RU2211704C2 - Модифицированный фактор vii - Google Patents
Модифицированный фактор vii Download PDFInfo
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- RU2211704C2 RU2211704C2 RU99100089/14A RU99100089A RU2211704C2 RU 2211704 C2 RU2211704 C2 RU 2211704C2 RU 99100089/14 A RU99100089/14 A RU 99100089/14A RU 99100089 A RU99100089 A RU 99100089A RU 2211704 C2 RU2211704 C2 RU 2211704C2
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- factor vii
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- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/745—Blood coagulation or fibrinolysis factors
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- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/14—Hydrolases (3)
- C12N9/48—Hydrolases (3) acting on peptide bonds (3.4)
- C12N9/50—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25)
- C12N9/64—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue
- C12N9/6421—Proteinases, e.g. Endopeptidases (3.4.21-3.4.25) derived from animal tissue from mammals
- C12N9/6424—Serine endopeptidases (3.4.21)
- C12N9/6437—Coagulation factor VIIa (3.4.21.21)
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/164—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- A61K38/166—Streptokinase
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- A61K38/46—Hydrolases (3)
- A61K38/48—Hydrolases (3) acting on peptide bonds (3.4)
- A61K38/482—Serine endopeptidases (3.4.21)
- A61K38/4846—Factor VII (3.4.21.21); Factor IX (3.4.21.22); Factor Xa (3.4.21.6); Factor XI (3.4.21.27); Factor XII (3.4.21.38)
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/43—Enzymes; Proenzymes; Derivatives thereof
- A61K38/46—Hydrolases (3)
- A61K38/48—Hydrolases (3) acting on peptide bonds (3.4)
- A61K38/49—Urokinase; Tissue plasminogen activator
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P7/00—Drugs for disorders of the blood or the extracellular fluid
- A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Y—ENZYMES
- C12Y304/00—Hydrolases acting on peptide bonds, i.e. peptidases (3.4)
- C12Y304/21—Serine endopeptidases (3.4.21)
- C12Y304/21021—Coagulation factor VIIa (3.4.21.21)
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- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
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Abstract
Изобретение относится к медицине, а именно к способам лечения, касающимся улучшения регионального миокардиального кровотока в процессе постишемической реперфузии, а также предупреждения или минимизации повреждений ткани, связанных с постишемической перфузией. Указанное назначение осуществляется путем введения пациенту композиции, которая содержит фармакологически приемлемый Фактор VII, имеющий в своем каталитическом центре по меньшей мере одну модификацию, которая существенно ингибирует способность модифицированного Фактора VII активировать плазменный Фактор Х или IX. Использование Фактора VII, модифицированного указанным образом, позволяет повысить эффективность лечения. 4 с. и 14 з.п. ф-лы, 22 табл., 11 ил.
Description
Текст описания в факсимильном виде (см. графическую часть). Т Тk
Claims (18)
1. Применение Фактора VII, имеющего в своем каталитическом центре по меньшей мере одну модификацию, которая существенно ингибирует способность модифицированного Фактора VII активировать плазменный Фактор Х или IX, для производства композиции для предупреждения или минимизации повреждения ткани, ассоциированного с постишемической реперфузией.
2. Применение по п. 1, где указанная модификация включает в себя взаимодействие Фактора VII с ингибитором сериновой протеиназы.
3. Применение по п. 2, где протеиназным ингибитором является фосфорорганическое соединение, сульфанилфторид, пептидный галогенметилкетон или азапептид.
4. Применение по п. 3, где протеиназным ингибитором является пептидный галогенметилкетон, выбранный из Дансил-Phe-Pro-Arg-хлорметилкетона, Дaнcил-Glu-Gly-Arg-xлopмeтилкeтoнa, Дансил-Phe-Phe-Arg-хлорметилкетона и Phe-Phe-Arg-хлорметилкетона.
5. Применение по пп. 1-4, где повреждение ткани представляет собой некроз.
