RU2706708C2 - Твердые лекарственные формы ондансетрона с пролонгированным высвобождением для лечения симптомов тошноты, рвоты и диареи - Google Patents
Твердые лекарственные формы ондансетрона с пролонгированным высвобождением для лечения симптомов тошноты, рвоты и диареи Download PDFInfo
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| US201462040136P | 2014-08-21 | 2014-08-21 | |
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| CA3051614A1 (en) | 2017-01-26 | 2018-08-02 | Triastek, Inc. | Dosage forms of controlled release at specific gastrointestinal sites |
| JP7315383B2 (ja) * | 2019-06-27 | 2023-07-26 | 株式会社Screenホールディングス | インクジェット用水性組成物及び固体製剤 |
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| US20080200508A1 (en) * | 2004-12-20 | 2008-08-21 | Collegium Pharmaceutical, Inc. | Pharmaceutical Compositions For Sleep Disorders |
| WO2009118763A1 (en) * | 2008-03-28 | 2009-10-01 | Panacea Biotec Limited | Multilayered pharmaceutical compositions and processes thereof |
| RU2490012C2 (ru) * | 2006-01-27 | 2013-08-20 | Апталис Фарматех Инк | Системы доставки лекарственного средства, содержащие слабощелочной селективный 5-ht3, серотониновый блокатор и органические кислоты |
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| DE60019334T2 (de) | 1999-12-09 | 2005-09-08 | Alza Corp., Mountain View | Antivirale arznei |
| WO2003024427A1 (en) | 1999-12-20 | 2003-03-27 | Temple University Of The Commonwealth System Of Higher Education | Tableted oral extended release dosage form |
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| US20050131045A1 (en) | 2002-04-30 | 2005-06-16 | Judith Aronhime | Novel crystal forms of ondansetron, processes for their preparation, pharmaceutical, compositions containing the novel forms and methods for treating nausea using them |
| US7704527B2 (en) | 2002-10-25 | 2010-04-27 | Collegium Pharmaceutical, Inc. | Modified release compositions of milnacipran |
| PL378369A1 (pl) * | 2003-01-13 | 2006-04-03 | Dynogen Pharmaceuticals, Inc. | Sposób leczenia mdłości, wymiotów, nudności lub ich dowolnej kombinacji |
| PL1683526T3 (pl) * | 2003-11-14 | 2012-09-28 | Senju Pharma Co | Preparat wodnego roztworu zawierający antybiotyk aminoglikozydowy i bromfenak |
| CA2635313C (en) | 2005-12-29 | 2013-12-31 | Osmotica Corp. | Triple combination release multi-layered tablet |
| US20070190141A1 (en) | 2006-02-16 | 2007-08-16 | Aaron Dely | Extended release opiate composition |
| US20080004260A1 (en) | 2006-06-29 | 2008-01-03 | Transcept Pharmaceuticals, Inc. | Compositions of 5-HT3 antagonists and dopamine D2 antagonists for treatment of dopamine-associated chronic conditions |
| BRPI0621996B8 (pt) * | 2006-08-18 | 2022-07-05 | Evonik Roehm Gmbh | preparação farmacêutica compreendendo um núcleo com um ingrediente ativo e com um ácido orgânico e/ou com o sal de um ácido orgânico, e um revestimento que envolve o núcleo e que compreende um ou mais copolímeros de (met)acrilato, e seu uso. |
| CN100584319C (zh) | 2006-10-16 | 2010-01-27 | 北京科信必成医药科技发展有限公司 | 群孔释放渗透泵控释片及其制备方法 |
| MX2009004439A (es) | 2006-10-25 | 2009-05-11 | Mcneil Ppc Inc | Composicion de ibuprofeno. |
| GB0624087D0 (en) | 2006-12-01 | 2007-01-10 | Selamine Ltd | Ramipril combination salt |
| JP2010514679A (ja) | 2006-12-22 | 2010-05-06 | スリーエム イノベイティブ プロパティズ カンパニー | 制御放出組成物及び方法 |
| US20100196291A1 (en) | 2009-01-30 | 2010-08-05 | Laurence Halimi | Personal care sunscreen compositions having reduced eye irritation |
