DK2766014T3 - METHODS OF TREATING PEDIATRIC PATIENTS USING DEXMEDETOMIDINE - Google Patents
METHODS OF TREATING PEDIATRIC PATIENTS USING DEXMEDETOMIDINE Download PDFInfo
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- DK2766014T3 DK2766014T3 DK12840033.0T DK12840033T DK2766014T3 DK 2766014 T3 DK2766014 T3 DK 2766014T3 DK 12840033 T DK12840033 T DK 12840033T DK 2766014 T3 DK2766014 T3 DK 2766014T3
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- dexmedetomidine
- dose
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- 239000003981 vehicle Substances 0.000 description 1
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Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/4164—1,3-Diazoles
- A61K31/4174—Arylalkylimidazoles, e.g. oxymetazolin, naphazoline, miconazole
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- 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
- A61K31/4164—1,3-Diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/20—Hypnotics; Sedatives
Landscapes
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Neurosurgery (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Organic Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Anesthesiology (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (4)
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| US201161547626P | 2011-10-14 | 2011-10-14 | |
| US13/343,693 US20130096170A1 (en) | 2011-10-14 | 2012-01-04 | Methods of treating pediatric patients using dexmedetomidine |
| US13/471,403 US8324260B1 (en) | 2011-10-14 | 2012-05-14 | Methods of treating pediatric patients using dexmedetomidine |
| PCT/US2012/057652 WO2013055528A1 (en) | 2011-10-14 | 2012-09-27 | Methods of treating pediatric patients using dexmedetomidine |
Publications (1)
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| DK2766014T3 true DK2766014T3 (en) | 2018-09-24 |
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| CA (2) | CA2851780C (enExample) |
| CY (1) | CY1121041T1 (enExample) |
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| ES (1) | ES2685814T3 (enExample) |
| HK (1) | HK1200333A1 (enExample) |
| HR (1) | HRP20181378T1 (enExample) |
| HU (1) | HUE039671T2 (enExample) |
| IL (2) | IL232070A0 (enExample) |
| IN (1) | IN2014KN00996A (enExample) |
| LT (1) | LT2766014T (enExample) |
| MX (1) | MX362626B (enExample) |
| PL (1) | PL2766014T3 (enExample) |
| PT (1) | PT2766014T (enExample) |
| RS (1) | RS57660B1 (enExample) |
| SI (1) | SI2766014T1 (enExample) |
| WO (1) | WO2013055528A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20130096170A1 (en) | 2011-10-14 | 2013-04-18 | Hospira, Inc. | Methods of treating pediatric patients using dexmedetomidine |
| US8242158B1 (en) * | 2012-01-04 | 2012-08-14 | Hospira, Inc. | Dexmedetomidine premix formulation |
| KR101831290B1 (ko) | 2013-10-07 | 2018-02-22 | 테이코쿠 팔마 유에스에이, 인코포레이티드 | 덱스메데토미딘 경피 조성물을 사용하여 주의력 결핍 과잉행동 장애, 불안 및 불면증을 치료하기 위한 방법 및 조성물 |
| TWI645866B (zh) | 2013-10-07 | 2019-01-01 | 美商帝國製藥美國股份有限公司 | 右美托咪啶經皮輸送裝置及使用其之方法 |
| EP3054931B1 (en) * | 2013-10-07 | 2020-12-23 | Teikoku Pharma USA, Inc. | Transdermal delivery device for managing pain comprising dexmedetomidine transdermal compositions |
| BR112016006848A2 (pt) * | 2013-10-07 | 2017-08-01 | Teikoku Pharma Usa Inc | métodos e composições para distribuição transdérmica de uma quantidade não sedativa de dexmedetomidina |
| US11017330B2 (en) * | 2014-05-20 | 2021-05-25 | Elasticsearch B.V. | Method and system for analysing data |
