HRP20240115T1 - Povećavanje bioraspoloživosti lijeka u terapiji naltreksonom - Google Patents

Povećavanje bioraspoloživosti lijeka u terapiji naltreksonom Download PDF

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Publication number
HRP20240115T1
HRP20240115T1 HRP20240115TT HRP20240115T HRP20240115T1 HR P20240115 T1 HRP20240115 T1 HR P20240115T1 HR P20240115T T HRP20240115T T HR P20240115TT HR P20240115 T HRP20240115 T HR P20240115T HR P20240115 T1 HRP20240115 T1 HR P20240115T1
Authority
HR
Croatia
Prior art keywords
pharmaceutically acceptable
acceptable salt
naltrexone
bupropion
use according
Prior art date
Application number
HRP20240115TT
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English (en)
Inventor
Shawn Flanagan
Eduardo Dunayevich
Original Assignee
Nalpropion Pharmaceuticals Llc
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.)
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Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=46172304&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=HRP20240115(T1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Nalpropion Pharmaceuticals Llc filed Critical Nalpropion Pharmaceuticals Llc
Publication of HRP20240115T1 publication Critical patent/HRP20240115T1/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
    • A61K31/33Heterocyclic 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
    • 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
    • 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)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Organic Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Diabetes (AREA)
  • Obesity (AREA)
  • Child & Adolescent Psychology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Acoustics & Sound (AREA)
  • Biomedical Technology (AREA)
  • Anesthesiology (AREA)
  • Physics & Mathematics (AREA)
  • Psychology (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 (14)

