RU2342929C2 - Способы лечения болезни паркинсона - Google Patents
Способы лечения болезни паркинсона Download PDFInfo
- Publication number
- RU2342929C2 RU2342929C2 RU2005131422/15A RU2005131422A RU2342929C2 RU 2342929 C2 RU2342929 C2 RU 2342929C2 RU 2005131422/15 A RU2005131422/15 A RU 2005131422/15A RU 2005131422 A RU2005131422 A RU 2005131422A RU 2342929 C2 RU2342929 C2 RU 2342929C2
- Authority
- RU
- Russia
- Prior art keywords
- safinamide
- treatment
- levodopa
- inhibitor
- disease
- Prior art date
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Landscapes
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2698330C2 (ru) * | 2014-04-21 | 2019-08-26 | Сивитас Терапьютикс, Инк. | Быстрое купирование двигательных флуктуаций при болезни паркинсона |
| US12458615B2 (en) | 2012-10-22 | 2025-11-04 | Merz Pharmaceuticals, Llc | Methods for providing rapid relief of motor fluctuations in a Parkinson's disease patient |
Families Citing this family (57)
| Publication number | Priority date | Publication date | Assignee | Title |
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| GB9727523D0 (en) | 1997-12-31 | 1998-02-25 | Pharmacia & Upjohn Spa | Alpha-aminoamide derivatives useful as analgesic agents |
| SI1423168T1 (sl) | 2001-09-03 | 2006-06-30 | Newron Pharm Spa | Farmacevtski sestavek, ki vsebuje gabapentin ali njegov analog in alfa-aminoamid, in njegova analgetska uporaba |
| EP1438956A1 (en) * | 2003-01-16 | 2004-07-21 | Newron Pharmaceuticals S.p.A. | Alpha-aminoamide derivatives useful as antimigraine agents |
| ES2339021T3 (es) * | 2003-08-25 | 2010-05-14 | Newron Pharmaceuticals S.P.A. | Derivados de alfa-aminoamida utiles como agentes antiinflamatorios. |
| EP1588704A1 (en) | 2004-04-22 | 2005-10-26 | Newron Pharmaceuticals S.p.A. | Alpha-aminoamide derivatives useful in the treatment of restless legs syndrome and addictive disorders |
| US20080096965A1 (en) * | 2004-09-10 | 2008-04-24 | Newron Pharmaceuticals S.P.A. | (Halobenzyloxy) Benzylamino-Propanamides as Sodium and/or Calcium Channel Selective Modulators |
| US20070004639A1 (en) * | 2005-07-01 | 2007-01-04 | Bodybio, Inc. | Methods and compositions for treating Parkinson's disease |
| WO2007069274A2 (en) * | 2005-11-09 | 2007-06-21 | Torrent Pharmaceuticals Limited | Pharmaceutical composition comprising a compound having a catechol moiety and an alkalising agent |
| EP1963280B1 (en) | 2005-12-22 | 2015-10-28 | Newron Pharmaceuticals S.p.A. | 2-phenylethylamino derivatives as calcium and/or sodium channel modulators |
| CN101032474B (zh) * | 2006-03-06 | 2011-02-16 | 重庆医药工业研究院有限责任公司 | 一种治疗或预防神经系统疾病的雷沙吉兰透皮贴片及其制备方法 |
| EP1870097A1 (en) * | 2006-06-15 | 2007-12-26 | Newron Pharmaceuticals S.p.A. | Alpha-aminoamide derivatives useful in the treatment of cognitive disorders |
| US8106056B2 (en) * | 2006-06-16 | 2012-01-31 | Solvay Pharmaceuticals B.V. | Combination preparations comprising bifeprunox and a dopamine agonist |
| DK2474521T3 (en) | 2006-06-19 | 2016-10-31 | Newron Pharm Spa | High-purity 2- [4- (3- and 2-fluorobenzyloxy) benzylamino] propanamides for use as pharmaceuticals and pharmaceutical formulations thus |
