CN118975972A - 用于治疗剂缓释的胃驻留系统及其使用方法 - Google Patents
用于治疗剂缓释的胃驻留系统及其使用方法 Download PDFInfo
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- CN118975972A CN118975972A CN202411064156.6A CN202411064156A CN118975972A CN 118975972 A CN118975972 A CN 118975972A CN 202411064156 A CN202411064156 A CN 202411064156A CN 118975972 A CN118975972 A CN 118975972A
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- therapeutic agent
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Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FI3725357T3 (fi) | 2014-06-11 | 2024-12-13 | Massachusetts Inst Technology | Pidättyviä rakenteita ja niihin liittyviä menetelmiä |
| US20170266112A1 (en) | 2014-06-11 | 2017-09-21 | Massachusetts Institute Of Technology | Residence structures and related methods |
| AU2016342374B2 (en) | 2015-10-23 | 2022-08-04 | Lyndra Therapeutics, Inc. | Gastric residence systems for sustained release of therapeutic agents and methods of use thereof |
| CN108697649A (zh) | 2015-12-08 | 2018-10-23 | 林德拉有限公司 | 用于胃驻留系统的几何构型 |
| JP7189772B2 (ja) * | 2016-05-27 | 2022-12-14 | リンドラ セラピューティクス, インコーポレイティド | 胃内滞留システムのための材料構造物 |
| CN118766834A (zh) | 2016-09-30 | 2024-10-15 | 林德拉治疗公司 | 用于金刚烷类药物缓释的胃驻留系统 |
| JP7045397B2 (ja) | 2017-05-17 | 2022-03-31 | マサチューセッツ インスティテュート オブ テクノロジー | 自己復元システムおよび関連構成要素 |
| US11541015B2 (en) | 2017-05-17 | 2023-01-03 | Massachusetts Institute Of Technology | Self-righting systems, methods, and related components |
| CA3066658A1 (en) * | 2017-06-09 | 2018-12-13 | Lyndra, Inc. | Gastric residence systems with release rate-modulating films |
| KR102046395B1 (ko) * | 2017-12-12 | 2019-11-19 | 동아에스티 주식회사 | 베포타스틴 또는 이의 약제학적으로 허용 가능한 염을 포함하는 서방성 제제 |
| CA3095460A1 (en) * | 2018-03-29 | 2019-10-03 | Mati Therapeutics, Inc. | Ophthalmic drug sustained release formulation and uses for dry eye syndrome treatment |
| AU2019269636A1 (en) | 2018-05-17 | 2020-11-19 | Massachusetts Institute Of Technology | Systems for electrical stimulation |
| KR20210031910A (ko) | 2018-06-19 | 2021-03-23 | 싱가포르국립대학교 | 다양한 적응증에 대한 향상된 생체 이용률을 위한 5-하이드록시트립토판의 제형 |
| WO2020117855A1 (en) * | 2018-12-03 | 2020-06-11 | Lyndra, Inc. | Stomach simulating device |
| WO2020160399A1 (en) | 2019-02-01 | 2020-08-06 | Massachusetts Institute Of Technology | Systems and methods for liquid injection |
| AU2020240108B2 (en) | 2019-03-20 | 2025-12-04 | Lyndra Therapeutics, Inc. | Capsules and capsule coatings for gastric residence dosage forms |
| EP4054641A4 (en) * | 2019-11-08 | 2023-12-27 | Lyndra Therapeutics, Inc. | POLYMERIC LINKERS FOR A STOMACH RESIDENCE SYSTEM |
| BR112022008908A2 (pt) * | 2019-11-08 | 2022-10-11 | Lyndra Therapeutics Inc | Sistemas de permanência gástrica para administração de agentes ativos |
| CA3160660A1 (en) * | 2019-11-08 | 2021-05-14 | Lyndra Therapeutics, Inc. | Formulations for release-rate modulating films for gastric residence systems |
| US11541216B2 (en) | 2019-11-21 | 2023-01-03 | Massachusetts Institute Of Technology | Methods for manufacturing tissue interfacing components |
| JP2023536456A (ja) | 2020-07-29 | 2023-08-25 | ザ・セカント・グループ・エルエルシー | 架橋ポリ(セバシン酸グリセロール)を含む構造を含む形状誘導型制御放出および保持 |
| CN117615755A (zh) * | 2021-05-05 | 2024-02-27 | 林德拉治疗公司 | 包含美沙酮的胃驻留系统 |