1. Farmaceutski pripravak za uporabu u terapiji, naznačen time, da sadrži formulaciju s produljenim otpuštanjem naltreksona ili njegove farmaceutski prihvatljive soli i formulaciju s produljenim otpuštanjem bupropiona ili njegove farmaceutski prihvatljive soli, pri čemu se navedeni pripravak daje s hranom.
2. Farmaceutski pripravak za uporabu prema patentnom zahtjevu 1, naznačen time, da se količina spomenutog bupropiona ili njegove farmaceutski prihvatljive soli nalazi u rasponu od oko 90 mg do oko 360 mg po danu, i količina naltreksona ili njegove farmaceutski prihvatljive soli nalazi se u rasponu od oko 4 mg do oko 32 mg po danu.
3. Farmaceutski pripravak za uporabu prema patentnom zahtjevu 1, naznačen time, da spomenuti naltrekson ili njegova farmaceutski prihvatljiva sol sadrži nesekvestriranu formulaciju naltreksona ili njegove farmaceutski prihvatljive soli.
4. Farmaceutski pripravak za uporabu prema patentnom zahtjevu 1, naznačen time, da se spomenuti naltrekson ili njegova farmaceutski prihvatljiva sol daje istovremeno s bupropionom ili njegovom farmaceutski prihvatljivom soli.
5. Farmaceutski pripravak za uporabu prema patentnom zahtjevu 1, naznačen time, da se spomenuti naltrekson ili njegova farmaceutski prihvatljiva sol daje prije od ili uzastopno nakon bupropiona ili njegove farmaceutski prihvatljive soli.
6. Farmaceutski pripravak za uporabu prema patentnom zahtjevu 1, naznačen time, da se spomenuti naltrekson ili njegova farmaceutski prihvatljiva sol i spomenuti bupropion ili njegova farmaceutski prihvatljiva sol nalaze u pojedinačnom obliku za doziranje.
7. Farmaceutski pripravak za uporabu prema bilo kojem od prethodnih patentnih zahtjeva, naznačen time, da spomenuta hrana sadrži jelo s visokim udjelom masti.
8. Farmaceutski pripravak za uporabu prema bilo kojem od patentnih zahtjeva 1 do 7, naznačen time, da spomenuta hrana sadrži obrok odabran iz skupine koju čine umjereno kaloričan, umjereno masan obrok od oko 575 kalorija i s procjenom masti od oko 23% od ukupnog kalorijskog sadržaja; visokokaloričan obrok s visokim sadržajem masti od oko 1000 kalorija i s procjenom masti od oko 50% od ukupnog kalorijskog sadržaja; i obrok koji potpada unutar raspona definiranog navedenim umjereno kaloričnim, umjereno masnim obrokom i navedenim visokokaloričnim obrokom s visokim sadržajem masti.
9. Farmaceutski pripravak za uporabu prema bilo kojem od patentnih zahtjeva 1 do 8, naznačen time, da spomenuta hrana sadrži umjereno kaloričan, umjereno masan obrok.
10. Farmaceutski pripravak za uporabu prema bilo kojem od prethodnih patentnih zahtjeva, naznačen time, da je plan liječenja za spomenuti naltrekson ili njegovu farmaceutski prihvatljivu sol i spomenuti bupropion ili njegovu farmaceutski prihvatljivu sol, kako slijedi: oko 8 mg spomenutog naltreksona ili njegove farmaceutski prihvatljive soli i oko 90 mg spomenutog bupropiona ili njegove farmaceutski prihvatljive soli za prvi tjedan liječenja; oko 16 mg spomenutog naltreksona ili njegove farmaceutski prihvatljive soli i oko 180 mg spomenutog bupropiona ili njegove farmaceutski prihvatljive soli za drugi tjedan liječenja; oko 24 mg spomenutog naltreksona ili njegove farmaceutski prihvatljive soli i oko 270 mg spomenutog bupropiona ili njegove farmaceutski prihvatljive soli za treći tjedan liječenja; i oko 32 mg spomenutog naltreksona ili njegove farmaceutski prihvatljive soli i oko 360 mg spomenutog bupropiona ili njegove farmaceutski prihvatljive soli za četvrti i bilo koji od naknadnih tjedana liječenja.
11. Farmaceutski pripravak za uporabu prema bilo kojem od prethodnih patentnih zahtjeva, naznačen time, da se spomenuti naltrekson ili njegova farmaceutski prihvatljiva sol i spomenuti bupropion ili njegova farmaceutski prihvatljiva sol daju kao dvije tablete od 8 mg naltreksona s produljenim otpuštanjem dva puta dnevno i dvije tablete od 90 mg bupropiona s produljenim otpuštanjem dva puta dnevno.
12. Farmaceutski pripravak za uporabu prema bilo kojem od prethodnih patentnih zahtjeva, naznačen time, da se spomenuti naltrekson ili njegova farmaceutski prihvatljiva sol i spomenuti bupropion ili njegova farmaceutski prihvatljiva sol daju u trajanju od najmanje 28 tjedana.
13. Farmaceutski pripravak za uporabu prema bilo kojem od prethodnih patentnih zahtjeva, naznačen time, da se spomenuti naltrekson ili njegova farmaceutski prihvatljiva sol i spomenuti bupropion ili njegova farmaceutski prihvatljiva sol daju u trajanju od najmanje 56 tjedana.
14. Farmaceutski pripravak za uporabu prema bilo kojem od prethodnih patentnih zahtjeva, naznačen time, da se pripravak koristi za utjecanje na gubljenje težine, smanjenje kardiovaskularnih rizičnih faktora, povećanje osjetljivosti na inzulin, smanjenje žudnje za hranom, liječenje stanja visceralne masnoće, olakšanje dobivanja na težini ili poticanje gubitka težine za vrijeme prestanka pušenja, i omogućavanje terapije za gubljenje težine kod pacijenata s teškom depresijom.
HRP20240115TT 2010-12-03 2011-12-02 Povećavanje bioraspoloživosti lijeka u terapiji naltreksonom HRP20240115T1 (hr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US41939510P 2010-12-03 2010-12-03
EP21152314.7A EP3884947B1 (en) 2010-12-03 2011-12-02 Increasing drug bioavailability in naltrexone therapy

Publications (1)

Publication Number Publication Date
HRP20240115T1 true HRP20240115T1 (hr) 2024-06-07

Family

ID=46172304

Family Applications (3)

Application Number Title Priority Date Filing Date
HRP20240115TT HRP20240115T1 (hr) 2010-12-03 2011-12-02 Povećavanje bioraspoloživosti lijeka u terapiji naltreksonom
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

Family Applications After (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

Country Status (26)

Country Link
US (1) US20130245056A1 (hr)
EP (4) EP2646031B9 (hr)
JP (5) JP6008866B2 (hr)
KR (5) KR102391511B1 (hr)
CN (1) CN103313711A (hr)
AR (2) AR093182A1 (hr)
AU (2) AU2011336304B2 (hr)
BR (1) BR112013013390A2 (hr)
CA (2) CA3239386A1 (hr)
CL (1) CL2013001564A1 (hr)
CY (2) CY1118968T1 (hr)
DK (3) DK2646031T3 (hr)
ES (2) ES2625527T3 (hr)
FI (1) FI3884947T3 (hr)
HR (3) HRP20240115T1 (hr)
HU (3) HUE034393T2 (hr)
IL (3) IL226504B (hr)
LT (3) LT2646031T (hr)
MX (1) MX356801B (hr)
PL (3) PL3884947T3 (hr)
PT (3) PT3884947T (hr)
RS (3) RS65198B1 (hr)
RU (1) RU2640561C2 (hr)
SI (3) SI3884947T1 (hr)
TW (1) TWI618536B (hr)
WO (1) WO2012075459A1 (hr)

