DK1948219T3 - Vegf-analoger og fremgangsmåder til anvendelse - Google Patents
Vegf-analoger og fremgangsmåder til anvendelse Download PDFInfo
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- DK1948219T3 DK1948219T3 DK06836213T DK06836213T DK1948219T3 DK 1948219 T3 DK1948219 T3 DK 1948219T3 DK 06836213 T DK06836213 T DK 06836213T DK 06836213 T DK06836213 T DK 06836213T DK 1948219 T3 DK1948219 T3 DK 1948219T3
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Claims (14)
1. Modificeret vaskulær endothelial vækstfaktor (VEGF) omfattende mindst en mutation som forårsager den modificerede VEGF til at agere som en receptorantagonist, hvor mutationen resulterer i en reduktion i bioaktivitet sammenlignet med vildtype VEGF, og hvor mutationen er en basisk aminosyre-substitution ved en position svarende til position 83 af SEQ ID Nr. :4, hvor substitutionen er valgt fra gruppen bestående af I83K og I83R.
2. VEGF-receptorantagonist ifølge krav 1, hvor antagonisten omfatter en eller flere yderligere basiske aminosyresubstitutioner svarende til gruppen bestående af positioner 44, 67, 72, 73 og 87 af SEQ ID Nr. :4, hvor den yderligere substitution er en eller flere substitutioner valgt fra gruppen bestående af E72R, E73R, E72K, E73K, E44R, E44K, Q87K, Q87L og E67K.
3. VEGF-receptorantagonist ifølge krav 1 og 2 endvidere omfattende en eller flere mutationer der forhindrer neutrophilin-1 binding, og endvidere omfattende en eller flere basiske aminosyresubstitutioner valgt fra gruppen bestående af E44, E67, E72, og Q87 af SEQ ID Nr.:4.
4. VEGF-receptorantagonist ifølge krav 1 og 2, hvor antagonisten omfatter en eller flere yderligere aminosyresubstitutioner i aminosyrer svarende til positionerne 111-165 af SEQ ID Nr.: 4 hvilke forhindrer neurophilin-1 binding, hvor substitutionen er ved positionen svarende til C146 eller C160 af SEQ ID Nr.: 4 og hvor substitutionen er valgt fra gruppen bestående af C146S og C160S.
5. VEGF-receptorantagonist ifølge krav 1 og 2, hvor antagonisten omfatter en eller flere yderligere aminosyresubstitutioner hvilke reducerer eller forhindrer proteasenedbrydning af antagonisten, hvor den ene eller flere yderligere aminosyresubstitutioner er valgt fra gruppen af positioner svarende til positionerne Alll og A148 af SEQ ID Nr.:4, hvor substitutionen er en eller flere valgt fra gruppen bestående af Al IIP og A148P.
6. VEGF-receptorantagonist ifølge krav 1, hvor antagonisten er udtrykt som fusionprotein omfattende en eller flere VEGF-subunits, hvor VEGF-receptorantagonisten yderligere omfatter et toksin.
7. VEGF-receptorantagonist ifølge krav 1 hvor antagonisten er udtrykt som en homodimer eller heterodimer, hvor en eller begge subunits af homodimeren eller heterodimeren indeholder mindst én mutation.
8. VEGF-receptorantagonist ifølge krav 6, hvor toksinet er valgt fra gruppen bestående af Pseudomonas exotoxin (PE), et Diphtheria toksin (DT), ricintoksin, abrintoksin, anthraxtoksin, shigatoksin, botulismetoksin, tetanustoksin, koleratoksin, maitotoksin, palytoksin, ciguatoksin, textilotoksin, batrachotoksin, alfa cono-toksin, taipoxin, tetrodotoksin, alfa tityustoksin, saxitoksin, anatoksin, microcystin, akonitin, exfoliatin toksiner A, exfoliatin B, et enterotoksin, toksisk choksyndromtoksin (TSST-1), Y. pestis toksin og gas koldbrand toksin.
9. VEGF-receptorantagonist ifølge krav 7 og 8, hvor mindst en af subunits er en VEGF-A subunit, VEGF-B subunit, en VEGF-C subunit, VEGF-D subunit eller en PIGF subunit, hvor VEGF-A subunitten er valgt fra gruppen bestående af VEGFi65, VEGFiesb, VEGFm, VEGF145, VEGF148, VEGFiss, VEGFisg, og VEGF206.
10. VEGF-receptorantagonist ifølge krav 1-9, hvor angiogenese er mindst delvist hæmmet.
11. VEGF-receptorantagonist ifølge krav 1, hvor en eller begge subunits af VEGF'en omfatter en modifikation til at forlænge halveringstid, hvor modifikationen til at forlænge halveringstid er en eller flere modifikationer valgt fra gruppen bestående afen N-terminalforlængelse, en C-terminalforlængelse og pegylering.
12. VEGF-receptorantagonist ifølge krav 1, hvor VEGF-receptorantagonist er VEGFiesb receptorantagonist omfattende en eller flere yderligere mutationer valgt fra gruppen bestående af E44B, E67B, E72B, E73B, og Q87B af SEQ ID Nr.: 13, hvor B er en basisk aminosyre.
