CN110152000A - 用于单独治疗肝脂肪变性或治疗伴有丙型肝炎病毒感染的肝脂肪变性的组合物 - Google Patents
用于单独治疗肝脂肪变性或治疗伴有丙型肝炎病毒感染的肝脂肪变性的组合物 Download PDFInfo
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- CN110152000A CN110152000A CN201910281848.9A CN201910281848A CN110152000A CN 110152000 A CN110152000 A CN 110152000A CN 201910281848 A CN201910281848 A CN 201910281848A CN 110152000 A CN110152000 A CN 110152000A
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Families Citing this family (40)
| Publication number | Priority date | Publication date | Assignee | Title |
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| US9155772B2 (en) | 2008-12-08 | 2015-10-13 | Philip Morris Usa Inc. | Soft, chewable and orally dissolvable and/or disintegrable products |
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| EA201391262A1 (ru) | 2011-03-02 | 2014-03-31 | Джером Шентаг | Композиция, способ лечения и диагностики стеатоза печени как самостоятельного заболевания или в комбинации с инфекцией гепатита с |
| US20180099001A1 (en) | 2011-04-29 | 2018-04-12 | Volant Holdings Gmbh | Diagnostics and methods for treatment of non-alcoholic hepatic steatosis and hepatic steatohepatitis, and prevention of complications thereof |
| JP6203816B2 (ja) | 2012-03-29 | 2017-09-27 | セラバイオーム,エルエルシー | 回腸及び虫垂に対して活性の胃腸部位特異的経口ワクチン接種製剤 |
| JP2016506371A (ja) | 2012-11-16 | 2016-03-03 | ユニバーシティ カレッジ カーディフ コンサルタンツ リミテッド | ヌクレオシドプロドラッグを調製する方法 |
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| BR112015022936A2 (pt) | 2013-03-14 | 2017-07-18 | J Schentag Jerome | vesículas de colestossoma para a incorporação de moléculas em quilomícrons |
| RU2015140610A (ru) | 2013-03-14 | 2017-04-17 | ТЕРАБАЙОМ, ЭлЭлСи | Направленная доставка в желудочно-кишечный тракт пробиотических микроорганизмов и/или терапевтических средств |
| CA2903493C (en) * | 2013-03-15 | 2022-05-31 | Cedars-Sinai Medical Center | Methods of diagnosis, selection, and treatment of diseases and conditions caused by or associated with methanogens |
| JP6797692B2 (ja) * | 2014-02-20 | 2020-12-09 | バクサート インコーポレイテッド | 小腸送達のための製剤 |
| EP3169331A4 (en) * | 2014-07-17 | 2018-01-17 | Jerome J. Schentag | Activation of the endogenous ileal brake hormone pathway for organ regeneration and related compositions, methods of treatment, diagnostics, and regulatory systems |
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| US10744070B2 (en) | 2015-06-19 | 2020-08-18 | University Of Southern California | Enteral fast access tract platform system |
| CA2990230A1 (en) | 2015-06-19 | 2016-12-22 | University Of Southern California | Compositions and methods for modified nutrient delivery |
| ES2928408T3 (es) | 2016-04-11 | 2022-11-17 | Genfit | Métodos para el tratamiento de enfermedades fibróticas |
| US11400078B2 (en) * | 2016-04-11 | 2022-08-02 | Genfit | Methods of treatment for cholestatic and fibrotic diseases |
| US10653678B2 (en) | 2016-04-11 | 2020-05-19 | Genfit | Methods of treatment for cholestatic and fibrotic diseases |
| WO2017203367A2 (en) * | 2016-05-22 | 2017-11-30 | Volant Holdings Gmbh | Diagnostics and methods for treatment of non-alcoholic hepatic steatosis and hepatic steatohepatitis, and prevention of complications thereof |
| US11040054B2 (en) | 2016-11-14 | 2021-06-22 | The Brigham And Women's Hospital, Inc. | Estrogen sensing through GPER1 regulates normal and malignant liver growth |
| US11033534B2 (en) | 2017-01-27 | 2021-06-15 | Genfit | Pharmaceutical compositions for combination therapy |
