PE20160529A1 - Uso de una combinacion de un inhibidor de mek y un inhibidor de erk para el tratamiento de enfermedades hiperproliferativas - Google Patents

Uso de una combinacion de un inhibidor de mek y un inhibidor de erk para el tratamiento de enfermedades hiperproliferativas

Info

Publication number
PE20160529A1
PE20160529A1 PE2016000076A PE2016000076A PE20160529A1 PE 20160529 A1 PE20160529 A1 PE 20160529A1 PE 2016000076 A PE2016000076 A PE 2016000076A PE 2016000076 A PE2016000076 A PE 2016000076A PE 20160529 A1 PE20160529 A1 PE 20160529A1
Authority
PE
Peru
Prior art keywords
inhibitor
treatment
combination
hyperproliferative diseases
gdc
Prior art date
Application number
PE2016000076A
Other languages
English (en)
Inventor
Mark Merchant
Marcia Belvin
John Moffat
Original Assignee
Hoffmann La Roche
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of PE20160529A1 publication Critical patent/PE20160529A1/es

Links

Classifications

    • 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
    • A61K31/397Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having four-membered rings, e.g. azetidine
    • 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
    • A61K31/435Heterocyclic 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
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/5025Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic ring systems
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

Abstract

La invencion proporciona combinaciones que comprenden un inhibidor de MEK tal como GDC-0973, GDC-0623, GSK-112 0212 (trametinib), AZD-6244 (selumetinib), etc; o una de sus sales farmaceuticamente aceptables y un inhibidor de ERK (tal como GDC-0994, [(S)-1-(1-(4-cloro-3-fluorofenil)-2-hidroxietil)-4-(2-((1-metil-1H-pirazol-5-il)amino)pirimidin-4-il)piridin-2(1H)-ona]. Las combinaciones son particularmente utiles para tratar trastornos hiperproliferativos, tal como el cancer
PE2016000076A 2013-09-05 2014-09-04 Uso de una combinacion de un inhibidor de mek y un inhibidor de erk para el tratamiento de enfermedades hiperproliferativas PE20160529A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201361874206P 2013-09-05 2013-09-05

Publications (1)

Publication Number Publication Date
PE20160529A1 true PE20160529A1 (es) 2016-05-21

Family

ID=51492945

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2016000076A PE20160529A1 (es) 2013-09-05 2014-09-04 Uso de una combinacion de un inhibidor de mek y un inhibidor de erk para el tratamiento de enfermedades hiperproliferativas

Country Status (21)

Country Link
US (1) US9532987B2 (es)
EP (1) EP3041471A1 (es)
JP (2) JP2016531139A (es)
KR (1) KR20160048807A (es)
CN (1) CN105517548B (es)
AR (1) AR097556A1 (es)
AU (1) AU2014317119B2 (es)
CA (1) CA2916619A1 (es)
CL (1) CL2016000042A1 (es)
EA (1) EA034872B1 (es)
HK (1) HK1218072A1 (es)
IL (1) IL243251B (es)
MA (1) MA38827A1 (es)
MX (1) MX370417B (es)
PE (1) PE20160529A1 (es)
PH (1) PH12016500270A1 (es)
SG (1) SG11201600989VA (es)
TW (1) TW201605477A (es)
UA (1) UA120423C2 (es)
WO (1) WO2015032840A1 (es)
ZA (1) ZA201600091B (es)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013130976A1 (en) * 2012-03-01 2013-09-06 Array Biopharma Inc. Serine/threonine kinase inhibitors
UA120506C2 (uk) 2013-12-06 2019-12-26 Дженентек, Інк. Інгібітори серин/треонінкіназ
KR102396710B1 (ko) * 2013-12-30 2022-05-10 어레이 바이오파마 인크. 세린/트레오닌 키나제 저해제
WO2016162325A1 (en) 2015-04-07 2016-10-13 Astrazeneca Ab Substituted 3,4-dihydropyrrolo[1,2-a]pyrazin-1 (2h)-one derivatives as kinase inhibitors
SI3374359T1 (sl) 2015-11-09 2020-04-30 Astrazeneca Ab Derivati dihidroimidazopirazinona uporabni pri zdravljenju raka
WO2017080980A1 (en) 2015-11-09 2017-05-18 Astrazeneca Ab Dihydropyrrolopyrazinone derivatives useful in the treatment of cancer
CN105330643B (zh) * 2015-12-09 2017-12-05 苏州明锐医药科技有限公司 卡比替尼的制备方法
KR20180134347A (ko) * 2016-04-15 2018-12-18 제넨테크, 인크. 암의 진단 및 치료 방법
WO2018039211A1 (en) * 2016-08-23 2018-03-01 Genentech, Inc. Combination therapy for the treatment of pancreatic cancer
MY194462A (en) * 2016-11-25 2022-11-30 Genuv Inc Composition for Promoting Differentiation of and Protecting Neural Stem Cells and Method for Inducing Neural Regeneration using same
JP2019019094A (ja) * 2017-07-19 2019-02-07 学校法人福岡大学 変異kras関連シグナル阻害用組成物
JP2020532982A (ja) 2017-09-08 2020-11-19 エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト がんの診断及び治療方法
WO2019139970A1 (en) * 2018-01-09 2019-07-18 Duke University Topical administration of mek inhibiting agents for the treatment of skin disorders
EP3752200A1 (en) 2018-02-13 2020-12-23 Vib Vzw Targeting minimal residual disease in cancer with rxr antagonists
WO2021007499A1 (en) * 2019-07-11 2021-01-14 Emory University Combination therapies for managing cancer

