JP7124234B2 - フェノルドパムの安定な局所用組成物 - Google Patents
フェノルドパムの安定な局所用組成物 Download PDFInfo
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- JP7124234B2 JP7124234B2 JP2021553117A JP2021553117A JP7124234B2 JP 7124234 B2 JP7124234 B2 JP 7124234B2 JP 2021553117 A JP2021553117 A JP 2021553117A JP 2021553117 A JP2021553117 A JP 2021553117A JP 7124234 B2 JP7124234 B2 JP 7124234B2
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- fenoldopam
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- topical composition
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/04—Antipruritics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/10—Anti-acne agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/14—Drugs for dermatological disorders for baldness or alopecia
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- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
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- Medicinal Preparation (AREA)
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Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2022127610A JP2022160648A (ja) | 2019-03-08 | 2022-08-10 | フェノルドパムの安定な局所用組成物 |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201962815893P | 2019-03-08 | 2019-03-08 | |
| US62/815,893 | 2019-03-08 | ||
| PCT/IB2020/051967 WO2020183322A1 (en) | 2019-03-08 | 2020-03-06 | Stable topical compositions of fenoldopam |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2022127610A Division JP2022160648A (ja) | 2019-03-08 | 2022-08-10 | フェノルドパムの安定な局所用組成物 |
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| Publication Number | Publication Date |
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| JP2022515569A JP2022515569A (ja) | 2022-02-18 |
| JP7124234B2 true JP7124234B2 (ja) | 2022-08-23 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2021553117A Active JP7124234B2 (ja) | 2019-03-08 | 2020-03-06 | フェノルドパムの安定な局所用組成物 |
| JP2022127610A Ceased JP2022160648A (ja) | 2019-03-08 | 2022-08-10 | フェノルドパムの安定な局所用組成物 |
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| Application Number | Title | Priority Date | Filing Date |
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| JP2022127610A Ceased JP2022160648A (ja) | 2019-03-08 | 2022-08-10 | フェノルドパムの安定な局所用組成物 |
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| Country | Link |
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| US (2) | US11446237B2 (https=) |
| EP (2) | EP3908255B1 (https=) |
| JP (2) | JP7124234B2 (https=) |
| CN (2) | CN116966129A (https=) |
| AU (2) | AU2020236525B2 (https=) |
| BR (1) | BR112021017140A2 (https=) |
| CA (1) | CA3131049A1 (https=) |
| ES (1) | ES2941241T3 (https=) |
| IL (1) | IL286197A (https=) |
| NZ (1) | NZ781774A (https=) |
| WO (1) | WO2020183322A1 (https=) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2023257375A1 (en) | 2022-04-21 | 2024-11-07 | Glaukos Corporation | Ophthalmic topical cream compositions |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002521324A (ja) | 1998-07-24 | 2002-07-16 | アルザ コーポレイション | フェノルドパムの経皮投与のための配合物 |
| US20110104287A1 (en) | 2007-10-18 | 2011-05-05 | Mia Levite | Fenoldopam formulations and pro-drug derivatives |
| WO2016116909A2 (en) | 2015-01-23 | 2016-07-28 | Dr. Reddy's Laboratories Limited | Non-staining topical gel compositions of nimesulide |