| CN117615754A (zh) * | 2021-05-05 | 2024-02-27 | 林德拉治疗公司 | 包含丁丙诺啡和纳洛酮的胃驻留系统 |
| EP4362919A1 (en) | 2021-07-30 | 2024-05-08 | Evecxia Therapeutics, Inc. | 5-hydroxytryptophan gastroretentive dosage forms |
| US12409163B2 (en) | 2021-07-30 | 2025-09-09 | Evecxia Therapeutics, Inc. | Method of enhancing 5-hydroxytryptophan (5-HTP) exposure |
| JP2024535585A (ja) | 2021-10-14 | 2024-09-30 | エヴェクシア セラピューティクス, インク. | 脳内5-ヒドロキシトリプタミンの機能を治療目的で最適化する方法 |
| WO2023141524A2 (en) * | 2022-01-19 | 2023-07-27 | Lyndra Therapeutics, Inc. | Dosage forms for gastric retention |
| WO2025195482A1 (zh) * | 2024-03-22 | 2025-09-25 | 厦门君德医药科技有限公司 | 一种胃滞留装置 |
Family Cites Families (150)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1957564A (en) | 1932-11-23 | 1934-05-08 | Aubra T West | Expanding capsule body |
| US3154461A (en) | 1960-03-07 | 1964-10-27 | Minnesota Mining & Mfg | Matte-finish polymeric film and method of forming the same |
| US3531368A (en) | 1966-01-07 | 1970-09-29 | Toray Industries | Synthetic filaments and the like |
| US3716614A (en) | 1969-05-12 | 1973-02-13 | Toray Industries | Process of manufacturing collagen fiber-like synthetic superfine filament bundles |
| AU449029B2 (en) | 1969-08-28 | 1974-04-17 | Commonwealth Scientific And Industrial Research Organisation | Device for administration to ruminants |
| JPS5512411B2 (enExample) | 1974-03-12 | 1980-04-02 | ||
| US4304767A (en) | 1980-05-15 | 1981-12-08 | Sri International | Polymers of di- (and higher functionality) ketene acetals and polyols |
| DK154078C (da) | 1981-02-06 | 1989-05-22 | Ucb Sa | Analogifremgangsmaade til fremstilling af 2-(2-(4-(diphenyl-methyl)-1-piperazinyl)ethoxy)-acetamider eller syreadditionssalte heraf |
| US4451260A (en) | 1982-03-26 | 1984-05-29 | Minnesota Mining And Manufacturing Company | Sustained release oral medicinal delivery device |
| US4676507A (en) | 1985-05-06 | 1987-06-30 | Patterson Bruce D | Puzzles forming platonic solids |
| DE3680024D1 (de) | 1985-05-10 | 1991-08-08 | Merck & Co Inc | Abgabesystem fuer arzneimittel, das waehrend einer kontrollierten zeitspanne im magen zurueckgehalten werden kann. |
| JPS6226215A (ja) * | 1985-05-10 | 1987-02-04 | メルク エンド カムパニ− インコ−ポレ−テツド | 一定に制御した時間内胃中に保持できる薬剤移送装置 |
| US4735804A (en) | 1985-05-10 | 1988-04-05 | Merck & Co., Inc. | Drug delivery device which can be retained in the stomach for a controlled period of time |
| US4767627A (en) | 1985-05-29 | 1988-08-30 | Merck & Co., Inc. | Drug delivery device which can be retained in the stomach for a controlled period of time |
| US4758436A (en) | 1985-05-29 | 1988-07-19 | Merck & Co., Inc. | Drug delivery device which can be retained in the stomach for a controlled period of time |
| EP0253554A3 (en) | 1986-07-15 | 1988-07-20 | Pfizer Inc. | Controlled release drug-containing fibers |
| CA1314742C (en) | 1986-12-12 | 1993-03-23 | Hiromu Terada | Optical fiber array |
| IL87710A (en) | 1987-09-18 | 1992-06-21 | Ciba Geigy Ag | Covered floating retard form for controlled release in gastric juice |
| US5002772A (en) | 1988-05-31 | 1991-03-26 | Pfizer Inc. | Gastric retention system for controlled drug release |
| NZ228382A (en) * | 1989-03-17 | 1992-08-26 | Carter Holt Harvey Plastic Pro | Drug administering coil-like device for insertion in body cavity of animal |