Family Cites Families (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1934174B1 (en) * 2005-10-07 2011-04-06 Exelixis, Inc. Azetidines as mek inhibitors for the treatment of proliferative diseases
US20080085886A1 (en) 2006-08-21 2008-04-10 Genentech, Inc. Aza-benzofuranyl compounds and methods of use
BRPI0714629A2 (pt) 2006-08-21 2013-05-07 Genentech Inc composto, composiÇço farmacÊutica, mÉtodo para inibir o crescimento celular, mÉtodo para tratar uma doenÇa inflamatària e mÉtodo para trataruma doenÇa auto-imune, lesço àsseo destrutiva, distérbios proliferativos, doenÇas infecciosas, doenÇas virais, doenÇas fibràticas ou doenÇas neurodegenerativas
PE20081354A1 (es) 2006-11-30 2008-11-14 Genentech Inc Compuestos de azaindolilo como inhibidores de mek
US7999006B2 (en) 2006-12-14 2011-08-16 Exelixis, Inc. Methods of using MEK inhibitors
WO2008157179A2 (en) 2007-06-12 2008-12-24 Genentech, Inc. N-substituted azaindoles and methods of use
PL2222675T3 (pl) 2007-12-19 2014-02-28 Genentech Inc 5-anilinoimidazopirydyny i sposoby zastosowania
EP2231662B1 (en) 2007-12-19 2011-06-22 Genentech, Inc. 8-anilinoimidazopyridines and their use as anti-cancer and/or anti-inflammatory agents
JP5710269B2 (ja) 2007-12-21 2015-04-30 ジェネンテック, インコーポレイテッド アザインドリジン類と使用方法
WO2010003025A1 (en) 2008-07-01 2010-01-07 Genentech, Inc. Bicyclic heterocycles as mek kinase inhibitors
CN102137843A (zh) 2008-07-01 2011-07-27 健泰科生物技术公司 作为mek激酶抑制剂的异吲哚酮衍生物及其使用方法
EP2470898A4 (en) 2009-08-24 2013-03-13 Genentech Inc DETERMINING SENSITIVITY OF CELLS TO B-RAF INHIBITOR TREATMENT IN DETECTION OF K-RAS MUTATIONS AND MEASURING RTK EXPRESSION LEVELS
TWI428336B (zh) 2009-10-12 2014-03-01 Hoffmann La Roche Pi3k抑制劑及mek抑制劑之組合
SG190361A1 (en) 2010-11-23 2013-06-28 Abbvie Inc Salts and crystalline forms of an apoptosis-inducing agent
US9133187B2 (en) 2011-02-28 2015-09-15 Array Biopharma Inc. Serine/threonine kinase inhibitors
WO2012145503A1 (en) 2011-04-21 2012-10-26 Novartis Ag Pharmaceutical combinations
BR112014002675A2 (pt) 2011-08-04 2017-02-21 Array Biopharma Inc "quinazolina como inibidores de serina/treonina quinase, seus usos, e composição"
WO2013130976A1 (en) 2012-03-01 2013-09-06 Array Biopharma Inc. Serine/threonine kinase inhibitors
US20130267517A1 (en) 2012-03-31 2013-10-10 Hoffmann-La Roche Inc. Novel 4-methyl-dihydropyrimidines for the treatment and prophylaxis of hepatitis b virus infection
KR20150023318A (ko) 2012-05-30 2015-03-05 에프. 호프만-라 로슈 아게 피롤리디노 헤테로사이클
MX367970B (es) 2012-08-17 2019-09-11 Hoffmann La Roche Tratamientos de combinación para melanoma que comprenden la administración de cobimetinib y vemurafinib.
MX369989B (es) 2012-08-27 2019-11-27 Array Biopharma Inc Inhibidores de serina/treonina cinasa para el tratamiento de enfermedades hiperproliferativas.
MX2015004660A (es) 2012-10-12 2015-08-07 Exelixis Inc Proceso novedoso para la elaboración de compuestos para su uso en el tratamiento del cáncer.
CN104755478B (zh) 2012-10-16 2017-10-10 霍夫曼-拉罗奇有限公司 丝氨酸/苏氨酸激酶抑制剂
UA120506C2 (uk) 2013-12-06 2019-12-26 Дженентек, Інк. Інгібітори серин/треонінкіназ
KR102396710B1 (ko) 2013-12-30 2022-05-10 어레이 바이오파마 인크. 세린/트레오닌 키나제 저해제
CN105848723B (zh) 2013-12-30 2019-08-02 基因泰克公司 丝氨酸/苏氨酸激酶抑制剂
EP3129025B1 (en) 2014-04-09 2019-05-15 Genentech, Inc. Process for the manufacturing of medicaments

