MA30807B1 - Compositions pharmaceutiques. - Google Patents

Compositions pharmaceutiques.

Info

Publication number
MA30807B1
MA30807B1 MA31809A MA31809A MA30807B1 MA 30807 B1 MA30807 B1 MA 30807B1 MA 31809 A MA31809 A MA 31809A MA 31809 A MA31809 A MA 31809A MA 30807 B1 MA30807 B1 MA 30807B1
Authority
MA
Morocco
Prior art keywords
pharmaceutical compositions
pellets
salt
produced
pharmaceutically acceptable
Prior art date
Application number
MA31809A
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=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA30807(B1) "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 MA30807B1 publication Critical patent/MA30807B1/fr

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)
  • General Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (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

LA PRÉSENTE INVENTION CONCERNE UNE COMPOSITION PHARMACEUTIQUE, EN PARTICULIER DES CAPSULES, COMPRENANT DES GRANULÉS CONTENANT DU NILOTINIB OU UN SEL DE CELUI-CI, AINSI QU'AU MOINS UN EXCIPIENT PHARMACEUTIQUEMENT ACCEPTABLE. CES GRANULÉS PEUVENT ÊTRE PRODUITS PAR UN PROCÉDÉ DE GRANULATION PAR VOIE HUMIDE.
MA31809A 2006-09-27 2009-04-22 Compositions pharmaceutiques. MA30807B1 (fr)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP06121371A EP1923053A1 (fr) 2006-09-27 2006-09-27 Composition pharmaceutique comprenant de la nilotinib ou son sel

Publications (1)

Publication Number Publication Date
MA30807B1 true MA30807B1 (fr) 2009-10-01

Family

ID=37684496

Family Applications (1)

Application Number Title Priority Date Filing Date
MA31809A MA30807B1 (fr) 2006-09-27 2009-04-22 Compositions pharmaceutiques.

Country Status (34)

Country Link
US (2) US8293756B2 (fr)
EP (4) EP1923053A1 (fr)
JP (2) JP5567340B2 (fr)
KR (2) KR20090076931A (fr)
CN (2) CN104306350A (fr)
AR (1) AR062980A1 (fr)
AU (1) AU2007301977B2 (fr)
BR (1) BRPI0719438B1 (fr)
CA (1) CA2662571C (fr)
CL (1) CL2007002766A1 (fr)
CO (1) CO6160288A2 (fr)
CY (2) CY1117021T1 (fr)
DK (2) DK3984528T3 (fr)
ES (3) ES2957912T3 (fr)
FI (2) FI2068839T4 (fr)
HR (2) HRP20151383T4 (fr)
HU (2) HUE063083T2 (fr)
IL (1) IL197496A (fr)
JO (1) JO3757B1 (fr)
LT (1) LT3984528T (fr)
MA (1) MA30807B1 (fr)
MX (1) MX2009003184A (fr)
MY (1) MY148237A (fr)
NO (2) NO347404B1 (fr)
NZ (1) NZ575317A (fr)
PE (2) PE20081379A1 (fr)
PL (2) PL2068839T5 (fr)
PT (2) PT2068839E (fr)
RU (1) RU2469707C2 (fr)
SI (2) SI3984528T1 (fr)
TN (1) TN2009000093A1 (fr)
TW (3) TW201418245A (fr)
WO (1) WO2008037716A2 (fr)
ZA (1) ZA200901511B (fr)