| DE102007014947B4 (de) * | 2007-03-23 | 2010-05-27 | Axxonis Pharma Ag | Stabilisierte wässrige Lösungen von Ergolinverbindungen |
| WO2008129043A1 (en) * | 2007-04-24 | 2008-10-30 | Boehringer Ingelheim International Gmbh | Combination with an extended release tablet formulation containing pramipexole or a pharmaceutically acceptable salt thereof |
| DK2155663T3 (en) | 2007-06-15 | 2018-01-22 | Newron Pharm Spa | SUBSTITUTED 2- [2- (PHENYL) ETHYLAMINO] ALKANAMIDE DERIVATIVES AND THEIR USE AS SODIUM AND / OR CALCIUM CHANNEL MODULATORS |
| GB2453770A (en) * | 2007-10-19 | 2009-04-22 | Reckitt Benckiser Healthcare | Oral composition comprising a cooling agent |
| WO2009054964A1 (en) * | 2007-10-22 | 2009-04-30 | Concert Pharmaceuticals, Inc. | Alpha-aminoamide derivatives |
| KR101593627B1 (ko) | 2007-12-11 | 2016-02-11 | 뉴론 파마슈티칼즈 에스. 피. 에이. | 고순도의 ２［４（３ 또는 ２플루오로벤질옥시）벤질아미노］프로판아미드의 제조방법 |
| CA2707646C (en) * | 2007-12-19 | 2016-09-13 | Newron Pharmaceuticals S.P.A. | Alpha-aminoamide derivatives useful in the treatment of psychiatric disorders |
| US20110027354A1 (en) * | 2008-04-01 | 2011-02-03 | Kim Hyoung-Chun | Anti-parkinsonian compounds |
| NZ589470A (en) * | 2008-06-02 | 2012-08-31 | Generics Uk Ltd | A process for the preparation of rasagiline and its analogues |
| AU2009254927B2 (en) * | 2008-06-02 | 2014-03-13 | Generics [Uk] Limited | A process for the preparation of enantiomerically pure amines |
| MX2010013393A (es) * | 2008-06-06 | 2011-06-21 | Pharma Two B Ltd | Composiciones farmaceuticas para el tratamiento de la enfermedad de parkinson. |
| BRPI0909894A2 (pt) * | 2008-06-13 | 2015-07-28 | Teva Pharma | "método de redução da velocidade de progressão de mal de parkinson em um paciente com mal de parkinson em estágio inicial, método de redução da velocidade de progressão de mal de parkinson, método de atraso da necessidade de terapia antiparkinsoniana sintomática em um paciente de mal de parkinson em estágio inicial, método de redução do risco de um paciente com mal de parkinson que necessita de terapia antiparkinsoniana, método de redução do declínio funcional de um paciente com mal de parkinson em estágio inicial, método de redução do declínio funcional em um paciente com mal de parkinson, método de tratamento de um paciente que exibe sinais iniciais de mal de parkinson, método de redução da fadiga em um paciente com mal de parkinson em estágio inicial, método de redução da velocidade de progressão clínica e tratamento de sintomas de mal de parkinson em um paciente com mal de parkinson, rasagilina ou um sal farmaceuticamente aceitável de rasagilina, composição farmacêutica. |
| WO2010010138A1 (en) * | 2008-07-24 | 2010-01-28 | Boehringer Ingelheim International Gmbh | Pharmaceutical composition comprising pramipexole and a calcium channel blocker for the treatment of parkinson's disease |
| EP2218444A3 (en) * | 2009-01-23 | 2010-08-25 | Teva Pharmaceutical Industries, Ltd. | Delayed release rasagiline formulation |
| US20100189791A1 (en) | 2009-01-23 | 2010-07-29 | Teva Pharmaceutical Industries, Ltd. | Delayed release rasagiline malate formulation |
