JP2009504748A - Ｒ（＋）プラミペキソールを用いた神経回復 - Google Patents
Ｒ（＋）プラミペキソールを用いた神経回復 Download PDFInfo
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- JP2009504748A JP2009504748A JP2008527061A JP2008527061A JP2009504748A JP 2009504748 A JP2009504748 A JP 2009504748A JP 2008527061 A JP2008527061 A JP 2008527061A JP 2008527061 A JP2008527061 A JP 2008527061A JP 2009504748 A JP2009504748 A JP 2009504748A
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- pramipexole
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- tetrahydrobenzathiazole
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- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
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- A61P25/00—Drugs for disorders of the nervous system
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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
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A—HUMAN NECESSITIES
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Landscapes
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- Chemical & Material Sciences (AREA)
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Applications Claiming Priority (2)
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| US70821305P | 2005-08-15 | 2005-08-15 | |
| PCT/US2006/031831 WO2007022182A1 (en) | 2005-08-15 | 2006-08-15 | Neurorestoration with r(+) pramipexole |
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| JP2012233610A Pending JP2013014629A (ja) | 2005-08-15 | 2012-10-23 | Ｒ（＋）プラミペキソールを用いた神経回復 |
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| EP (1) | EP1917014B1 (enExample) |
| JP (2) | JP2009504748A (enExample) |
| AT (1) | ATE444750T1 (enExample) |
| AU (1) | AU2006279643B2 (enExample) |
| CA (1) | CA2619217A1 (enExample) |
| DE (1) | DE602006009670D1 (enExample) |
| ES (1) | ES2334061T3 (enExample) |
| IL (1) | IL189512A (enExample) |
| WO (1) | WO2007022182A1 (enExample) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8017598B2 (en) | 2006-05-16 | 2011-09-13 | Knopp Neurosciences, Inc. | Compositions of R(+) and S(−) pramipexole and methods of using the same |
| JP2012530723A (ja) * | 2009-06-19 | 2012-12-06 | ノップ ニューロサイエンシーズ、インク． | 筋萎縮性側索硬化症を治療するための組成物及び方法 |
| US8518926B2 (en) | 2006-04-10 | 2013-08-27 | Knopp Neurosciences, Inc. | Compositions and methods of using (R)-pramipexole |
| US8524695B2 (en) | 2006-12-14 | 2013-09-03 | Knopp Neurosciences, Inc. | Modified release formulations of (6R)-4,5,6,7-tetrahydro-N6-propyl-2,6-benzothiazole-diamine and methods of using the same |
| JP2016523981A (ja) * | 2013-07-12 | 2016-08-12 | ノップ バイオサイエンシーズ エルエルシー | 高好酸球値および／または高好塩基球値の治療 |
| US9468630B2 (en) | 2013-07-12 | 2016-10-18 | Knopp Biosciences Llc | Compositions and methods for treating conditions related to increased eosinophils |
| US9642840B2 (en) | 2013-08-13 | 2017-05-09 | Knopp Biosciences, Llc | Compositions and methods for treating plasma cell disorders and B-cell prolymphocytic disorders |
| US9662313B2 (en) | 2013-02-28 | 2017-05-30 | Knopp Biosciences Llc | Compositions and methods for treating amyotrophic lateral sclerosis in responders |
| US9763918B2 (en) | 2013-08-13 | 2017-09-19 | Knopp Biosciences Llc | Compositions and methods for treating chronic urticaria |
| US10179774B2 (en) | 2007-03-14 | 2019-01-15 | Knopp Biosciences Llc | Synthesis of chirally purified substituted benzothiazole diamines |
