JP2003525028A5 - - Google Patents

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JP2003525028A5
JP2003525028A5 JP2001510411A JP2001510411A JP2003525028A5 JP 2003525028 A5 JP2003525028 A5 JP 2003525028A5 JP 2001510411 A JP2001510411 A JP 2001510411A JP 2001510411 A JP2001510411 A JP 2001510411A JP 2003525028 A5 JP2003525028 A5 JP 2003525028A5
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JP
Japan
Prior art keywords
pharmaceutical composition
phe
tissue factor
composition according
arg
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Pending
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JP2001510411A
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English (en)
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JP2003525028A (ja
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Priority claimed from PCT/DK2000/000401 external-priority patent/WO2001005353A2/en
Publication of JP2003525028A publication Critical patent/JP2003525028A/ja
Publication of JP2003525028A5 publication Critical patent/JP2003525028A5/ja
Pending legal-status Critical Current

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【特許請求の範囲】
【請求項1】 組織因子アゴニストを含んで成る、細胞移動を誘発または増強するための医薬組成物。
【請求項2】 組織因子アゴニストがFVllまたはFVllaである請求項1記載の医薬組成物。
【請求項3】 組織因子アンタゴニストを含んで成る、細胞移動の減少または阻害するための医薬組成物。
【請求項4】 組織因子アンタゴニストが修飾されたFVllである請求項3記載の医薬組成物。
【請求項5】 前記細胞が、線維芽細胞、平滑筋細胞、腫瘍細胞、造血細胞、単球、マクロファージおよび上皮細胞を含む、ヒト細胞発現組織因子である請求項1または請求項3に記載の医薬組成物。
【請求項6】 前記細胞がさらにPDGFおよびPDGF受容体、特にPDGFベータ受容体を発現する請求項5記載の医薬組成物。
【請求項7】 前記修飾因子Vllが、Dansyl-Phe-Phe-Arg chloromethl ketone、Phe-Phe-Arg chloromethyl ketone、Dansyl-D-Phe-Phe-Arg chloromethl ketoneおよびD-Phe-Phe-Arg chloromethl ketoneから選択される、請求項4記載の医薬組成物。
【請求項8】 因子Vllaまたは因子Vllあるいは他の組織因子アゴニストを含んで成る、創傷治癒の促進または増強するための医薬組成物。
【請求項9】 望ましくない細胞移動、侵入、移動を誘発する細胞増殖または血管新成に関連した疾患または症状を有する患者の細胞移動、侵入、移動を誘発する細胞増殖または血管新成を阻害または減少させるための、組織因子アンタゴニストを含む医薬組成物。
【請求項10】 前記疾患または症状が、原発性腫瘍増殖、腫瘍の侵入または転移である請求項9記載の医薬組成物。
【請求項11】 前記組織因子アンタゴニストが修飾因子Vllであることを特徴とする請求項9記載の医薬組成物。
【請求項12】 細胞移動を誘発または増強するための投与薬を製造するための組織因子アゴニストの使用。
【請求項13】 前記組織因子アゴニストがFVllまたはFVllaあるいはその組み合わせである請求項12記載の使用。
【請求項14】 細胞移動を減少または阻害する投与薬を製造するための組織因子アンタゴニストの使用。
【請求項15】 前記組織因子アンタゴニストが修飾因子Vllである請求項14記載の使用。
【請求項16】 修飾因子VllがDANSYL-Phe-Phe-Arg chloromethl ketone、Phe-Phe-Arg chloromethl ketone、Dansyl-D-Phe-Phe-Arg chloromethl ketoneおよびD-Phe-Phe-Arg chloromethl ketoneで修飾因子Vllから選択される請求項15記載の使用。
【請求項17】 細胞内の少なくとも1つの遺伝子の発現を調節するための、組織因子アンタゴニストを含んでなる医薬組成物。
【請求項18】 前記組織因子アゴニストがFVllまたはFVllaである請求項17記載の医薬組成物。
【請求項19】 前記組織因子アンタゴニストが修飾されたFVllである請求項17記載の医薬組成物。
【請求項20】 前記遺伝子がCyr61、CCN遺伝子ファミリーに属する遺伝子である請求項17記載の医薬組成物。
【請求項21】 前記遺伝子が、CTFG、ドーパミンD2受容体、EST incyte PD 395116またはP2Uヌクレオチド受容体からなる群より選択される請求項17記載の医薬組成物。
【請求項22】 遺伝子がCyr61遺伝子である請求項21記載の医薬組成物。
JP2001510411A 1999-07-14 2000-07-14 遺伝子発現および細胞移動または走化を調節するためのFVllaまたは組織因子アンタゴニストの使用 Pending JP2003525028A (ja)

Applications Claiming Priority (7)

Application Number Priority Date Filing Date Title
DK199901023 1999-07-14
DKPA199901023 1999-07-14
US14830099P 1999-08-11 1999-08-11
US60/148,300 1999-08-11
DK199901117 1999-08-12
DKPA199901117 1999-08-12
PCT/DK2000/000401 WO2001005353A2 (en) 1999-07-14 2000-07-14 USE OF FVIIa OR A TISSUE FACTOR ANTAGONIST FOR REGULATING GENE EXPRESSION AND CELL MIGRATION OR CHEMOTAXIS

Publications (2)

Publication Number Publication Date
JP2003525028A JP2003525028A (ja) 2003-08-26
JP2003525028A5 true JP2003525028A5 (ja) 2007-06-28

Family

ID=27221063

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2001510411A Pending JP2003525028A (ja) 1999-07-14 2000-07-14 遺伝子発現および細胞移動または走化を調節するためのFVllaまたは組織因子アンタゴニストの使用

