HRP20150848T1 - Morfinski spojevi - Google Patents

Morfinski spojevi Download PDF

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Publication number
HRP20150848T1
HRP20150848T1 HRP20150848TT HRP20150848T HRP20150848T1 HR P20150848 T1 HRP20150848 T1 HR P20150848T1 HR P20150848T T HRP20150848T T HR P20150848TT HR P20150848 T HRP20150848 T HR P20150848T HR P20150848 T1 HRP20150848 T1 HR P20150848T1
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HR
Croatia
Prior art keywords
disorders
diseases
pain
homocysteine
caused
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HRP20150848TT
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English (en)
Inventor
Roger Tung
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Concert Pharmaceuticals Inc.
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Publication of HRP20150848T1 publication Critical patent/HRP20150848T1/hr

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    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12QMEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
    • C12Q1/00Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
    • C12Q1/26Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase
    • C12Q1/28Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving oxidoreductase involving peroxidase
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • 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
    • A61K31/4709Non-condensed quinolines and containing further heterocyclic rings
    • 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
    • A61K31/33Heterocyclic 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
    • A61K31/49Cinchonan derivatives, e.g. quinine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/14Antitussive agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B59/00Introduction of isotopes of elements into organic compounds ; Labelled organic compounds per se
    • C07B59/002Heterocyclic compounds
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/08Bridged systems
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483Physical analysis of biological material
    • G01N33/487Physical analysis of biological material of liquid biological material
    • G01N33/49Blood
    • G01N33/491Blood by separating the blood components
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483Physical analysis of biological material
    • G01N33/487Physical analysis of biological material of liquid biological material
    • G01N33/493Physical analysis of biological material of liquid biological material urine

Claims (22)

