DK2515900T3 - Fremgangsmåde til behandling af atriefibrillation - Google Patents

Fremgangsmåde til behandling af atriefibrillation Download PDF

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Publication number
DK2515900T3
DK2515900T3 DK10798436.1T DK10798436T DK2515900T3 DK 2515900 T3 DK2515900 T3 DK 2515900T3 DK 10798436 T DK10798436 T DK 10798436T DK 2515900 T3 DK2515900 T3 DK 2515900T3
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DK
Denmark
Prior art keywords
ranolazine
dronedarone
atrial
approx
ventricular
Prior art date
Application number
DK10798436.1T
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English (en)
Inventor
Charles Antzelevitch
Luiz Belardinelli
Alexander Burashnikov
John Shryock
Dewan Zeng
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Gilead Sciences Inc
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Application filed by Gilead Sciences Inc filed Critical Gilead Sciences Inc
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Publication of DK2515900T3 publication Critical patent/DK2515900T3/da

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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
    • A61K31/495Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/04Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/06Antiarrhythmics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

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  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hospice & Palliative Care (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicinal Preparation (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Epoxy Compounds (AREA)

Claims (17)

  1. FREMGANGSMÅDE TIL BEHANDLING AF ATRIEFIBRILLATION
    1. Ranolazin til anvendelse i en fremgangsmåde til behandling eller forebyggelse af atriefibrillation eller atrieflagren hos en human patient med behov derfor, hvilken fremgangsmåde omfatter administration til patienten af en terapeutisk effektiv mængde af dronedaron eller et farmaceutisk acceptabelt salt deraf og en terapeutisk effektiv mængde ranolazin
  2. 2. Ranolazin til anvendelse ifølge krav 1, hvor dronedaron eller saltet deraf og ranolazin administreres separat eller sammen som en kombineret doseringsenhed, hvor den kombinerede doseringsenhed fortrinsvis er en tablet.
  3. 3. Ranolazin til anvendelse ifølge krav 1, hvor dronedaron eller saltet deraf og ranolazin administreres intravenøst eller oralt.
  4. 4. Ranolazin til anvendelse ifølge et hvilket som helst af kravene 1-3, hvor mængden af administreret ranolazin er fra ca. 50 mg til ca. 3000 mg dagligt, fortrinsvis fra ca. 50 mg til ca. 1500 mg dagligt.
  5. 5. Ranolazin til anvendelse ifølge et hvilket som helst af kravene 1-4, hvor mængden af administreret dronedaron eller saltet deraf er fra ca. 50 mg til ca. 800 mg dagligt, fortrinsvis fra ca. 50 mg til ca. 600 mg dagligt og mere fortrinsvis fra ca. 50 mg til ca. 400 mg dagligt.
  6. 6. Ranolazin til anvendelse ifølge et hvilket som helst af kravene 1-5, hvor mængden af administreret dronedaron eller saltet deraf er fra ca. 50 mg til ca. 300 mg dagligt, og mængden af administreret ranolazin er fra ca. 300 mg til ca. 1000 mg dagligt.
  7. 7. Ranolazin til anvendelse ifølge krav 6, hvor mængden af administreret dronedaron eller saltet deraf er fra ca. 50 mg til ca. 200 mg dagligt.
  8. 8. Ranolazin til anvendelse ifølge et hvilket som helst af kravene 1-7, hvor saltet af dronedaron er dronedaronhydrochlorid.
  9. 9. Farmaceutisk formulering omfattende ranolazin og dronedaron eller et farmaceutisk acceptabelt salt deraf og en farmaceutisk acceptabel bærer.
  10. 10. Farmaceutisk formulering ifølge krav 9, der er formuleret til intravenøs administration eller oral administration.
  11. 11. Farmaceutisk formulering ifølge krav 9, hvor formuleringen er i en tabletform eller en kapselform.
  12. 12. Formulering ifølge krav 11, hvor tabletten eller kapslen omfatter fra ca. 25 mg til ca. 600 mg, fortrinsvis fra ca. 50 mg til ca. 200 mg dronedaron eller saltet deraf.
  13. 13. Formulering ifølge krav 11 eller 12, hvor tabletten eller kapslen omfatter fra ca. 50 mg til ca. 1000 mg, fortrinsvis fra ca. 100 mg til ca. 750 mg ranolazin.
  14. 14. Formulering ifølge krav 11, hvor tabletten eller kapslen omfatter fra ca. 100 mg til ca. 750 mg ranolazin og ca. 50 mg til ca. 200 mg dronedaron eller saltet deraf.
  15. 15. Formulering ifølge et hvilket som helst af kravene 9-14, hvor saltet af dronedaron er dronedaronhydrochlorid.
  16. 16. Formulering ifølge et hvilket som helst af kravene 9-15, hvor ranolazin er formuleret som depotmedicin.
  17. 17. Formulering ifølge et hvilket som helst af kravene 9-15, hvor dronedaron eller saltet deraf er formuleret til øjeblikkelig frigivelse eller depotmedicin.
DK10798436.1T 2009-12-21 2010-12-20 Fremgangsmåde til behandling af atriefibrillation DK2515900T3 (da)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US28873909P 2009-12-21 2009-12-21
PCT/US2010/061257 WO2011084733A1 (en) 2009-12-21 2010-12-20 Method of treating atrial fibrillation