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EP1923053A1 (fr) * 2006-09-27 2008-05-21 Novartis AG Composition pharmaceutique comprenant de la nilotinib ou son sel
US8933037B2 (en) 2009-09-28 2015-01-13 Medizinische Universitat Wien Methods involving PDGFRBETA inhibitors
JP5948246B2 (ja) 2009-10-23 2016-07-06 ノバルティス アーゲー Bcr−abl、c−kit、ddr1、ddr2またはpdgf−rのキナーゼ活性によって仲介される増殖性障害およびその他の病態の治療方法
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
IN2011CH01887A (fr) * 2011-06-02 2012-12-14
AR086913A1 (es) * 2011-06-14 2014-01-29 Novartis Ag 4-metil-3-[[4-(3-piridinil)-2-pirimidinil]-amino]-n-[5-(4-metil-1h-imidazol-1-il)-3-(trifluoro-metil)-fenil]-benzamida amorfa, forma de dosificacion que la contiene y metodo para prepararlas
CN102321073A (zh) * 2011-08-12 2012-01-18 西安交通大学 一种尼罗替尼的制备方法
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WO2013063003A1 (fr) 2011-10-28 2013-05-02 Novartis Ag Méthode de traitement des tumeurs stromales gastro-intestinales
US9301957B2 (en) 2011-11-14 2016-04-05 Novartis Ag Immediate release 4-methyl-3-4[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-N-[5-(4-methyl-1H-imidazol-1-YL)-3-(trifluoromethyl)phenyl] benzamide formulation
SG11201401476TA (en) * 2011-11-14 2014-10-30 Novartis Ag Immediate release 4-methyl-3-[[4-(3-pyridinyl)-2-pyrimidinyl]amino]-n-[5-(4-methyl- 1h-imidazol-1-yl)-3-(trifluoromethyl)phenyl] benzamide formulation
IN2014DN10801A (fr) 2012-07-11 2015-09-04 Novartis Ag
EP2988729A1 (fr) 2013-04-25 2016-03-02 Sun Pharmaceutical Industries Limited Forme posologique orale solide de produit pharmaceutique à rétention gastrique de nilotinib
US9636340B2 (en) 2013-11-12 2017-05-02 Ayyappan K. Rajasekaran Kinase inhibitors
EP3189045B1 (fr) * 2014-08-11 2022-02-09 Sun Pharmaceutical Industries Limited Nouveaux sels de nilotinib et leurs polymorphes
US10045987B2 (en) * 2014-08-28 2018-08-14 Codexis, Inc. Imidazoyl anilide derivatives and methods of use
IL315294A (en) 2015-03-03 2024-10-01 Pharmacyclics Llc Pharmaceutical formulations of bruton's tyrosine kinase inhibitor
EP3429589B1 (fr) * 2016-03-17 2022-12-14 Sun Pharmaceutical Industries Ltd Composition pharmaceutique du nilotinib
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
CZ2017821A3 (cs) 2017-12-20 2019-07-03 Zentiva, K.S. Léková forma obsahující krystalický nilotinib
TWI831259B (zh) 2018-06-15 2024-02-01 漢達生技醫藥股份有限公司 包含達沙替尼十二烷基硫酸鹽組合物的膠囊
EP4096791A1 (fr) 2020-01-31 2022-12-07 Nanocopoeia LLC Microparticules de nilotinib amorphe et leurs utilisations
WO2021222739A1 (fr) 2020-04-30 2021-11-04 Nanocopoeia, Llc Comprimé à désintégration orale comprenant une dispersion solide amorphe de nilotinib
JP7489849B2 (ja) * 2020-07-20 2024-05-24 日本化薬株式会社 ニロチニブ錠剤
MX2023003556A (es) 2020-09-29 2023-06-13 Shenzhen Pharmacin Co Ltd Composiciones farmaceuticas.
CN115154437A (zh) * 2021-04-01 2022-10-11 齐鲁制药有限公司 一种含有盐酸尼洛替尼的药物组合物及其制备方法
MX2023015480A (es) 2021-06-19 2024-01-19 Helm Ag Composicion granulada que comprende nilotinib.
WO2023285981A1 (fr) * 2021-07-15 2023-01-19 Torrent Pharmaceuticals Limited Composition pharmaceutique liquide stable de nilotinib
EP4122452A1 (fr) 2021-07-23 2023-01-25 KRKA, d.d., Novo mesto Composition pharmaceutique comprenant du nilotinib et son procédé de fabrication
EP4260848A1 (fr) 2022-04-11 2023-10-18 Lotus Pharmaceutical Co., Ltd. Composition pharmaceutique pour forme posologique solide contenant du nilotinib et son procédé de préparation
EP4642435A1 (fr) 2022-12-29 2025-11-05 Renata Pharmaceuticals (Ireland) Limited Suspension pharmaceutique de nilotinib
WO2024194718A1 (fr) * 2023-03-22 2024-09-26 Unichem Laboratories Limited Composition pharmaceutique stable et son procédé de préparation
CN116854638A (zh) * 2023-06-05 2023-10-10 南华大学 一种含烷基链的氨基酸甲酯类化合物及其用途

