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

Info

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)
Spanish (es)
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

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic 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
    • A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427—Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439—Non 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
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    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41—Heterocyclic 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
    • A61K31/425—Thiazoles
    • A61K31/427—Thiazoles not condensed and containing further heterocyclic rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K31/33—Heterocyclic compounds
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    • A61K31/435—Heterocyclic 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
    • A61K31/4353—Heterocyclic 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
    • A61K31/436—Heterocyclic 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
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    • A61K31/435—Heterocyclic 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
    • A61K31/439—Heterocyclic 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
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    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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  • Public Health (AREA)
  • Chemical & Material Sciences (AREA)
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  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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  • Bioinformatics & Cheminformatics (AREA)
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  • Endocrinology (AREA)
  • Neurology (AREA)
  • Urology & Nephrology (AREA)
  • Diabetes (AREA)
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  • Neurosurgery (AREA)
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  • Oncology (AREA)
  • Biomedical Technology (AREA)
  • Reproductive Health (AREA)
  • Hematology (AREA)
  • Communicable Diseases (AREA)
  • Dermatology (AREA)
  • Gynecology & Obstetrics (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Virology (AREA)
  • Pulmonology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Transplantation (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Physical Education & Sports Medicine (AREA)
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 (26)

Country Link
US (3) US20140066474A1 (enExample)
EP (1) EP2701703A1 (enExample)
JP (2) JP6086902B2 (enExample)
KR (1) KR101925656B1 (enExample)
CN (1) CN103491955B (enExample)
AR (1) AR086481A1 (enExample)
AU (2) AU2012250010A1 (enExample)
BR (1) BR112013027486A2 (enExample)
CA (1) CA2833962A1 (enExample)
CL (1) CL2013003078A1 (enExample)
CO (1) CO6801759A2 (enExample)
EA (1) EA025948B1 (enExample)
EC (1) ECSP13012994A (enExample)
GT (1) GT201300263A (enExample)
IL (1) IL229008A (enExample)
MA (1) MA35038B1 (enExample)
MX (1) MX2013012385A (enExample)
NZ (1) NZ615593A (enExample)
PE (1) PE20140601A1 (enExample)
PH (1) PH12013502077A1 (enExample)
SG (1) SG193919A1 (enExample)
TN (1) TN2013000392A1 (enExample)
TW (1) TWI602567B (enExample)
UA (1) UA110961C2 (enExample)
WO (1) WO2012148846A1 (enExample)
ZA (1) ZA201306973B (enExample)

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MX2014005414A (es) * 2011-11-02 2014-09-22 Novartis Ag Derivados de 2-carboxamida-cicloamino-urea para su uso en el tratamiento de las enfermedades dependientes del factor de crecimiento endotelial vascular (vegf).
HK1219421A1 (zh) * 2013-03-15 2017-04-07 因特利凯有限责任公司 激酶抑制剂的组合及其用途
EA201690987A1 (ru) * 2013-11-13 2016-10-31 Новартис Аг Низкодозовые иммуностимулирующие ингибиторы mtor и их применения
AU2015216590A1 (en) * 2014-02-11 2016-06-30 Novartis Ag Pharmaceutical combinations comprising a PI3K inhibitor for the treatment of cancer
WO2015148626A1 (en) * 2014-03-26 2015-10-01 Millennium Pharmaceuticals, Inc. Treatment of fibrotic disorders
EP3200772B1 (en) * 2014-10-03 2022-08-03 Novartis AG Pharmaceutical compositions comprising alpelisib
US20160339030A1 (en) * 2015-05-19 2016-11-24 University Of Maryland, Baltimore Treatment agents for inhibiting hiv and cancer in hiv infected patients
JP6691337B2 (ja) * 2016-02-29 2020-04-28 学校法人北里研究所 膀胱癌患者の予後を予測するための方法
GB202010627D0 (en) * 2020-07-10 2020-08-26 Qbd (Qs-Ip) Ltd Blocking method

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EP0729471A1 (en) 1993-11-19 1996-09-04 Abbott Laboratories Semisynthetic analogs of rapamycin (macrolides) being immunomodulators
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AR044519A1 (es) * 2003-05-02 2005-09-14 Novartis Ag Derivados de piridin-tiazol amina y de pirimidin-tiazol amina
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CA2736361C (en) * 2008-10-31 2017-10-10 Novartis Ag Combination of a phosphatidylinositol-3-kinase (pi3k) inhibitor and a mtor inhibitor

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CN103491955B (zh) 2015-12-23
ZA201306973B (en) 2014-06-25
PH12013502077A1 (en) 2013-12-16
BR112013027486A2 (pt) 2017-02-14
MX2013012385A (es) 2013-11-04
SG193919A1 (en) 2013-11-29
US20170095463A1 (en) 2017-04-06
AU2016202372B2 (en) 2017-07-20
MA35038B1 (fr) 2014-04-03
CA2833962A1 (en) 2012-11-01
UA110961C2 (uk) 2016-03-10
AR086481A1 (es) 2013-12-18
ECSP13012994A (es) 2013-12-31
WO2012148846A1 (en) 2012-11-01
AU2012250010A1 (en) 2013-10-10
IL229008A0 (en) 2013-12-31
JP2014513097A (ja) 2014-05-29
TWI602567B (zh) 2017-10-21
EA025948B1 (ru) 2017-02-28
US20180085362A1 (en) 2018-03-29
EA201391565A1 (ru) 2014-02-28
JP2017061527A (ja) 2017-03-30
GT201300263A (es) 2015-11-24
US20140066474A1 (en) 2014-03-06
TN2013000392A1 (en) 2015-01-20
CO6801759A2 (es) 2013-11-29
JP6086902B2 (ja) 2017-03-01
IL229008A (en) 2017-11-30
NZ615593A (en) 2015-05-29
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EP2701703A1 (en) 2014-03-05
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KR101925656B1 (ko) 2018-12-05
TW201244716A (en) 2012-11-16

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