CA2777384A1 - Combination therapy treatment for viral infections - Google Patents
Combination therapy treatment for viral infections Download PDFInfo
- Publication number
- CA2777384A1 CA2777384A1 CA2777384A CA2777384A CA2777384A1 CA 2777384 A1 CA2777384 A1 CA 2777384A1 CA 2777384 A CA2777384 A CA 2777384A CA 2777384 A CA2777384 A CA 2777384A CA 2777384 A1 CA2777384 A1 CA 2777384A1
- Authority
- CA
- Canada
- Prior art keywords
- receptor agonist
- antiviral agent
- hydroxy
- day
- hydroxyl
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
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- A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
- A61K31/7056—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing five-membered rings with nitrogen as a ring hetero atom
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- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/235—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group
- A61K31/24—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids having an aromatic ring attached to a carboxyl group having an amino or nitro group
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- A61K31/34—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
- A61K31/343—Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
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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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Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
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- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US25156109P | 2009-10-14 | 2009-10-14 | |
| US61/251,561 | 2009-10-14 | ||
| PCT/US2010/052506 WO2011047048A1 (en) | 2009-10-14 | 2010-10-13 | Combination therapy treatment for viral infections |
Publications (1)
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| CA2777384A1 true CA2777384A1 (en) | 2011-04-21 |
Family
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Family Applications (1)
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|---|---|---|---|
| CA2777384A Abandoned CA2777384A1 (en) | 2009-10-14 | 2010-10-13 | Combination therapy treatment for viral infections |
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| Country | Link |
|---|---|
| US (2) | US20120190637A1 (enExample) |
| EP (1) | EP2488168A1 (enExample) |
| JP (1) | JP2013508282A (enExample) |
| KR (1) | KR20120093955A (enExample) |
| CN (1) | CN102655859A (enExample) |
| BR (1) | BR112012008959A2 (enExample) |
| CA (1) | CA2777384A1 (enExample) |
| NZ (1) | NZ599128A (enExample) |
| WO (1) | WO2011047048A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2269611B1 (en) | 2006-11-16 | 2016-03-23 | Gemmus Pharma Inc. | EP2 and EP4 agonists as agents for the treatment of influenza A viral infection |
| JP2016512833A (ja) * | 2013-03-15 | 2016-05-09 | ゲームス・ファーマ・インコーポレイテッド | ウイルス感染症の治療薬としてのベラプロスト異性体 |
| WO2015109112A1 (en) * | 2014-01-16 | 2015-07-23 | Gemmus Pharma Inc. | Combination treatment of antibiotic and gpcr agonist for viral/bacterial co-infections |
| CN110603041A (zh) * | 2017-04-12 | 2019-12-20 | 沃泰克斯药物股份有限公司 | 用于治疗流感病毒感染的组合治疗 |
| CN111265528A (zh) * | 2020-01-21 | 2020-06-12 | 中国人民解放军军事科学院军事医学研究院 | 法匹拉韦在治疗冠状病毒感染方面的应用 |
| US12042503B2 (en) | 2020-02-12 | 2024-07-23 | Cytoagents, Inc. | Compositions and methods for treating coronavirus infections |
| CN111184707B (zh) * | 2020-02-20 | 2021-04-27 | 中山大学 | 托芬那酸或其药学上可接受的盐在制备预防和/或治疗新型冠状病毒炎症药物中的应用 |
| JP2023525981A (ja) * | 2020-04-30 | 2023-06-20 | ミノリックス セラピューティクス エセ．エレ． | 肺炎症および間質性肺疾患を処置するためのレリグリタゾン |
| JP7715353B2 (ja) * | 2020-04-30 | 2025-07-30 | 国立大学法人京都大学 | Ｒｎａウイルス関連疾患の予防又は治療剤 |
| US20210386725A1 (en) * | 2020-06-11 | 2021-12-16 | Chang Gung University | Method for inhibiting coronavirus infection and replication |
| WO2022118020A1 (en) | 2020-12-02 | 2022-06-09 | Cipla Limited | Method of treating viral infection |
