HRP20170734T1 - Povećana biodostupnost lijeka u terapiji naltreksonom - Google Patents

Povećana biodostupnost lijeka u terapiji naltreksonom Download PDF

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Publication number
HRP20170734T1
HRP20170734T1 HRP20170734TT HRP20170734T HRP20170734T1 HR P20170734 T1 HRP20170734 T1 HR P20170734T1 HR P20170734T T HRP20170734T T HR P20170734TT HR P20170734 T HRP20170734 T HR P20170734T HR P20170734 T1 HRP20170734 T1 HR P20170734T1
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HR
Croatia
Prior art keywords
pharmaceutically acceptable
acceptable salt
naltrexone
bupropion
use according
Prior art date
Application number
HRP20170734TT
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English (en)
Inventor
Shawn Flanagan
Eduardo Dunayevich
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Orexigen Therapeutics, Inc.
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46172304&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HRP20170734(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Orexigen Therapeutics, Inc. filed Critical Orexigen Therapeutics, Inc.
Publication of HRP20170734T1 publication Critical patent/HRP20170734T1/hr

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M21/00Other devices or methods to cause a change in the state of consciousness; Devices for producing or ending sleep by mechanical, optical, or acoustical means, e.g. for hypnosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/13Amines
    • A61K31/135Amines having aromatic rings, e.g. ketamine, nortriptyline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/13Amines
    • A61K31/135Amines having aromatic rings, e.g. ketamine, nortriptyline
    • A61K31/137Arylalkylamines, e.g. amphetamine, epinephrine, salbutamol, ephedrine or methadone
    • 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/485Morphinan derivatives, e.g. morphine, codeine
    • 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
    • A61P3/00Drugs for disorders of the metabolism
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00Drugs for disorders of the metabolism
    • A61P3/04Anorexiants; Antiobesity agents
    • 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
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

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  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Organic Chemistry (AREA)
  • Hematology (AREA)
  • Obesity (AREA)
  • Diabetes (AREA)
  • Child & Adolescent Psychology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Psychology (AREA)
  • Acoustics & Sound (AREA)
  • Physics & Mathematics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Coloring Foods And Improving Nutritive Qualities (AREA)
  • Medicinal Preparation (AREA)

Claims (13)