1. Tvar formule I: [image] ili njena farmaceutski prihvatljiva sol, pri čemu: R1 je CD3; i R2 je CH3, za uporabu u liječenju subjekta koji pati od ili je podložan bolesti ili stanju odabranih između emocionalne labilnosti; pseudobulbarnog afekta; autizma; neuroloških poremećaja; neurodegenerativnih bolesti; ozljeda mozga; poremećaja narušavanja svijesti; kardiovaskularnih bolesti; glaukoma; tardivne diskinezije; dijabetičke neuropatije; retinopatskih bolesti; bolesti ili poremećaja uzrokovanih homocisteinom induciranom apoptozom; bolesti ili poremećaja uzrokovanih povećanom razinom homocisteina; kronične boli; tvrdokorne boli; neuropatske boli; simpatički posredovane boli; boli povezane s gastrointestinalnom disfunkcijom; epileptičkih napada; tinitusa; seksualne disfunkcije; tvrdokornog kašlja; dermatitisa; poremećaja ovisnosti; Rett sindroma (RTT); poremećaja glasa zbog nekontroliranog spazma mišića larinksa; neurotoksičnosti metotreksata; i umora uzrokovanog karcinomom.
2. Tvar ili njena farmaceutski prihvatljiva sol iz patentnog zahtjeva 1, pri čemu je bilo koji atom koji nije utvrđen da je deuterij prisutan u svom prirodno zastupljenom izotopnom obliku.
3. Apirogeni sastav koji obuhvaća: tvar ili njenu farmaceutski prihvatljivu sol iz bilo kojeg od prethodnih patentnih zahtjeva, za uporabu u liječenju subjekta koji pati od ili je podložan bolesti ili stanju odabranih između emocionalne labilnosti; pseudobulbarnog afekta; autizma; neuroloških poremećaja; neurodegenerativnih bolesti; ozljeda mozga; poremećaja narušavanja svijesti; kardiovaskularnih bolesti; glaukoma; tardivne diskinezije; dijabetičke neuropatije; retinopatskih bolesti; bolesti ili poremećaja uzrokovanih homocisteinom induciranom apoptozom; bolesti ili poremećaja uzrokovanih povećanom razinom homocisteina; kronične boli; tvrdokorne boli; neuropatske boli; simpatički posredovane boli; boli povezane s gastrointestinalnom disfunkcijom; epileptičkih napada; tinitusa; seksualne disfunkcije; tvrdokornog kašlja; dermatitisa; poremećaja ovisnosti; Rett sindroma (RTT); poremećaja glasa zbog nekontroliranog spazma mišića larinksa; neurotoksičnosti metotreksata; i umora uzrokovanog karcinomom; i prihvatljivi nosač.
4. Sastav iz patentnog zahtjeva 3 formuliran za farmaceutsku primjenu i pri čemu je nosač farmaceutski prihvatljivi nosač.
5. Tvar, njena farmaceutski prihvatljiva sol ili sastav prema patentnom zahtjevu 4, za uporabu u liječenju neuropatske boli ili pseudobulbarnog afekta.
6. Tvar, njena farmaceutski prihvatljiva sol ili sastav prema patentnom zahtjevu 5, za uporabu u liječenju pseudobulbarnog afekta.
7. Sastav u skladu s bilo kojim od patentnih zahtjeva 3-6, nadalje obuhvaća drugi terapijski agens koristan u liječenju ili sprečavanju bolesti ili stanja odabranih između emocionalne labilnosti; pseudobulbarnog afekta; autizma; neuroloških poremećaja; neurodegenerativnih bolesti; ozljeda mozga; poremećaja narušavanja svijesti; kardiovaskularnih bolesti; glaukoma; tardivne diskinezije; dijabetičke neuropatije; retinopatskih bolesti; bolesti ili poremećaja uzrokovanih homocisteinom induciranom apoptozom; bolesti ili poremećaja uzrokovanih povećanom razinom homocisteina; kronične boli; tvrdokorne boli; neuropatske boli; simpatički posredovane boli; boli povezane s gastrointestinalnom disfunkcijom; epileptičkih napada; tinitusa; seksualne disfunkcije; tvrdokornog kašlja; dermatitisa; poremećaja ovisnosti; Rett sindroma (RTT); poremećaja glasa zbog nekontroliranog spazma mišića larinksa; neurotoksičnosti metotreksata; i umora uzrokovanog karcinomom.
8. Sastav iz patentnog zahtjeva 7, pri čemu je drugi terapijski agens odabran između kinidina, kinidin sulfata, oksikodona i gabapentina.
9. Zasebni oblici doziranja: I. tvari, njena farmaceutski prihvatljiva sol ili sastav prema bilo kojem od patentnih zahtjeva 1-4; i II. drugi terapijski agens koristan u liječenju ili sprečavanju bolesti ili stanja odabranih između emocionalne labilnosti; pseudobulbarnog afekta; autizma; neuroloških poremećaja; neurodegenerativnih bolesti; ozljeda mozga; poremećaja narušavanja svijesti; kardiovaskularnih bolesti; glaukoma; tardivne diskinezije; dijabetičke neuropatije; retinopatskih bolesti; bolesti ili poremećaja uzrokovanih homocisteinom induciranom apoptozom; bolesti ili poremećaja uzrokovanih povećanom razinom homocisteina; kronične boli; tvrdokorne boli; neuropatske boli; simpatički posredovane boli; boli povezane s gastrointestinalnom disfunkcijom; epileptičkih napada; tinitusa; seksualne disfunkcije; tvrdokornog kašlja; dermatitisa; poremećaja ovisnosti; Rett sindroma (RTT); poremećaja glasa zbog nekontroliranog spazma mišića larinksa; neurotoksičnosti metotreksata; i umora uzrokovanog karcinomom, pri čemu navedena tvar, njena farmaceutski prihvatljiva sol ili sastav i drugi terapijski agens nisu međusobno povezani.
10. Zasebni oblici doziranja u skladu s patentnim zahtjevom 9, pri čemu je navedeni drugi terapijski agens odabran između kinidina, kinidin sulfata, oksikodona i gabapentina.
11. Pakiranje koje obuhvaća zasebne oblike doziranja u skladu s patentnim zahtjevom 9 ili 10.
12. Zasebni oblici doziranja ili pakiranje u skladu s bilo kojim od patentnih zahtjeva 9-11, pri čemu je navedeni drugi terapijski agens za istovremenu primjenu.
13. Zasebni oblici doziranja ili pakiranje u skladu s bilo kojim od patentnih zahtjeva 9-11, pri čemu je navedeni drugi terapijski agens za zasebnu primjenu.
14. Sastav, zasebni oblici doziranja ili pakiranje u skladu s bilo kojim od patentnih zahtjeva 7-13, za uporabu u liječenju subjekta subjekta koji pati od ili je podložan dijabetičkoj neuropatiji, pri čemu je drugi agens kinidin sulfat.
15. Sastav, zasebni oblici doziranja ili pakiranje u skladu s bilo kojim od patentnih zahtjeva 7-14, koji obuhvaćaju 10-60 mg tvari formule I ili njene farmaceutski prihvatljive soli, i 2.5-30 mg kinidina.
16. Uporaba tvari formule I [image] ili njene farmaceutski prihvatljive soli, pri čemu: R1 je CD3; i R2 je CH3, za uporabu u proizvodnji lijeka za liječenje subjekta koji pati od ili je podložan bolesti ili stanju odabranih između emocionalne labilnosti; pseudobulbarnog afekta; autizma; neuroloških poremećaja; neurodegenerativnih bolesti; ozljeda mozga; poremećaja narušavanja svijesti; kardiovaskularnih bolesti; glaukoma; tardivne diskinezije; dijabetičke neuropatije; retinopatskih bolesti; bolesti ili poremećaja uzrokovanih homocisteinom induciranom apoptozom; bolesti ili poremećaja uzrokovanih povećanom razinom homocisteina; kronične boli; tvrdokorne boli; neuropatske boli; simpatički posredovane boli; boli povezane s gastrointestinalnom disfunkcijom; epileptičkih napada; tinitusa; seksualne disfunkcije; tvrdokornog kašlja; dermatitisa; poremećaja ovisnosti; Rett sindroma (RTT); poremećaja glasa zbog nekontroliranog spazma mišića larinksa; neurotoksičnosti metotreksata; i umora uzrokovanog karcinomom.
17. Uporaba u skladu s patentnim zahtjevom 16, pri čemu je bilo koji atom koji nije utvrđen da je deuterij prisutan u svom prirodno zastupljenom izotopnom obliku.
18. Uporaba u skladu s patentnim zahtjevom 16 ili 17, pri čemu je bolest ili stanje neuropatska bol ili pseudobulbarni afekt.
19. Uporaba u skladu s patentnim zahtjevom 18, pri čemu je bolest ili stanje pseudobulbarni afekt.
20. Uporaba iz bilo kojeg od patentnih zahtjeva 16-19, zajedno s drugim terapijskim agensom korisnim u liječenju ili prevenciji bolesti ili stanja odabranih između emocionalne labilnosti; pseudobulbarnog afekta; autizma; neuroloških poremećaja; neurodegenerativnih bolesti; ozljeda mozga; poremećaja narušavanja svijesti; kardiovaskularnih bolesti; glaukoma; tardivne diskinezije; dijabetičke neuropatije; retinopatskih bolesti; bolesti ili poremećaja uzrokovanih homocisteinom induciranom apoptozom; bolesti ili poremećaja uzrokovanih povećanom razinom homocisteina; kronične boli; tvrdokorne boli; neuropatske boli; simpatički posredovane boli; boli povezane s gastrointestinalnom disfunkcijom; epileptičkih napada; tinitusa; seksualne disfunkcije; tvrdokornog kašlja; dermatitisa; poremećaja ovisnosti; Rett sindroma (RTT); poremećaja glasa zbog nekontroliranog spazma mišića larinksa; neurotoksičnosti metotreksata; i umora uzrokovanog karcinomom.
21. Uporaba u skladu s patentnim zahtjevom 20, pri čemu je drugi terapijski agens odabran između kinidina, kinidin sulfata, oksikodona i gabapentina.
22. Uporaba u skladu s patentnim zahtjevom 20 ili 21, pri čemu je drugi terapijski agens kinidin, i pri čemu je količina doziranja tvari formule I ili njene farmaceutski prihvatljive soli 10-60 mg, a količina doziranja kinidina je 2.5-30 mg.
HRP20150848TT 2007-05-01 2015-08-10 Morfinski spojevi HRP20150848T1 (hr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US91513007P 2007-05-01 2007-05-01
US91666207P 2007-05-08 2007-05-08
US97604407P 2007-09-28 2007-09-28
EP11000764.8A EP2357183B1 (en) 2007-05-01 2008-04-30 Morphinan compounds