| US10208003B2 (en) | 2011-12-22 | 2019-02-19 | Knopp Biosciences Llc | Synthesis of amine substituted 4,5,6,7-tetrahydrobenzothiazole compounds |
| JP2020512390A (ja) * | 2017-03-27 | 2020-04-23 | チェイス セラピューティクス コーポレイション | シヌクレイノパチーを処置するための組成物および方法 |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2246053B1 (en) * | 2001-12-11 | 2013-09-18 | University Of Virginia Patent Foundation | Use of pramipexole to treat amyotrophic lateral sclerosis |
| US20060281797A1 (en) * | 2001-12-11 | 2006-12-14 | University Of Virginia Patent Foundation | Neurorestoration with R(+) Pramipexole |
| US20050226926A1 (en) | 2002-07-25 | 2005-10-13 | Pfizer Inc | Sustained-release tablet composition of pramipexole |
| BRPI0513848A (pt) | 2004-08-13 | 2008-05-20 | Boehringer Ingelheim Int | formulação de pélete de liberação prolongada contendo pramipexol ou um sal farmaceuticamente aceitável deste, método para fabricação da mesma e uso desta |
| PH12012501282A1 (en) | 2004-08-13 | 2019-03-22 | Boehringer Ingelheim Int | Extended release tablet formulation containing pramipexole or a pharmaceutically acceptable salt thereof, method for manufacturing the same and use thereof |
| DE602006009670D1 (de) * | 2005-08-15 | 2009-11-19 | Univ Virginia | Neurorestauration mit r(+) pramipexol |
| WO2007090882A2 (en) * | 2006-02-10 | 2007-08-16 | Boehringer Ingelheim International Gmbh | Pharmaceutical extended release compositions comprising pramipexole |
| EP2497472A1 (en) * | 2006-05-16 | 2012-09-12 | Knopp Neurosciences, Inc. | Therapeutically effective amounts of R(+) and S(-) pramipexole for use in the treatment of Parkinson's disease and their pharmaceutical compositions |
| JP2010513316A (ja) * | 2006-12-14 | 2010-04-30 | ノップ ニューロサイエンシーズ、インク． | （ｒ）−プラミペキソール組成物およびその使用法 |
| EP2136638A4 (en) * | 2007-03-14 | 2010-05-12 | Knopp Neurosciences Inc | MODIFIED RELEASE FORMULATIONS OF (6R) -4,5,6,7-TETRAHYDRO-N6-PROPYL-2,6-BENZOTHIAZOLE DIAMINE AND METHODS OF USE THEREOF |
| US20100130569A1 (en) * | 2007-05-11 | 2010-05-27 | Saten Pharmaceutical Co., Ltd. | Prophylactic or therapeutic agent for posterior ocular disease comprising non-ergot selective d2 receptor agonist as active ingredient |
| GB0721333D0 (en) * | 2007-10-31 | 2007-12-12 | Motac Neuroscience Ltd | Medicaments |
| CA2734491A1 (en) | 2008-08-19 | 2010-02-25 | Knopp Neurosciences, Inc. | Compositions and methods of using (r)-pramipexole |
| AU2010234244A1 (en) * | 2009-04-09 | 2011-10-13 | Purdue Pharma | Once-daily oral IR/CR pramipexole formulation |
| KR101799429B1 (ko) | 2010-05-03 | 2017-11-21 | 에스케이바이오팜 주식회사 | 신경 세포 사멸 또는 신경 퇴화를 억제하기 위한 약학적 조성물 |
| WO2016194015A2 (en) * | 2015-06-04 | 2016-12-08 | Chiarugi Alberto | Use of r(+)-pramipexole (dexpramipexole) for the treatment of cerebral ischemia of the focal type |
| IL312486B2 (en) | 2017-04-10 | 2025-05-01 | Chase Therapeutics Corp | NK1 antagonist combination and method for treating synucleinopathies |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005516911A (ja) * | 2001-12-11 | 2005-06-09 | ユニバーシティ オブ バージニア パテント ファウンデーション | 筋萎縮性側索硬化症を処置するためのプラミペキソールの使用 |
Family Cites Families (27)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE45735T1 (de) * | 1984-12-22 | 1989-09-15 | Thomae Gmbh Dr K | Tetrahydro-benzthiazole, deren herstellung und deren verwendung als zwischenprodukte oder als arnzneimittel. |
| DE3937271A1 (de) * | 1989-11-09 | 1991-05-16 | Boehringer Ingelheim Kg | Transdermale applikation von 2-amino-6-n-propylamino-4,5,6,7-tetrahydrobenzothiazol |