| EP2314569A1 (en) | 2009-10-22 | 2011-04-27 | Merck Patent GmbH | Novel polymorphic forms of (S)-2-[4-(3-Fluoro-benzyloxy)-benzylamino]-propionamide mesylate salt and processes of manufacturing thereof |
| CN102048717B (zh) * | 2009-10-29 | 2014-02-19 | 重庆医药工业研究院有限责任公司 | 一种稳定的雷沙吉兰组合物 |
| WO2011098456A1 (en) * | 2010-02-09 | 2011-08-18 | Merck Serono S.A. | Safinamide in the treatment of dyskinesia |
| NZ602648A (en) | 2010-04-27 | 2014-10-31 | Newron Pharm Spa | Process for the production of ralfinamide methanesulfonate salts or their r-enantiomers |
| JP5820469B2 (ja) | 2010-04-30 | 2015-11-24 | テイコク ファーマ ユーエスエー インコーポレーテッド | プロピニルアミノインダンの経皮組成物 |
| CN103476404B (zh) | 2011-03-24 | 2017-09-29 | 帝国制药美国公司 | 包含活性剂层和活性剂转化层的透皮组合物 |
| US20150031768A1 (en) * | 2011-08-19 | 2015-01-29 | The Trustees Of Princeton University | C-halogen bond formation |
| WO2013081685A1 (en) | 2011-08-19 | 2013-06-06 | The Trustees Of Princeton University | C-halogen bond formation |
| WO2013070526A1 (en) | 2011-11-09 | 2013-05-16 | Teikoku Pharma Usa, Inc. | Methods for the treatment of skin neoplasms |
| AU2013338243B2 (en) | 2012-11-02 | 2016-09-29 | Teikoku Seiyaku Co., Ltd. | Propynylaminoindan transdermal compositions |
| US9155695B2 (en) | 2013-03-14 | 2015-10-13 | Medtronic, Inc. | Injectable ropinirole compositions and methods for making and using same |
| KR20160026897A (ko) | 2013-06-27 | 2016-03-09 | 세다르스-신나이 메디칼 센터 | 신경퇴행성 질환의 예방 및 치료를 위한 아드레날린 수용체 길항제 |
| CA2963371C (en) * | 2014-10-02 | 2020-06-02 | Korea Institute Of Science And Technology | Alpha-aminoamide derivative compound and pharmaceutical composition containing the same |
| WO2017032874A1 (en) * | 2015-08-27 | 2017-03-02 | Prexton Therapeutics Sa | Brain-penetrant chromone oxime derivative for the therapy of levodopa-induced dyskinesia |
| KR102889062B1 (ko) * | 2016-03-17 | 2025-11-21 | 더 존스 홉킨스 유니버시티 | Paris의 파네실화에 의해 파킨슨병을 예방 또는 치료하기 위한 방법 |
| ITUA20163981A1 (it) | 2016-05-31 | 2017-12-01 | Zambon Spa | Composizioni farmaceutiche comprendenti safinamide |
| WO2018132746A1 (en) * | 2017-01-14 | 2018-07-19 | Mischley Laurie Kathern | Method of using human excrement and secretions for early detection of parkinson's disease |
| CN109251155A (zh) * | 2017-07-14 | 2019-01-22 | 广东东阳光药业有限公司 | α-氨基酰胺衍生物及其用途 |
| US11234961B2 (en) * | 2017-08-17 | 2022-02-01 | Zi-Qiang Gu | Pamoate salt of monoamine anti-Parkinson's agents, method of preparation and use thereof |
| MX2020004403A (es) | 2017-11-02 | 2020-08-06 | Zambon Spa | Composiciones farmaceuticas que comprenden safinamida. |
| KR102005019B1 (ko) * | 2018-04-04 | 2019-07-31 | 한국과학기술연구원 | 뇌졸중의 예방 및 치료용 조성물 |
| KR20220074895A (ko) * | 2019-09-12 | 2022-06-03 | 어치브 라이프 사이언시즈, 인크. | 필요로 하는 대상체의 중독 치료 및/또는 예방을 위한 시티신을 포함하는 조성물 |
| LU101477B1 (en) * | 2019-11-12 | 2021-05-14 | Univ Luxembourg | An inhibitor of an iron-containing hydrogenase of a methanogenic archaeon for use in the treatment or prevention of a parkinsonian condition |
| CN110938014A (zh) * | 2019-11-28 | 2020-03-31 | 岳千奥 | 取代苯氧酰胺衍生物、应用及用于治疗帕金森病的药物 |
| JP2023504876A (ja) * | 2019-12-06 | 2023-02-07 | シャンハイ ファーマシューティカルズ ホールディング カンパニー，リミティド | 薬物組成物、キット及びその応用 |
| CN110999980A (zh) * | 2019-12-19 | 2020-04-14 | 新疆石河子职业技术学院（石河子市技工学校） | 一种葡萄酒洗浸奶酪加工方法 |
