ES2663709T3 - Métodos para la prevención y el tratamiento de la isquemia cerebral - Google Patents
Métodos para la prevención y el tratamiento de la isquemia cerebral Download PDFInfo
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- ES2663709T3 ES2663709T3 ES10747777.0T ES10747777T ES2663709T3 ES 2663709 T3 ES2663709 T3 ES 2663709T3 ES 10747777 T ES10747777 T ES 10747777T ES 2663709 T3 ES2663709 T3 ES 2663709T3
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- tocotrienol quinone
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/12—Ketones
- A61K31/122—Ketones having the oxygen directly attached to a ring, e.g. quinones, vitamin K1, anthralin
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- A—HUMAN NECESSITIES
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- A—HUMAN NECESSITIES
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- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
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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
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- A61P9/00—Drugs for disorders of the cardiovascular system
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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
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
Landscapes
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- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
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| PCT/US2010/046503 WO2011025785A1 (en) | 2009-08-26 | 2010-08-24 | Methods for the prevention and treatment of cerebral ischemia |
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| WO2005033092A1 (en) | 2003-09-19 | 2005-04-14 | Galileo Pharmaceuticals, Inc. | Chroman derivatives |
| PL2471530T3 (pl) * | 2005-06-01 | 2017-07-31 | Edison Pharmaceuticals, Inc. | Środki terapeutyczne o aktywności redoks do leczenia chorób mitochondrialnych i innych stanów oraz modulacja biomarkerów energetycznych |
| US9278085B2 (en) | 2006-02-22 | 2016-03-08 | Edison Pharmaceuticals, Inc. | Side-chain variants of redox-active therapeutics for treatment of mitochondrial diseases and other conditions and modulation of energy biomarkers |
| PL3456707T3 (pl) | 2007-11-06 | 2020-09-21 | Ptc Therapeutics, Inc. | Pochodne 4-(p-chinonylo)-2-hydroksybutanamidu do leczenia chorób mitochondrialnych |
| EA023618B1 (ru) * | 2008-01-08 | 2016-06-30 | Эдисон Фармасьютикалз, Инк. | Производные (гет)арил-п-хинона для лечения митохондриальных болезней |
| US8716527B2 (en) | 2008-03-05 | 2014-05-06 | Edison Pharmaceuticals, Inc. | 2-substituted-p-quinone derivatives for treatment of oxidative stress diseases |
| JP5798481B2 (ja) | 2008-06-25 | 2015-10-21 | エジソン ファーマシューティカルズ， インコーポレイテッド | 酸化ストレス疾患を治療するための２−ヘテロシクリルアミノアルキル−（ｐ−キノン）誘導体 |
| BRPI0918139B1 (pt) | 2008-09-10 | 2024-04-30 | Ptc Therapeutics, Inc | Composição, alimento medicinal ou funcional, suplemento alimentar ou dietético para tratamento de distúrbios de desenvolvimento pervasivos com terapêuticos redox-ativos |
| WO2010045220A1 (en) | 2008-10-14 | 2010-04-22 | Edison Pharmaceuticals, Inc. | Treatment of oxidative stress disorders including contrast nephropathy, radiation damage and disruptions in the function of red cells |
| PL2362875T3 (pl) | 2008-10-28 | 2016-01-29 | Bioelectron Tech Corp | Proces do wytwarzania alfa-tokotrienolu i pochodnych |
| MX336800B (es) | 2009-04-28 | 2016-02-02 | Edison Pharmaceuticals Inc | Tratamiento de neuropatia optica hereditaria de leber y atrofia optica dominante con tocotrienol quinonas. |