1. Farmaceutski pripravak za upotrebu za liječenje prekomjerne težine ili pretilosti koji sadrži formulaciju naltreksona s usporenim oslobađanjem ili njegove farmaceutski prihvatljive soli i formulaciju bupropiona s usporenim oslobađanjem ili njegove farmaceutski prihvatljive soli, naznačen time da se navedeni pripravak daje u kombinaciji s hranom.
2. Farmaceutski pripravak za upotrebu prema zahtjevu 1, naznačen time da je količina navedenog bupropiona ili njegove farmaceutski prihvatljive soli u opsegu od oko 90 mg do oko 360 mg dnevno, te je količina naltreksona ili njegove farmaceutski prihvatljive soli u opsegu od oko 4 mg do oko 32 mg dnevno.
3. Farmaceutski pripravka za upotrebu prema zahtjevu 1, naznačen time da navedeni naltrekson ili njegova farmaceutski prihvatljiva sol sadrži nesekvestriranu formulaciju naltreksona ili njegove farmaceutski prihvatljive soli.
4. Farmaceutski pripravka za upotrebu prema zahtjevu 1, naznačen time da se navedeni naltrekson ili njegova farmaceutski prihvatljiva sol, daje istovremeno s bupropionom ili njegovom farmaceutski prihvatljivom soli.
5. Farmaceutski pripravka za upotrebu prema zahtjevu 1, naznačen time da se navedeni naltrekson ili njegova farmaceutski prihvatljiva sol, daje prije ili poslije bupropiona ili njegove farmaceutski prihvatljive soli.
6. Farmaceutski pripravka za upotrebu prema zahtjevu 1, naznačen time da su navedeni naltrekson ili njegova farmaceutski prihvatljiva sol i bupropion ili njegova farmaceutski prihvatljiva sol u jednom obliku doziranja.
7. Farmaceutski pripravak za upotrebu prema bilo kojem od prethodnih zahtjeva, naznačen time da navedena hrana sadrži obrok s visokim sadržajem masti.
8. Farmaceutski pripravak za upotrebu prema bilo kojem od zahtjeva 1 do 7, naznačen time da navedena hrana sadrži obrok izabran iz skupine koju čine umjereno kaloričan obrok s umjerenim sadržajem masti od oko 575 kalorija, a mast iznosi oko 23% ukupnog kalorijskog sadržaja; visoko kalorijski obrok sa visokim sadržajem masti od oko 1000 kalorija, a mast čini oko 50% ukupnog kalorijskog sadržaja; i obrok koji pripada u okvir opsega definiranog navedenim umjereno kaloričnim obrokom s umjerenim sadržajem masti i navedenim visoko kaloričnim obrokom sa visokim sadržajem masti.
9. Farmaceutski pripravak za upotrebu prema bilo kojem od zahtjeva 1 do 8, naznačen time da je navedena hrana umjereno kaloričan obrok s umjerenim sadržajem masti.
10. Farmaceutski pripravak za upotrebu prema bilo kojem od prethodnih zahtjeva, naznačen time da raspored davanja navedenog naltreksona ili njegove farmaceutski prihvatljive soli i navedenog bupropiona ili njegove farmaceutski prihvatljive soli je: oko 8 mg navedenog naltreksona ili njegove farmaceutski prihvatljive soli i oko 90 mg navedenog bupropiona ili njegove farmaceutski prihvatljive soli u toku prvog tjedna tretmana; oko 16 mg navedenog naltreksona ili njegove farmaceutski prihvatljive soli i oko 180 mg navedenog bupropiona ili njegove farmaceutski prihvatljive soli u toku drugog tjedna tretmana; oko 24 mg naltreksona ili njegove farmaceutski prihvatljive soli i oko 270 mg navedenog bupropiona ili njegove farmaceutski prihvatljive soli u toku trećeg tjedna tretmana; i oko 32 mg navedenog naltreksona ili njegove farmaceutski prihvatljive soli i oko 360 mg navedenog bupropiona ili njegove farmaceutski prihvatljive soli u toku četvrtog tjedna tretmana i bilo kojeg slijedećeg tjedna tretmana.
11. Farmaceutski pripravak za upotrebu prema bilo kojem od prethodnih zahtjeva, naznačen time da se navedeni naltrekson ili njegova farmaceutski prihvatljiva sol i navedeni bupropion ili njegova farmaceutski prihvatljiva sol daju kao dvije tablete od 8 mg naltreksona s usporenim oslobađanjem dva puta dnevno i dvije tablete od 90 mg bupropiona s usporenim oslobađanjem dva puta dnevno.
12. Farmaceutski pripravak za upotrebu prema bilo kojem od prethodnih zahtjeva, naznačen time da se navedeni naltrekson ili njegova farmaceutski prihvatljiva sol i navedeni bupropion ili njegova farmaceutski prihvatljiva sol daju tijekom najmanje 28 tjedana.
13. Farmaceutski pripravak za upotrebu prema bilo kojem od prethodnih zahtjeva, naznačen time da se navedeni naltrekson ili njegova farmaceutski prihvatljiva sol i navedeni bupropion ili njegova farmaceutski prihvatljiva sol daju tijekom najmanje 56 tjedana.
HRP20170734TT 2010-12-03 2017-05-16 Povećana biodostupnost lijeka u terapiji naltreksonom HRP20170734T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US41939510P 2010-12-03 2010-12-03
EP11845186.3A EP2646031B9 (en) 2010-12-03 2011-12-02 Increasing drug bioavailability in naltrexone therapy
PCT/US2011/063177 WO2012075459A1 (en) 2010-12-03 2011-12-02 Increasing drug bioavailability in naltrexone therapy

Publications (1)

Publication Number Publication Date
HRP20170734T1 true HRP20170734T1 (hr) 2017-08-11

Family

ID=46172304

Family Applications (2)

Application Number Title Priority Date Filing Date
HRP20170734TT HRP20170734T1 (hr) 2010-12-03 2017-05-16 Povećana biodostupnost lijeka u terapiji naltreksonom
HRP20210618TT HRP20210618T1 (hr) 2010-12-03 2021-04-19 Povećavanje bioraspoloživosti lijeka u terapiji naltreksonom

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HRP20210618TT HRP20210618T1 (hr) 2010-12-03 2021-04-19 Povećavanje bioraspoloživosti lijeka u terapiji naltreksonom

Country Status (26)

Country Link
US (1) US20130245056A1 (hr)
EP (4) EP2646031B9 (hr)
JP (5) JP6008866B2 (hr)
KR (5) KR102258043B1 (hr)
CN (1) CN103313711A (hr)
AR (2) AR093182A1 (hr)
AU (2) AU2011336304B2 (hr)
BR (1) BR112013013390A2 (hr)
CA (1) CA2819262A1 (hr)
CL (1) CL2013001564A1 (hr)
CY (2) CY1118968T1 (hr)
DK (3) DK2646031T3 (hr)
ES (2) ES2625527T3 (hr)
FI (1) FI3884947T3 (hr)
HR (2) HRP20170734T1 (hr)
HU (2) HUE053831T2 (hr)
IL (3) IL226504B (hr)
LT (3) LT3222280T (hr)
MX (1) MX356801B (hr)
PL (3) PL3884947T3 (hr)
PT (3) PT3884947T (hr)
RS (3) RS65198B1 (hr)
RU (1) RU2640561C2 (hr)
SI (2) SI2646031T1 (hr)
TW (1) TWI618536B (hr)
WO (1) WO2012075459A1 (hr)