6. Способ предупреждения или минимизации повреждения ткани, ассоциированного с постишемической реперфузией у индивидуума, включающий в себя введение индивидууму композиции, которая содержит фармакологически приемлемый Фактор VII, имеющий в своем каталитическом центре по меньшей мере одну модификацию, которая существенно ингибирует способность модифицированного Фактора VII активировать плазменный Фактор Х или IX.
7. Способ по п. 6, где модификация включает в себя взаимодействие Фактора VII с ингибитором сериновой протеиназы.
8. Способ по п. 7, где протеиназным ингибитором является фосфорорганическое соединение, сульфанилфторид, пептидный галогенметилкетон или азапептид.
9. Способ по п. 8, где протеиназным ингибитором является пептидный галогенметилкетон, выбранный из Дансил-Phe-Pro-Arg-хлорметилкетона, Дансил-Glu-Gly-Аrg-хлорметилкетона, Дансил-Phe-Phe-Arg-хлорметилкетона и Phe-Phe-Arg-хлорметилкетона.
10. Способ по любому из пп. 6-9, где повреждение ткани представляет собой некроз.
11. Применение Фактора VII, имеющего в своем каталитическом центре по меньшей мере одну модификацию, которая существенно ингибирует способность модифицированного Фактора VII активировать плазменный Фактор Х или IX, для производства композиции для улучшения регионального миокардиального кровотока в процессе постишемической реперфузии.
12. Применение по п. 11, где модификация включает в себя взаимодействие Фактора VII с ингибитором сериновой протеиназы.
13. Применение по п. 12, где протеиназным ингибитором является фосфорорганическое соединение, сульфанилфторид, пептидный галогенметилкетон или азапептид.
14. Применение по п. 13, где протеиназным ингибитором является пептидный галогенметилкетон, выбранный из Дансил-Phe-Pro-Arg-хлорметилкетона, Дансил-Glu-Gly-Аrg-хлорметилкетона, Дансил-Phe-Phe-Arg-хлорметилкетона и Phe-Phe-Arg-хлорметилкетона.
15. Способ улучшения регионального миокардиального кровотока в процессе постишемической реперфузии у индивидуума, включающий в себя введение индивидууму композиции, которая содержит фармакологически приемлемый Фактор VII, имеющий в своем каталитическом центре по меньшей мере одну модификацию, которая существенно ингибирует способность модифицированного Фактора VII активировать плазменный Фактор Х или IX.
16. Способ по п. 15, где модификация включает в себя взаимодействие Фактора VII с ингибитором сериновой протеиназы.
17. Способ по п. 16, где протеиназным ингибитором является фосфорорганическое соединение, сульфанилфторид, пептидный галогенметилкетон или азапептид.
18. Способ по п. 17, где протеиназным ингибитором является пептидный галогенметилкетон, выбранный из Дансил-Phe-Pro-Arg-хлорметилкетона, Дансил-Glu-Gly-Аrg-хлорметилкетона, Дансил-Phe-Phe-Arg-хлорметилкетона и Phe-Phe-Arg-хлорметилкетона.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/660,289 US5833982A (en) | 1991-02-28 | 1996-06-07 | Modified factor VII |
US08/660,289 | 1996-06-07 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU99100089A RU99100089A (ru) | 2000-11-27 |
RU2211704C2 true RU2211704C2 (ru) | 2003-09-10 |
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ID=24648892
