionan, de modo independiente, de O, S y N(H).
ARP140103456A 2013-09-17 2014-09-17 Métodos de uso de anticuerpos anti-lgr5 AR097685A1 (es)

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US201361879089P 2013-09-17 2013-09-17

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US (1) US10246515B2 (es)
EP (1) EP3046940B1 (es)
JP (1) JP2016537399A (es)
KR (1) KR20160055252A (es)
CN (1) CN105518027A (es)
AR (1) AR097685A1 (es)
BR (1) BR112016004450A2 (es)
CA (1) CA2922889A1 (es)
HK (1) HK1218124A1 (es)
MX (1) MX2016003248A (es)
RU (1) RU2016109247A (es)
WO (1) WO2015042108A1 (es)

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WO2018049474A1 (en) * 2016-09-16 2018-03-22 Bionomics Limited Antibody and checkpoint inhibitor combination therapy
WO2019059707A1 (ko) 2017-09-21 2019-03-28 엘지전자 주식회사 무선 통신 시스템에서 사이드링크 통신을 위한 방법 및 장치
US20240207457A1 (en) * 2021-05-11 2024-06-27 The Catholic University Of Korea Industry-Academic Cooperation Foundation Cancer-specific polypeptide and use thereof
KR102838739B1 (ko) * 2021-05-11 2025-07-25 가톨릭대학교 산학협력단 암 특이적인 폴리펩티드 및 이의 용도
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