| US20230181508A1 (en) * | 2020-08-31 | 2023-06-15 | Purdue Pharma L.P. | Compositions and methods for levodopa delivery |
| WO2022192173A1 (en) * | 2021-03-08 | 2022-09-15 | Prothena Biosciences Limited | Treatment of parkinson's disease |
| KR102790040B1 (ko) * | 2021-06-24 | 2025-04-01 | 연세대학교 산학협력단 | 도파민 미모톱 기능 합성 펩티드 및 이를 포함하는 mao-b 억제제 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1990014334A1 (en) * | 1989-05-25 | 1990-11-29 | Farmitalia Carlo Erba S.R.L. | N-PHENYLALKYL SUBSTITUTED α-AMINO CARBOXAMIDE DERIVATIVES AND PROCESS FOR THEIR PREPARATION |
| US5945454A (en) * | 1995-07-27 | 1999-08-31 | Pharmacia & Upjohn, S.P.A. | 2-(4-substituted)-benzylamino-2-methyl-propanamide derivatives |
| US6306903B1 (en) * | 1997-12-31 | 2001-10-23 | Newron Pharmaceuticals S.P.A. | Alpha-aminoamide derivatives useful as analgesic agents |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1140748A (en) | 1966-06-23 | 1969-01-22 | Ici Ltd | New carboxylic acid derivatives |
| US3795739A (en) * | 1972-02-14 | 1974-03-05 | Hoffmann La Roche | Treatment of parkinson disease |
| US4049663A (en) | 1972-06-06 | 1977-09-20 | Allen & Hanburys Limited | Ethylene diamine derivatives |
| FR2480747A1 (fr) | 1980-04-17 | 1981-10-23 | Roques Bernard | Derives d'acides amines et leur application therapeutique |
| US4935429A (en) | 1985-10-25 | 1990-06-19 | Dackis Charles A | Method of treating psychostimulant addiction |
| ES2042520T3 (es) * | 1986-06-10 | 1993-12-16 | Chiesi Farma Spa | Composiciones farmaceuticas que contienen el ester metilico de levodopa, preparacion y aplicaciones terapeuticas del mismo. |
| CA1336169C (en) | 1988-03-01 | 1995-07-04 | Walther Birkmayer | Agent for treatment of parkinson's disease |
| US5221536A (en) * | 1990-05-07 | 1993-06-22 | Alza Corporation | Dosage form indicated for the management of abnormal posture, tremor and involuntary movement |
| US5502658A (en) | 1990-12-27 | 1996-03-26 | Relin; Arkadi | Sampled-continuous probability method of velocity measurement of the object having informatively-structural inhomogeneity |
| GB9306886D0 (en) | 1993-04-01 | 1993-05-26 | Erba Carlo Spa | Substituted (arylakoxybenzyl) aminopropanamide derivatives and process for their preparation |
| IL111240A (en) * | 1993-10-18 | 2001-10-31 | Teva Pharma | Salts of r(+) - enantiomers of n- propargyl-1-aminoindan and pharmaceutical compositions comprising them |
| ES2211904T3 (es) * | 1995-05-26 | 2004-07-16 | Pfizer Inc. | Combinaciones para el tratamiento del parkinsonismo que contienen antagonistas selectivos de nmda. |
| FI109453B (fi) | 1999-06-30 | 2002-08-15 | Orion Yhtymae Oyj | Farmaseuttinen koostumus |
| US20020019421A1 (en) * | 2000-07-05 | 2002-02-14 | Roni Biberman | Compositions and therapy for substance addiction |
| DE10041479A1 (de) * | 2000-08-24 | 2002-03-14 | Sanol Arznei Schwarz Gmbh | Neue pharmazeutische Zusammensetzung zur Verabreichung von N-0923 |
| FR2829027A1 (fr) * | 2001-08-29 | 2003-03-07 | Aventis Pharma Sa | Association avec un antagoniste du recepteur cb1, les compositions pharmaceutiques les contenant et leur utilisation pour le traitement de la maladie de parkinson |