| WO2018042352A1 (en) | 2016-08-31 | 2018-03-08 | Taro Pharmaceutical Industries | Fenoldopam topical formulations for treating skin disorders |
Family Cites Families (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4666828A (en) | 1984-08-15 | 1987-05-19 | The General Hospital Corporation | Test for Huntington's disease |
| US4683202A (en) | 1985-03-28 | 1987-07-28 | Cetus Corporation | Process for amplifying nucleic acid sequences |
| US4801531A (en) | 1985-04-17 | 1989-01-31 | Biotechnology Research Partners, Ltd. | Apo AI/CIII genomic polymorphisms predictive of atherosclerosis |
| US5272057A (en) | 1988-10-14 | 1993-12-21 | Georgetown University | Method of detecting a predisposition to cancer by the use of restriction fragment length polymorphism of the gene for human poly (ADP-ribose) polymerase |
| US5192659A (en) | 1989-08-25 | 1993-03-09 | Genetype Ag | Intron sequence analysis method for detection of adjacent and remote locus alleles as haplotypes |
| ATE210975T1 (de) | 1994-06-23 | 2002-01-15 | Procter & Gamble | Topisch anzuwendende zubereitungen enthaltend n- acetyl-l-cystein |
| US6054429A (en) | 1996-03-08 | 2000-04-25 | Elan Pharmaceuticals, Inc. | Epidural method of producing analgesia |
| AU3869399A (en) | 1998-04-27 | 1999-11-16 | Elan Pharmaceuticals, Inc. | Transdermal administration of fenoldopam |
| JPH11335236A (ja) | 1998-05-22 | 1999-12-07 | Shiseido Co Ltd | 皮膚外用剤 |
| US6699497B1 (en) | 1998-07-24 | 2004-03-02 | Alza Corporation | Formulations for the transdermal administration of fenoldopam |
| US7442369B1 (en) * | 2000-08-09 | 2008-10-28 | Mcneil Ab | Compositions of minoxidil |
| US7358236B1 (en) | 2002-06-21 | 2008-04-15 | Oxigene, Inc. | Control of acute hypertension and cardiotoxicity in patients treated with vascular targeting agents |
| US7820145B2 (en) | 2003-08-04 | 2010-10-26 | Foamix Ltd. | Oleaginous pharmaceutical and cosmetic foam |
| WO2005079851A2 (en) | 2004-02-18 | 2005-09-01 | Sepracor, Inc. | Dopamine-agonist combination therapy with sedatives for improving sleep quality |
| WO2005108387A2 (en) | 2004-05-03 | 2005-11-17 | Boehringer Ingelheim Pharmaceuticals, Inc. | Cytokine inhibitors |
| CN101151028A (zh) * | 2005-03-03 | 2008-03-26 | Isw集团公司 | 局部用凝胶组合物 |
| AU2006265002B2 (en) | 2005-06-30 | 2012-09-20 | Centocor, Inc. | Anti-IL-23 antibodies, compositions, methods and uses |
| JP2009502206A (ja) | 2005-08-03 | 2009-01-29 | ミニュー・セラピューティクス・リミテッド | 腫瘍壊死因子アルファ(TNF−α)合成および分泌を調節するための、T細胞におけるKv1.1電位依存性カリウムチャンネルのモデュレーション、およびTNF−αの有害な高または低レベルを介しての人の疾患または傷害の治療 |
| WO2009072007A2 (en) | 2007-12-07 | 2009-06-11 | Foamix Ltd. | Carriers, formulations, methods for formulating unstable active agents for external application and uses thereof |
| WO2009076553A1 (en) | 2007-12-11 | 2009-06-18 | Monroe Stephen H | Composition of aqueous buffer solution for the treatment of cellular environment and ion channels and methods for using same |
| CA2732439A1 (en) | 2008-07-31 | 2010-02-04 | Case Western Reserve University | Halogen-stabilized insulin |
| JP2011144143A (ja) | 2010-01-15 | 2011-07-28 | Shiseido Co Ltd | 皮膚外用剤 |
| RU2571277C2 (ru) | 2010-10-21 | 2015-12-20 | Галдерма С.А. | Композиции геля с бримонидином и способы применения |