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Also Published As

Publication number Publication date
TWI540128B (zh) 2016-07-01
BRPI0719438B1 (pt) 2022-04-19
CN104306350A (zh) 2015-01-28
HUE063083T2 (hu) 2023-12-28
SI2068839T2 (sl) 2023-01-31
AU2007301977A1 (en) 2008-04-03
TW201418245A (zh) 2014-05-16
CY1126116T1 (el) 2023-11-15
HRP20151383T1 (hr) 2016-01-15
PL2068839T3 (pl) 2016-06-30
ES2957912T3 (es) 2024-01-29
LT3984528T (lt) 2023-08-10
WO2008037716A3 (fr) 2008-07-17
CA2662571A1 (fr) 2008-04-03
EP3984528A1 (fr) 2022-04-20
EP2068839A2 (fr) 2009-06-17
CL2007002766A1 (es) 2008-08-08
SI2068839T1 (sl) 2016-02-29
US20130023549A1 (en) 2013-01-24
TWI428333B (zh) 2014-03-01
HUE028204T2 (en) 2016-12-28
KR20090076931A (ko) 2009-07-13
RU2469707C2 (ru) 2012-12-20
EP3984528B1 (fr) 2023-07-05
NO20220946A1 (no) 2009-04-24
HRP20151383T4 (hr) 2023-03-03
HK1133193A1 (en) 2010-03-19
CY1117021T1 (el) 2017-04-05
BRPI0719438A2 (pt) 2013-12-10
NO347404B1 (no) 2023-10-16
RU2009115782A (ru) 2010-11-10
US20100087463A1 (en) 2010-04-08
DK2068839T3 (da) 2016-01-11
DK3984528T3 (da) 2023-07-31
IL197496A0 (en) 2009-12-24
AU2007301977B2 (en) 2011-09-08
MX2009003184A (es) 2009-04-03
CO6160288A2 (es) 2010-05-20
TW200821298A (en) 2008-05-16
CA2662571C (fr) 2016-09-27
FI2068839T4 (fi) 2023-01-31
US8293756B2 (en) 2012-10-23
JP2010504942A (ja) 2010-02-18
ZA200901511B (en) 2010-02-24
TW201418244A (zh) 2014-05-16
WO2008037716A2 (fr) 2008-04-03
EP1923053A1 (fr) 2008-05-21
IL197496A (en) 2016-04-21
JP5567340B2 (ja) 2014-08-06
JO3757B1 (ar) 2021-01-31
ES2556625T3 (es) 2016-01-19
EP2068839B2 (fr) 2022-10-12
FI3984528T3 (fi) 2023-07-27
EP3009128A1 (fr) 2016-04-20
PT3984528T (pt) 2023-08-07
PT2068839E (pt) 2015-12-30
KR101598747B1 (ko) 2016-03-02
JP2014065715A (ja) 2014-04-17
NZ575317A (en) 2011-12-22
ES2951547T3 (es) 2023-10-23
PL2068839T5 (pl) 2023-01-30
MY148237A (en) 2013-03-29
HRP20230753T3 (hr) 2023-10-27
CN101516344A (zh) 2009-08-26
TN2009000093A1 (en) 2010-08-19
NO346639B1 (no) 2022-11-07
KR20140121903A (ko) 2014-10-16
AR062980A1 (es) 2008-12-17
PE20081379A1 (es) 2008-11-27
PE20120626A1 (es) 2012-06-07
EP3009128B1 (fr) 2023-07-05
SI3984528T1 (sl) 2023-09-29
NO20091501L (no) 2009-04-24
PL3984528T3 (pl) 2023-08-28
ES2556625T5 (es) 2023-03-02
US8501760B2 (en) 2013-08-06
EP2068839B1 (fr) 2015-09-23

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