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU99100089/14A RU2211704C2 (ru) | 1996-06-07 | 1997-06-06 | Модифицированный фактор vii |
Country Status (17)
Country | Link |
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US (2) | US5833982A (ru) |
EP (1) | EP0910580A1 (ru) |
JP (1) | JP2000513720A (ru) |
KR (1) | KR20000016415A (ru) |
CN (2) | CN1131872C (ru) |
AU (1) | AU735012B2 (ru) |
BR (1) | BR9709661A (ru) |
CA (1) | CA2256761A1 (ru) |
CZ (1) | CZ394698A3 (ru) |
HU (1) | HUP0003077A3 (ru) |
IL (1) | IL127099A0 (ru) |
NO (1) | NO985668L (ru) |
PL (1) | PL330365A1 (ru) |
RU (1) | RU2211704C2 (ru) |
UA (1) | UA68333C2 (ru) |
WO (1) | WO1997047651A1 (ru) |
ZA (1) | ZA975013B (ru) |
Families Citing this family (87)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5997864A (en) | 1995-06-07 | 1999-12-07 | Novo Nordisk A/S | Modified factor VII |
US20040087498A1 (en) * | 1991-02-28 | 2004-05-06 | Novo Nordisk Health Care Ag | Modified factor VII |
EP1005361B1 (en) * | 1997-07-18 | 2010-01-06 | Novo Nordisk Health Care AG | USE OF FVIIa OR FVIIai FOR THE TREATMENT OF ENDOTHELIAL DYSFUNKTION AND FOR THE INHIBITION OF ANGIOGENESIS RESPECTIVELY |
US7247708B2 (en) * | 1997-10-23 | 2007-07-24 | Regents Of The University Of Minnesota | Modified vitamin K-dependent polypeptides |
US6693075B1 (en) | 1997-10-23 | 2004-02-17 | Regents Of The University Of Minnesota | Modified vitamin K-dependent polypeptides |
US6747003B1 (en) | 1997-10-23 | 2004-06-08 | Regents Of The University Of Minnesota | Modified vitamin K-dependent polypeptides |
US6406488B1 (en) * | 1998-08-27 | 2002-06-18 | Heartstent Corporation | Healing transmyocardial implant |
EP0987274A1 (en) | 1998-09-15 | 2000-03-22 | Hoechst Marion Roussel Deutschland GmbH | Factor VIIa Inhibitors |
EP1059302A1 (en) | 1999-06-08 | 2000-12-13 | Aventis Pharma Deutschland GmbH | Factor VIIa inhibitors |
US6924359B1 (en) * | 1999-07-01 | 2005-08-02 | Yale University | Neovascular-targeted immunoconjugates |
EP1095933A1 (en) | 1999-10-30 | 2001-05-02 | Aventis Pharma Deutschland GmbH | Novel N-guanidinoalkylamides, their preparation, their use, and pharmaceutical preparations comprising them |
RU2278123C2 (ru) * | 2000-02-11 | 2006-06-20 | Максиджен Холдингз Лтд. | Молекулы, подобные фактору vii или viia |
AU2001259063A1 (en) * | 2000-04-12 | 2001-10-30 | Human Genome Sciences, Inc. | Albumin fusion proteins |
US7220837B1 (en) | 2000-04-28 | 2007-05-22 | Regents Of The University Of Minnesota | Modified vitamin K-dependent polypeptides |
US7812132B2 (en) * | 2000-04-28 | 2010-10-12 | Regents Of The University Of Minnesota | Modified vitamin K-dependent polypeptides |
EP1162194A1 (en) | 2000-06-06 | 2001-12-12 | Aventis Pharma Deutschland GmbH | Factor VIIa inhibitory (thio)urea derivatives, their preparation and their use |
WO2001097752A2 (en) * | 2000-06-20 | 2001-12-27 | The Trustees Of The University Of Pennsylvania | Compositions comprising urokinase for modulating muscle contractility and angiogenisis |
US6423826B1 (en) | 2000-06-30 | 2002-07-23 | Regents Of The University Of Minnesota | High molecular weight derivatives of vitamin K-dependent polypeptides |
