JP2014525476A5 - - Google Patents
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- JP2014525476A5 JP2014525476A5 JP2014529840A JP2014529840A JP2014525476A5 JP 2014525476 A5 JP2014525476 A5 JP 2014525476A5 JP 2014529840 A JP2014529840 A JP 2014529840A JP 2014529840 A JP2014529840 A JP 2014529840A JP 2014525476 A5 JP2014525476 A5 JP 2014525476A5
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- JP
- Japan
- Prior art keywords
- pharmaceutical composition
- serpinf2
- composition according
- binding molecule
- inhibitor
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- 239000008194 pharmaceutical composition Substances 0.000 claims 32
- 239000003112 inhibitor Substances 0.000 claims 12
- 230000002401 inhibitory effect Effects 0.000 claims 12
- 102000003801 alpha-2-Antiplasmin Human genes 0.000 claims 9
- 108090000183 alpha-2-Antiplasmin Proteins 0.000 claims 9
- 102000003978 Tissue plasminogen activator Human genes 0.000 claims 8
- 108090000373 Tissue plasminogen activator Proteins 0.000 claims 8
- 102000004965 antibodies Human genes 0.000 claims 8
- 108090001123 antibodies Proteins 0.000 claims 8
- 229960000187 tissue plasminogen activator Drugs 0.000 claims 8
- 206010018987 Haemorrhage Diseases 0.000 claims 5
- 206010061255 Ischaemia Diseases 0.000 claims 5
- 206010030113 Oedema Diseases 0.000 claims 5
- 231100000419 toxicity Toxicity 0.000 claims 5
- 230000001988 toxicity Effects 0.000 claims 5
- 206010059512 Apoptosis Diseases 0.000 claims 4
- 229920002395 Aptamer Polymers 0.000 claims 4
- 210000002216 Heart Anatomy 0.000 claims 4
- 210000004185 Liver Anatomy 0.000 claims 4
- 210000000496 Pancreas Anatomy 0.000 claims 4
- 230000006907 apoptotic process Effects 0.000 claims 4
- 230000034994 death Effects 0.000 claims 4
- 229920003013 deoxyribonucleic acid Polymers 0.000 claims 4
- 230000000694 effects Effects 0.000 claims 4
- 102000004196 processed proteins & peptides Human genes 0.000 claims 4
- 108090000765 processed proteins & peptides Proteins 0.000 claims 4
- 150000003384 small molecules Chemical class 0.000 claims 4
- 206010022114 Injury Diseases 0.000 claims 3
- 210000003734 Kidney Anatomy 0.000 claims 3
- 210000004072 Lung Anatomy 0.000 claims 2
- 206010060860 Neurological symptom Diseases 0.000 claims 2
- 230000000740 bleeding Effects 0.000 claims 2
- 231100000319 bleeding Toxicity 0.000 claims 2
- 201000010099 disease Diseases 0.000 claims 2
- 210000000056 organs Anatomy 0.000 claims 2
- 230000000241 respiratory Effects 0.000 claims 2
- 206010052639 Nerve injury Diseases 0.000 claims 1
- 102000001938 Plasminogen Activators Human genes 0.000 claims 1
- 108010001014 Plasminogen Activators Proteins 0.000 claims 1
- 102000012479 Serine Proteases Human genes 0.000 claims 1
- 108010022999 Serine Proteases Proteins 0.000 claims 1
- 210000003292 kidney cell Anatomy 0.000 claims 1
- 230000002265 prevention Effects 0.000 claims 1
- 230000002035 prolonged Effects 0.000 claims 1
- 210000001519 tissues Anatomy 0.000 claims 1
Claims (28)
- 必要とされる患者において、出血または浮腫による障害または死亡を防止するための医薬組成物であって、SerpinF2活性または濃度を低減させる有効量のSerpinF2結合分子を含み、前記SerpinF2結合分子の投与が、前記患者における出血または浮腫による障害または死亡を防止する、医薬組成物。
- 前記出血または浮腫は、神経、心臓、肝臓、膵臓、呼吸器、または腎臓の出血または浮腫である、請求項1に記載の医薬組成物。
- 前記結合分子は、抗体、ペプチド、DNAアプタマー、または小分子から選択される、SerpinF2阻害剤である、請求項1に記載の医薬組成物。
