PE20140601A1 - COMBINACION DE UN INHIBIDOR DE CINASA DE FOSFATIDIL-INOSITOL-3 (PI3K) Y UN INHIBIDOR DE mTOR - Google Patents

COMBINACION DE UN INHIBIDOR DE CINASA DE FOSFATIDIL-INOSITOL-3 (PI3K) Y UN INHIBIDOR DE mTOR

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Publication number
PE20140601A1
PE20140601A1 PE2013002391A PE2013002391A PE20140601A1 PE 20140601 A1 PE20140601 A1 PE 20140601A1 PE 2013002391 A PE2013002391 A PE 2013002391A PE 2013002391 A PE2013002391 A PE 2013002391A PE 20140601 A1 PE20140601 A1 PE 20140601A1
Authority
PE
Peru
Prior art keywords
pi3k
phosphatidyl
inositol
inhibitor
combination
Prior art date
Application number
PE2013002391A
Other languages
English (en)
Inventor
Christine Fritsch
Carlos Garcia-Echeverria
Xizhong Huang
Sauveur-Michel Maira
Original Assignee
Novartis Ag
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46018130&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20140601(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of PE20140601A1 publication Critical patent/PE20140601A1/es

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    • 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
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
    • 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
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/425Thiazoles
    • A61K31/427Thiazoles not condensed and containing further heterocyclic rings
    • 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
    • A61K31/436Heterocyclic 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 six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
    • AHUMAN NECESSITIES
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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
    • A61K31/439Heterocyclic 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 the ring forming part of a bridged ring system, e.g. quinuclidine
    • AHUMAN NECESSITIES
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    • 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
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Abstract

SE REFIERE A UNA COMBINACION FARMACEUTICA QUE COMPRENDE: A) UN INHIBIDOR DE CINASA DE FOSFATIDIL-INOSITOL-3 (PI3K) TAL COMO EL COMPUESTO 1-({4-METIL-5-[2-(2,2,2-TRIFLUORO-1,1-DIMETIL-ETIL)-PIRIDIN-4-IL]-TIAZOL-2-IL}-AMIDA) DE 2-AMIDA DEL ACIDO (S)-PIRROLIDIN-1,2-DICARBOXILICO; Y B) UN INHIBIDOR DE mTOR TAL COMO EVEROLIMUS (RAD001), TEMSIROLIMUS (CCI-779), ZOTAROLIMUS (ABT578), DEFEROLIMUS, ENTRE OTROS. DICHA COMBINACION ES UTIL EN EL TRATAMIENTO DE ENFERMEDAD DEL INJERTO CONTRA EL HUESPED, RESTENOSIS, RETINITIS PIGMENTOSA, ESCLEROSIS MULTIPLE
PE2013002391A 2011-04-25 2012-04-23 COMBINACION DE UN INHIBIDOR DE CINASA DE FOSFATIDIL-INOSITOL-3 (PI3K) Y UN INHIBIDOR DE mTOR PE20140601A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201161478572P 2011-04-25 2011-04-25

Publications (1)

Publication Number Publication Date
PE20140601A1 true PE20140601A1 (es) 2014-05-24

Family

ID=46018130

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2013002391A PE20140601A1 (es) 2011-04-25 2012-04-23 COMBINACION DE UN INHIBIDOR DE CINASA DE FOSFATIDIL-INOSITOL-3 (PI3K) Y UN INHIBIDOR DE mTOR

Country Status (25)

Country Link
US (3) US20140066474A1 (es)
EP (1) EP2701703A1 (es)
JP (2) JP6086902B2 (es)
KR (1) KR101925656B1 (es)
CN (1) CN103491955B (es)
AR (1) AR086481A1 (es)
AU (2) AU2012250010A1 (es)
BR (1) BR112013027486A2 (es)
CA (1) CA2833962A1 (es)
CL (1) CL2013003078A1 (es)
CO (1) CO6801759A2 (es)
EA (1) EA025948B1 (es)
EC (1) ECSP13012994A (es)
GT (1) GT201300263A (es)
IL (1) IL229008A (es)
MA (1) MA35038B1 (es)
MX (1) MX2013012385A (es)
NZ (1) NZ615593A (es)
PE (1) PE20140601A1 (es)
SG (1) SG193919A1 (es)
TN (1) TN2013000392A1 (es)
TW (1) TWI602567B (es)
UA (1) UA110961C2 (es)
WO (1) WO2012148846A1 (es)
ZA (1) ZA201306973B (es)

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KR20160110963A (ko) * 2014-02-11 2016-09-23 노파르티스 아게 암 치료를 위한 pi3k 억제제를 포함하는 제약 조합물
WO2015148626A1 (en) * 2014-03-26 2015-10-01 Millennium Pharmaceuticals, Inc. Treatment of fibrotic disorders
MX2017004359A (es) * 2014-10-03 2017-06-23 Novartis Ag Composiciones farmaceuticas que comprenden alpelisib.
US20160339030A1 (en) 2015-05-19 2016-11-24 University Of Maryland, Baltimore Treatment agents for inhibiting hiv and cancer in hiv infected patients
GB202010627D0 (en) * 2020-07-10 2020-08-26 Qbd (Qs-Ip) Ltd Blocking method

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US20140066474A1 (en) 2014-03-06
TN2013000392A1 (en) 2015-01-20
US20170095463A1 (en) 2017-04-06
ECSP13012994A (es) 2013-12-31
AU2012250010A1 (en) 2013-10-10
CA2833962A1 (en) 2012-11-01
AU2016202372B2 (en) 2017-07-20
EP2701703A1 (en) 2014-03-05
MA35038B1 (fr) 2014-04-03
IL229008A (en) 2017-11-30
JP2014513097A (ja) 2014-05-29
TW201244716A (en) 2012-11-16
KR101925656B1 (ko) 2018-12-05
IL229008A0 (en) 2013-12-31
BR112013027486A2 (pt) 2017-02-14
SG193919A1 (en) 2013-11-29
WO2012148846A1 (en) 2012-11-01
NZ615593A (en) 2015-05-29
US20180085362A1 (en) 2018-03-29
UA110961C2 (uk) 2016-03-10
MX2013012385A (es) 2013-11-04
CO6801759A2 (es) 2013-11-29
CL2013003078A1 (es) 2014-05-30
AR086481A1 (es) 2013-12-18
CN103491955A (zh) 2014-01-01
KR20140012147A (ko) 2014-01-29
EA025948B1 (ru) 2017-02-28
TWI602567B (zh) 2017-10-21
JP6086902B2 (ja) 2017-03-01
JP2017061527A (ja) 2017-03-30
AU2016202372A1 (en) 2016-05-05
ZA201306973B (en) 2014-06-25
CN103491955B (zh) 2015-12-23
EA201391565A1 (ru) 2014-02-28
GT201300263A (es) 2015-11-24

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