US7160540B2 (en) * | 2000-06-30 | 2007-01-09 | Regents Of The University Of Minnesota | Methods for detecting activity of clottings factors |
US20030211094A1 (en) * | 2001-06-26 | 2003-11-13 | Nelsestuen Gary L. | High molecular weight derivatives of vitamin k-dependent polypeptides |
RU2003120070A (ru) | 2000-12-06 | 2004-12-27 | Авентис Фармаа Дойчланд Гмбх (De) | Производные гуанидина и амидина в качестве ингибиторов фактора ха |
US6825323B2 (en) * | 2001-01-10 | 2004-11-30 | The United States Of America As Represented By The Secretary Of The Army | Compositions for treatment of hemorrhaging with activated factor VIIa in combination with fibrinogen and methods of using same |
US7235638B2 (en) | 2001-03-22 | 2007-06-26 | Novo Nordisk Healthcare A/G | Coagulation factor VII derivatives |
AU2002249096B2 (en) * | 2001-03-22 | 2007-06-28 | Novo Nordisk Health Care Ag | Coagulation factor VII derivatives |
PL366564A1 (en) * | 2001-05-02 | 2005-02-07 | Novo Nordisk A/S | Modified fvii in treatment of ards |
EP1270551A1 (en) | 2001-06-26 | 2003-01-02 | Aventis Pharma Deutschland GmbH | Urea derivatives with antiproteolytic activity |
AU2002326135A1 (en) * | 2001-09-10 | 2003-03-24 | Florence Medical Ltd. | Individual ffr determination for lesions of a multi-lesioned blood vessel |
US7214660B2 (en) | 2001-10-10 | 2007-05-08 | Neose Technologies, Inc. | Erythropoietin: remodeling and glycoconjugation of erythropoietin |
CN105131104B (zh) | 2001-10-10 | 2018-11-16 | 诺和诺德公司 | 肽的重构和糖缀合 |
US7173003B2 (en) | 2001-10-10 | 2007-02-06 | Neose Technologies, Inc. | Granulocyte colony stimulating factor: remodeling and glycoconjugation of G-CSF |
AU2002336920A1 (en) * | 2001-11-02 | 2003-05-12 | Novo Nordisk Health Care Ag | Use of tissue factor agonist or tissue factor antagonist for treatment of conditions related to apoptosis |
EP1314733A1 (en) | 2001-11-22 | 2003-05-28 | Aventis Pharma Deutschland GmbH | Indole-2-carboxamides as factor Xa inhibitors |
IL162239A0 (en) * | 2001-12-21 | 2005-11-20 | Novo Nordisk Healthcare Ag | Liquid composition of factor vii polypeptides |
KR20040065278A (ko) * | 2001-12-21 | 2004-07-21 | 노보 노르디스크 에이/에스 | 변경된 인자 ⅶ 폴리펩티드의 액체 조성물 |
RU2004122430A (ru) * | 2001-12-21 | 2005-04-20 | Ново Нордиск А/С (DK) | Жидкая композиция полипептидов модифицированного фактора vii |
SI1499719T1 (sl) * | 2002-04-30 | 2011-03-31 | Bayer Healthcare Llc | Polipeptidne variante faktorja VII ali VIIa |
US20040009918A1 (en) * | 2002-05-03 | 2004-01-15 | Hanne Nedergaard | Stabilised solid compositions of modified factor VII |
ATE536886T1 (de) * | 2002-05-03 | 2011-12-15 | Novo Nordisk As | Stabilisierte feste zusammensetzungen von modifizierter faktor vii |
ES2523655T5 (es) * | 2002-06-21 | 2018-04-23 | Novo Nordisk Health Care Ag | Composiciones sólidas estabilizadas de polipéptidos del Factor VIIa |
US20060166874A1 (en) * | 2002-09-30 | 2006-07-27 | Haaning Jesper M | Fvii or fviia variants having increased clotting activity |
US7358268B2 (en) | 2002-12-04 | 2008-04-15 | Sanofi-Aventis Deutschland Gmbh | Imidazole derivatives as factor Xa inhibitors |