| US5007790A (en) | 1989-04-11 | 1991-04-16 | Depomed Systems, Inc. | Sustained-release oral drug dosage form |
| JPH03163011A (ja) | 1989-08-31 | 1991-07-15 | Yamanouchi Pharmaceut Co Ltd | 胃内滞留デバイス |
| US5047464A (en) | 1989-09-20 | 1991-09-10 | Merck & Co., Inc. | Bioerodible thermoset elastomers |
| US5121329A (en) | 1989-10-30 | 1992-06-09 | Stratasys, Inc. | Apparatus and method for creating three-dimensional objects |
| JP2648897B2 (ja) | 1991-07-01 | 1997-09-03 | 塩野義製薬株式会社 | ピリミジン誘導体 |
| US5939467A (en) | 1992-06-26 | 1999-08-17 | The Procter & Gamble Company | Biodegradable polymeric compositions and products thereof |
| US5369142A (en) | 1993-01-15 | 1994-11-29 | The Ohio State University | Water soluble polymers containing amino acid residues for dental restoratives |
| JP2750802B2 (ja) | 1993-01-29 | 1998-05-13 | 日進工業 株式会社 | 物体表面の洗滌・剥離方法とその装置 |
| JP2983800B2 (ja) | 1993-05-17 | 1999-11-29 | 三洋電機株式会社 | 部品位置認識装置 |
| WO1995003558A1 (en) | 1993-07-19 | 1995-02-02 | Reflexite Corporation | Retroreflective structure |
| DE4406424A1 (de) * | 1994-02-28 | 1995-08-31 | Bayer Ag | Expandierbare Arzneiformen |
| US5837276A (en) | 1994-09-02 | 1998-11-17 | Delab | Apparatus for the delivery of elongate solid drug compositions |
| DE69625831T2 (de) | 1995-03-23 | 2003-11-20 | Advanced Animal Technology Ltd., Hamilton | Vorrichtung zur Verabreichung einer Substanz |
| US6962579B2 (en) | 1995-03-23 | 2005-11-08 | Advanced Animal Technology Limited | Substance delivery device |
| US5840332A (en) | 1996-01-18 | 1998-11-24 | Perio Products Ltd. | Gastrointestinal drug delivery system |
| AU2521797A (en) | 1996-04-12 | 1997-11-07 | Japan Atomic Energy Research Institute | Ph-sensitive polymers |
| WO1999007342A1 (en) * | 1997-08-11 | 1999-02-18 | Alza Corporation | Prolonged release active agent dosage form adapted for gastric retention |
| DE19850309A1 (de) | 1998-10-30 | 2000-05-04 | Lohmann Therapie Syst Lts | Expandierbares gastroretensives Therapiesystem mit verlängerter Magenverweildauer |
| IL133196A0 (en) | 1999-11-29 | 2001-03-19 | Yissum Res Dev Co | Gastroretentive controlled release pharmaceutical dosage forms |
| GB0001621D0 (en) | 2000-01-26 | 2000-03-15 | Astrazeneca Ab | Pharmaceutical compositions |
| DE60116758T2 (de) | 2000-05-18 | 2006-11-02 | Therics, Inc. | Einkapselung eines toxischen kerns in einen nicht-toxischen bereich in einer oralen darreichungsform |
| US20020022048A1 (en) | 2000-05-26 | 2002-02-21 | Bromberg Lev E. | Composite wafer for controlled drug delivery |
| US6488962B1 (en) | 2000-06-20 | 2002-12-03 | Depomed, Inc. | Tablet shapes to enhance gastric retention of swellable controlled-release oral dosage forms |
| US8158143B2 (en) | 2000-07-14 | 2012-04-17 | Helmholtz-Zentrum Geesthacht Zentrum Fuer Material- Und Kuestenforschung Gmbh | Systems for releasing active ingredients, based on biodegradable or biocompatible polymers with a shape memory effect |
| US7803392B2 (en) | 2000-12-27 | 2010-09-28 | University Of Kentucky Research Foundation | pH-Sensitive mucoadhesive film-forming gels and wax-film composites suitable for topical and mucosal delivery of molecules |