| US11191749B2 (en) * | 2017-03-13 | 2021-12-07 | Genfit | Pharmaceutical compositions for combination therapy |
| GB2571749A (en) * | 2018-03-07 | 2019-09-11 | Anabio Tech Limited | A method inducing satiety in a mammal |
| WO2020120519A1 (en) | 2018-12-10 | 2020-06-18 | Aphaia Pharma Ag | Combinatorial oral treatment of metabolic disorders through orchestrated release of enterokines |
| HUE057346T2 (hu) | 2018-12-10 | 2022-05-28 | Aphaia Ip Ag | Orális gyógyászati adagolási forma metabolikus rendellenességek és rokon betegségek enterokinek megtervezett felszabadításával történõ kezelésére |
| CN109568284B (zh) * | 2018-12-29 | 2020-04-24 | 广东中润药物研发有限公司 | 一种替诺福韦艾拉酚胺肠溶片及其制备方法 |
| CN110478357A (zh) * | 2019-07-23 | 2019-11-22 | 哈尔滨医科大学 | 硝唑尼特及其体内代谢物在抗肥胖、降血脂、抗脂肪肝及抗动脉粥样硬化中的应用 |
| TWI775313B (zh) | 2020-02-18 | 2022-08-21 | 美商基利科學股份有限公司 | 抗病毒化合物 |
| TWI883391B (zh) | 2020-02-18 | 2025-05-11 | 美商基利科學股份有限公司 | 抗病毒化合物 |
| CN115135383B (zh) | 2020-02-18 | 2024-06-11 | 吉利德科学公司 | 抗病毒化合物 |
| JP2023537461A (ja) | 2020-06-10 | 2023-09-01 | アファイア アイピー アーゲー | ゲル化剤と組み合わせて複数の剤形のエンテロカイン放出物質を含有する医薬組成物 |
| JP7688152B2 (ja) | 2021-04-16 | 2025-06-03 | ギリアード サイエンシーズ, インコーポレイテッド | アミドを使用してカルバヌクレオシドを調製する方法 |
| KR20240049311A (ko) | 2021-08-18 | 2024-04-16 | 길리애드 사이언시즈, 인코포레이티드 | 인지질 화합물 및 이의 제조 및 사용 방법 |
| JP7109827B1 (ja) * | 2021-11-16 | 2022-08-01 | 株式会社ハニック・ホワイトラボ | 抗ウイルス剤 |
| CN120500345A (zh) * | 2022-09-01 | 2025-08-15 | Hlb吉尼克斯股份有限公司 | 表达超氧化物歧化酶的芽孢杆菌属菌株、芽孢杆菌属菌株孢子和/或超氧化物歧化酶以及其用于预防或治疗纤维化疾病的用途 |
| WO2025119939A1 (en) | 2023-12-03 | 2025-06-12 | Aphaia Pharma Ag | Treatment of obesity and related conditions by circadian administration of enterokine-stimulating compositions |
| LU103233B1 (en) | 2023-12-21 | 2025-06-24 | Aphaia Ip Ag | Treatment of obesity and related conditions by circadian administration of enterokine-stimulating compositions |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1194831A (zh) * | 1997-04-01 | 1998-10-07 | 李春华 | 利巴韦林大输液系列制剂 |
| CN101291685A (zh) * | 2005-08-19 | 2008-10-22 | 安米林药品公司 | 治疗糖尿病和降低体重的毒蜥外泌肽 |
| WO2010027498A2 (en) * | 2008-09-03 | 2010-03-11 | New Science Holdings, Llc | Compositions and methods for inducing satiety and treating non-insulin dependent diabetes emillitus, pre-diabetic symptoms, insulin resistance and related disease states and conditions |
Family Cites Families (40)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51133489A (en) * | 1975-05-14 | 1976-11-19 | Tokyo Daigaku | Process for producing microbial components of pseudomonas aeruginosa h aving antimicrobial and antitumor activities |
| US4544550A (en) | 1982-10-05 | 1985-10-01 | Rodolfo Almanzor Y | Method for the treatment of diabetes |
| US5194464A (en) | 1988-09-27 | 1993-03-16 | Takeda Chemical Industries, Ltd. | Enteric film and preparatoin thereof |
| US5769793A (en) | 1989-09-08 | 1998-06-23 | Steven M. Pincus | System to determine a relative amount of patternness |
| US5120563A (en) * | 1989-12-21 | 1992-06-09 | The Procter & Gamble Company | Food compositions containing reduced calorie fats and reduced calorie sugars |
| ATE219522T1 (de) * | 1992-02-04 | 2002-07-15 | Chiron Corp | Hepatistherapeutikum |
| US5322697A (en) | 1992-05-28 | 1994-06-21 | Meyer James H | Composition and method for inducing satiety |
| US5976548A (en) | 1994-11-08 | 1999-11-02 | Viva America Marketing, Inc. | Nutritional supplement composition and use |
