PE20081379A1 - Composiciones farmaceuticas que comprende nilotinib - Google Patents

Composiciones farmaceuticas que comprende nilotinib

Info

Publication number
PE20081379A1
PE20081379A1 PE2007001294A PE2007001294A PE20081379A1 PE 20081379 A1 PE20081379 A1 PE 20081379A1 PE 2007001294 A PE2007001294 A PE 2007001294A PE 2007001294 A PE2007001294 A PE 2007001294A PE 20081379 A1 PE20081379 A1 PE 20081379A1
Authority
PE
Peru
Prior art keywords
methyl
nilotinib
tensioactive
benzamide
amino
Prior art date
Application number
PE2007001294A
Other languages
English (en)
Inventor
Nathalie Bruneau
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=37684496&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20081379(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 PE20081379A1 publication Critical patent/PE20081379A1/es

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1617Organic compounds, e.g. phospholipids, fats
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/48Preparations in capsules, e.g. of gelatin, of chocolate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1629Organic macromolecular compounds
    • A61K9/1641Organic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, poloxamers
    • 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
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • 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
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1617Organic compounds, e.g. phospholipids, fats
    • A61K9/1623Sugars or sugar alcohols, e.g. lactose; Derivatives thereof; Homeopathic globules
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1605Excipients; Inactive ingredients
    • A61K9/1629Organic macromolecular compounds
    • A61K9/1635Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates

Landscapes

  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

SE REFIERE A UNA COMPOSICION FARMACEUTICA QUE COMPRENDE UN COMPUESTO INHIBIDOR DE LA CINASA DE PROTEINA TIROSINA (TK) DERIVADO DE PIRIMIDIL-AMINO-BENZAMIDA DE FORMULA (I), SIENDO PREFERIDO 4-METIL-3-[[4-(3-PIRIDINIL)-2-PIRIMIDINIL]-AMINO]-N-[5-(4-METIL-1H-IMIDAZOL-1-IL)-3-(TRIFLUORO-METIL)-FENIL]-BENZAMIDA O NILOTINIB COMO SAL MONOHIDRATO DE CLORHIDRATO. ESTA COMPOSICION SE PRESENTA BAJO LA FORMA DE DOSIFICACION SOLIDA, EN ESPECIAL COMO CAPSULA, LAS CUALES SE RELLENAN CON GRANULOS QUE CONTIENEN DICHO COMPUESTO, MEZCLADO CON UNA FASE EXTERNA QUE COMRENDE AL MENOS UN EXCIPIENTE TAL COMO UN TENSIOACTIVO SIENDO PREFERIDO UN POLOXAMERO 188, AMASADOS EN HUMEDO. TAMBIEN SE REFIERE UN PROCEDIMIENTO DE PREPARACION DE GRANULACION HUMEDA; SIENDO UTILES EN EL TRATAMIENTO DE LEUCEMIA MIELOIDE Y TUMORES GASTROINTESTINALES
PE2007001294A 2006-09-27 2007-09-25 Composiciones farmaceuticas que comprende nilotinib PE20081379A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP06121371A EP1923053A1 (en) 2006-09-27 2006-09-27 Pharmaceutical compositions comprising nilotinib or its salt

Publications (1)

Publication Number Publication Date
PE20081379A1 true PE20081379A1 (es) 2008-11-27

Family

ID=37684496

Family Applications (2)

Application Number Title Priority Date Filing Date
PE2012000043A PE20120626A1 (es) 2006-09-27 2007-09-25 Composiciones farmaceuticas que comprende nilotinib
PE2007001294A PE20081379A1 (es) 2006-09-27 2007-09-25 Composiciones farmaceuticas que comprende nilotinib

Family Applications Before (1)

Application Number Title Priority Date Filing Date
PE2012000043A PE20120626A1 (es) 2006-09-27 2007-09-25 Composiciones farmaceuticas que comprende nilotinib

Country Status (35)

Country Link
US (2) US8293756B2 (es)
EP (4) EP1923053A1 (es)
JP (2) JP5567340B2 (es)
KR (2) KR20090076931A (es)
CN (2) CN104306350A (es)
AR (1) AR062980A1 (es)
AU (1) AU2007301977B2 (es)
BR (1) BRPI0719438B1 (es)
CA (1) CA2662571C (es)
CL (1) CL2007002766A1 (es)
CO (1) CO6160288A2 (es)
CY (2) CY1117021T1 (es)
DK (2) DK3984528T3 (es)
ES (3) ES2951547T3 (es)
FI (2) FI2068839T4 (es)
HK (1) HK1133193A1 (es)
HR (2) HRP20151383T4 (es)
HU (2) HUE028204T2 (es)
IL (1) IL197496A (es)
JO (1) JO3757B1 (es)
LT (1) LT3984528T (es)
MA (1) MA30807B1 (es)
MX (1) MX2009003184A (es)
MY (1) MY148237A (es)
NO (2) NO346639B1 (es)
NZ (1) NZ575317A (es)
PE (2) PE20120626A1 (es)
PL (2) PL3984528T3 (es)
PT (2) PT3984528T (es)
RU (1) RU2469707C2 (es)
SI (2) SI2068839T2 (es)
TN (1) TN2009000093A1 (es)
TW (3) TWI540128B (es)
WO (1) WO2008037716A2 (es)
ZA (1) ZA200901511B (es)