US7429581B2 (en) | 2002-12-23 | 2008-09-30 | Sanofi-Aventis Deutschland Gmbh | Pyrazole-derivatives as factor Xa inhibitors |
US20040176704A1 (en) * | 2003-03-04 | 2004-09-09 | Stevens Timothy A | Collection device adapted to accept cartridge for point of care system |
WO2004082708A2 (en) * | 2003-03-18 | 2004-09-30 | Novo Nordisk Health Care Ag | Liquid, aqueous, pharmaceutical compositions of factor vii polypeptides |
DK2085470T3 (da) * | 2003-03-20 | 2012-08-06 | Bayer Healthcare Llc | FVII- eller FVIIa-varianter |
US7897734B2 (en) * | 2003-03-26 | 2011-03-01 | Novo Nordisk Healthcare Ag | Method for the production of proteins |
EP2338333B1 (en) | 2003-04-09 | 2017-09-06 | ratiopharm GmbH | Glycopegylation methods and proteins/peptides produced by the methods |
US20040202726A1 (en) * | 2003-04-10 | 2004-10-14 | Deshay Samuel L. | Topical blood pressure composition |
US7741341B2 (en) | 2003-05-19 | 2010-06-22 | Sanofi-Aventis Deutschland Gmbh | Benzimidazole-derivatives as factor Xa inhibitors |
US7223780B2 (en) | 2003-05-19 | 2007-05-29 | Sanofi-Aventis Deutschland Gmbh | Triazole-derivatives as blood clotting enzyme factor Xa inhibitors |
US7317027B2 (en) | 2003-05-19 | 2008-01-08 | Sanofi-Aventis Deutschland Gmbh | Azaindole-derivatives as factor Xa inhibitors |
EP1479677A1 (en) | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | New indole derivatives as factor xa inhibitors |
EP1479680A1 (en) | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Azaindole derivatives as Factor Xa inhibitors |
EP1479675A1 (en) | 2003-05-19 | 2004-11-24 | Aventis Pharma Deutschland GmbH | Indazole-derivatives as factor Xa inhibitors |
RU2364609C2 (ru) * | 2003-05-23 | 2009-08-20 | Ново Нордиск Хелт Кэр Аг | Стабилизация белка в растворе |
US7029675B1 (en) * | 2003-06-04 | 2006-04-18 | Shu-Wha Lin | Hepsin antagonist and methods of use |
CN1839203B (zh) * | 2003-06-19 | 2011-11-16 | 拜耳医药保健有限公司 | 因子VII或VIIa的GLA结构域变体 |
ATE547114T1 (de) | 2003-06-25 | 2012-03-15 | Novo Nordisk Healthcare Ag | Flüssige zusammensetzungen von factor vii polypeptiden |
DE602004023848D1 (de) * | 2003-07-01 | 2009-12-10 | Novo Nordisk Healthcare Ag | Von factor vii polypeptiden |
WO2005012484A2 (en) | 2003-07-25 | 2005-02-10 | Neose Technologies, Inc. | Antibody-toxin conjugates |
CN102872451A (zh) * | 2003-08-14 | 2013-01-16 | 诺和诺德医疗保健公司 | 因子vii多肽类的含水液体药物组合物 |
US20080305992A1 (en) | 2003-11-24 | 2008-12-11 | Neose Technologies, Inc. | Glycopegylated erythropoietin |
RU2373953C2 (ru) * | 2003-12-19 | 2009-11-27 | Ново Нордиск Хелс Кеа Аг | Стабилизированная композиция, содержащая полипептид фактора vii |
EP1568698A1 (en) | 2004-02-27 | 2005-08-31 | Aventis Pharma Deutschland GmbH | Pyrrole-derivatives as factor Xa inhibitors |
JP2008514216A (ja) * | 2004-09-29 | 2008-05-08 | ノボ ノルディスク ヘルス ケア アクチェンゲゼルシャフト | Desgla−vii因子ポリペプチド構造の除去による、vii因子ポリペプチドの原体の精製 |
SI2586456T1 (sl) | 2004-10-29 | 2016-05-31 | Ratiopharm Gmbh | Preoblikovanje in glikopegliacija fibroblastnega rastnega faktorja (FGF) |
EP1858543B1 (en) | 2005-01-10 | 2013-11-27 | BioGeneriX AG | Glycopegylated granulocyte colony stimulating factor |