- 前記SerpinF2阻害剤は、抗体である、請求項3に記載の医薬組成物。
- 前記SerpinF2阻害剤は、28〜91ナノモル/kgの用量範囲で投与される、請求項4に記載の医薬組成物。
- 必要とされる患者において、組織プラスミノーゲン活性化因子(TPA)毒性による障害または死亡を防止するための医薬組成物であって、SerpinF2活性または濃度を低減させる有効量のSerpinF2結合分子を含み、前記SerpinF2結合分子の投与が、TPA毒性による障害または死亡を防止する、医薬組成物。
- 前記TPA毒性は、出血、器官浮腫、またはアポトーシスを引き起こす、請求項6に記載の医薬組成物。
- 前記投与が、前記患者がTPAに誘発される損傷の危険性にあることを判定する先行ステップを含む、請求項6に記載の医薬組成物。
- 前記TPA毒性は、虚血または外傷に起因する、請求項6に記載の医薬組成物。
- 前記TPA毒性は、神経、心臓、肝臓、膵臓、呼吸器、または腎臓の損傷を引き起こす、請求項6に記載の医薬組成物。
- 前記TPAは、48時間以内に事前に前記患者に投与されている、請求項6に記載の医薬組成物。
- プラスミノーゲン活性化因子またはセリンプロテアーゼ酵素は、48時間以内に事前に前記患者に投与されている、請求項6に記載の医薬組成物。
- 前記結合分子は、抗体、ペプチド、DNAアプタマー、または小分子から選択される、SerpinF2阻害剤である、請求項6に記載の医薬組成物。
- 前記SerpinF2阻害剤は、抗体である、請求項13に記載の医薬組成物。
- 前記SerpinF2阻害剤は、28〜91ナノモル/kgの用量範囲で投与される、請求項14に記載の医薬組成物。
- アポトーシスの予防を、それを必要とする患者において行うための医薬組成物であって、SerpinF2活性または濃度を低下させる有効量のSerpinF2結合分子を含み、前記SerpinF2結合分子の投与が、前記患者におけるアポトーシスを予防する、医薬組成物。
- 前記アポトーシスは、神経、心臓、肝臓、膵臓、肺、または腎臓の細胞に生じる、請求項16に記載の医薬組成物。
- 前記結合分子は、抗体、ペプチド、DNAアプタマー、または小分子から選択される、SerpinF2阻害剤である、請求項16に記載の医薬組成物。
- 前記SerpinF2阻害剤は、抗体である、請求項18に記載の医薬組成物。
- 前記SerpinF2阻害剤は、28〜91ナノモル/kgの用量範囲で投与される、請求項19に記載の医薬組成物。
- 必要とされる患者において、長期虚血を防止するための医薬組成物であって、前記患者においてSerpinF2濃度または活性を低減させる有効量のSerpinF2結合分子を含み、前記SerpinF2結合分子の投与が前記長期虚血を防止する、医薬組成物。
- 前記長期虚血は、少なくとも40分間現れている、請求項21に記載の医薬組成物。
- 前記長期虚血は、神経、心臓、肝臓、膵臓、肺、または腎臓の組織に生じる、請求項21に記載の医薬組成物。
- 前記投与が、前記患者が神経損傷を示す神経症状を有することを判定する先行ステップを含む、請求項21に記載の医薬組成物。
- 前記神経症状は、Rankin 1またはNIH Stroke Scale 4よりも重度かまたはそれと同等として分類される、請求項24に記載の医薬組成物。
- 前記結合分子は、抗体、ペプチド、DNAアプタマー、または小分子から選択される、SerpinF2阻害剤である、請求項21に記載の医薬組成物。
- 前記SerpinF2阻害剤は、抗体である、請求項26に記載の医薬組成物。
- 前記SerpinF2阻害剤は、28〜91ナノモル/kgの用量範囲で投与される、請求項27に記載の医薬組成物。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201161531278P | 2011-09-06 | 2011-09-06 | |
US61/531,278 | 2011-09-06 | ||
PCT/US2012/053900 WO2013036596A2 (en) | 2011-09-06 | 2012-09-06 | Serpinf2-binding molecules and methods of use |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2014525476A JP2014525476A (ja) | 2014-09-29 |
JP2014525476A5 true JP2014525476A5 (ja) | 2015-08-13 |
JP6184410B2 JP6184410B2 (ja) | 2017-08-23 |
Family
ID=47832762
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2014529840A Active JP6184410B2 (ja) | 2011-09-06 | 2012-09-06 | Serpinf2結合分子および使用方法 |
Country Status (6)
Country | Link |
---|---|
US (2) | US11236176B2 (ja) |
EP (1) | EP2753359B1 (ja) |
JP (1) | JP6184410B2 (ja) |
AU (1) | AU2012304635B2 (ja) |
CA (1) | CA2846667A1 (ja) |
WO (1) | WO2013036596A2 (ja) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2016106186A1 (en) * | 2014-12-22 | 2016-06-30 | Translational Sciences, Inc. | Prophylaxis of thrombosis |
EP4007812A1 (en) * | 2019-08-01 | 2022-06-08 | Alnylam Pharmaceuticals, Inc. | Serpin family f member 2 (serpinf2) irna compositions and methods of use thereof |
KR20230005333A (ko) | 2020-04-30 | 2023-01-09 | 라리마 테라퓨틱스, 인코포레이티드 | 미엘린 관련 질환 및 미토콘드리아 관련 질환을 치료하기 위한 방법 |
Family Cites Families (22)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6147500A (ja) | 1984-08-15 | 1986-03-07 | Res Dev Corp Of Japan | キメラモノクロ−ナル抗体及びその製造法 |
EP0173494A3 (en) | 1984-08-27 | 1987-11-25 | The Board Of Trustees Of The Leland Stanford Junior University | Chimeric receptors by dna splicing and expression |
GB8422238D0 (en) | 1984-09-03 | 1984-10-10 | Neuberger M S | Chimeric proteins |