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WO2011050120A1 (en) * 2009-10-23 2011-04-28 Novartis Ag Method of treating proliferative disorders and other pathological conditions mediated by bcr-abl, c-kit, ddr1, ddr2 or pdgf-r kinase activity
JO3634B1 (ar) 2009-11-17 2020-08-27 Novartis Ag طريقة لعلاج اضطرابات تكاثرية وحالات مرضية أخرى متوسطة بنشاط كيناز bcr-abl، c-kit، ddr1، ddr2، أو pdgf-r
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CN107582531B (zh) * 2016-07-06 2020-12-29 四川科伦药物研究院有限公司 一种利伐沙班固体制剂及其制备方法
CN107320460B (zh) * 2017-08-04 2020-11-03 北京化工大学 一种尼罗替尼口服纳米制剂及其制备方法
CN107441094B (zh) * 2017-08-08 2020-05-22 南方医科大学 尼罗替尼作为治疗登革病毒感染的药物及其制药用途
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CN113292537B (zh) 2018-06-15 2024-04-05 汉达癌症医药责任有限公司 激酶抑制剂的盐类及其组合物
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Also Published As

Publication number Publication date
HRP20151383T4 (hr) 2023-03-03
JO3757B1 (ar) 2021-01-31
PT2068839E (pt) 2015-12-30
ES2951547T3 (es) 2023-10-23
EP2068839B2 (en) 2022-10-12
IL197496A0 (en) 2009-12-24
FI2068839T4 (fi) 2023-01-31
EP2068839A2 (en) 2009-06-17
US8501760B2 (en) 2013-08-06
MX2009003184A (es) 2009-04-03
TN2009000093A1 (en) 2010-08-19
HRP20151383T1 (hr) 2016-01-15
KR101598747B1 (ko) 2016-03-02
CL2007002766A1 (es) 2008-08-08
BRPI0719438B1 (pt) 2022-04-19
MY148237A (en) 2013-03-29
ES2957912T3 (es) 2024-01-29
SI2068839T2 (sl) 2023-01-31
US20100087463A1 (en) 2010-04-08
TWI428333B (zh) 2014-03-01
HK1133193A1 (en) 2010-03-19
KR20090076931A (ko) 2009-07-13
ES2556625T5 (es) 2023-03-02
CO6160288A2 (es) 2010-05-20
AU2007301977B2 (en) 2011-09-08
WO2008037716A2 (en) 2008-04-03
CY1126116T1 (el) 2023-11-15
NZ575317A (en) 2011-12-22
EP3984528B1 (en) 2023-07-05
LT3984528T (lt) 2023-08-10
NO347404B1 (no) 2023-10-16
WO2008037716A3 (en) 2008-07-17
PL2068839T5 (pl) 2023-01-30
EP1923053A1 (en) 2008-05-21
TW200821298A (en) 2008-05-16
EP3984528A1 (en) 2022-04-20
EP3009128B1 (en) 2023-07-05
CY1117021T1 (el) 2017-04-05
NO346639B1 (no) 2022-11-07
FI3984528T3 (fi) 2023-07-27
CN104306350A (zh) 2015-01-28
SI2068839T1 (sl) 2016-02-29
HUE063083T2 (hu) 2023-12-28
US8293756B2 (en) 2012-10-23
JP2014065715A (ja) 2014-04-17
DK2068839T3 (da) 2016-01-11
AU2007301977A1 (en) 2008-04-03
JP2010504942A (ja) 2010-02-18
ES2556625T3 (es) 2016-01-19
HUE028204T2 (en) 2016-12-28
PL2068839T3 (pl) 2016-06-30
TWI540128B (zh) 2016-07-01
DK3984528T3 (da) 2023-07-31
RU2469707C2 (ru) 2012-12-20
PT3984528T (pt) 2023-08-07
EP3009128A1 (en) 2016-04-20
TW201418244A (zh) 2014-05-16
AR062980A1 (es) 2008-12-17
NO20220946A1 (no) 2009-04-24
RU2009115782A (ru) 2010-11-10
CN101516344A (zh) 2009-08-26
IL197496A (en) 2016-04-21
NO20091501L (no) 2009-04-24
KR20140121903A (ko) 2014-10-16
MA30807B1 (fr) 2009-10-01
BRPI0719438A2 (pt) 2013-12-10
PE20120626A1 (es) 2012-06-07
CA2662571A1 (en) 2008-04-03
HRP20230753T3 (hr) 2023-10-27
JP5567340B2 (ja) 2014-08-06
EP2068839B1 (en) 2015-09-23
SI3984528T1 (sl) 2023-09-29
PL3984528T3 (pl) 2023-08-28
CA2662571C (en) 2016-09-27
US20130023549A1 (en) 2013-01-24
ZA200901511B (en) 2010-02-24
TW201418245A (zh) 2014-05-16

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