| WO2011082355A1 (en) * | 2009-12-31 | 2011-07-07 | Edison Pharmaceuticals, Inc. | Treatment of leigh syndrome and leigh-like syndrome with tocotrienol quinones |
| SG185046A1 (en) * | 2010-04-27 | 2012-12-28 | Edison Pharmaceuticals Inc | Formulations of quinones for the treatment of ophthalmic diseases |
| PT2680873T (pt) | 2011-03-03 | 2017-11-01 | Cidara Therapeutics Inc | Agentes antifúngicos e suas utilizações |
| US9464016B2 (en) | 2011-06-14 | 2016-10-11 | Edison Pharmaceuticals, Inc. | Catechol derivatives for treatment of oxidative stress diseases |
| JP2014520894A (ja) | 2011-07-19 | 2014-08-25 | エジソン ファーマシューティカルズ， インコーポレイテッド | 非アルファトコトリエノールの存在下でのアルファトコトリエノールの選択的酸化のための方法 |
| GB201117808D0 (en) * | 2011-10-14 | 2011-11-30 | Siemens Medical Solutions | SUV correction following dose infiltration |
| WO2013142279A1 (en) * | 2012-03-19 | 2013-09-26 | Seachaid Pharmaceuticals, Inc. | Dosing regimens for echinocandin class compounds |
| WO2014039917A1 (en) * | 2012-09-07 | 2014-03-13 | Edison Pharmaceuticals, Inc. | Benzoquinone derivatives for treating oxidative stress disorders |
| CN112451518B (zh) * | 2012-11-13 | 2025-02-21 | 因维克特斯生物技术有限公司 | 生育三烯酚的经粘膜递送 |
| US9670170B2 (en) | 2013-03-15 | 2017-06-06 | Bioelectron Technology Corporation | Resorufin derivatives for treatment of oxidative stress disorders |
| WO2014145116A2 (en) | 2013-03-15 | 2014-09-18 | Edison Pharmaceuticals, Inc. | Alkyl-heteroaryl substituted quinone derivatives for treatment of oxidative stress disorders |
| US9868711B2 (en) | 2013-03-15 | 2018-01-16 | Bioelectron Technology Corporation | Phenazine-3-one and phenothiazine-3-one derivatives for treatment of oxidative stress disorders |
| US9296712B2 (en) | 2013-03-15 | 2016-03-29 | Edison Pharmaceuticals, Inc. | Resorufin derivatives for treatment of oxidative stress disorders |
| RU2578451C1 (ru) * | 2014-12-09 | 2016-03-27 | Государственное Бюджетное Образовательное Учреждение Высшего Профессионального Образования "Амурская Государственная Медицинская Академия" Министерства Здравоохранения Российской Федерации | Способ повышения устойчивости головного мозга к ишемии во время реконструктивных операций на брахиоцефальных артериях |
| US10251847B2 (en) | 2014-12-16 | 2019-04-09 | Bioelectron Technology Corporation | Polymorphic and amorphous forms of (R)-2-hydroxy-2-methyl-4-(2,4,5-trimethyl-3,6-dioxocyclohexa-1,4-dienyl)butanamide |
| EP3390377A1 (en) | 2015-12-16 | 2018-10-24 | BioElectron Technology Corporation | Improved methods for enriching alpha-tocotrienol from mixed tocol compositions |
| AU2016369616B2 (en) | 2015-12-17 | 2021-03-25 | Ptc Therapeutics, Inc. | Fluoroalkyl, fluoroalkoxy, phenoxy, heteroaryloxy, alkoxy, and amine 1,4-benzoquinone derivatives for treatment of oxidative stress disorders |
| CA3017485A1 (en) | 2016-03-16 | 2017-09-21 | Cidara Therapeutics, Inc. | Dosing regimens for treatment of fungal infections |
| US10707531B1 (en) | 2016-09-27 | 2020-07-07 | New Dominion Enterprises Inc. | All-inorganic solvents for electrolytes |
| JP2018083799A (ja) | 2016-11-15 | 2018-05-31 | バイオエレクトロン テクノロジー コーポレイション | ２−置換アミノ−ナフト［１，２−ｄ］イミダゾール−５−オン化合物またはその製薬学上許容される塩 |
| CN111050798A (zh) | 2017-07-12 | 2020-04-21 | 奇达拉治疗公司 | 用于治疗真菌感染的组合物和方法 |
| WO2020010180A1 (en) * | 2018-07-03 | 2020-01-09 | Cardio Vascular Bio Therapeutics, Inc. | Compositions and methods for treating stroke |
| KR102337954B1 (ko) * | 2018-08-16 | 2021-12-10 | 차의과학대학교 산학협력단 | 뇌졸중 치료용 조성물 및 이를 스크리닝하는 방법 |