| AU766597B2 (en) * | 1998-05-15 | 2003-10-16 | Schering Corporation | Combination therapy comprising ribavirin and interferon alpha in antiviral treatment naive patients having chronic hepatitis C infection |
| US6248363B1 (en) | 1999-11-23 | 2001-06-19 | Lipocine, Inc. | Solid carriers for improved delivery of active ingredients in pharmaceutical compositions |
| ES2350330T3 (es) | 2000-06-07 | 2011-01-21 | Watson Pharmaceuticals, Inc. | Tratamiento de la hiperactividad del músculo liso con (r)-oxibutinina y (r)-desetiloxibutinina. |
| EP1499300B1 (en) | 2002-04-29 | 2009-03-18 | Supernus Pharmaceuticals, Inc. | Pharmaceutical formulations with improved bioavailability |
| US20040062778A1 (en) | 2002-09-26 | 2004-04-01 | Adi Shefer | Surface dissolution and/or bulk erosion controlled release compositions and devices |
| EP1462116A1 (en) | 2003-03-29 | 2004-09-29 | Villitech SARL | Composition for treating the gastrointestinal tract |
| CA2566677A1 (en) | 2004-05-13 | 2005-11-24 | Intermune, Inc. | Combination therapy for treating hepatitis virus infection |
| WO2006034463A2 (en) | 2004-09-23 | 2006-03-30 | Herbalife International, Inc. | Herbal supplement to support weight loss |
| US20080064632A1 (en) | 2004-09-24 | 2008-03-13 | Amatruda John M | Combination Therapy for the Treatment of Obesity |
| US20060093592A1 (en) | 2004-10-04 | 2006-05-04 | Nutracea | Synbiotics |
| KR101174966B1 (ko) * | 2005-05-31 | 2012-08-17 | 노파르티스 아게 | 철이 발병에 관여하는 간질환의 치료 |
| JP2007001945A (ja) | 2005-06-24 | 2007-01-11 | Tsuneo Ozeki | 癌治療剤 |
| WO2007022518A2 (en) * | 2005-08-19 | 2007-02-22 | Amylin Pharmaceuticals, Inc. | New uses of glucoregulatory proteins |
| ES2670856T3 (es) | 2005-09-06 | 2018-06-01 | Oramed Pharmaceuticals Inc. | Métodos y composiciones para la administración oral de proteínas |
| US8394845B2 (en) | 2006-10-30 | 2013-03-12 | Hanall Biopharma Co., Ltd. | Method of using combination preparation comprising angiotensin-II-receptor blocker and HMG-CoA reductase inhibitor |
| JP2010509363A (ja) | 2006-11-08 | 2010-03-25 | ノババックス,インコーポレイテッド | 固体剤形の多相医薬組成物の製造方法 |
| US7951789B2 (en) * | 2006-12-28 | 2011-05-31 | Idenix Pharmaceuticals, Inc. | Compounds and pharmaceutical compositions for the treatment of viral infections |
| US20070172525A1 (en) | 2007-03-15 | 2007-07-26 | Ramesh Sesha | Anti-diabetic combinations |
| BRPI0908292B1 (pt) | 2008-05-05 | 2022-09-20 | Oramed Ltd | Métodos e composições para administração oral de exenatida |
| US9757346B2 (en) | 2008-09-03 | 2017-09-12 | Volant Holdings Gmbh | Compositions and methods for treating insulin resistance and non-insulin dependent diabetes mellitus (type II diabetes) |
| WO2010045361A1 (en) | 2008-10-17 | 2010-04-22 | Metabolex, Inc. | Methods of reducing small, dense ldl particles |
| US9339480B2 (en) | 2008-11-26 | 2016-05-17 | Satiogen Pharmaceuticals, Inc. | Bile acid recycling inhibitors for treatment of obesity and diabetes |
| CA2752232C (en) | 2009-02-12 | 2016-11-22 | Arqule, Inc. | A composition comprising (-)-trans-3-(5,6-dihydro-4h-pyrrolo [3,2,1-ij] quinolin-1-yl)-4-(1h-indol-3-yl) pyrrolidine-2, 5-dione in combination with a second anti-proliferative agent |
| CN102438599B (zh) | 2009-03-04 | 2015-01-21 | 迈雅营养品有限公司 | 通过降低血糖水平来控制糖尿病的营养组合物和方法 |
| RU2410108C1 (ru) | 2009-08-03 | 2011-01-27 | Государственное образовательное учреждение высшего профессионального образования "Орловский государственный технический университет" (ОрелГТУ) | Способ скармливания пробиотика поросятам-сосунам |