Families Citing this family (10)

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WO2007067341A2 (en) 2005-11-22 2007-06-14 Orexigen Therapeutics, Inc. Compositions and methods for increasing insulin sensitivity
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EP3482751A1 (en) * 2017-11-14 2019-05-15 LDN Pharma Limited Cancer treatment

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PT3884947T (pt) 2010-12-03 2024-02-16 Nalpropion Pharmaceuticals Llc Aumento da biodisponibilidade farmacológica numa terapêutica com naltrexona

Also Published As

Publication number Publication date
ES2866879T3 (es) 2021-10-20
IL279626A (en) 2021-03-01
TW201304780A (zh) 2013-02-01
AU2017204309A1 (en) 2017-07-13
SI3222280T1 (sl) 2021-11-30
RU2017144631A (ru) 2019-02-18
AR124500A2 (es) 2023-04-05
JP6008866B2 (ja) 2016-10-19
AU2011336304B2 (en) 2017-03-30
JP2013544290A (ja) 2013-12-12
EP3884947A1 (en) 2021-09-29
TWI618536B (zh) 2018-03-21
RU2640561C2 (ru) 2018-01-09
ES2625527T3 (es) 2017-07-19
HUE053831T2 (hu) 2021-07-28
EP4349369A2 (en) 2024-04-10
DK3884947T3 (da) 2024-01-22
EP2646031B1 (en) 2017-02-22
BR112013013390A2 (pt) 2016-09-06
CA2819262A1 (en) 2012-06-07
KR102258043B1 (ko) 2021-05-28
KR102391511B1 (ko) 2022-04-26
AR093182A1 (es) 2015-05-27
ES2625527T9 (es) 2018-09-25
JP2022060331A (ja) 2022-04-14
US20130245056A1 (en) 2013-09-19
PL2646031T3 (pl) 2017-08-31
RS56014B1 (sr) 2017-09-29
IL226504B (en) 2021-01-31
JP7025319B2 (ja) 2022-02-24
EP3222280A1 (en) 2017-09-27
PL3222280T3 (pl) 2021-11-29
CY1124331T1 (el) 2022-07-22
HRP20210618T1 (hr) 2021-09-17
CY1118968T1 (el) 2018-01-10
EP4349369A3 (en) 2024-05-15
EP2646031A4 (en) 2014-04-23
PT3222280T (pt) 2021-04-22
IL270841A (en) 2020-01-30
EP3222280B1 (en) 2021-01-20
RS62149B1 (sr) 2021-08-31
EP3884947B1 (en) 2023-11-15
CL2013001564A1 (es) 2014-05-02
KR20210063473A (ko) 2021-06-01
CN103313711A (zh) 2013-09-18
DK2646031T3 (en) 2017-05-22
SI2646031T1 (sl) 2017-07-31
WO2012075459A1 (en) 2012-06-07
EP2646031A1 (en) 2013-10-09
HUE034393T2 (en) 2018-02-28
KR102105857B1 (ko) 2020-05-04
KR20190058702A (ko) 2019-05-29
LT2646031T (lt) 2017-06-26
JP2024071605A (ja) 2024-05-24
RU2017144631A3 (hr) 2021-04-13
RU2013127423A (ru) 2015-01-10
KR20180069089A (ko) 2018-06-22
PT3884947T (pt) 2024-02-16
LT3222280T (lt) 2021-05-10
LT3884947T (lt) 2024-03-12
JP6456890B2 (ja) 2019-01-23
PT2646031T (pt) 2017-05-25
PL3884947T3 (pl) 2024-05-06
MX356801B (es) 2018-06-13
RS65198B1 (sr) 2024-03-29
FI3884947T3 (fi) 2024-01-30
DK3222280T3 (da) 2021-04-19
JP2019056004A (ja) 2019-04-11
KR20200044158A (ko) 2020-04-28
KR20140035320A (ko) 2014-03-21
KR101984500B1 (ko) 2019-05-31
JP2016210809A (ja) 2016-12-15
MX2013006071A (es) 2013-10-01
AU2011336304A1 (en) 2013-07-11
EP2646031B9 (en) 2018-01-10

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