| US6627206B2 (en) | 2001-07-25 | 2003-09-30 | Greg A. Lloyd | Method and apparatus for treating obesity and for delivering time-released medicaments |
| IL160363A0 (en) | 2001-08-16 | 2004-07-25 | Oregon State | Expandable gastric retention device |
| US20040219186A1 (en) | 2001-08-16 | 2004-11-04 | Ayres James W. | Expandable gastric retention device |
| US20050165136A1 (en) | 2002-01-23 | 2005-07-28 | Uab Research Foundation | Glass-ionomer cements containing amino acids |
| AU2003234159A1 (en) | 2002-04-22 | 2003-11-03 | Purdue Research Foundation | Hydrogels having enhanced elasticity and mechanical strength properties |
| DE10224352A1 (de) | 2002-06-01 | 2003-12-11 | Mueller Schulte Detlef | Thermosensitive Polymerträger mit veränderbarer physikalischer Struktur für die biochemische Analytik, Diagnostik und Therapie |
| GB0214013D0 (en) * | 2002-06-18 | 2002-07-31 | Euro Celtique Sa | Pharmaceutical product |
| MY142179A (en) | 2002-07-25 | 2010-10-15 | Glaxo Group Ltd | Multicomponent pharmaceutical dosage form |
| WO2004032906A1 (en) | 2002-10-11 | 2004-04-22 | Depomed Development, Ltd. | Gastro-retentive levodopa delivery form |
| EP1594475A1 (en) * | 2003-02-19 | 2005-11-16 | Mnemoscience GmbH | Self-expanding device for the gastrointestinal or urogenital area |
| JP4497833B2 (ja) | 2003-04-21 | 2010-07-07 | 富士フイルム株式会社 | ポジ型平版印刷版原版 |
| US7662864B2 (en) * | 2003-06-04 | 2010-02-16 | Rutgers, The State University Of New Jersey | Solution polymerization processes to prepare a polymer that degrades to release a physiologically active agent |
| CA2527976C (en) | 2003-06-13 | 2011-11-22 | Mnemoscience Gmbh | Stents |
| WO2004112755A1 (en) | 2003-06-18 | 2004-12-29 | John Michael Newton | Controlled release devices with lumens |
| US20090259236A2 (en) | 2003-07-28 | 2009-10-15 | Baronova, Inc. | Gastric retaining devices and methods |
| US8048169B2 (en) | 2003-07-28 | 2011-11-01 | Baronova, Inc. | Pyloric valve obstructing devices and methods |
| DE10350556A1 (de) | 2003-10-29 | 2005-06-02 | Clariant Gmbh | Wasserbasierende Pigmentpräparationen |
| US6825308B1 (en) | 2003-10-29 | 2004-11-30 | Council Of Scientific And Industrial Research | Copolymers and preparation thereof |
| WO2005056708A2 (en) | 2003-12-09 | 2005-06-23 | Spherics, Inc. | Bioadhesive polymers with catechol functionality |
| US20050163858A1 (en) * | 2003-12-31 | 2005-07-28 | Garth Boehm | Ziprasidone formulations |
| US20080089933A1 (en) | 2006-10-16 | 2008-04-17 | Amir Alon | Device and method for reducing calorie intake |
| TW201240679A (en) * | 2004-03-12 | 2012-10-16 | Capsugel Belgium Nv | Pharmaceutical formulations |
| EP1773303A2 (en) | 2004-05-25 | 2007-04-18 | Chimeracore, Inc. | Self-assembling nanoparticle drug delivery system |
| DE102004047076A1 (de) | 2004-09-28 | 2006-04-06 | Zimmer Ag | Verfahren zur Herstellung von Polyestern |
| IL166183A0 (en) | 2005-01-06 | 2006-01-15 | Yissum Res Dev Co | Novel diagnostic and imaging techniques of the gi tract |
| US20060182788A1 (en) | 2005-01-27 | 2006-08-17 | Parminder Singh | Hydrophilic biocompatible adhesive formulations and uses |
| EP1843755B1 (en) | 2005-02-01 | 2015-04-01 | Emisphere Technologies, Inc. | Gastric retention and controlled release delivery system |
| US7785291B2 (en) | 2005-03-01 | 2010-08-31 | Tulip Medical Ltd. | Bioerodible self-deployable intragastric implants |
