DK2800563T3 - Dpa-berigede sammensætninger af flerumættede omega-3-fedtsyrer i fri syreform - Google Patents
Dpa-berigede sammensætninger af flerumættede omega-3-fedtsyrer i fri syreform Download PDFInfo
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- DK2800563T3 DK2800563T3 DK13733671.5T DK13733671T DK2800563T3 DK 2800563 T3 DK2800563 T3 DK 2800563T3 DK 13733671 T DK13733671 T DK 13733671T DK 2800563 T3 DK2800563 T3 DK 2800563T3
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- A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
- A61K47/32—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. carbomers, poly(meth)acrylates, or polyvinyl pyrrolidone
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Claims (16)
1. Farmaceutisk sammensætning omfattende: eicosapentaensyre (omega-3) (EPA), i fri syreform, i en mængde på 50 % (m/m) til 60 % (m/m); docosahexaensyre (omega-3) (DHA), i fri syreform, i en mængde på 17 % (m/m) til 23 % (m/m) og docosapentaensyre (omega-3) (DPA), i fri syreform, i en mængde på mindst 1 % (m/m); hvor m/m betegner den procentvise vægtandel af alle fedtsyrer i sammensætningen.
2. Farmaceutisk sammensætning ifølge krav 1, hvor mindst 95 vægt-% af den flerumættede fedtsyre i sammensætningen er til stede i fri syreform.
3. Farmaceutisk sammensætning ifølge krav 1, hvor DPA er til stede i en mængde på højst 10 % (m/m).
4. Farmaceutisk sammensætning ifølge krav 1, hvor DPA er til stede i en mængde på 1 % (m/m) til 8 % (m/m).
5. Farmaceutisk sammensætning ifølge krav 1, hvor EPA er til stede i en mængde på 55 % (m/m).
6. Farmaceutisk sammensætning ifølge krav 1, hvor DHA er til stede i en mængde på 20 % (m/m).
7. Farmaceutisk sammensætning ifølge krav 1, hvor mindst 90 vægt-% af den samlede flerumættede fedtsyre i sammensætningen er til stede i fri syreform.
8. Enhedsdoseringsform, der egner sig til oral administration, omfattende en kapsel, hvor kapslen indkapsler mindst 500 mg af den farmaceutiske sammensætning ifølge krav 1.
9. Enhedsdoseringsform ifølge krav 8, hvor kapslen indkapsler mindst 1000 mg af den farmaceutiske sammensætning ifølge krav 1.
10. Enhedsdoseringsform ifølge krav 9, hvor kapslen er en blød gelatinekapsel.
11. Farmaceutisk sammensætning ifølge krav 1 til anvendelse til behandling af svær hypertriglyceridæmi hos en patient, der før behandling har serum- eller plasmatriglyceridniveauer >500 mg/dl, hvilken behandling omfatter oral administration af den farmaceutiske sammensætning ifølge krav 1 i en mængde på mindst 2 g pr. dag og har en varighed på mindst 30 dage.
12. Farmaceutisk sammensætning til anvendelse ifølge krav 11, hvor behandlingen endvidere omfatter oral administration af en effektiv mængde af et statin.
13. Farmaceutisk sammensætning til anvendelse ifølge krav 12, hvor statinet er udvalgt fra gruppen bestående af pravastatin, lovastatin, simvastatin, atorvastatin, fluvastatin, rosuvastatin og pitavastatin.
14. Farmaceutisk sammensætning ifølge krav 1 til anvendelse til behandling af hypertriglyceridæmi hos patienter, der har serum- eller plasmatriglyceridniveauer på 200 mg/dl til 500 mg/dl på statinbehandling, hvilken behandling omfatter oral administration af en effektiv mængde af et statin og mindst 2 g pr. dag af den farmaceutiske sammensætning ifølge krav 1.
15. Farmaceutisk sammensætning til anvendelse ifølge krav 11 eller krav 14, hvor mængden af den farmaceutiske sammensætning ifølge krav 1 er mindst 3 g pr. dag.
16. Farmaceutisk sammensætning til anvendelse ifølge krav 11 eller krav 14, hvor mængden af den farmaceutiske sammensætning ifølge krav 1 er mindst 4 g pr. dag.
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| PCT/US2013/020398 WO2013103902A1 (en) | 2012-01-06 | 2013-01-04 | Dpa-enriched compositions of omega-3 polyunsaturated fatty acids in free acid form |
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