DK2777695T3 - Formuleringer til en tight-junction-effektor - Google Patents
Formuleringer til en tight-junction-effektor Download PDFInfo
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- DK2777695T3 DK2777695T3 DK14150323.5T DK14150323T DK2777695T3 DK 2777695 T3 DK2777695 T3 DK 2777695T3 DK 14150323 T DK14150323 T DK 14150323T DK 2777695 T3 DK2777695 T3 DK 2777695T3
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Claims (13)
1. Sammensætning til oral dosering omfattende en virksom mængde af et peptid ifølge SEQ ID NO:1, og omfattende første partikler med forsinket frigivelse, som frigiver peptidet i en patients tolvfingertarm efter indgivelse, hvor de første partikler med forsinket frigivelse omfatter: en kernepartikel; en coating omfattende peptidet ifølge SEQ ID NO:1 over kernepartiklen; og en coating med forsinket frigivelse uden om coatingen omfattende peptidet, hvor coatingen med forsinket frigivelse omfatter 1:1 co-polymer af poly-methacrylsyre og ethylacrylat; hvor coatingen med forsinket frigivelse er stabil i simuleret mavevæske og frigiver mindst 70 % af peptidet i de første partikler med forsinket frigivelse med ca. 90 minutters eksposition for simuleret tarmvæske med en pH-værdi på mere end 5.
2. Sammensætning til oral dosering ifølge krav 1, omfattende andre partikler med forsinket frigivelse, som frigiver peptidet i jejunum af en patient, hvor de andre partikler med forsinket frigivelse omfatter: en kernepartikel; en coating omfattende peptidet ifølge SEQ ID NO:1 over kernepartiklen; og en coating med forsinket frigivelse uden om coatingen omfattende peptidet, hvor coatingen med forsinket frigivelse omfatter 1:1 co-polymer af poly-methacrylsyre og ethylacrylat; hvor coatingen med forsinket frigivelse er stabil i simuleret mavevæske.
3. Sammensætning ifølge krav 1, hvor kernepartiklerne har en gennemsnitlig størrelse på fra 15 til 40 mesh.
4. Sammensætning ifølge krav 1, hvor kernepartikelmaterialet omfatter et sukkerstof, en oxid, cellulose, en organisk polymer eller et uorganisk salt.
5. Sammensætning ifølge krav 1, yderligere omfattende et overcoat-lag, der er påført over coatingen med forsinket frigivelse.
6. Sammensætning ifølge krav 5, hvor overcoat-laget omfatter hydroxypropylmethylcellulose (HPMC), sukker, polyethylenglycol, polyvinylpyrrolidon, poly-vinylalkohol, polyvinylacetat, hydroxypropylcellulose, methylcellulose og/eller ethylcellulose.
7. Sammensætning ifølge krav 1, hvor coatingen omfattende peptidet ifølge SEQ ID NO:1 yderligere omfatter et farmaceutisk acceptabelt bindemiddel, hvor bindemidlet eventuelt omfatter et sukkerstof, methylcellulose, polyvinylpyrrolidon, hydroxypropylcellulose, hydroxymethylcellulose og mikrokry-stallinsk cellulose.
8. Sammensætning ifølge krav 1, hvor coatingen med forsinket frigivelse yderligere omfatter talkum, et inert forarbejdningshjælpestof og/eller blødgører, eventuelt hvor det inerte forarbejdningshjælpestof omfatter siliconedioxid, talkum og/eller magnesiumstearat, og eventuelt hvor blødgøreren omfatter en citronsyreester, triacetin, phthalsyreester, dibutylsebacat, cetylalkohol, polyethylenglycol og/eller polysorbat.
9. Sammensætning ifølge krav 1, hvor sammensætningen er en kapsel.
10. Sammensætning ifølge krav 1, hvor den simulerede mavevæske og den simulerede tarmvæske ikke indeholder enzymer.
11. Sammensætning ifølge krav 1, hvor sammensætningen omfatter peptidet med fra 0,1 % til ca. 6 % baseret på sammensætningens samlede vægt.
12. Sammensætning ifølge krav 1, hvor den simulerede mavevæske har en pH-værdi på ca. 1,2, og eventuelt hvor mindre end 8 % af peptidet frigives i nærvær af simuleret mavevæske på ca. 60 minutter.
13. Sammensætning ifølge krav 1 til anvendelse ved en fremgangsmåde til behandling af gastrointestinal inflammation, hvor fremgangsmåden omfatter at indgive sammensætningen til et individ med behov herfor, eventuelt hvor individet har cøliaki eller har inflammatorisk tarmsygdom.
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| DE10332160A1 (de) * | 2003-07-15 | 2005-02-03 | Röhm GmbH & Co. KG | Multipartikuläre Arzneiform, enthaltend mucoadhaesiv formulierte Peptid- oder Protein-Wirkstoffe, sowie ein Verfahren zur Herstellung der Arzneiform |
| EP1648917A4 (en) * | 2003-07-15 | 2008-11-12 | Univ Maryland | AGONISTPOLYPEPTIDE OF THE RECEPTOR FOR ZOT AND ZONULIN |
| PE20060003A1 (es) * | 2004-03-12 | 2006-03-01 | Smithkline Beecham Plc | Formulacion farmaceutica polimerica para moldear por inyeccion |
| AU2006247731A1 (en) * | 2005-05-13 | 2006-11-23 | University Of Maryland - Baltimore | Method for assessing the effectiveness of a treatment regimen by determining zonulin |
| ES2459018T3 (es) | 2006-02-09 | 2014-05-07 | Alba Therapeutics Corporation | Formulaciones de efectores de la unión estrecha |
| WO2008043107A2 (en) * | 2006-10-06 | 2008-04-10 | Alba Therapeutics Corporation | Use of tight junction antagonists to treat inflammatory bowel disease |
| US8034776B2 (en) * | 2006-10-26 | 2011-10-11 | Alba Therapeutics Corporation | Materials and methods for the treatment of celiac disease |
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2007
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- 2007-02-09 MX MX2008010221A patent/MX2008010221A/es active IP Right Grant
- 2007-02-09 WO PCT/US2007/003486 patent/WO2007095092A2/en not_active Ceased
- 2007-02-09 CN CN2013101516785A patent/CN103301070A/zh active Pending
- 2007-02-09 KR KR1020087022059A patent/KR101393652B1/ko not_active Expired - Fee Related
- 2007-02-09 DK DK14150323.5T patent/DK2777695T3/da active
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- 2007-02-09 ZA ZA200807111A patent/ZA200807111B/xx unknown
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