WO2006121569A2 (en) | 2005-04-08 | 2006-11-16 | Neose Technologies, Inc. | Compositions and methods for the preparation of protease resistant human growth hormone glycosylation mutants |
US20070105755A1 (en) | 2005-10-26 | 2007-05-10 | Neose Technologies, Inc. | One pot desialylation and glycopegylation of therapeutic peptides |
US20090048440A1 (en) | 2005-11-03 | 2009-02-19 | Neose Technologies, Inc. | Nucleotide Sugar Purification Using Membranes |
CN101516388B (zh) | 2006-07-21 | 2012-10-31 | 诺和诺德公司 | 通过o-联糖基化序列的肽的糖基化 |
EP2054521A4 (en) | 2006-10-03 | 2012-12-19 | Novo Nordisk As | METHODS OF PURIFYING CONJUGATES OF POLYPEPTIDES |
ES2406267T3 (es) | 2007-04-03 | 2013-06-06 | Biogenerix Ag | Métodos de tratamiento usando G-CSF glicopegilado |
WO2008154639A2 (en) | 2007-06-12 | 2008-12-18 | Neose Technologies, Inc. | Improved process for the production of nucleotide sugars |
PL2257311T3 (pl) | 2008-02-27 | 2014-09-30 | Novo Nordisk As | Koniugaty cząsteczek czynnika VIII |
BR122021014783B1 (pt) | 2008-12-19 | 2023-03-14 | Baxalta GmbH | Peptídeo que se liga a tfpi, uso do peptídeo, composição farmacêutica e método para purificação de tfpi |
AU2010290077C1 (en) | 2009-08-24 | 2015-12-03 | Bioverativ Therapeutics Inc. | Coagulation factor IX compositions and methods of making and using same |
CN103025345B (zh) | 2010-03-19 | 2016-01-20 | 巴克斯特国际公司 | Tfpi抑制剂及使用方法 |
KR101294351B1 (ko) * | 2010-05-27 | 2013-08-07 | 동국대학교 산학협력단 | 뇌혈전 형광영상기술을 이용한 뇌졸중 동물모델의 뇌경색 영역의 크기 예측 방법 |
ES2771208T3 (es) | 2012-02-15 | 2020-07-06 | Bioverativ Therapeutics Inc | Composiciones de factor VIII y métodos de preparación y uso de las mismas |
EP3549953A1 (en) | 2012-02-15 | 2019-10-09 | Bioverativ Therapeutics Inc. | Recombinant factor viii proteins |
AU2013235741C1 (en) | 2012-03-21 | 2017-12-21 | Takeda Pharmaceutical Company Limited | TFPI inhibitors and methods of use |
WO2015023891A2 (en) | 2013-08-14 | 2015-02-19 | Biogen Idec Ma Inc. | Factor viii-xten fusions and uses thereof |
CA2990837A1 (en) * | 2015-07-22 | 2017-01-26 | Iconic Therapeutics, Inc. | Methods for treating disorders associated with angiogenesis and neovascularization |
EA201890423A1 (ru) | 2015-08-03 | 2018-07-31 | Биовератив Терапьютикс Инк. | Слитые белки фактора ix, способы их получения и применения |
AU2017206445B2 (en) | 2016-01-15 | 2019-07-18 | Rigshospitalet | Quantitative pet imaging of tissue factor expression using 18F-labled active site inhibited factor VII |
WO2018091058A1 (en) | 2016-11-17 | 2018-05-24 | Rigshospitalet | 177-lu labeled active site inhibited factor vii |
Family Cites Families (25)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4775624A (en) * | 1985-02-08 | 1988-10-04 | Eli Lilly And Company | Vectors and compounds for expression of human protein C |
GR860984B (en) * | 1985-04-17 | 1986-08-18 | Zymogenetics Inc | Expression of factor vii and ix activities in mammalian cells |
US4770999A (en) * | 1985-04-22 | 1988-09-13 | Genetics Institute, Inc. | High yield production of active Factor IX |
US4959318A (en) * | 1985-06-27 | 1990-09-25 | Zymogenetics, Inc. | Expression of protein C |
US4829052A (en) * | 1986-06-11 | 1989-05-09 | Monsanto Company | Serine protease inhibitors |