| JP2006323082A (ja) | 2005-05-18 | 2006-11-30 | Canon Inc | 現像剤補給容器 |
| US8021384B2 (en) | 2005-07-26 | 2011-09-20 | Ram Weiss | Extending intrabody capsule |
| JP4981671B2 (ja) | 2005-08-05 | 2012-07-25 | 滋賀県 | ポリマーブレンドを含んでなる液中物質捕集材料 |
| US20070048383A1 (en) | 2005-08-25 | 2007-03-01 | Helmus Michael N | Self-assembled endovascular structures |
| WO2007048223A2 (en) | 2005-10-25 | 2007-05-03 | Pharmascience Inc. | A gastric retention drug delivery system |
| US8187633B2 (en) | 2005-11-03 | 2012-05-29 | Sun Pharma Advanced Research Company Limited | Controlled release coated tablets having prolonged gastric retention |
| US7674396B2 (en) | 2005-11-08 | 2010-03-09 | Plensat Llc | Method and system for treatment of eating disorders |
| US8298574B2 (en) | 2006-01-18 | 2012-10-30 | Intec Pharma Ltd. | Method and apparatus for forming delivery devices for oral intake of an agent |
| WO2007093999A1 (en) | 2006-02-15 | 2007-08-23 | Intec Pharma Ltd. | A gastro-retentive system for the delivery of macromolecules |
| US20090246142A1 (en) | 2006-03-10 | 2009-10-01 | Massachusetts Institute Of Technology | Triggered Self-Assembly of Nanoparticles In Vivo |
| US7691151B2 (en) | 2006-03-31 | 2010-04-06 | Spiration, Inc. | Articulable Anchor |
| US20070264307A1 (en) | 2006-05-15 | 2007-11-15 | Medtronic Vascular, Inc. | Biodegradable Modified Caprolactone Polymers for Fabricating and Coating Medical Devices |
| EP1886665A1 (en) | 2006-08-01 | 2008-02-13 | Boehringer Ingelheim Pharma GmbH & Co. KG | Gastro retentive delivery system |
| CN101511346B (zh) | 2006-09-04 | 2012-07-04 | 万能药生物有限公司 | 可编制的漂浮递送技术 |
| US20080075766A1 (en) | 2006-09-25 | 2008-03-27 | Shun-Por Li | Multi-core dosage form having transparent outer coating |
| CA2673511A1 (en) | 2006-12-22 | 2008-07-03 | Combinatorx, Incorporated | Pharmaceutical compositions for treatment of parkinson's disease and related disorders |
| US8507778B2 (en) | 2007-03-13 | 2013-08-13 | Arthur J. Olson | Self-assembled polyhedra |
| WO2008111077A2 (en) | 2007-03-13 | 2008-09-18 | Technion Research & Development Foundation Ltd. | Self-assembled polyhedral multimeric chemical structures |
| WO2008124122A1 (en) | 2007-04-09 | 2008-10-16 | Scidose, Llc | Combinations of statins and anti-obesity agent and glitazones |
| JP2010527712A (ja) | 2007-05-25 | 2010-08-19 | ゴーラム エンタープライゼス エルエルシー | 肥満症用の磁気装置およびその製造方法 |
| MX354603B (es) | 2007-05-25 | 2018-03-13 | Indivior Uk Ltd | Formulaciones de transferencia sostenida de compuestos de risperidona. |
| US8038659B2 (en) | 2007-10-17 | 2011-10-18 | The Invention Science Fund I, Llc | Disintegrating digestive tract interaction system |
| US8637455B2 (en) | 2007-10-22 | 2014-01-28 | Affinergy, Llc | Compositions and methods for delivery of glycopeptide antibiotics to medical device surfaces |
| EP2262367A4 (en) | 2008-03-08 | 2011-04-20 | Theraquest Biosciences Inc | PHARMACEUTICAL ORAL COMPOSITIONS OF BUPRENORPHINE AND METHOD FOR THEIR USE |
| CN102105136B (zh) | 2008-03-11 | 2014-11-26 | 蒂宝制药公司 | 包含非-阿片类止痛剂和阿片类止痛剂的组合的胃滞留型缓释剂型 |
| US20130273135A1 (en) | 2008-03-25 | 2013-10-17 | University Of Utah Research Foundation | Controlled Release Combination Biomaterials |
