DK2608670T3 - Fremgangsmåde til behandling af antipsykotikum-induceret vægtstigning - Google Patents
Fremgangsmåde til behandling af antipsykotikum-induceret vægtstigning Download PDFInfo
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- DK2608670T3 DK2608670T3 DK11820517.8T DK11820517T DK2608670T3 DK 2608670 T3 DK2608670 T3 DK 2608670T3 DK 11820517 T DK11820517 T DK 11820517T DK 2608670 T3 DK2608670 T3 DK 2608670T3
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- compound
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- atypical
- antipsychotic
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Claims (20)
1. Forbindelse med strukturen:
eller et farmaceutisk acceptabelt salt deraf, til anvendelse i en fremgangsmåde til reducering af antipsykotikum-induceret vægtstigning.
2. Sammensætning, der omfatter et atypisk antipsykotikum og en forbindelse med strukturen: eller et farmaceutisk acceptabelt salt deraf.
3. Sammensætning ifølge krav 2, hvor det atypiske antipsykotikum er valgt blandt olanzapin, clozapin, risperidon, quetiapin, aripiprazol, ziprasidon og farmaceutisk acceptable salte deraf.
4. Sammensætning ifølge krav 2 eller 3, hvor sammensætningen er i form af en oral tablet.
5. Forbindelse til anvendelse ifølge krav 1, hvor vægtstigningen er induceret af indgivelse af et atypisk antipsykotikum.
6. Forbindelse til anvendelse ifølge krav 5, hvor det atypiske antipsykotikum er valgt fra gruppen bestående af olanzapin, clozapin, risperidon, quetiapin, aripiprazol, ziprasidon og farmaceutisk acceptable salte deraf.
7. Forbindelse til anvendelse ifølge krav 6, hvor det atypiske antipsykotikum anvendes i behandlingen af skizofreni, bipolar sygdom, demens, akut mani, alvorlig depression og psykotisk agitation.
8. Forbindelse til anvendelse ifølge et hvilket som helst af kravene 1 eller 5 til 7, hvor forbindelsen indgives i en daglig dosis på fra ca. 3 til ca. 30 mg om dagen.
9. Forbindelse til anvendelse ifølge krav 8, hvor forbindelsen indgives i en daglig dosis på fra ca. 3 til ca. 15 mg om dagen.
10. Forbindelse til anvendelse ifølge krav 9, hvor den daglige dosis er ca. 5 mg om dagen.
11. Forbindelse til anvendelse ifølge krav 9 eller krav 10, hvor den daglige dosis indgives peroralt.
12. Forbindelse til anvendelse ifølge et hvilket som helst af kravene 5 til 11, hvor patienten har taget ca. 2, 3, 4, 5, 10, 15 eller 20 % kropsvægt på inden for en periode på en uge fra starten af behandlingen med atypisk antipsykotikum, inden for en periode på en uge under behandlingen med atypisk antipsykotikum, inden for en periode på en måned fra starten af behandlingen med atypisk antipsykotikum eller inden for en periode på en måned under behandlingen med atypisk antipsykotikum.
13. Forbindelse til anvendelse ifølge et hvilket som helst af kravene 5 til 11, hvor patienten har taget ca. 2, 3, 4, 5, 10, 15 eller 20 % kropsvægt på inden for en periode på en uge umiddelbart forud for starten på indgivelsen af forbindelsen eller inden for en periode på en måned umiddelbart forud for starten på indgivelsen af forbindelsen.
14. Forbindelse til anvendelse ifølge et hvilket som helst af kravene 5 til 11, hvor patienten inden for et års behandling med atypisk antipsykotikum har taget ca. 5, 10, 15, eller 20 % kropsvægt på.
15. Forbindelse til anvendelse ifølge et hvilket som helst af kravene 5 til 11, hvor forbindelsen indgives forud for den daglige dosis af det atypiske antipsykotikum, eller hvor forbindelsen indgives efter den daglige dosis af atypisk antipsykotikum.
16. Forbindelse til anvendelse ifølge krav 1,hvor forbindelsen indgives til patienten forud for begyndelsen på den antipsykotikum-inducerede vægtstigning, eller hvor forbindelsen indgives i starten af patientens behandling med atypisk antipsykotikum.
17. Forbindelse med strukturen eller et farmaceutisk acceptabelt salt deraf, til anvendelse i en fremgangsmåde til dæmpning affødeindtaget eller en fremgangsmåde til reducering af ghrelin-niveauerne, hvor den forhøjede appetit eller de forhøjede ghrelin-niveauer er induceret af indgivelse af et atypisk antipsykotikum.
18. Forbindelse med strukturen
eller et farmaceutisk acceptabelt salt deraf, til anvendelse i en fremgangsmåde til reducering af ghrelin-niveauet i mavetarmkanalen.
19. Forbindelse til anvendelse ifølge krav 17 eller krav 18, hvor forbindelsen indgives i en daglig dosis på fra ca. 3 til ca. 30 mg om dagen, fortrinsvis i en daglig dosis på fra ca. 3 til ca. 15 mg om dagen.
20. Forbindelse til anvendelse ifølge krav 19, hvor den daglige dosis er ca. 5 mg om dagen.
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