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HRP20150848T1 true HRP20150848T1 (hr) 2015-09-25

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Family Applications (5)

Application Number Title Priority Date Filing Date
HRP20230745TT HRP20230745T3 (hr) 2007-05-01 2008-04-30 Spojevi morfina
HRP20140903AT HRP20140903T1 (hr) 2007-05-01 2014-09-22 Morfinski spojevi
HRP20150809TT HRP20150809T1 (hr) 2007-05-01 2015-07-24 Spojevi morfinana
HRP20150848TT HRP20150848T1 (hr) 2007-05-01 2015-08-10 Morfinski spojevi
HRP20160521TT HRP20160521T8 (hr) 2007-05-01 2016-05-16 Morfinski spojevi

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HRP20230745TT HRP20230745T3 (hr) 2007-05-01 2008-04-30 Spojevi morfina
HRP20140903AT HRP20140903T1 (hr) 2007-05-01 2014-09-22 Morfinski spojevi
HRP20150809TT HRP20150809T1 (hr) 2007-05-01 2015-07-24 Spojevi morfinana

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HRP20160521TT HRP20160521T8 (hr) 2007-05-01 2016-05-16 Morfinski spojevi

Country Status (15)

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US (6) US9314440B2 (hr)
EP (5) EP3093290B1 (hr)
BR (1) BRPI0811478B8 (hr)
CA (3) CA2945581C (hr)
CY (1) CY1117826T1 (hr)
DK (4) DK2357183T3 (hr)
ES (5) ES2523286T3 (hr)
FI (1) FI3825306T3 (hr)
HK (5) HK1178154A1 (hr)
HR (5) HRP20230745T3 (hr)
HU (3) HUE025569T2 (hr)
LT (1) LT3825306T (hr)
PL (3) PL2357183T3 (hr)
PT (5) PT2792662T (hr)
SI (2) SI2792662T1 (hr)

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PT2792662T (pt) 2007-05-01 2016-07-07 Concert Pharmaceuticals Inc Compostos de morfinano
WO2017020002A1 (en) * 2015-07-30 2017-02-02 Concert Pharmaceuticals, Inc. Deuterated morphinan compounds for use in treating agitation
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