13. Farmaceutisk sammensætning omfattende VEGF-receptorantagonist ifølge krav 1-12.
14. Farmaceutisk sammensætning omfattende VEGF-receptorantagonist ifølge krav 1-12 til anvendelse i behandling afen patient diagnosticeret med a) cancer, hvor canceren er en solid tumorcancer valgt fra gruppen bestående af blære, bryst, lever, knogle, nyre, tarm, æggestok, prostata, bugspytkirtel, lunge, hjerne, og hud; eller b) en angiogenese-associeret øjensygdom, hvor den angiogenese-associerede øjensygdom er valgt fra gruppen bestående af retinopati af præmaturitet, diabetisk retinopati, retinal veneokklusion, makulær degeneration, og neovaskularisering; eller c) en angiogenese-relateret sygdom eller tilstand, hvor den angiogenese-relaterede tilstand er valgt fra gruppen bestående af hæmangiomer, rheumatoid arthritis, osteoarthritis, septisk arthritis, astma, atherosclerose, idiopatisk lungefibrose, vaskulær restenose, arteriovenøs misdannelser, meningiomer, neovaskulær glaukom, psoriasis, Kaposi's syndrom, angiofibrom, hæmofiliske led, hypertrofiske ar, Osler-Weber syndrom, pyogent granulom, retrolental fibroplasia, sklerodermi, trakom, von-Hippel-Lindau sygdom, vaskulære adhesionspatologier, synovitis, dermatitis, uforklarlig ufrugtbarhed hos kvinder, endometriose, uforklarlig ufrugtbarhed hos mænd, pterygium, sår, betændelse, skindsår, gastriske sår, og ulcus duodeni.
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| US72391705P | 2005-10-06 | 2005-10-06 | |
| US80810606P | 2006-05-25 | 2006-05-25 | |
| PCT/US2006/039181 WO2007044534A2 (en) | 2005-10-06 | 2006-10-06 | Vegf analogs and methods of use |
Publications (1)
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| DK1948219T3 true DK1948219T3 (da) | 2015-03-30 |
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| TW (1) | TW200732347A (da) |
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-
2006
- 2006-10-05 TW TW095137144A patent/TW200732347A/zh unknown
- 2006-10-06 EP EP12152289A patent/EP2447280A3/en not_active Withdrawn
- 2006-10-06 EP EP06836213.6A patent/EP1948219B1/en active Active
- 2006-10-06 AU AU2006302345A patent/AU2006302345B2/en not_active Ceased
- 2006-10-06 RU RU2008118000/13A patent/RU2008118000A/ru not_active Application Discontinuation
- 2006-10-06 CA CA002625395A patent/CA2625395A1/en not_active Abandoned
- 2006-10-06 EP EP14177415.8A patent/EP2799446B1/en not_active Not-in-force
- 2006-10-06 JP JP2008534722A patent/JP5567271B2/ja not_active Expired - Fee Related
- 2006-10-06 ES ES06836213.6T patent/ES2533466T3/es active Active
- 2006-10-06 KR KR1020087010925A patent/KR20080082608A/ko not_active Ceased
- 2006-10-06 PL PL06836213T patent/PL1948219T3/pl unknown
- 2006-10-06 US US12/089,296 patent/US8759285B2/en active Active
- 2006-10-06 WO PCT/US2006/039181 patent/WO2007044534A2/en not_active Ceased
- 2006-10-06 DK DK06836213T patent/DK1948219T3/da active
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2013
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2014
- 2014-06-23 US US14/312,446 patent/US9078860B2/en not_active Expired - Fee Related
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2015
- 2015-04-28 HK HK15104083.3A patent/HK1203527A1/en unknown
- 2015-06-12 US US14/738,549 patent/US20150274793A1/en not_active Abandoned
Also Published As
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| HK1203527A1 (en) | 2015-10-30 |
| EP2799446A1 (en) | 2014-11-05 |
| US20140308264A1 (en) | 2014-10-16 |
| JP2009511492A (ja) | 2009-03-19 |
| PL1948219T3 (pl) | 2015-07-31 |
| JP5567271B2 (ja) | 2014-08-06 |
| KR20080082608A (ko) | 2008-09-11 |
| US8759285B2 (en) | 2014-06-24 |
| EP1948219B1 (en) | 2014-12-24 |
| ES2533466T3 (es) | 2015-04-10 |
| WO2007044534A3 (en) | 2009-04-23 |
| AU2006302345A1 (en) | 2007-04-19 |
| EP2447280A2 (en) | 2012-05-02 |
| JP2013177458A (ja) | 2013-09-09 |
| US20100216702A1 (en) | 2010-08-26 |
| CA2625395A1 (en) | 2007-04-19 |
| RU2008118000A (ru) | 2009-11-20 |
| AU2006302345B2 (en) | 2013-09-05 |
| EP2799446B1 (en) | 2016-05-11 |
| EP1948219A4 (en) | 2009-10-28 |
| JP5840650B2 (ja) | 2016-01-06 |
| US9078860B2 (en) | 2015-07-14 |
| US20150274793A1 (en) | 2015-10-01 |
| TW200732347A (en) | 2007-09-01 |
| WO2007044534A2 (en) | 2007-04-19 |
| EP1948219A2 (en) | 2008-07-30 |
| EP2447280A3 (en) | 2012-06-20 |
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