| EP4257190A3 (en) | 2018-10-17 | 2024-01-03 | PTC Therapeutics, Inc. | 2,3,5-trimethyl-6-nonylcyclohexa-2,5-diene-1,4-dione for suppressing and treating alpha-synucleinopathies, tauopathies, and other disorders |
| KR20220078644A (ko) | 2019-10-04 | 2022-06-10 | 스텔스 바이오테라퓨틱스 인코포레이티드 | 미토콘드리아 질환 치료를 위한 바티퀴논의 퀴논-, 히드로퀴논- 및 나프토퀴논-유사체 |
| WO2021076951A1 (en) * | 2019-10-17 | 2021-04-22 | The Penn State Research Foundation | Regenerating functional neurons for treatment of hemorrhagic stroke |
| WO2021202986A1 (en) | 2020-04-03 | 2021-10-07 | Stealth Biotherapeutics Corp | Compositions and methods for the prevention and/or treatment of mitochondrial disease, including friedreich's ataxia |
| CN116762096A (zh) * | 2020-12-22 | 2023-09-15 | 皇家飞利浦有限公司 | 定位血管收缩 |
| CN113066113B (zh) * | 2021-04-27 | 2022-01-11 | 河北医科大学第二医院 | 自发性高血压大鼠脑模板和地图集的构建方法及设备 |
| US11786486B2 (en) | 2021-07-08 | 2023-10-17 | Ptc Therapeutics, Inc. | Pharmaceutical compositions comprising 2,3,5-trimethyl-6-nonylcyclohexa-2,5-diene-1,4-dione |
Family Cites Families (49)
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| US5872108A (en) | 1995-03-06 | 1999-02-16 | Interneuron Pharmaceuticals, Inc. | Reduction of infarct volume using citicoline |
| US6232060B1 (en) * | 1996-01-19 | 2001-05-15 | Galileo Laboratories, Inc. | Assay system for anti-stress agents |
| US5801159A (en) * | 1996-02-23 | 1998-09-01 | Galileo Laboratories, Inc. | Method and composition for inhibiting cellular irreversible changes due to stress |
| FR2753098B1 (fr) * | 1996-09-06 | 1998-11-27 | Sod Conseils Rech Applic | Composition pharmaceutique comprenant au moins un inhibiteur de no synthase et au moins un piegeur des formes reactives de l'oxygene |
| ID26335A (id) | 1997-11-17 | 2000-12-14 | Lipogenic Inc | Metoda untuk mencegah restenosis dengan menggunakan tokotrienol |
| US6048891A (en) * | 1998-12-17 | 2000-04-11 | Loma Linda University Medical Center | Use of γ-tocopherol and its oxidative metabolite LLU-α in the treatment of natriuretic disease |
| WO2000078296A2 (en) | 1999-06-17 | 2000-12-28 | Basf Aktiengesellschaft | Tocotrienol and/or tocotrienol derivatives for the treatment or prophylaxis of glutamate- and/or calcium-induced disorders |
| US6426362B1 (en) * | 1999-10-08 | 2002-07-30 | Galileo Laboratories, Inc. | Formulations of tocopherols and methods of making and using them |
| US6528042B1 (en) * | 1999-10-08 | 2003-03-04 | Galileo Laboratories, Inc. | Compositions of flavonoids for use as cytoprotectants and methods of making and using them |
| US6346544B2 (en) * | 2000-03-02 | 2002-02-12 | Oklahoma Medical Research Foundation | Desmethyl tocopherols for protecting cardiovascular tissue |
| DE10034233A1 (de) * | 2000-07-14 | 2002-01-24 | Basf Ag | Tocotrienolchinon-Cyclisierungsprodukte |
| US7034054B2 (en) * | 2000-12-15 | 2006-04-25 | Galileo Pharmaceuticals, Inc. | Methods for the prevention and treatment of cerebral ischemia using non-alpha tocopherols |
| WO2002047680A2 (en) * | 2000-12-15 | 2002-06-20 | Galileo Laboratories, Inc. | Use of tocopherol, metabolites or derivatives thereof or flavonoid metabolites or derivatives thereof in the manufacture of a medicament for the treatment of tissue ischemia |
| US6608196B2 (en) * | 2001-05-03 | 2003-08-19 | Galileo Pharmaceuticals, Inc. | Process for solid supported synthesis of pyruvate-derived compounds |
| US7119117B2 (en) * | 2001-08-21 | 2006-10-10 | Galileo Pharmaceuticals, Inc. | Tocopherol enriched compositions and amelioration of inflammatory symptoms |