| HUE034480T2 (en) | 2011-04-28 | 2018-02-28 | Platform Brightworks Two Ltd | Improved parenteral formulations of lipophilic pharmaceutical agents and methods for preparing and using the same |
| FR2991177B1 (fr) | 2012-06-01 | 2014-12-19 | Galderma Res & Dev | Compositions topiques, contenant un retinoide, de type emulsion huile dans eau sans emulsionnant |
| AU2014227996B2 (en) * | 2013-03-15 | 2018-08-23 | Vapogenix, Inc. | Novel analgesic compositions |
| JP6893075B2 (ja) | 2014-08-04 | 2021-06-23 | 日東電工株式会社 | 液性免疫誘導促進用組成物及びワクチン医薬組成物 |
| MX2020004187A (es) * | 2017-10-24 | 2020-09-21 | Glenmark Pharmaceuticals Ltd | Composicion farmaceutica topica de adapaleno y minociclina. |
-
2020
- 2020-03-06 NZ NZ781774A patent/NZ781774A/en not_active IP Right Cessation
- 2020-03-06 US US17/430,264 patent/US11446237B2/en active Active
- 2020-03-06 EP EP20712690.5A patent/EP3908255B1/en active Active
- 2020-03-06 ES ES20712690T patent/ES2941241T3/es active Active
- 2020-03-06 CN CN202310774370.XA patent/CN116966129A/zh active Pending
- 2020-03-06 CA CA3131049A patent/CA3131049A1/en active Pending
- 2020-03-06 AU AU2020236525A patent/AU2020236525B2/en not_active Ceased
- 2020-03-06 JP JP2021553117A patent/JP7124234B2/ja active Active
- 2020-03-06 WO PCT/IB2020/051967 patent/WO2020183322A1/en not_active Ceased
- 2020-03-06 EP EP23150539.7A patent/EP4218719A3/en not_active Withdrawn
- 2020-03-06 BR BR112021017140A patent/BR112021017140A2/pt active Search and Examination
- 2020-03-06 CN CN202080019392.XA patent/CN113543773B/zh not_active Expired - Fee Related
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2021
- 2021-09-06 IL IL286197A patent/IL286197A/en unknown
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2022
- 2022-05-03 AU AU2022202941A patent/AU2022202941A1/en not_active Abandoned
- 2022-08-09 US US17/883,687 patent/US20230059107A1/en not_active Abandoned
- 2022-08-10 JP JP2022127610A patent/JP2022160648A/ja not_active Ceased
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2002521324A (ja) | 1998-07-24 | 2002-07-16 | アルザ コーポレイション | フェノルドパムの経皮投与のための配合物 |
| US20110104287A1 (en) | 2007-10-18 | 2011-05-05 | Mia Levite | Fenoldopam formulations and pro-drug derivatives |
| WO2016116909A2 (en) | 2015-01-23 | 2016-07-28 | Dr. Reddy's Laboratories Limited | Non-staining topical gel compositions of nimesulide |
| WO2018042352A1 (en) | 2016-08-31 | 2018-03-08 | Taro Pharmaceutical Industries | Fenoldopam topical formulations for treating skin disorders |
Also Published As
| Publication number | Publication date |
|---|---|
| EP4218719A2 (en) | 2023-08-02 |
| EP3908255B1 (en) | 2023-01-11 |
| WO2020183322A1 (en) | 2020-09-17 |
| ES2941241T3 (es) | 2023-05-19 |
| JP2022160648A (ja) | 2022-10-19 |
| CN113543773B (zh) | 2023-07-14 |
| EP3908255A1 (en) | 2021-11-17 |
| BR112021017140A2 (pt) | 2021-11-09 |
| US20230059107A1 (en) | 2023-02-23 |
| AU2022202941A1 (en) | 2022-05-26 |
| EP4218719A3 (en) | 2023-09-20 |
| US11446237B2 (en) | 2022-09-20 |
| CN116966129A (zh) | 2023-10-31 |
| JP2022515569A (ja) | 2022-02-18 |
| AU2020236525B2 (en) | 2022-02-03 |
| CA3131049A1 (en) | 2020-09-17 |
| IL286197A (en) | 2021-10-31 |
| NZ781774A (en) | 2023-03-31 |
| CN113543773A (zh) | 2021-10-22 |
| AU2020236525A1 (en) | 2021-11-04 |
| US20220040089A1 (en) | 2022-02-10 |
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