| EP2403487A2 (en) | 2009-03-04 | 2012-01-11 | Fdc Limited | Oral controlled release dosage forms for water soluble drugs |
| US20110003005A1 (en) | 2009-07-06 | 2011-01-06 | Gopi Venkatesh | Methods of Treating PDNV and PONV with Extended Release Ondansetron Compositions |
| US20110108058A1 (en) * | 2009-11-11 | 2011-05-12 | Axcelis Technologies, Inc. | Method and apparatus for cleaning residue from an ion source component |
| AU2010343147A1 (en) | 2009-12-28 | 2012-07-19 | Monosol Rx, Llc | Orally administrable film dosage forms containing ondansetron |
| WO2012028922A2 (en) | 2010-08-30 | 2012-03-08 | Lupin Limited | Controlled release pharmaceutical compositions of milnacipran |
| US20120128730A1 (en) | 2010-11-23 | 2012-05-24 | Nipun Davar | Compositions and methods for once-daily treatment of obsessive compulsive disorder with ondansetron |
| KR102270521B1 (ko) | 2013-03-14 | 2021-06-30 | 레드힐 바이오파마 엘티디 | 구토억제 서방형 고체 제형 |
-
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- 2015-03-11 CA CA2941829A patent/CA2941829C/en active Active
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- 2015-03-11 UA UAA201610250A patent/UA121209C2/uk unknown
- 2015-03-11 RU RU2016139474A patent/RU2706708C2/ru active
- 2015-03-11 CN CN201580024541.0A patent/CN106456611B/zh not_active Expired - Fee Related
- 2015-03-11 EP EP15761030.4A patent/EP3116500B1/en active Active
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-
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-
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- 2020-04-29 US US16/861,752 patent/US20200253933A1/en not_active Abandoned
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20080200508A1 (en) * | 2004-12-20 | 2008-08-21 | Collegium Pharmaceutical, Inc. | Pharmaceutical Compositions For Sleep Disorders |
| RU2490012C2 (ru) * | 2006-01-27 | 2013-08-20 | Апталис Фарматех Инк | Системы доставки лекарственного средства, содержащие слабощелочной селективный 5-ht3, серотониновый блокатор и органические кислоты |
| WO2009118763A1 (en) * | 2008-03-28 | 2009-10-01 | Panacea Biotec Limited | Multilayered pharmaceutical compositions and processes thereof |
Non-Patent Citations (3)
| Title |
|---|
| AL-ANSARI K. et al. Metoclopramide versus ondansetron for the treatment of vomiting in children with acute gastroenteritis. J.Pediatr. Gastroenterol Nutr. 2011 Aug; 53(2): 156-60 * |
| MAXTON DG et al. Selective 5-hydroxytryptamine antagonism: a role in irritable bowel syndrome and functional dyspepsia? Aliment. Pharmacol. Ther. 1996 Aug; 10(4): 595-9. * |
| MAXTON DG et al. Selective 5-hydroxytryptamine antagonism: a role in irritable bowel syndrome and functional dyspepsia? Aliment. Pharmacol. Ther. 1996 Aug; 10(4): 595-9. AL-ANSARI K. et al. Metoclopramide versus ondansetron for the treatment of vomiting in children with acute gastroenteritis. J.Pediatr. Gastroenterol Nutr. 2011 Aug; 53(2): 156-60 Реферат [он лайн] [найдено 24.10.2018] (найдено из интернет: www.ncbi.nlm.nih.gov/pubmed/21788756). * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2818947C1 (ru) * | 2023-05-15 | 2024-05-07 | федеральное государственное бюджетное учреждение "Национальный медицинский исследовательский центр детской гематологии, онкологии и иммунологии имени Дмитрия Рогачева" Министерства здравоохранения Российской Федерации | Способ профилактики и лечения тошноты и рвоты у детей и подростков, получающих высокоэметогенную химиотерапию |
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