Family Cites Families (52)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2845770A1 (de) | 1978-10-19 | 1980-04-30 | Schering Ag | Neue prostacyclin-derivate und verfahren zu ihrer herstellung |
| DE3048906A1 (de) | 1980-12-19 | 1982-07-15 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Neue carbacycline, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
| JPS58124778A (ja) | 1982-01-20 | 1983-07-25 | Toray Ind Inc | ５，６，７−トリノル−４，８−インタ−ｍ−フエニレンＰＧＩ↓２誘導体 |
| DE3226550A1 (de) | 1982-07-13 | 1984-01-19 | Schering AG, 1000 Berlin und 4709 Bergkamen | Neue carbacycline, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
| DE3306123A1 (de) | 1983-02-18 | 1984-09-06 | Schering AG, 1000 Berlin und 4709 Bergkamen | Neue carbacycline, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel |
| DE3740838A1 (de) | 1987-11-27 | 1989-06-08 | Schering Ag | Cyclodextrinclathrate von 5-cyano-prostacyclinderivaten und ihre verwendung als arzneimittel |
| OA12533A (en) | 2000-11-27 | 2006-06-05 | Pfizer Prod Inc | Ep4 receptor selective agonists in the treatment of osteoporosis. |
| GB0031302D0 (en) | 2000-12-21 | 2001-01-31 | Glaxo Group Ltd | Napthalene derivatives |
| GB0031295D0 (en) | 2000-12-21 | 2001-01-31 | Glaxo Group Ltd | Naphthalene derivatives |
| US20030027853A1 (en) | 2001-06-14 | 2003-02-06 | Allergan Sales, Inc. | 3, 7or3 and 7 thia or oxa prostanoic acid derivatives as agents for lowering intraocular pressure |
| KR100826866B1 (ko) | 2001-07-23 | 2008-05-06 | 오노 야꾸힝 고교 가부시키가이샤 | Ｅｐ４ 아고니스트를 유효 성분으로 하는 골량 저하질환의 치료제 |
| CA2466751A1 (en) | 2001-12-03 | 2003-06-12 | Merck And Co., Inc. | Ep4 receptor agonist, compositions and methods thereof |
| CA2466757A1 (en) | 2001-12-03 | 2003-06-12 | Merck & Co., Inc. | Method for treating ocular hypertension |
| KR100592007B1 (ko) | 2002-04-12 | 2006-06-21 | 화이자 인코포레이티드 | Ｉｌ-６ 관련 질환 치료에서의 ｅｐ４ 수용체 리간드의용도 |
| EP1513589B1 (en) | 2002-06-06 | 2010-11-10 | Merck Frosst Canada Ltd. | 1,5-disubstituted pyrrolid-2-one derivatives for use as ep4 receptor agonists in the treatment of eye diseases such as glaucoma |
| WO2003103664A1 (en) | 2002-06-06 | 2003-12-18 | Merck Frosst Canada & Co. | 1,5-disubstituted imidazolidin-2-one derivatives for use as ep4 receptor agonists in the treatment of eye and bone diseases |
| AU2003258433A1 (en) | 2002-08-28 | 2004-03-19 | Merck Frosst Canada Ltd | Oxazolidin-2-one and thiazolidin-2-one derivatives for use as ep4 receptor agonists in the treatment of glaucoma |
| CA2502914A1 (en) | 2002-10-25 | 2004-05-06 | Merck Frosst Canada & Co. | 2-pyrrolidones as ep4 receptor agonists |
| US7053085B2 (en) | 2003-03-26 | 2006-05-30 | Merck & Co. Inc. | EP4 receptor agonist, compositions and methods thereof |
| EP1586564B1 (en) | 2003-01-21 | 2012-11-28 | Ono Pharmaceutical Co., Ltd. | 8-azaprostaglandin derivatives and medicinal uses thereof |
| JP5319065B2 (ja) | 2003-02-11 | 2013-10-16 | アラーガン インコーポレイテッド | 眼圧降下剤としての１０，１０−ジアルキルプロスタン酸誘導体 |
| GB0306907D0 (en) | 2003-03-26 | 2003-04-30 | Angiogene Pharm Ltd | Boireductively-activated prodrugs |
| US7326716B2 (en) | 2003-06-06 | 2008-02-05 | Allergan, Inc. | Treatment of inflammatory bowel disease |
| US6747037B1 (en) | 2003-06-06 | 2004-06-08 | Allergan, Inc. | Piperidinyl prostaglandin E analogs |
| US7015243B2 (en) | 2003-08-28 | 2006-03-21 | Allergan, Inc. | Cyclohexyl prostaglandin analogs as EP4-receptor agonists |
| WO2005027931A1 (en) | 2003-09-19 | 2005-03-31 | Pfizer Products Inc. | Pharmaceutical compositions and methods comprising combinations of 2-alkylidene-19-nor-vitamin d derivatives and an ep2 or ep4 selective agonist |
| MXPA06006810A (es) | 2003-12-17 | 2006-08-23 | Pfizer Prod Inc | Tratamiento de afecciones que se presentan con un nivel bajo de masa osea por terapia de combinacion continua con agonistas selectivos del receptor de prostaglandina ep4 y un estrogeno. |
| US7169807B2 (en) | 2004-04-09 | 2007-01-30 | Allergan, Inc. | 10-Hydroxy-11-dihydroprostaglandin analogs as selective EP4 agonists |
| WO2005116010A1 (en) | 2004-05-26 | 2005-12-08 | Merck Frosst Canada Ltd. | Ep4 receptor agonist, compositions and methods thereof |