EP0247091B1 (en) | 1985-11-01 | 1993-09-29 | Xoma Corporation | Modular assembly of antibody genes, antibodies prepared thereby and use |
US4946778A (en) | 1987-09-21 | 1990-08-07 | Genex Corporation | Single polypeptide chain binding molecules |
US5260203A (en) | 1986-09-02 | 1993-11-09 | Enzon, Inc. | Single polypeptide chain binding molecules |
DE3777359D1 (de) | 1986-12-19 | 1992-04-16 | Teijin Ltd | Aminosaeuresequenz des menschlichen alpha 2-plasmininhibitors und cdns sowie diese aminosaeuresequenz codierende genomische dns. |
US5091513A (en) | 1987-05-21 | 1992-02-25 | Creative Biomolecules, Inc. | Biosynthetic antibody binding sites |
US5530101A (en) | 1988-12-28 | 1996-06-25 | Protein Design Labs, Inc. | Humanized immunoglobulins |
US5565332A (en) | 1991-09-23 | 1996-10-15 | Medical Research Council | Production of chimeric antibodies - a combinatorial approach |
EP0941345A2 (en) * | 1996-09-20 | 1999-09-15 | The General Hospital Corporation | Chimeric, humanized and single chain antibodies to alpha-2-antiplasmin |
US6534035B1 (en) | 1998-05-29 | 2003-03-18 | President And Fellows Of Harvard College | Methods of inhibiting clot formation |
AU6200599A (en) * | 1998-09-29 | 2000-04-17 | Leuven Research & Development Vzw | Use of compounds that reduce alpha2-antiplasmin in vivo for the preparation of acomposition for the treatment of ischemic stroke |
US6411506B1 (en) | 2000-07-20 | 2002-06-25 | Rlx Technologies, Inc. | High density web server chassis system and method |
EP1572864A4 (en) * | 2001-03-08 | 2008-02-13 | Immunex Corp | HUMAN SERPIN POLYPEPTIDE |
AU2003301843A1 (en) | 2002-05-17 | 2004-06-07 | Human Genome Sciences, Inc. | 157 human secreted proteins |
US7309774B2 (en) | 2003-02-07 | 2007-12-18 | The Board Of Regents Of The University Of Oklahoma | Antiplasmin cleaving enzyme |
WO2006005583A2 (en) | 2004-07-12 | 2006-01-19 | Geneprot Inc. | Secreted polypeptide species involved in multiple sclerosis |
US20090118162A1 (en) * | 2005-06-07 | 2009-05-07 | Regents Of The University Of Colorado | Inhibitors of serine protease activity and their use in methods and compositions for treatment of graft rejection and promotion of graft survival |
US9150903B2 (en) | 2007-04-25 | 2015-10-06 | Translational Sciences Inc. | Method of increasing plasmin activity through antiplasmin conversion |
WO2010071787A1 (en) * | 2008-12-17 | 2010-06-24 | Arizona Board Regents, A Body Corporate Acting For And On Behalf Of Arizona State University | Pancreatic cancer markers and uses thereof |
EP2521918B1 (en) * | 2010-01-08 | 2015-03-25 | Cavadis B.V. | Determination of exosomal biomarkers for predicting cardiovascular events |
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2012
- 2012-09-06 AU AU2012304635A patent/AU2012304635B2/en active Active
- 2012-09-06 JP JP2014529840A patent/JP6184410B2/ja active Active
- 2012-09-06 WO PCT/US2012/053900 patent/WO2013036596A2/en active Application Filing
- 2012-09-06 CA CA2846667A patent/CA2846667A1/en active Pending
- 2012-09-06 EP EP12830126.4A patent/EP2753359B1/en active Active
-
2014
- 2014-03-06 US US14/198,804 patent/US11236176B2/en active Active
-
2022
- 2022-02-01 US US17/590,744 patent/US20220298261A1/en active Pending
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