CA2977367A1 - Methods and compositions for decreasing gastric emptying - Google Patents
Methods and compositions for decreasing gastric emptying Download PDFInfo
- Publication number
- CA2977367A1 CA2977367A1 CA2977367A CA2977367A CA2977367A1 CA 2977367 A1 CA2977367 A1 CA 2977367A1 CA 2977367 A CA2977367 A CA 2977367A CA 2977367 A CA2977367 A CA 2977367A CA 2977367 A1 CA2977367 A1 CA 2977367A1
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- alkyl
- group
- agent
- optionally substituted
- treating
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| PH12013501258A1 (en) | 2010-12-22 | 2013-08-28 | Purdue Pharma Lp | Substituted pyridines as sodium channel blockers |
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| US9120786B2 (en) | 2013-03-04 | 2015-09-01 | Purdue Pharma, L.P. | Triazine carboxamides as sodium channel blockers |
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| CN105612152A (zh) | 2013-08-26 | 2016-05-25 | 普渡制药公司 | 氮杂螺[4.5]癸烷衍生物及其用途 |
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| EA202092627A1 (ru) | 2013-11-18 | 2021-09-30 | Глобал Блад Терапьютикс, Инк. | Соединения и их применения для модуляции гемоглобина |
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| RU2017490C1 (ru) * | 1990-01-18 | 1994-08-15 | Назаренко Петр Михайлович | Способ лечения демпин-синдрома после резекции желудка по способу бильрот-1 |
| ATE301457T1 (de) | 1995-06-12 | 2005-08-15 | Searle & Co | Mittel, enthaltend einen cyclooxygenase-2 inhibitor und einen 5-lipoxygenase inhibitor |
| US20040038970A1 (en) * | 1998-06-12 | 2004-02-26 | Societe De Conseils De Recherches Etd' Application Scientifiques, S.A.S. A Paris, France Corp. | Beta-carboline compounds |
| AR029489A1 (es) | 2000-03-10 | 2003-07-02 | Euro Celtique Sa | Piridinas, pirimidinas, pirazinas, triazinas sustituidas por arilo, composiciones farmaceuticas y el uso de las mismas para la manufactura de un medicamento |
| EP1292577B1 (en) | 2000-03-24 | 2012-10-24 | Euro-Celtique S.A. | Aryl substituted pyrazoles, triazoles and tetrazoles as sodium channel blocker |
| EP1268427A1 (en) | 2000-03-31 | 2003-01-02 | Cocensys, Inc. | Aminopyridines and their use as anticonvulsants and sodium channel blockers |
| JP2004538285A (ja) | 2001-07-16 | 2004-12-24 | ユーロ−セルティック エス． ア． | アリール置換チアゾリジノンおよびその使用 |
| AR036873A1 (es) | 2001-09-07 | 2004-10-13 | Euro Celtique Sa | Piridinas aril sustituidas a, composiciones farmaceuticas y el uso de las mismas para la preparacion de un medicamento |
| ATE434610T1 (de) | 2002-03-13 | 2009-07-15 | Euro Celtique Sa | Aryl substituierte pyrimidine und deren verwendung |
| JP2006504660A (ja) | 2002-07-31 | 2006-02-09 | ユーロ−セルティーク エス．エイ． | アリール置換ベンゾイミダゾール類およびナトリウムチャネルブロッカーとしてのそれらの使用 |
| JP2006515326A (ja) * | 2003-01-30 | 2006-05-25 | ダイノジェン ファーマシューティカルズ， インコーポレイテッド | 胃腸管障害を処置するためのナトリウムチャネルモジュレーターの使用 |
| EP1533298A1 (en) * | 2003-11-21 | 2005-05-25 | Newron Pharmaceuticals S.p.A. | 3-aminopyrrolidone derivatives |
| AU2006206274A1 (en) | 2005-01-20 | 2006-07-27 | Sirtris Pharmaceuticals, Inc. | Use of sirtuin-activating compounds for treating flushing and drug induced weight gain |
| US20070020194A1 (en) | 2005-06-08 | 2007-01-25 | Greenway Frank L Iii | Nasally administered appetite suppressant |
| JP2009523842A (ja) | 2006-01-23 | 2009-06-25 | ファイザー・リミテッド | ナトリウムチャネルモジュレーターとしてのピリジン誘導体 |
| EP2078523A4 (en) * | 2006-10-13 | 2010-02-10 | Ajinomoto Kk | AGENT COMPRISING 4-HYDROXYISOLEUCINE FOR THE SUPPRESSION OF GASTRIC DRAIN |
| MX2009004822A (es) | 2006-11-01 | 2009-10-19 | Purdue Pharma Lp | Compuestos de fenilpropionamida y usos de los mismos. |
| WO2009012242A2 (en) | 2007-07-13 | 2009-01-22 | Icagen, Inc. | Sodium channel inhibitors |
