ES2856698T3 - Fotosensibilizadores de (bacterio)clorofila para el tratamiento de enfermedades y trastornos oculares - Google Patents
Fotosensibilizadores de (bacterio)clorofila para el tratamiento de enfermedades y trastornos oculares Download PDFInfo
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- ES2856698T3 ES2856698T3 ES12762405T ES12762405T ES2856698T3 ES 2856698 T3 ES2856698 T3 ES 2856698T3 ES 12762405 T ES12762405 T ES 12762405T ES 12762405 T ES12762405 T ES 12762405T ES 2856698 T3 ES2856698 T3 ES 2856698T3
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- amide
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- rhodobacteriochlorin
- methoxycarbonylmethyl
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Classifications
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- A61K41/0071—PDT with porphyrins having exactly 20 ring atoms, i.e. based on the non-expanded tetrapyrrolic ring system, e.g. bacteriochlorin, chlorin-e6, or phthalocyanines
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- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/409—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil having four such rings, e.g. porphine derivatives, bilirubin, biliverdine
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- A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
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- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
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Landscapes
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Applications Claiming Priority (2)
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| US201161526414P | 2011-08-23 | 2011-08-23 | |
| PCT/IL2012/050325 WO2013027222A1 (en) | 2011-08-23 | 2012-08-23 | (bacterio)chlorophyll photosensitizers for treatment of eye diseases and disorders |
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| ES2856698T3 true ES2856698T3 (es) | 2021-09-28 |
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| Application Number | Title | Priority Date | Filing Date |
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| ES12762405T Active ES2856698T3 (es) | 2011-08-23 | 2012-08-23 | Fotosensibilizadores de (bacterio)clorofila para el tratamiento de enfermedades y trastornos oculares |
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| US9622911B2 (en) | 2010-09-30 | 2017-04-18 | Cxl Ophthalmics, Llc | Ophthalmic treatment device, system, and method of use |
| JP6049712B2 (ja) | 2011-07-08 | 2016-12-21 | ザ ユニバーシティ オブ ノース カロライナ アット チャペル ヒルＴｈｅ Ｕｎｉｖｅｒｓｉｔｙ Ｏｆ Ｎｏｒｔｈ Ｃａｒｏｌｉｎａ Ａｔ Ｃｈａｐｅｌ Ｈｉｌｌ | 抗癌治療及び画像化並びに骨障害治療のための金属ビスホスホネートナノ粒子 |
| EP2830637B1 (en) | 2012-03-29 | 2024-08-21 | Epion Therapeutics, Inc. | Compositions and methods for treating or preventing diseases associated with oxidative stress |
| EP2830627B1 (en) | 2012-03-29 | 2024-05-01 | Epion Therapeutics, Inc. | Ocular treatment solutions, delivery devices and delivery augmentation methods |
| RU2635185C2 (ru) * | 2013-12-17 | 2017-11-09 | Иван Дмитриевич Захаров | Фармацевтический препарат для профилактики и лечения прогрессирующей близорукости |
| CN116832158A (zh) | 2015-07-21 | 2023-10-03 | 艾维德洛公司 | 用光敏剂治疗眼睛的系统和方法 |
| CN106620893B (zh) | 2015-07-23 | 2021-07-30 | 爱博诺德(北京)医疗科技股份有限公司 | 用于眼部疾病光治疗的材料 |
| US10449090B2 (en) | 2015-07-31 | 2019-10-22 | Allotex, Inc. | Corneal implant systems and methods |
| CN105601638B (zh) * | 2016-01-28 | 2018-10-26 | 东北林业大学 | 一种叶绿酸衍生物及其制备方法、作为光敏抑菌剂及光敏杀虫剂的应用 |
| EP3442481B1 (en) | 2016-04-13 | 2023-06-28 | Avedro, Inc. | Systems for delivering drugs to an eye |
| US20170319329A1 (en) * | 2016-05-05 | 2017-11-09 | David Muller | Corneal Implant Systems and Methods |
| CA3046668A1 (en) * | 2017-01-03 | 2018-07-12 | Vitrean, Inc. | Methods and devices for treating a retinal detachment |
| CN111194232B (zh) * | 2017-08-02 | 2023-01-31 | 芝加哥大学 | 纳米级金属有机层和金属有机纳米片 |
| CN109091685A (zh) * | 2018-08-10 | 2018-12-28 | 北京市眼科研究所 | 一种对角膜炎提取细菌病原体的灭活方法 |
| WO2020086697A1 (en) * | 2018-10-24 | 2020-04-30 | California Institute Of Technology | Treatment of myopia and other ocular conditions using singlet oxygen |
| US11702546B2 (en) | 2018-10-24 | 2023-07-18 | California Institute Of Technology | Near-infrared heptamethine dyes for generation of singlet oxygen |
| EP3890741A1 (en) * | 2018-12-04 | 2021-10-13 | Avedro Inc. | Compounds and compositions for eye treatments |
Family Cites Families (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IL102645A (en) | 1992-07-26 | 1998-02-22 | Yeda Res & Dev | Chlorophyll and bacteriochlorophyll derivatives, their preparation and pharmaceutical compositions comprising them |
| US5756541A (en) * | 1996-03-11 | 1998-05-26 | Qlt Phototherapeutics Inc | Vision through photodynamic therapy of the eye |
| IL133253A0 (en) * | 1999-12-01 | 2001-04-30 | Yeda Res & Dev | Chlorophyll and bacteriochlorophyll esters, their preparation and pharmaceutical compositions comprising them |
| RU2201219C2 (ru) * | 2001-04-24 | 2003-03-27 | Макаров Константин Алексеевич | Фармакологическая композиция пролонгированного действия |
| WO2003028628A2 (en) | 2001-10-03 | 2003-04-10 | Miravant Pharmaceuticals, Inc. | Photosensitizing carbamate derivatives |
| IL152900A0 (en) | 2002-11-17 | 2003-06-24 | Yeda Res & Dev | Water-soluble bacteriochlorophyll derivatives and their pharmaceutical uses |
| CN1980661B (zh) * | 2004-06-07 | 2011-09-28 | 耶达研究及发展有限公司 | 阳离子细菌叶绿素衍生物及其用途 |
| JP2010502574A (ja) * | 2006-08-23 | 2010-01-28 | イエダ リサーチ アンド デベロップメント カンパニー リミテッド | Ｒｇｄペプチドとポルフィリン又は（バクテリオ）クロロフィル光合成剤とのコンジュゲート及びその使用 |
| KR101551590B1 (ko) | 2006-10-24 | 2015-09-08 | 캘리포니아 인스티튜트 오브 테크놀로지 | 신체 조직의 물리적 및/또는 화학적 성질에 영향을 주는 광화학적 요법 |
| RU2404768C1 (ru) * | 2009-10-28 | 2010-11-27 | Федеральное агентство по науке и инновациям | Глазные капли |
| WO2011099602A1 (ja) * | 2010-02-12 | 2011-08-18 | 学校法人日本大学 | ポルフィリン誘導体および放射線力学療法におけるその使用 |
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| BR112014004306A2 (pt) | 2017-03-28 |
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| MX2014002107A (es) | 2015-04-16 |
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| JP6215203B2 (ja) | 2017-10-18 |
| MX360683B (es) | 2018-11-13 |
| US11058772B2 (en) | 2021-07-13 |
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