| US8367418B2 (en) | 2009-10-23 | 2013-02-05 | Therasyn Sensors, Inc. | Method and system to provide personalized pharmaceutical compositions and dosages |
| US8999721B2 (en) | 2009-10-23 | 2015-04-07 | Therabrake, Inc. | Method and system to provide personalized pharmaceutical compositions and dosages |
| US20140294951A1 (en) | 2011-10-26 | 2014-10-02 | Joseph M. Fayad | Oral formulations mimetic of Roux-en-Y gastric bypass actions on the ileal brake; Compositions, methods of treatment, diagnostics and systems for treatment of metabolic syndrome manifestations including insulin resistance, fatty liver disease, hyperlipidemia, and T2D |
| US20130273154A1 (en) | 2011-03-02 | 2013-10-17 | Joseph M. Fayad | Oral formulations Mimetic of Roux-en-Y gastric bypass actions on the ileal brake; Compositions, Methods of Treatment, Diagnostics and Systems for treatment of metabolic syndrome manifestations including insulin resistance, fatty liver disease, hpperlipidemia, and type 2 diabetes |
| EA201391262A1 (ru) | 2011-03-02 | 2014-03-31 | Джером Шентаг | Композиция, способ лечения и диагностики стеатоза печени как самостоятельного заболевания или в комбинации с инфекцией гепатита с |
| JP6203816B2 (ja) | 2012-03-29 | 2017-09-27 | セラバイオーム,エルエルシー | 回腸及び虫垂に対して活性の胃腸部位特異的経口ワクチン接種製剤 |
| CA2897448A1 (en) | 2013-01-08 | 2014-07-17 | Jerome Schentag | Activation of the endogenous ileal brake hormone pathway for organ regeneration and related compositions, methods of treatment, diagnostics, and regulatory systems |
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- 2012-02-24 KR KR1020197014958A patent/KR20190060879A/ko not_active Ceased
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Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1194831A (zh) * | 1997-04-01 | 1998-10-07 | 李春华 | 利巴韦林大输液系列制剂 |
| CN101291685A (zh) * | 2005-08-19 | 2008-10-22 | 安米林药品公司 | 治疗糖尿病和降低体重的毒蜥外泌肽 |
| WO2010027498A2 (en) * | 2008-09-03 | 2010-03-11 | New Science Holdings, Llc | Compositions and methods for inducing satiety and treating non-insulin dependent diabetes emillitus, pre-diabetic symptoms, insulin resistance and related disease states and conditions |
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| EP2680859A2 (en) | 2014-01-08 |
| EP2680859A4 (en) | 2014-12-17 |
| US20130337055A1 (en) | 2013-12-19 |
| US9370528B2 (en) | 2016-06-21 |
| KR20200006177A (ko) | 2020-01-17 |
| WO2012118712A2 (en) | 2012-09-07 |
| AU2012223528A1 (en) | 2013-10-24 |
| KR20190060879A (ko) | 2019-06-03 |
| AU2012223528A8 (en) | 2017-05-11 |
| JP2014506928A (ja) | 2014-03-20 |
| JP2019123716A (ja) | 2019-07-25 |
| JP2018065840A (ja) | 2018-04-26 |
| EP2680859B1 (en) | 2022-04-27 |
| AU2019201917A1 (en) | 2019-04-11 |
| WO2012118712A3 (en) | 2013-04-04 |
| IL228259B (en) | 2019-05-30 |
| IL258450A (en) | 2018-05-31 |
| BR112013022391A2 (pt) | 2018-01-16 |
| KR102198749B1 (ko) | 2021-01-06 |
| CN103635196A (zh) | 2014-03-12 |
| JP6253991B2 (ja) | 2017-12-27 |
| AU2017202713A1 (en) | 2017-05-18 |
| US10245277B2 (en) | 2019-04-02 |
| CN103635196B (zh) | 2019-05-07 |
| KR20140147657A (ko) | 2014-12-30 |
| EA201391262A1 (ru) | 2014-03-31 |
| US9730951B2 (en) | 2017-08-15 |
| KR20180118236A (ko) | 2018-10-30 |
| US20160279157A1 (en) | 2016-09-29 |
| US20180125870A1 (en) | 2018-05-10 |
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