| EP1450787A4 (en) * | 2001-11-15 | 2006-01-25 | Galileo Pharmaceuticals Inc | FORMULATIONS AND METHODS FOR THE TREATMENT OR AMELIORATION OF INFLAMMATORY CONDITIONS |
| US20040152764A1 (en) * | 2001-12-14 | 2004-08-05 | Miller Guy M. | Compositions and methods for the prevention and treatment of cerebral ischemia |
| US6653346B1 (en) * | 2002-02-07 | 2003-11-25 | Galileo Pharmaceuticals, Inc. | Cytoprotective benzofuran derivatives |
| US7078541B2 (en) * | 2002-02-07 | 2006-07-18 | Galileo Pharmaceuticals, Inc. | Benzofuran derivatives |
| JP4599292B2 (ja) * | 2002-10-30 | 2010-12-15 | エジソン ファーマシューティカルズ， インコーポレイテッド | 物理的−化学的特性に基づく治療用化合物の同定 |
| WO2005033092A1 (en) * | 2003-09-19 | 2005-04-14 | Galileo Pharmaceuticals, Inc. | Chroman derivatives |
| US7393662B2 (en) * | 2004-09-03 | 2008-07-01 | Centocor, Inc. | Human EPO mimetic hinge core mimetibodies, compositions, methods and uses |
| PL2471530T3 (pl) * | 2005-06-01 | 2017-07-31 | Edison Pharmaceuticals, Inc. | Środki terapeutyczne o aktywności redoks do leczenia chorób mitochondrialnych i innych stanów oraz modulacja biomarkerów energetycznych |
| CA2622523C (en) * | 2005-09-15 | 2014-02-18 | Edison Pharmaceuticals, Inc. | Tail variants of redox-active therapeutics for treatment of mitochondrial diseases and other conditions and modulation of energy biomarkers |
| US9278085B2 (en) * | 2006-02-22 | 2016-03-08 | Edison Pharmaceuticals, Inc. | Side-chain variants of redox-active therapeutics for treatment of mitochondrial diseases and other conditions and modulation of energy biomarkers |
| US20100056429A1 (en) * | 2007-01-10 | 2010-03-04 | Miller Guy M | Treatment of respiratory chain disorders using compounds having erythropoietin or thrombopoietin activity |
| PL3456707T3 (pl) * | 2007-11-06 | 2020-09-21 | Ptc Therapeutics, Inc. | Pochodne 4-(p-chinonylo)-2-hydroksybutanamidu do leczenia chorób mitochondrialnych |
| US20100266591A1 (en) * | 2008-01-07 | 2010-10-21 | Peter Bugelski | Method of treating erythropoietin hyporesponsive anemias |
| EA023618B1 (ru) * | 2008-01-08 | 2016-06-30 | Эдисон Фармасьютикалз, Инк. | Производные (гет)арил-п-хинона для лечения митохондриальных болезней |
| JP2011513420A (ja) * | 2008-03-05 | 2011-04-28 | エジソン ファーマシューティカルズ， インコーポレイテッド | レドックス活性治療薬を用いる聴覚機能障害および平衡機能障害の処置 |
| US8716527B2 (en) * | 2008-03-05 | 2014-05-06 | Edison Pharmaceuticals, Inc. | 2-substituted-p-quinone derivatives for treatment of oxidative stress diseases |
| CA2723621A1 (en) * | 2008-05-15 | 2009-11-19 | Edison Pharmaceuticals, Inc | Treatment of hearing and balance impairments using compounds having erythropoietin activity |
| CA2724841A1 (en) * | 2008-05-22 | 2009-11-26 | Edison Pharmaceuticals, Inc. | Treatment of mitochondrial diseases with an erythropoietin mimetic |
| JP5798481B2 (ja) * | 2008-06-25 | 2015-10-21 | エジソン ファーマシューティカルズ， インコーポレイテッド | 酸化ストレス疾患を治療するための２−ヘテロシクリルアミノアルキル−（ｐ−キノン）誘導体 |
| WO2010005989A1 (en) * | 2008-07-09 | 2010-01-14 | Edison Pharmaceuticals, Inc. | Dermatological compositions with anti-aging and skin even-toning properties |
| US20100029784A1 (en) * | 2008-07-30 | 2010-02-04 | Hinman Andrew W | Naphthoquinone compositions with anti-aging, anti-inflammatory and skin even-toning properties |
| BRPI0918139B1 (pt) * | 2008-09-10 | 2024-04-30 | Ptc Therapeutics, Inc | Composição, alimento medicinal ou funcional, suplemento alimentar ou dietético para tratamento de distúrbios de desenvolvimento pervasivos com terapêuticos redox-ativos |