| US5650420A (en) * | 1994-12-15 | 1997-07-22 | Pharmacia & Upjohn Company | Pramipexole as a neuroprotective agent |
| US6156777A (en) * | 1994-12-15 | 2000-12-05 | Pharmacia & Upjohn Company | Use of pramipexole as a neuroprotective agent |
| CA2235747C (en) * | 1995-10-26 | 2006-01-03 | Sanofi | Use of 1-(2-naphth-2-ylethyl)-4-(3-trifluoromethylphenyl)-1,2,3,6-tetrahydropyridine for preparing drugs for treating amyotrophic lateral sclerosis |
| GB9705428D0 (en) * | 1997-03-15 | 1997-04-30 | Knoll Ag | Therapeutic agents |
| US6197339B1 (en) * | 1997-09-30 | 2001-03-06 | Pharmacia & Upjohn Company | Sustained release tablet formulation to treat Parkinson's disease |
| PE20000728A1 (es) * | 1998-06-26 | 2000-08-21 | Cocensys Inc | Heterociclos 4-bencil piperidina alquilsulfoxido y su uso como antagonistas receptores subtipo-selectivo nmda |
| DE19830201A1 (de) * | 1998-07-07 | 2000-01-13 | Boehringer Ingelheim Pharma | Mittel mit antidepressiver Wirkung |
| CA2301899C (en) * | 1998-07-27 | 2008-11-18 | Boehringer Ingelheim Pharma Kg | Agent with an antidepressant activity |
| CA2653839A1 (en) * | 1998-11-02 | 2000-05-11 | John G. Devane | Multiparticulate modified release composition |
| AU2001278875B2 (en) * | 2000-07-06 | 2007-06-07 | The Government Of The United States Of America, As Represented By The Secretary, Department Of Health And Human Services | Tetrahydrobenzothiazole analogues as neuroprotective agents |
| DE10037619A1 (de) * | 2000-08-02 | 2002-02-14 | Daimler Chrysler Ag | Anordnung von Bedienelementen |
| ES2187249B1 (es) * | 2000-09-18 | 2004-09-16 | Synthon Bv | Procedimiento para la preparacion de 2-amino-6-(alquil)amino-4,5,6,7-tetrahidrobenzotiazoles. |
| US20020151526A1 (en) * | 2000-10-06 | 2002-10-17 | Gallop Mark A. | Bile-acid prodrugs of L-dopa and their use in the sustained treatment of parkinsonism |
| DE10137082A1 (de) * | 2001-07-28 | 2003-02-13 | Hexal Ag | Matrixkontrolliertes transdermales therapeutisches System zur Anwendung von Pramiprexol und Ropinirol |
| US20060281797A1 (en) * | 2001-12-11 | 2006-12-14 | University Of Virginia Patent Foundation | Neurorestoration with R(+) Pramipexole |
| AU2002316231A1 (en) * | 2002-02-19 | 2003-09-29 | Xenoport, Inc. | Methods for synthesis of prodrugs from 1-acyl-alkyl derivatives and compositions thereof |
| WO2003077897A1 (en) * | 2002-03-15 | 2003-09-25 | Cypress Bioscience, Inc. | Ne and 5-ht reuptake inhibitors for treating visceral pain syndromes |
| US20050226926A1 (en) * | 2002-07-25 | 2005-10-13 | Pfizer Inc | Sustained-release tablet composition of pramipexole |
| US20040132826A1 (en) * | 2002-10-25 | 2004-07-08 | Collegium Pharmaceutical, Inc. | Modified release compositions of milnacipran |
| ATE499100T1 (de) * | 2003-03-31 | 2011-03-15 | Titan Pharmaceuticals Inc | Polymeres implantat zur verzögerten freisetzung von dopamin antagonisten |
| US7662987B2 (en) * | 2003-07-15 | 2010-02-16 | Xenoport, Inc. | Methods for synthesis of acyloxyalkyl compounds |
| DE10333393A1 (de) * | 2003-07-23 | 2005-02-24 | Lts Lohmann Therapie-Systeme Ag | Transdermales Therapeutisches System mit dem Wirkstoff Pramipexol |
| BRPI0513848A (pt) * | 2004-08-13 | 2008-05-20 | Boehringer Ingelheim Int | formulação de pélete de liberação prolongada contendo pramipexol ou um sal farmaceuticamente aceitável deste, método para fabricação da mesma e uso desta |