| KR101601649B1 (ko) | 2008-04-18 | 2016-03-09 | 인텍 파마 리미티드 | 카르비도파/레보도파 위체류 약물 전달 |
| US9066877B2 (en) | 2008-04-28 | 2015-06-30 | Eat Little Inc. | Bezoar-forming units for weight control |
| US20100256342A1 (en) | 2008-08-12 | 2010-10-07 | Francis Raymond Salemme | Protein nodes for controlled nanoscale assembly |
| KR20110042366A (ko) | 2008-08-18 | 2011-04-26 | 팀 아카데미 오브 파마슈티컬 사이언스 | 위장체류 약물 전달 시스템, 제작 방법 및 그것들의 사용 |
| US20110268666A1 (en) | 2008-09-29 | 2011-11-03 | Yissum Research Development Company of the Research University of Jerusalem, Ltd. | Novel gastroretentive delivery system |
| JP5559798B2 (ja) | 2008-10-10 | 2014-07-23 | レヴァ メディカル、 インコーポレイテッド | 拡張可能スライドとロックステント |
| EP2378883B1 (en) | 2008-12-04 | 2015-12-23 | Intec Pharma Ltd. | Zaleplon gastroretentive drug delivery system |
| EP2373232A2 (en) | 2008-12-27 | 2011-10-12 | Chandra S. Duggirala | Devices for treating obesity and methods of using those devices |
| EP2401225B1 (en) | 2009-02-26 | 2014-10-22 | The Regents of The University of California | A supramolecular approach for preparation of size controllable nanoparticles |
| US8414559B2 (en) | 2009-05-07 | 2013-04-09 | Rainbow Medical Ltd. | Gastroretentive duodenal pill |
| DE102009028076A1 (de) | 2009-07-29 | 2011-02-03 | Evonik Röhm Gmbh | Beschichtungsmittel zum Tauchbeschichten von Kapselhälften |
| US20110052700A1 (en) | 2009-08-31 | 2011-03-03 | Depomed, Inc. | Gastric retentive pharmaceutical compositions for immediate and extended release of levosulpiride |
| WO2011032087A2 (en) | 2009-09-11 | 2011-03-17 | Replication Medical Inc. | Swellable polymeric device for dietary regulation |
| US20120321706A1 (en) | 2009-10-19 | 2012-12-20 | Intec Pharma Ltd. | Novel gastroretentive dosage forms of poorly soluble drugs |
| US9421169B2 (en) | 2009-11-20 | 2016-08-23 | Covidien Lp | Oral dosage forms for delivery of therapeutic agents |
| CN101711752B (zh) | 2009-11-26 | 2011-09-21 | 中国科学院上海药物研究所 | 一种苯并异噁唑类衍生物的控释制剂及其制备方法 |
| US11535510B2 (en) | 2010-04-27 | 2022-12-27 | The Johns Hopkins University | Self-folding sub-centimeter structures |
| JP6005636B2 (ja) | 2010-07-06 | 2016-10-12 | グリュネンタール・ゲゼルシャフト・ミト・ベシュレンクテル・ハフツング | Gaba類似体及びオピオイドを含む新規胃内滞留型剤形 |
| WO2012018923A1 (en) | 2010-08-05 | 2012-02-09 | Taris Biomedical, Inc. | Implantable drug delivery devices for genitourinary sites |
| US20120165794A1 (en) | 2010-12-22 | 2012-06-28 | Ethicon Endo-Surgery, Inc. | Pill Catchers |
| US20120165793A1 (en) | 2010-12-22 | 2012-06-28 | Ethicon Endo-Surgery, Inc. | Pill Catchers |
| US20120165792A1 (en) | 2010-12-22 | 2012-06-28 | Ethicon Endo-Surgery, Inc. | Pill Catchers |
| CA2825399A1 (en) | 2011-02-04 | 2012-08-09 | Taris Biomedical, Inc. | Implantable device for controlled release of low solubility drug |
| WO2014014348A1 (en) | 2012-07-16 | 2014-01-23 | APET Holding B.V. | Gastro-retentive drug delivery system |
| JP2014533975A (ja) | 2011-09-26 | 2014-12-18 | ノースイースタン・ユニバーシティ | カスタマイズ可能な埋め込みセンサ |
| ES2603278T3 (es) | 2011-12-09 | 2017-02-24 | Purdue Pharma Lp | Formas farmacéuticas de dosificación que comprenden poli (epsilon-caprolactona) y óxido de polietileno |
| US8986337B2 (en) | 2012-02-24 | 2015-03-24 | Elwha Llc | Devices, systems, and methods to control stomach volume |