US5258288A (en) * | 1986-07-25 | 1993-11-02 | Genzyme Corporation | Vector containing DNA encoding mature human protein S |
EP0278727A3 (en) | 1987-02-10 | 1990-03-14 | Glaxo Group Limited | 1-(4-amino-3-chloro-5-trifluoromethylphenyl)-2-(substituted amino)ethanol derivatives and their use in the treatment of respiratory disease |
FR2619314B1 (fr) * | 1987-08-11 | 1990-06-15 | Transgene Sa | Analogue du facteur viii, procede de preparation et composition pharmaceutique le contenant |
US4994371A (en) * | 1987-08-28 | 1991-02-19 | Davie Earl W | DNA preparation of Christmas factor and use of DNA sequences |
US5023236A (en) * | 1988-04-07 | 1991-06-11 | Corvas, Inc. | Factor VII/VIIA active site inhibitors |
US5258180A (en) * | 1988-09-02 | 1993-11-02 | Genetech, Inc. | Tissue plasminogen activator having fibrin specific properties and deletion of amino acids 466-970, compositions and methods of treatment |
AU4338689A (en) * | 1988-09-23 | 1990-04-18 | Corvas, Inc. | Peptidyl inhibitors of the initiation of coagulation |
US5120537A (en) * | 1989-06-14 | 1992-06-09 | Oklahoma Medical Research Foundation | Factor xa based anticoagulant compositions |
US5190919A (en) * | 1989-11-13 | 1993-03-02 | Board Of Regents, The University Of Texas System | Antihemostatic factor vii peptides |
ATE180834T1 (de) | 1990-01-29 | 1999-06-15 | Zymogenetics Inc | Antikoagulierende proteine |
US5278144A (en) * | 1990-09-04 | 1994-01-11 | Cor Therapeutics, Inc. | Antithrombosis agents |
US5817788A (en) | 1991-02-28 | 1998-10-06 | Zymogenetics, Inc. | Modified factor VII |
US5861374A (en) | 1991-02-28 | 1999-01-19 | Novo Nordisk A/S | Modified Factor VII |
JP3459416B2 (ja) * | 1991-02-28 | 2003-10-20 | ザイモジェネティクス,インコーポレイティド | 修飾されたファクター▲vii▼ |
US5788965A (en) | 1991-02-28 | 1998-08-04 | Novo Nordisk A/S | Modified factor VII |
US5326559A (en) * | 1991-05-16 | 1994-07-05 | Miller D Douglas | Treatment of accelerated atheosclerosis with interleukin-2 receptor targeted molecules |
US5419760A (en) * | 1993-01-08 | 1995-05-30 | Pdt Systems, Inc. | Medicament dispensing stent for prevention of restenosis of a blood vessel |
GB9301093D0 (en) * | 1993-01-20 | 1993-03-10 | Rca Thomson Licensing Corp | Digital video tape recorder for digital hdtv |
HU219682B (hu) * | 1993-05-21 | 2001-06-28 | Novo Nordisk A/S. | Módosított VII faktor |
US5648331A (en) * | 1994-08-26 | 1997-07-15 | G.D. Searle & Co. | Method of inhibiting tissue ischemia and reperfusion injury |
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AU3090697A (en) | 1998-01-07 |
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JP2000513720A (ja) | 2000-10-17 |
PL330365A1 (en) | 1999-05-10 |
EP0910580A1 (en) | 1999-04-28 |
HUP0003077A3 (en) | 2003-01-28 |
ZA975013B (en) | 1997-12-08 |
BR9709661A (pt) | 2000-04-25 |
CN1515318A (zh) | 2004-07-28 |
CZ394698A3 (cs) | 1999-04-14 |
KR20000016415A (ko) | 2000-03-25 |
NO985668L (no) | 1999-02-04 |
CN1221427A (zh) | 1999-06-30 |
HUP0003077A2 (hu) | 2000-12-28 |
US5833982A (en) | 1998-11-10 |
CN1131872C (zh) | 2003-12-24 |
WO1997047651A1 (en) | 1997-12-18 |
UA68333C2 (en) | 2004-08-16 |
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