| TW200616604A (en) * | 2004-08-26 | 2006-06-01 | Nicholas Piramal India Ltd | Nitric oxide releasing prodrugs containing bio-cleavable linker |
| DE602006009670D1 (de) * | 2005-08-15 | 2009-11-19 | Univ Virginia | Neurorestauration mit r(+) pramipexol |
-
2006
- 2006-08-15 DE DE602006009670T patent/DE602006009670D1/de active Active
- 2006-08-15 AU AU2006279643A patent/AU2006279643B2/en not_active Ceased
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- 2006-08-15 EP EP06801521A patent/EP1917014B1/en not_active Not-in-force
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- 2006-08-15 CA CA002619217A patent/CA2619217A1/en not_active Abandoned
- 2006-08-15 AT AT06801521T patent/ATE444750T1/de not_active IP Right Cessation
- 2006-08-15 ES ES06801521T patent/ES2334061T3/es active Active
- 2006-08-15 JP JP2008527061A patent/JP2009504748A/ja not_active Withdrawn
-
2008
- 2008-02-13 IL IL189512A patent/IL189512A/en not_active IP Right Cessation
-
2011
- 2011-05-06 US US13/102,757 patent/US20110218222A1/en not_active Abandoned
-
2012
- 2012-10-23 JP JP2012233610A patent/JP2013014629A/ja active Pending
- 2012-12-27 US US13/728,504 patent/US20130116292A1/en not_active Abandoned
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2005516911A (ja) * | 2001-12-11 | 2005-06-09 | ユニバーシティ オブ バージニア パテント ファウンデーション | 筋萎縮性側索硬化症を処置するためのプラミペキソールの使用 |
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| US8518926B2 (en) | 2006-04-10 | 2013-08-27 | Knopp Neurosciences, Inc. | Compositions and methods of using (R)-pramipexole |
| US8445474B2 (en) | 2006-05-16 | 2013-05-21 | Knopp Neurosciences, Inc. | Compositions of R(+) and S(−) pramipexole and methods of using the same |
| US8017598B2 (en) | 2006-05-16 | 2011-09-13 | Knopp Neurosciences, Inc. | Compositions of R(+) and S(−) pramipexole and methods of using the same |
| US8524695B2 (en) | 2006-12-14 | 2013-09-03 | Knopp Neurosciences, Inc. | Modified release formulations of (6R)-4,5,6,7-tetrahydro-N6-propyl-2,6-benzothiazole-diamine and methods of using the same |
| US10179774B2 (en) | 2007-03-14 | 2019-01-15 | Knopp Biosciences Llc | Synthesis of chirally purified substituted benzothiazole diamines |
| JP2012530723A (ja) * | 2009-06-19 | 2012-12-06 | ノップ ニューロサイエンシーズ、インク． | 筋萎縮性側索硬化症を治療するための組成物及び方法 |
| US10208003B2 (en) | 2011-12-22 | 2019-02-19 | Knopp Biosciences Llc | Synthesis of amine substituted 4,5,6,7-tetrahydrobenzothiazole compounds |
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| JP2023071825A (ja) * | 2017-03-27 | 2023-05-23 | チェイス セラピューティクス コーポレイション | シヌクレイノパチーを処置するための組成物および方法 |
| JP7557939B2 (ja) | 2017-03-27 | 2024-09-30 | チェイス セラピューティクス コーポレイション | シヌクレイノパチーを処置するための組成物および方法 |
| JP7711113B2 (ja) | 2017-03-27 | 2025-07-22 | チェイス セラピューティクス コーポレイション | シヌクレイノパチーを処置するための組成物および方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| IL189512A0 (en) | 2011-08-01 |
| US20080234338A1 (en) | 2008-09-25 |
| AU2006279643A1 (en) | 2007-02-22 |
| IL189512A (en) | 2013-03-24 |
| ATE444750T1 (de) | 2009-10-15 |
| WO2007022182A1 (en) | 2007-02-22 |
| AU2006279643B2 (en) | 2010-06-17 |
| EP1917014B1 (en) | 2009-10-07 |
| US20110218222A1 (en) | 2011-09-08 |
| DE602006009670D1 (de) | 2009-11-19 |
| US20130116292A1 (en) | 2013-05-09 |
| JP2013014629A (ja) | 2013-01-24 |
| EP1917014A1 (en) | 2008-05-07 |
| CA2619217A1 (en) | 2007-02-22 |
| ES2334061T3 (es) | 2010-03-04 |
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