Publications (1)

Publication Number Publication Date
DK2515900T3 true DK2515900T3 (da) 2015-07-27

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ID=43736345

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DK10798436.1T DK2515900T3 (da) 2009-12-21 2010-12-20 Fremgangsmåde til behandling af atriefibrillation

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US (3) US8513254B2 (da)
EP (2) EP2515900B1 (da)
JP (2) JP5723889B2 (da)
KR (2) KR20120107995A (da)
CN (3) CN102665713B (da)
AP (1) AP3536A (da)
AR (1) AR079552A1 (da)
AU (1) AU2010339753B2 (da)
BR (1) BR112012015499A2 (da)
CA (1) CA2784028C (da)
CL (1) CL2012001597A1 (da)
CR (1) CR20120353A (da)
CY (1) CY1116511T1 (da)
DK (1) DK2515900T3 (da)
EA (2) EA025445B1 (da)
EC (1) ECSP12012004A (da)
ES (2) ES2540093T3 (da)
HK (1) HK1170675A1 (da)
HR (1) HRP20150644T1 (da)
HU (1) HUE026916T2 (da)
IL (1) IL220152A (da)
ME (1) ME02179B (da)
MX (2) MX2012007052A (da)
NO (1) NO2749282T3 (da)
NZ (2) NZ627181A (da)
PE (1) PE20121520A1 (da)
PL (2) PL2749282T3 (da)
PT (2) PT2749282T (da)
RS (1) RS54118B1 (da)
SG (3) SG181541A1 (da)
SI (2) SI2515900T1 (da)
SM (1) SMT201500171B (da)
TW (1) TWI508726B (da)
UA (1) UA109887C2 (da)
UY (1) UY33119A (da)
WO (1) WO2011084733A1 (da)
ZA (1) ZA201204608B (da)

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Also Published As

Publication number Publication date
CY1116511T1 (el) 2017-03-15
UY33119A (es) 2011-07-29
SG10201710751TA (en) 2018-02-27
TW201136586A (en) 2011-11-01
EP2749282B1 (en) 2017-08-09
PL2515900T3 (pl) 2015-10-30
CN102665713B (zh) 2015-02-18
JP2015057449A (ja) 2015-03-26
IL220152A (en) 2016-11-30
CR20120353A (es) 2014-10-07
RS54118B1 (en) 2015-12-31
US20140323493A1 (en) 2014-10-30
NZ627181A (en) 2016-02-26
SI2515900T1 (sl) 2015-07-31
CA2784028A1 (en) 2011-07-14
PL2749282T3 (pl) 2018-01-31
ZA201204608B (en) 2013-02-27
WO2011084733A1 (en) 2011-07-14
AU2010339753B2 (en) 2015-01-22
SG181541A1 (en) 2012-07-30
KR20120107995A (ko) 2012-10-04
US8513254B2 (en) 2013-08-20
UA109887C2 (uk) 2015-10-26
EA201290451A1 (ru) 2013-01-30
AR079552A1 (es) 2012-02-01
AP2012006331A0 (en) 2012-06-30
MX2012007052A (es) 2012-07-30
SI2749282T1 (sl) 2017-12-29
AU2010339753A1 (en) 2012-07-12
PE20121520A1 (es) 2012-11-26
JP2013515007A (ja) 2013-05-02
CN104147010A (zh) 2014-11-19
AP3536A (en) 2016-01-13
EA025445B1 (ru) 2016-12-30
EA201691336A1 (ru) 2017-05-31
US20110183990A1 (en) 2011-07-28
US9056108B2 (en) 2015-06-16
IL220152A0 (en) 2012-07-31
NZ600718A (en) 2014-08-29
HUE026916T2 (en) 2016-08-29
NO2749282T3 (da) 2018-01-06
US20130317038A1 (en) 2013-11-28
ES2646603T3 (es) 2017-12-14
ES2540093T3 (es) 2015-07-08
EP2515900A1 (en) 2012-10-31
ECSP12012004A (es) 2012-08-31
PT2749282T (pt) 2017-11-15
CN104688739A (zh) 2015-06-10
HRP20150644T1 (hr) 2015-07-31
SG10201408528RA (en) 2015-04-29
TWI508726B (zh) 2015-11-21
CL2012001597A1 (es) 2013-06-28
PT2515900E (pt) 2015-07-30
KR20160108611A (ko) 2016-09-19
ME02179B (me) 2015-10-20
EP2749282A1 (en) 2014-07-02
US8754087B2 (en) 2014-06-17
HK1170675A1 (en) 2013-03-08
CA2784028C (en) 2016-08-23
EP2515900B1 (en) 2015-04-29
BR112012015499A2 (pt) 2016-05-03
MX344329B (es) 2016-12-13
CN102665713A (zh) 2012-09-12
SMT201500171B (it) 2015-09-07
JP5723889B2 (ja) 2015-05-27

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