HRP20191029T1 - Derivati morfinana radi liječenja predoziranja lijekom - Google Patents

Derivati morfinana radi liječenja predoziranja lijekom Download PDF

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Publication number
HRP20191029T1
HRP20191029T1 HRP20191029TT HRP20191029T HRP20191029T1 HR P20191029 T1 HRP20191029 T1 HR P20191029T1 HR P20191029T T HRP20191029T T HR P20191029TT HR P20191029 T HRP20191029 T HR P20191029T HR P20191029 T1 HRP20191029 T1 HR P20191029T1
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HR
Croatia
Prior art keywords
compound
use according
period
overdose
opioid
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HRP20191029TT
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English (en)
Inventor
Bernard Silverman
Fu Fen-Ni
Guo Chengyun
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Alkermes Pharma Ireland Limited
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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Application filed by Alkermes Pharma Ireland Limited filed Critical Alkermes Pharma Ireland Limited
Publication of HRP20191029T1 publication Critical patent/HRP20191029T1/hr

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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
    • A61K31/435Heterocyclic 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
    • A61K31/4748Quinolines; Isoquinolines forming part of bridged ring systems
    • 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
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/36Opioid-abuse
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D221/00Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • C07D221/02Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
    • C07D221/22Bridged ring systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D221/00Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00
    • C07D221/02Heterocyclic compounds containing six-membered rings having one nitrogen atom as the only ring hetero atom, not provided for by groups C07D211/00 - C07D219/00 condensed with carbocyclic rings or ring systems
    • C07D221/22Bridged ring systems
    • C07D221/28Morphinans

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Addiction (AREA)
  • Epidemiology (AREA)
  • Neurology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Psychiatry (AREA)
  • Emergency Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)

Claims (21)

1. Spoj koji sadrži formulu: za uporabu u postupku liječenja toksičnosti lijeka ili predoziranja lijekom kod subjekta kojem je nužno.
2. Spoj za uporabu sukladno patentnom zahtjevu 1, pri čemu navedena toksičnost ili predoziranje lijekom nastaje kao rezultat primjene opioida pacijentu koji nije ovisnik.
3. Spoj za uporabu sukladno patentnom zahtjevu 1 ili patentnom zahtjevu 2, pri čemu navedeni subjekt ima iskustvo s opioidom, a nije ovisnik o opoidima.
4. Spoj za uporabu sukladno patentnom zahtjevu 1, pri čemu se navedeni spoj primjenjuje u dnevnoj dozi od oko 3 do oko 20 mg/dnevno.
5. Spoj za uporabu sukladno patentnom zahtjevu 4, pri čemu je navedena dnevna doza oko 10 mg/dan.
6. Spoj za uporabu sukladno patentnom zahtjevu 1, pri čemu primjena spoja smanjuje simptome toksičnosti ili predoziranja lijekom tijekom perioda od najmanje 15 do oko 30 minuta.
7. Spoj za uporabu sukladno patentnom 6, pri čemu su simptomi predoziranja lijekom smanjeni za period od najmanje jednog sata, period od najmanje dva sata, period od najmanje tri sata, period od najmanje četiri sata ili period od najmanje osam sati.
8. Spoj za uporabu sukladno patentnom zahtjevu 6 ili patentnom zahtjevu 7, pri čemu navedena primjena sadrži oko 3 mg do oko 20 mg spoja.
9. Spoj za uporabu sukladno patentnom zahtjevu 6 ili patentnom zahtjevu 7, pri čemu su navedeni simptomi predoziranja odabrani iz smanjene brzine disanja, smanjene dubine disanja, apnee, komatoze, hipoksije, delirijske hipotenzije, bradikardije, smanjene temperature tijela, zadržavanja urina i suženja zjenica.
10. Spoj koji sadrži formulu: za uporabu u postupku liječenja opioidne toksičnosti ili predoziranja kod subjekta kojem je potrebno sadrži isporuku prvog antagonista receptora opioida nakon čega slijedi taj spoj.
11. Spoj za uporabu sukladno patentnom zahtjevu 10, pri čemu je prvi antagonist receptora opioida nalokson.
12. Spoj za uporabu sukladno patentnom zahtjevu 10 ili patentnom zahtjevu 11, pri čemu je navedeni subjekt korisnik opoida koji ima iskustvo s opioidom ali nije ovisnik.
13. Spoj za uporabu sukladno patentnom zahtjevu 11, pri čemu nabedenoj primjeni prethodi navedena primjena naloksona.
14. Spoj za uporabu sukladno patentnom zahtjevu 13, pri čemu navedena primjena naloksona smanjuje simptome predoziranja ili toksičnosti prije primjene spoja.
15. Spoj za uporabu sukladno patentnom zahtjevu 11, pri čemu se nalokson primjenjuje istodobno s tim spojem.
16. Spoj od formule: za uporabu u postupku liječenja akutne opioidne toksičnosti ili predoziranja tijemom razdoblja od preko jednog sata sadrži jednokratnu primjenu navedenog spoja subjektu kojem je nužno.
17. Spoj za uporabu sukladno patentnom zahtjevu 16, pri čemu je navedeni subjekt opioidno iskusan pacijent koji nije ovisnik.
18. Spoj za uporabu sukladno patentnom zahtjevu 16, pri čemu su simptomi opioidne toksičnosti ili predoziranja smanjeni tijekom razdoblja od više od jednog sata, tijekom razdoblja od više od četiri sata, tijekom razdoblja od više od osam sati ili tijekom razdoblja od više od dvadeset četiri sata.
19. Spoj od formule: radi uporabe u postupku za nekontrolirano liječenje opioidne toksičnosti ili predoziranja opioidom kod pacijenta kojem je nužno.
20. Spoj za uporabu sukladno patentnom zahtjevu 19, pri čemu je navedeno nekontrolirano liječenje djelotvorno tijekom razdoblja od preko jedog sata..
21. Sol L-malata koja sadrži formulu:
HRP20191029TT 2009-12-04 2019-06-07 Derivati morfinana radi liječenja predoziranja lijekom HRP20191029T1 (hr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US26688109P 2009-12-04 2009-12-04
PCT/US2010/052437 WO2011068594A1 (en) 2009-12-04 2010-10-13 Morphinan derivatives for the treatment of drug overdose
EP10834900.2A EP2506712B8 (en) 2009-12-04 2010-10-13 Morphinan derivatives for the treatment of drug overdose