Country Status (19)

Country Link
US (3) US20020193302A1 (ja)
EP (1) EP1200116B1 (ja)
JP (1) JP2003525028A (ja)
KR (1) KR100821644B1 (ja)
CN (1) CN100411684C (ja)
AT (1) ATE411041T1 (ja)
AU (1) AU5807500A (ja)
BR (1) BR0012408A (ja)
CA (1) CA2378249A1 (ja)
CZ (1) CZ200240A3 (ja)
DE (1) DE60040539D1 (ja)
ES (1) ES2316372T3 (ja)
HU (1) HUP0302052A3 (ja)
IL (1) IL147294A0 (ja)
MX (1) MXPA02000468A (ja)
NO (1) NO20020130L (ja)
PL (1) PL353035A1 (ja)
RU (1) RU2268744C2 (ja)
WO (1) WO2001005353A2 (ja)

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WO2001098359A2 (en) * 2000-06-21 2001-12-27 Wyeth Cyr61 as a target for treatment and diagnosis of breast cancer
DE10238429A1 (de) 2002-03-19 2003-10-30 Aventis Behring Gmbh Intellect Marburg I Mutante der Faktor VII aktivierenden Protease (FSAP) als Risikofaktor für Atherosklerose
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
US6858587B2 (en) 2001-11-02 2005-02-22 Novo Nordisk Pharmaceuticals, Inc. Use of tissue factor agonist or tissue factor antagonist for treatment of conditions related to apoptosis
AU2003214920A1 (en) * 2002-02-04 2003-09-02 Millennium Pharmaceuticals Inc. Methods and compositions for treating hematological disorders
AU2004284013A1 (en) * 2003-08-06 2005-05-06 Sirnasense As The use of siRNA silencing in the prevention of metastasis
MXPA06011952A (es) * 2004-04-16 2007-01-16 Scripps Research Inst Metodo para modulacion de vascularizacion.
EP1945261A4 (en) * 2005-11-07 2010-05-12 Scripps Research Inst COMPOSITIONS AND METHODS FOR CONTROLLING THE SPECIFICITY OF TISSUE FACTOR SIGNALING
US20100015160A1 (en) * 2007-02-21 2010-01-21 Yale University Compositions and methods for diagnosing and treating endometriosis
US10391137B2 (en) 2011-07-01 2019-08-27 Shiseido Company, Ltd. Platelet-derived growth factor-BB production promotor, and mesenchymal stem cell production accelerator, stem cell stabilizer and dermal regenerator comprising the same
CN109381478A (zh) * 2018-10-31 2019-02-26 青岛大学附属医院 一种miRNA在制备抑制新生血管生成和抑制VEGF-A因子表达的试剂中的应用

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HUT67693A (en) 1991-10-11 1995-04-28 Novo Nordisk As Hemostatic composition for arresting local bleedings
DE19538715A1 (de) * 1995-10-18 1997-04-30 Behringwerke Ag Verfahren zur Reinigung von Faktor VII und aktiviertem Faktor VII
US6413735B1 (en) 1996-03-15 2002-07-02 Munin Corporation Method of screening for a modulator of angiogenesis
AU7907398A (en) 1997-06-23 1999-01-04 Novo Nordisk A/S Use of fviia for the treatment of bleedings in patients with a normal blood clotting cascade and normal platelet function
ATE454161T1 (de) * 1997-07-18 2010-01-15 Novo Nordisk Healthcare Ag Verwendung von fviia oder fviiai zur behandlung von endothelialer fehlfunktion bzw zur inhibierung der angiogenese
US20030040481A1 (en) * 1997-07-18 2003-02-27 Lars Kongsbak Methods for modifying cell motility using a factor VIIa antagonist
AT408613B (de) * 1998-06-17 2002-01-25 Immuno Ag Pharmazeutisches faktor vii-präparat
US7015194B2 (en) * 2000-05-10 2006-03-21 Novo Nordisk A/S Pharmaceutical composition comprising factor VIIa and anti-TFPI
PL371800A1 (en) 2001-03-22 2005-06-27 Novo Nordisk Health Care Ag Coagulation factor vii derivatives
IL158615A0 (en) 2001-05-02 2004-05-12 Novo Nordisk As Modified factor vii in treatment of acute lung injury or acute respiratory distress syndrome
PL369077A1 (en) 2001-07-20 2005-04-18 Novo Nordisk Health Care Ag Pharmaceutical composition comprising factor vii polypeptides and factor xi polypeptides
WO2003039581A1 (en) 2001-11-09 2003-05-15 Novo Nordisk Health Care Ag Pharmaceutical composition comprising factor vii polypeptides and tranexamic acid
JP2006510568A (ja) 2001-11-09 2006-03-30 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 Vii因子ポリペプチドおよびイプシロン―アミノカプロン酸を含む薬学的組成物
EP1446155A1 (en) 2001-11-09 2004-08-18 Novo Nordisk A/S Pharmaceutical composition comprising factor vii polypeptides and aprotinin polypeptides
BR0213953A (pt) 2001-11-09 2004-08-31 Novo Nordisk Healthcare Ag Composição farmacêutica, kit de partes, uso de fator vii ou um polipeptìdeo relacionado com fator vii em combinação com um fator v ou um polipeptìdeo relacionado com fator v, uso de uma composição, métodos para tratar episódios de sangramento em um sujeito, para reduzir o tempo de coagulação, para intensificar hemóstase, para prolongar o tempo de lise de coágulos em um sujeito, e para incrementar a resistência do coágulo em um sujeito, kit contendo um tratamento para episódios de sangramento

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