| WO2009012241A1 (en) | 2007-07-13 | 2009-01-22 | Icagen, Inc. | Sodium channel inhibitors |
| JP2013530180A (ja) | 2010-06-16 | 2013-07-25 | パーデュー、ファーマ、リミテッド、パートナーシップ | アリール置換インドールおよびその使用 |
| US9279003B2 (en) | 2010-07-07 | 2016-03-08 | Purdue Pharma L.P. | Analogs of sodium channel peptide toxin |
| WO2012007836A1 (en) | 2010-07-16 | 2012-01-19 | Purdue Pharma .Lp. | Pyridine compounds as sodium channel blockers |
| MX2013003101A (es) | 2010-09-17 | 2013-09-26 | Purdue Pharma Lp | Compuestos de piridina y sus usos. |
| ES2540562T3 (es) | 2010-10-05 | 2015-07-10 | Purdue Pharma L.P. | Compuestos de quinazolina como bloqueadores de canales de sodio |
| PH12013501258A1 (en) | 2010-12-22 | 2013-08-28 | Purdue Pharma Lp | Substituted pyridines as sodium channel blockers |
| TW201331186A (zh) * | 2011-09-02 | 2013-08-01 | Purdue Pharma Lp | 作為鈉通道阻斷劑之嘧啶類 |
| JP5946538B2 (ja) | 2011-10-26 | 2016-07-06 | ファイザー・リミテッドＰｆｉｚｅｒ Ｌｉｍｉｔｅｄ | ナトリウムチャネルモジュレーターとして有用な（４−フェニルイミダゾール−２−イル）エチルアミン誘導体 |
| US9388137B2 (en) | 2011-10-31 | 2016-07-12 | Purdue Pharma L.P. | Quaternized amines as sodium channel blockers |
| WO2013072758A1 (en) | 2011-11-15 | 2013-05-23 | Purdue Pharma L.P. | Pyrimidine diol amides as sodium channel blockers |
| JP5938219B2 (ja) * | 2012-01-23 | 2016-06-22 | 株式会社明治 | 胃排出遅延のための食品用の剤または医療用の剤 |
| AU2013203824A1 (en) | 2012-03-16 | 2013-10-03 | Purdue Pharma L.P. | Substituted pyridines and pryimidines as sodium channel blockers |
| WO2014016673A1 (en) | 2012-07-27 | 2014-01-30 | Purdue Pharma L.P. | Sodium channel blocking peptides and the use thereof |
| JP6110516B2 (ja) * | 2013-03-04 | 2017-04-05 | パーデュー、ファーマ、リミテッド、パートナーシップ | ナトリウムチャネル遮断剤としてのピリミジンカルボキサミド |
| EP3666274A1 (en) | 2013-03-15 | 2020-06-17 | Purdue Pharma LP | Carboxamide derivatives and use thereof |
| JP6762308B2 (ja) * | 2015-02-19 | 2020-09-30 | パーデュー、ファーマ、リミテッド、パートナーシップ | 胃排出の減少方法及び組成物 |
-
2016
- 2016-02-19 JP JP2017543916A patent/JP6762308B2/ja active Active
- 2016-02-19 AU AU2016219879A patent/AU2016219879A1/en not_active Abandoned
- 2016-02-19 US US15/048,530 patent/US9763955B2/en active Active
- 2016-02-19 EP EP16753165.6A patent/EP3258925B1/en active Active
- 2016-02-19 KR KR1020177025621A patent/KR20170117170A/ko not_active Withdrawn
- 2016-02-19 CA CA2977367A patent/CA2977367A1/en not_active Abandoned
- 2016-02-19 BR BR112017017619A patent/BR112017017619A2/pt not_active Application Discontinuation
- 2016-02-19 CN CN201680021578.2A patent/CN107613965A/zh active Pending
- 2016-02-19 MX MX2017010682A patent/MX2017010682A/es unknown
- 2016-02-19 WO PCT/US2016/018715 patent/WO2016134283A1/en not_active Ceased
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2017
- 2017-08-03 PH PH12017501393A patent/PH12017501393A1/en unknown
- 2017-08-10 IL IL253949A patent/IL253949A0/en unknown
- 2017-08-18 US US15/680,737 patent/US10143696B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| MX2017010682A (es) | 2018-04-24 |
| EP3258925A4 (en) | 2019-01-09 |
| IL253949A0 (en) | 2017-10-31 |
| EP3258925B1 (en) | 2023-03-29 |
| AU2016219879A1 (en) | 2017-08-24 |
| PH12017501393A1 (en) | 2018-01-08 |
| US20160243129A1 (en) | 2016-08-25 |
| JP6762308B2 (ja) | 2020-09-30 |
| US20170340646A1 (en) | 2017-11-30 |
| JP2018509397A (ja) | 2018-04-05 |
| US10143696B2 (en) | 2018-12-04 |
| BR112017017619A2 (pt) | 2018-05-08 |
| US9763955B2 (en) | 2017-09-19 |
| WO2016134283A1 (en) | 2016-08-25 |
| EP3258925A1 (en) | 2017-12-27 |
| KR20170117170A (ko) | 2017-10-20 |
| CN107613965A (zh) | 2018-01-19 |
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| FZDE | Discontinued |
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