| JPWO2006016695A1 (ja) | 2004-08-10 | 2008-05-01 | 小野薬品工業株式会社 | Ｅｐ４アゴニストを含有してなる高カリウム血症の予防および／または治療剤 |
| AU2005299473B2 (en) | 2004-10-26 | 2012-06-28 | Allergan, Inc. | Therapeutic and delivery methods of prostaglandin EP4 agonists |
| US7994195B2 (en) | 2004-11-04 | 2011-08-09 | Allergan, Inc. | Therapeutic substituted piperidone compounds |
| US7101906B2 (en) | 2004-11-16 | 2006-09-05 | Allergan, Inc. | 2,3,4-substituted cyclopentanones as therapeutic agents |
| US7183324B2 (en) | 2004-11-23 | 2007-02-27 | Allergan, Inc. | 2,3,4-substituted cyclopentanones as therapeutic agents |
| KR100890490B1 (ko) | 2005-01-27 | 2009-03-26 | 아사히 가세이 파마 가부시키가이샤 | 헤테로 6원환 화합물 및 그의 용도 |
| JP4985400B2 (ja) | 2005-06-24 | 2012-07-25 | 大正製薬株式会社 | プロスタグランジン誘導体 |
| WO2007014454A1 (en) | 2005-08-03 | 2007-02-08 | Merck Frosst Canada Ltd. | Ep4 receptor agonist, compositions and methods thereof |
| WO2007014462A1 (en) | 2005-08-03 | 2007-02-08 | Merck Frosst Canada Ltd. | Ep4 receptor agonist, compositions and methods thereof |
| US7893107B2 (en) | 2005-11-30 | 2011-02-22 | Allergan, Inc. | Therapeutic methods using prostaglandin EP4 agonist components |
| GB0602900D0 (en) | 2006-02-13 | 2006-03-22 | Glaxo Group Ltd | Novel Compounds |
| WO2007139150A1 (ja) * | 2006-05-30 | 2007-12-06 | The University Of Tokushima | ＴＮＦα阻害物質を含有してなる抗インフルエンザウイルス剤 |
| CA2654811A1 (en) | 2006-06-12 | 2007-12-21 | Merck Frosst Canada Ltd. | Indoline amide derivatives as ep4 receptor ligands |
| GB0615105D0 (en) | 2006-07-28 | 2006-09-06 | Glaxo Group Ltd | Novel compounds |
| GB0615111D0 (en) | 2006-07-28 | 2006-09-06 | Glaxo Group Ltd | Novel compounds |
| WO2008017164A1 (en) | 2006-08-11 | 2008-02-14 | Merck Frosst Canada Ltd. | Thiophenecarboxamide derivatives as ep4 receptor ligands |
| GB0620619D0 (en) | 2006-10-17 | 2006-11-29 | Glaxo Group Ltd | Novel compounds |
| EP2269611B1 (en) * | 2006-11-16 | 2016-03-23 | Gemmus Pharma Inc. | EP2 and EP4 agonists as agents for the treatment of influenza A viral infection |
| GB0623203D0 (en) | 2006-11-21 | 2007-01-03 | Glaxo Group Ltd | Novel compounds |
| WO2008071736A1 (en) | 2006-12-15 | 2008-06-19 | Glaxo Group Limited | Benzamide derivatives as ep4 receptor agonists |
| EP1975163A1 (en) * | 2007-03-28 | 2008-10-01 | Bayer Schering Pharma Aktiengesellschaft | Novel 5-cyano-prostacyclin derivatives and their use as agents for the treatment of influenza a viral infection |
| US7776896B2 (en) | 2007-03-28 | 2010-08-17 | Bayer Schering Pharma Aktiengesellschaft | 5-cyano-prostacyclin derivatives as agents for the treatment of influenza a viral infection |
| MX2009012043A (es) | 2007-05-08 | 2010-02-18 | Nat Univ Corp Hamamatsu | Activador de celulas t citotoxicas que comprende agonista ep4. |
-
2010
- 2010-10-13 BR BR112012008959A patent/BR112012008959A2/pt not_active IP Right Cessation
- 2010-10-13 WO PCT/US2010/052506 patent/WO2011047048A1/en not_active Ceased
- 2010-10-13 CA CA2777384A patent/CA2777384A1/en not_active Abandoned
- 2010-10-13 JP JP2012534324A patent/JP2013508282A/ja active Pending
- 2010-10-13 KR KR1020127012323A patent/KR20120093955A/ko not_active Ceased
- 2010-10-13 CN CN2010800567360A patent/CN102655859A/zh active Pending
- 2010-10-13 US US13/129,108 patent/US20120190637A1/en not_active Abandoned
- 2010-10-13 NZ NZ599128A patent/NZ599128A/en not_active IP Right Cessation
- 2010-10-13 EP EP10768160A patent/EP2488168A1/en not_active Withdrawn
-
2014
- 2014-12-10 US US14/566,354 patent/US20150196578A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| BR112012008959A2 (pt) | 2019-09-24 |
| KR20120093955A (ko) | 2012-08-23 |
| CN102655859A (zh) | 2012-09-05 |
| NZ599128A (en) | 2014-02-28 |
| WO2011047048A1 (en) | 2011-04-21 |
| US20150196578A1 (en) | 2015-07-16 |
| JP2013508282A (ja) | 2013-03-07 |
| US20120190637A1 (en) | 2012-07-26 |
| EP2488168A1 (en) | 2012-08-22 |
| AU2010306914A1 (en) | 2012-04-19 |
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