Also Published As

Publication number Publication date
SG11201600989VA (en) 2016-03-30
JP2016531139A (ja) 2016-10-06
JP2019031517A (ja) 2019-02-28
US9532987B2 (en) 2017-01-03
HK1218072A1 (zh) 2017-02-03
AR097556A1 (es) 2016-03-23
MA38827A1 (fr) 2017-10-31
EA201690513A1 (ru) 2016-07-29
WO2015032840A1 (en) 2015-03-12
ZA201600091B (en) 2017-04-26
MX370417B (es) 2019-12-10
AU2014317119B2 (en) 2019-12-05
CL2016000042A1 (es) 2016-08-05
CA2916619A1 (en) 2015-03-12
TW201605477A (zh) 2016-02-16
CN105517548B (zh) 2020-01-21
KR20160048807A (ko) 2016-05-04
MX2016002857A (es) 2016-06-22
US20150111869A1 (en) 2015-04-23
EA034872B1 (ru) 2020-03-31
CN105517548A (zh) 2016-04-20
EP3041471A1 (en) 2016-07-13
AU2014317119A1 (en) 2016-03-03
UA120423C2 (uk) 2019-12-10
PH12016500270A1 (en) 2016-05-16
IL243251B (en) 2019-02-28

Similar Documents

Publication Publication Date Title
PE20160529A1 (es) Uso de una combinacion de un inhibidor de mek y un inhibidor de erk para el tratamiento de enfermedades hiperproliferativas
CL2017001566A1 (es) Derivados de azabiciclootano como agonistas de fxr para el uso en el tratamiento de enfermedades hepáticas y gastrointestinales.
CY1123810T1 (el) Τριφθορομεθυλ υποκατεστημενα πυραζολια ως αναστολεις καλλικρεϊνης στο ανθρωπινο πλασμα
CY1122279T1 (el) Ενωσεις ναφθυριδινης αναστολεις κινασης jak
MX2019007256A (es) Inhibidores de las fosfodiesterasas y métodos de tratamiento microbiano.
CO2017004525A2 (es) Dihidropirrolopiridinas inhibidoras de ror-gamma
CL2016002072A1 (es) 2-amino-3,5,5-trifluoro-3,4,5,6-tetrahidropiridinas como inhibidores de bace1 para el tratamiento de la enfermedad de alzheimer
CR20160036A (es) Inhibidores cristalinos de bromodominios
MY196243A (en) Dihydropyrimidine Compounds and Their Application In Pharmaceuticals
BR112017024917A2 (pt) síntese de compostos heterocíclicos
MX2017013797A (es) Inhibidor de janus quinasa.
CU24419B1 (es) 2-(morfolin-4-il)-1,7-naftiridinas útiles en el tratamiento o la profilaxis de enfermedades hiperproliferativas
UY37205A (es) Inhibidores de bromodominios
EA202192151A1 (ru) Применение пиразолпиримидиновых производных для лечения нарушений, связанных с pi3k
AU2018347307A1 (en) Heterocyclic compounds and uses thereof
NI201800042A (es) Nuevos derivados de pirrolo[2,3-d]pirimidina como inhibidores duales de dyrk1/clk1
CY1121806T1 (el) Ιμιδαζοπυραζινονες ως αναστολεις pde1
AR103680A1 (es) Inhibidores selectivos de bace1
UY36713A (es) Triazoles para el tratamiento de enfermedades desmielinizantes
AR100818A1 (es) N-(cianometil)-4-(2-(4-morfolinofenilamino)pirimidin-4-il)benzamida
MX2014013855A (es) Proceso para hacer compuestos de ciclopentapirimidina hidroxilada y sus sales.
TW201625535A (en) Inhibitors of histone demethylases
EP3492468A4 (en) HETEROCYCLIC COMPOUND AS A JAK INHIBITOR, SALTS AND THERAPEUTIC USE THEREOF
CO2019001181A2 (es) Compuestos de heteroarilcarboxamida como inhibidores de ripk2
CY1122587T1 (el) 1-[2-(αμινομεθυλο)βενζυλο]-2-θειοξο-1,2,3,5-τετραϋδρο-4η-πυρρολο[3,2-d]πυριμιδιν-4-ονες ως αναστολεις της μυελοϋπεροξειδασης