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Also Published As

Publication number Publication date
RU2017144631A3 (hr) 2021-04-13
HUE053831T2 (hu) 2021-07-28
RS62149B1 (sr) 2021-08-31
KR101984500B1 (ko) 2019-05-31
IL226504B (en) 2021-01-31
HRP20170734T1 (hr) 2017-08-11
RU2640561C2 (ru) 2018-01-09
ES2625527T9 (es) 2018-09-25
JP2024071605A (ja) 2024-05-24
SI3222280T1 (sl) 2021-11-30
EP3884947B1 (en) 2023-11-15
LT3884947T (lt) 2024-03-12
EP2646031A4 (en) 2014-04-23
EP3222280B1 (en) 2021-01-20
EP2646031B1 (en) 2017-02-22
JP7025319B2 (ja) 2022-02-24
LT3222280T (lt) 2021-05-10
CA2819262C (en) 2024-05-28
FI3884947T3 (fi) 2024-01-30
ES2625527T3 (es) 2017-07-19
LT2646031T (lt) 2017-06-26
TW201304780A (zh) 2013-02-01
PT3222280T (pt) 2021-04-22
PT3884947T (pt) 2024-02-16
AU2011336304A1 (en) 2013-07-11
ES2866879T3 (es) 2021-10-20
JP6008866B2 (ja) 2016-10-19
US20130245056A1 (en) 2013-09-19
KR20200044158A (ko) 2020-04-28
CA3239386A1 (en) 2012-06-07
JP2022060331A (ja) 2022-04-14
EP2646031A1 (en) 2013-10-09
AU2011336304B2 (en) 2017-03-30
PL2646031T3 (pl) 2017-08-31
RS56014B1 (sr) 2017-09-29
CL2013001564A1 (es) 2014-05-02
BR112013013390A2 (pt) 2016-09-06
CA2819262A1 (en) 2012-06-07
IL279626A (en) 2021-03-01
MX2013006071A (es) 2013-10-01
RU2017144631A (ru) 2019-02-18
JP2019056004A (ja) 2019-04-11
EP4349369A2 (en) 2024-04-10
JP2013544290A (ja) 2013-12-12
AR093182A1 (es) 2015-05-27
JP2016210809A (ja) 2016-12-15
MX356801B (es) 2018-06-13
IL270841A (en) 2020-01-30
TWI618536B (zh) 2018-03-21
KR20190058702A (ko) 2019-05-29
EP3884947A1 (en) 2021-09-29
RS65198B1 (sr) 2024-03-29
DK3222280T3 (da) 2021-04-19
PL3884947T3 (pl) 2024-05-06
RU2013127423A (ru) 2015-01-10
EP4349369A3 (en) 2024-05-15
CY1118968T1 (el) 2018-01-10
JP6456890B2 (ja) 2019-01-23
KR20210063473A (ko) 2021-06-01
AR124500A2 (es) 2023-04-05
KR102105857B1 (ko) 2020-05-04
EP2646031B9 (en) 2018-01-10
SI2646031T1 (sl) 2017-07-31
DK2646031T3 (en) 2017-05-22
HUE065852T2 (hu) 2024-06-28
PT2646031T (pt) 2017-05-25
KR20140035320A (ko) 2014-03-21
SI3884947T1 (sl) 2024-06-28
WO2012075459A1 (en) 2012-06-07
HRP20210618T1 (hr) 2021-09-17
CN103313711A (zh) 2013-09-18
EP3222280A1 (en) 2017-09-27
KR20180069089A (ko) 2018-06-22
AU2017204309A1 (en) 2017-07-13
CY1124331T1 (el) 2022-07-22
DK3884947T3 (da) 2024-01-22
PL3222280T3 (pl) 2021-11-29
HUE034393T2 (en) 2018-02-28
KR102258043B1 (ko) 2021-05-28
KR102391511B1 (ko) 2022-04-26

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