| WO2010045220A1 (en) * | 2008-10-14 | 2010-04-22 | Edison Pharmaceuticals, Inc. | Treatment of oxidative stress disorders including contrast nephropathy, radiation damage and disruptions in the function of red cells |
| PL2362875T3 (pl) * | 2008-10-28 | 2016-01-29 | Bioelectron Tech Corp | Proces do wytwarzania alfa-tokotrienolu i pochodnych |
| WO2010126910A1 (en) * | 2009-04-28 | 2010-11-04 | Edison Pharmaceuticals, Inc. | Topical, periocular, or intraocular use of tocotrienols for the treatment of ophthalmic diseases |
| MX336800B (es) * | 2009-04-28 | 2016-02-02 | Edison Pharmaceuticals Inc | Tratamiento de neuropatia optica hereditaria de leber y atrofia optica dominante con tocotrienol quinonas. |
| EP2424494A1 (en) * | 2009-04-28 | 2012-03-07 | Edison Pharmaceuticals, Inc. | Formulation of tocotrienol quinones for the treatment of ophthalmic diseases |
| EA201200054A1 (ru) * | 2009-06-25 | 2012-05-30 | Эмпэр Лайф Сайнсиз, Инк. | Лечение токотриенолами или экстрактами, богатыми токотриенолами, первазивных расстройств развития |
| WO2011082355A1 (en) * | 2009-12-31 | 2011-07-07 | Edison Pharmaceuticals, Inc. | Treatment of leigh syndrome and leigh-like syndrome with tocotrienol quinones |
| EP2555765A4 (en) * | 2010-04-06 | 2013-08-14 | Edison Pharmaceuticals Inc | TREATMENT OF ATAXIE TÉLANGIECTASIE |
| SG185046A1 (en) * | 2010-04-27 | 2012-12-28 | Edison Pharmaceuticals Inc | Formulations of quinones for the treatment of ophthalmic diseases |
| WO2012009271A1 (en) * | 2010-07-14 | 2012-01-19 | Penwest Pharmaceuticals Co. | Methods of providing anticoagulation effects in subjects |
| WO2012068552A1 (en) * | 2010-11-19 | 2012-05-24 | Edison Pharmaceuticals, Inc. | Methods for improving blood glucose control |
-
2010
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- 2010-08-24 MX MX2012002374A patent/MX337990B/es active IP Right Grant
- 2010-08-24 NO NO10747777A patent/NO2470168T3/no unknown
- 2010-08-24 WO PCT/US2010/046503 patent/WO2011025785A1/en active Application Filing
- 2010-08-24 PL PL10747777T patent/PL2470168T3/pl unknown
- 2010-08-24 SI SI201031644T patent/SI2470168T1/en unknown
- 2010-08-24 PT PT107477770T patent/PT2470168T/pt unknown
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- 2010-08-24 CA CA2772294A patent/CA2772294C/en active Active
- 2010-08-24 DK DK10747777.0T patent/DK2470168T3/en active
- 2010-08-24 AU AU2010286704A patent/AU2010286704B2/en not_active Ceased
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Also Published As
| Publication number | Publication date |
|---|---|
| DK2470168T3 (en) | 2018-05-07 |
| NO2470168T3 (en:Method) | 2018-06-30 |
| JP5785546B2 (ja) | 2015-09-30 |
| CA2772294A1 (en) | 2011-03-03 |
| JP2013503168A (ja) | 2013-01-31 |
| EP2470168A1 (en) | 2012-07-04 |
| PT2470168T (pt) | 2018-03-28 |
| AU2010286704B2 (en) | 2016-10-20 |
| CN102647981A (zh) | 2012-08-22 |
| EA201200355A1 (ru) | 2012-07-30 |
| AU2010286704A1 (en) | 2012-03-22 |
| PL2470168T3 (pl) | 2018-06-29 |
| MX2012002374A (es) | 2012-04-10 |
| CN102647981B (zh) | 2016-09-28 |
| CA2772294C (en) | 2018-08-21 |
| US20170007553A1 (en) | 2017-01-12 |
| JP2015091899A (ja) | 2015-05-14 |
| EA028677B1 (ru) | 2017-12-29 |
| US20180344667A1 (en) | 2018-12-06 |
| SI2470168T1 (en) | 2018-05-31 |
| WO2011025785A1 (en) | 2011-03-03 |
| US20110207828A1 (en) | 2011-08-25 |
| MX337990B (es) | 2016-03-30 |
| EP2470168B1 (en) | 2018-01-31 |
| HUE037592T2 (hu) | 2018-09-28 |
| BR112012004167A2 (pt) | 2016-03-29 |
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