Publications (1)

Publication Number Publication Date
HRP20191029T1 true HRP20191029T1 (hr) 2019-09-20

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
HRP20191029TT HRP20191029T1 (hr) 2009-12-04 2019-06-07 Derivati morfinana radi liječenja predoziranja lijekom

Country Status (19)

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US (4) US9119848B2 (hr)
EP (2) EP3569234A1 (hr)
JP (2) JP5691042B2 (hr)
AU (1) AU2010326676B2 (hr)
CA (1) CA2782529C (hr)
CY (1) CY1121646T1 (hr)
DK (1) DK2506712T3 (hr)
ES (1) ES2729679T3 (hr)
HR (1) HRP20191029T1 (hr)
HU (1) HUE043963T2 (hr)
LT (1) LT2506712T (hr)
ME (1) ME03468B (hr)
NZ (1) NZ600379A (hr)
PL (1) PL2506712T3 (hr)
PT (1) PT2506712T (hr)
RS (1) RS58894B1 (hr)
SI (1) SI2506712T1 (hr)
TR (1) TR201908514T4 (hr)
WO (1) WO2011068594A1 (hr)

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CA2782529A1 (en) 2011-06-09
JP2013512901A (ja) 2013-04-18
SI2506712T1 (sl) 2019-06-28
NZ600379A (en) 2014-05-30
AU2010326676A1 (en) 2012-06-21
EP2506712A1 (en) 2012-10-10
US9119848B2 (en) 2015-09-01
PL2506712T3 (pl) 2019-09-30
JP2015038139A (ja) 2015-02-26
US20110136848A1 (en) 2011-06-09
AU2010326676A2 (en) 2012-08-30
US20160051535A1 (en) 2016-02-25
EP2506712A4 (en) 2013-07-10
ME03468B (me) 2020-01-20
JP5691042B2 (ja) 2015-04-01
TR201908514T4 (tr) 2019-07-22
CY1121646T1 (el) 2020-07-31
RS58894B1 (sr) 2019-08-30
JP6216305B2 (ja) 2017-10-18
DK2506712T3 (da) 2019-06-03
US20200345718A1 (en) 2020-11-05
EP2506712B8 (en) 2019-06-19
CA2782529C (en) 2015-05-26
LT2506712T (lt) 2019-06-25
US20170333422A1 (en) 2017-11-23
WO2011068594A1 (en) 2011-06-09
HUE043963T2 (hu) 2019-09-30
PT2506712T (pt) 2019-05-31
ES2729679T3 (es) 2019-11-05
AU2010326676B2 (en) 2013-03-14
EP3569234A1 (en) 2019-11-20
EP2506712B1 (en) 2019-03-27

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