-
2004
- 2004-04-07 AR ARP040101189A patent/AR044007A1/es unknown
- 2004-04-08 TW TW093109755A patent/TWI340640B/zh not_active IP Right Cessation
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- 2004-04-08 JP JP2006506582A patent/JP2006522800A/ja active Pending
- 2004-04-08 US US10/559,982 patent/US8283380B2/en active Active
- 2004-04-08 BR BRPI0409364-0A patent/BRPI0409364A/pt not_active Application Discontinuation
- 2004-04-08 EP EP09154864.4A patent/EP2070526B1/en not_active Expired - Lifetime
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- 2004-04-08 DE DE602004021790T patent/DE602004021790D1/de not_active Expired - Lifetime
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- 2004-04-08 KR KR1020117013555A patent/KR20110070929A/ko not_active Ceased
- 2004-04-08 DK DK04726590T patent/DK1613296T3/da active
-
2005
- 2005-10-10 IL IL171331A patent/IL171331A/en active Protection Beyond IP Right Term
- 2005-10-10 NO NO20054640A patent/NO334316B1/no active Protection Beyond IP Right Term
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- 2009-08-12 CY CY20091100857T patent/CY1109295T1/el unknown
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- 2012-08-24 US US13/594,621 patent/US8901176B2/en not_active Expired - Lifetime
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- 2015-07-23 NO NO2015018C patent/NO2015018I1/no not_active IP Right Cessation
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1990014334A1 (en) * | 1989-05-25 | 1990-11-29 | Farmitalia Carlo Erba S.R.L. | N-PHENYLALKYL SUBSTITUTED α-AMINO CARBOXAMIDE DERIVATIVES AND PROCESS FOR THEIR PREPARATION |
| US5391577A (en) * | 1989-05-25 | 1995-02-21 | Farmitalia Carlo Erba S R L | N-phenylalkyl substituted α-amino carboxamide derivatives and process for their preparation |
| US5945454A (en) * | 1995-07-27 | 1999-08-31 | Pharmacia & Upjohn, S.P.A. | 2-(4-substituted)-benzylamino-2-methyl-propanamide derivatives |
| US6306903B1 (en) * | 1997-12-31 | 2001-10-23 | Newron Pharmaceuticals S.P.A. | Alpha-aminoamide derivatives useful as analgesic agents |
Non-Patent Citations (2)
| Title |
|---|
| МИХАЙЛОВ И.Б. Настольная книга врача по клинической фармакологии. - СПб.: Фолиант, 2001, с.473. МАШКОВСКИЙ М.Д. Лекарственные средства. - М.: Медицина 1993 12-е изд. т.1 с.173-177. Newron releases positive preliminary phase II data for safinamide in Parkinson's desease 09/01/2003 [найдено 12.12.2007]. Найдено из Интернет: <URL:http://www.newron.com/test/news_2003.html. Руководство по медицине THE MERCK MANUAL. - М.: Мир 1997, т.1, с.1022-1023. * |
| Харкевич Д.А. Фармакология. - М.: Медицина, 1987, с.47-48. Беликов В.Г. Фармацевтическая химия. - М.: Высшая школа, 1993, т.1, с.43-47. * |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12458615B2 (en) | 2012-10-22 | 2025-11-04 | Merz Pharmaceuticals, Llc | Methods for providing rapid relief of motor fluctuations in a Parkinson's disease patient |
| RU2698330C2 (ru) * | 2014-04-21 | 2019-08-26 | Сивитас Терапьютикс, Инк. | Быстрое купирование двигательных флуктуаций при болезни паркинсона |
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