| US9307966B2 (en) | 2012-08-15 | 2016-04-12 | St. Jude Medical Puerto Rico Llc | Vascular closure device anchor |
| US20140050784A1 (en) | 2012-08-16 | 2014-02-20 | Teva Pharmaceuticals Usa, Inc. | Pharmaceutical compositions of memantine |
| US10441760B2 (en) | 2013-03-01 | 2019-10-15 | The Johns Hopkins University | Self-actuating chemomechanical devices for delivery and extended release of therapeutic agents in the gastrointestinal tract |
| CN103654903A (zh) | 2013-11-27 | 2014-03-26 | 西安交通大学 | 一种用于人体消化道吻合的磁性可降解装置 |
| AU2014358675B2 (en) | 2013-12-05 | 2019-10-03 | Epitomee Medical Ltd | Retentive devices and systems for in-situ release of pharmaceutical active agents |
| WO2015168297A1 (en) | 2014-04-29 | 2015-11-05 | Massachusetts Institute Of Technology | Polymeric materials for bio-applications |
| MX2016015417A (es) | 2014-05-26 | 2017-02-22 | Gruenenthal Gmbh | Multiparticulas protegidas contra vertido de dosis etanolico. |
| KR20170015389A (ko) | 2014-06-02 | 2017-02-08 | 테바 파마슈티컬 인더스트리즈 리미티드 | 확장 가능한 위체류 투여 형태 |
| US20170266112A1 (en) | 2014-06-11 | 2017-09-21 | Massachusetts Institute Of Technology | Residence structures and related methods |
| FI3725357T3 (fi) | 2014-06-11 | 2024-12-13 | Massachusetts Inst Technology | Pidättyviä rakenteita ja niihin liittyviä menetelmiä |
| WO2016178971A1 (en) | 2015-05-01 | 2016-11-10 | Massachusetts Institute Of Technology | Triggerable shape memory induction devices |
| AU2016342374B2 (en) | 2015-10-23 | 2022-08-04 | Lyndra Therapeutics, Inc. | Gastric residence systems for sustained release of therapeutic agents and methods of use thereof |
| CN108601724A (zh) | 2015-12-01 | 2018-09-28 | 克雷西奥生物科技有限公司 | 胃滞留装置 |
| AU2016362794B2 (en) | 2015-12-02 | 2019-05-09 | Clexio Biosciences Ltd. | Device for preparing gastroretentive dosage forms |
| CN108697649A (zh) | 2015-12-08 | 2018-10-23 | 林德拉有限公司 | 用于胃驻留系统的几何构型 |
| JP7189772B2 (ja) | 2016-05-27 | 2022-12-14 | リンドラ セラピューティクス, インコーポレイティド | 胃内滞留システムのための材料構造物 |
| CN118766834A (zh) | 2016-09-30 | 2024-10-15 | 林德拉治疗公司 | 用于金刚烷类药物缓释的胃驻留系统 |
| WO2018089684A1 (en) | 2016-11-09 | 2018-05-17 | Massachusetts Institute Of Technology | Triggerable hydrogel compositions and related methods |
| US10737079B2 (en) | 2016-12-02 | 2020-08-11 | Clexio Biosciences Ltd. | Gastric residence system |
| CA3066658A1 (en) | 2017-06-09 | 2018-12-13 | Lyndra, Inc. | Gastric residence systems with release rate-modulating films |
| CA3076330A1 (en) | 2017-09-20 | 2019-03-28 | Lyndra, Inc. | Encapsulation of gastric residence systems |
| JP7296084B2 (ja) | 2017-12-04 | 2023-06-22 | クレキシオ バイオサイエンシーズ エルティーディー. | 長時間作用型胃滞留システム |
| US20190365645A1 (en) | 2018-05-31 | 2019-12-05 | Massachusetts Institute Of Technology | Drug delivery articles for gram-level dosing |
| WO2020102648A1 (en) | 2018-11-15 | 2020-05-22 | Massachusetts Institute Of Technology | Millineedle systems for esophageal drug delivery |
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| HK1258050A1 (zh) | 2019-11-01 |
| EP3364946A1 (en) | 2018-08-29 |
| AU2016342374A1 (en) | 2018-06-07 |
| JP7085473B2 (ja) | 2022-06-16 |
| CA3002916A1 (en) | 2017-04-27 |
| CN108472249A (zh) | 2018-08-31 |
| JP7448587B2 (ja) | 2024-03-12 |
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