| EP3182893B1 (en) | 2014-08-18 | 2024-02-07 | Electronic Pain Assessment Technologies (EPAT) Pty Ltd | A pain assessment system |
| CN104784174A (zh) * | 2015-03-06 | 2015-07-22 | 北京大学第一医院 | 右美托咪定的药物新用途 |
| US9717796B1 (en) * | 2016-04-20 | 2017-08-01 | Slypharma, Llc | Heat sterilizeable, premixed, ready to use dexmedetomidine solution packaged in a flexible plastic container |
| CA3038354C (en) * | 2016-10-31 | 2021-08-17 | Teikoku Pharma Usa, Inc. | Methods of managing pain using dexmedetomidine transdermal delivery devices |
| CN106539778A (zh) * | 2016-12-08 | 2017-03-29 | 武汉大学 | 一种小儿麻醉术前含服口腔泡腾片及其制备方法 |
| WO2018126182A1 (en) | 2016-12-31 | 2018-07-05 | Bioxcel Therapeutics, Inc. | Use of sublingual dexmedetomidine for the treatment of agitation |
| US11621969B2 (en) | 2017-04-26 | 2023-04-04 | Elasticsearch B.V. | Clustering and outlier detection in anomaly and causation detection for computing environments |
| US11783046B2 (en) | 2017-04-26 | 2023-10-10 | Elasticsearch B.V. | Anomaly and causation detection in computing environments |
| CN108042533B (zh) * | 2017-12-25 | 2020-11-13 | 苏州格兰科医药科技有限公司 | 右美托米定在制备用于预防和/或抑制创伤性脑损伤后的神经元死亡的药物组合物中的用途 |
| WO2020006119A1 (en) * | 2018-06-27 | 2020-01-02 | Bioxcel Therapeutics, Inc. | Methods for treating agitation using dexmedetomidine hydrochloride |
| CN114983979A (zh) | 2018-06-27 | 2022-09-02 | 比奥克斯塞尔医疗股份有限公司 | 含右美托咪定的膜制剂及其制造方法 |
| AU2019339352B2 (en) * | 2018-09-12 | 2025-05-22 | Hough Ear Institute | Methods for treating hearing loss incident to cochlear implant surgery |
| EP3849532A4 (en) * | 2018-09-13 | 2022-06-08 | Taiwan Liposome Company, Ltd. | SUSTAINED-RELEASE PHARMACEUTICAL COMPOSITIONS COMPRISING A SEDATIVE MEDICINE AND THEIR USES |
| US20220051802A1 (en) * | 2018-12-13 | 2022-02-17 | Dignity Health | System and method for detection and monitoring of over sedation to prevent harm to patients |
| US10817669B2 (en) | 2019-01-14 | 2020-10-27 | International Business Machines Corporation | Automatic classification of adverse event text fragments |
| CN109793709A (zh) * | 2019-02-22 | 2019-05-24 | 青岛农业大学 | 一种斑海豹用复方注射剂及其制备方法 |
| US11000488B2 (en) * | 2019-03-22 | 2021-05-11 | Syntrix Biosystems Inc. | Treating pain using desmetramadol |
| KR20220049526A (ko) | 2019-07-19 | 2022-04-21 | 바이오엑셀 테라퓨틱스 인코포레이티드 | 비-진정성 덱스메데토미딘 치료 양생법 |
| WO2021211507A1 (en) * | 2020-04-17 | 2021-10-21 | Bioventures, Llc | Methods and systems for predicting the effect of inhaled and infused anesthetics |
| KR102815903B1 (ko) | 2021-12-21 | 2025-05-30 | 충남대학교산학협력단 | 감염 환자에서 반코마이신 최적 용량을 결정하는 방법 |
| EP4386768A1 (en) * | 2022-12-13 | 2024-06-19 | Koninklijke Philips N.V. | Active sleep apnea case finding and scheduling system and method of operation thereof |
| US11806334B1 (en) | 2023-01-12 | 2023-11-07 | Bioxcel Therapeutics, Inc. | Non-sedating dexmedetomidine treatment regimens |
| WO2025176701A1 (en) * | 2024-02-19 | 2025-08-28 | Rigshospitalet | Novel pediatric composition of nasal dexmedetomidine |
Family Cites Families (37)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4407957A (en) | 1981-03-13 | 1983-10-04 | Damon Corporation | Reversible microencapsulation of a core material |
| JPS6058890A (ja) | 1983-09-13 | 1985-04-05 | Mizusawa Ind Chem Ltd | 感熱記録紙用填剤 |
| FI844786A0 (fi) | 1984-12-04 | 1984-12-04 | Farmos Oy | Terapeutiskt utnyttjbar foerening. |
| GB2206880B (en) | 1987-07-16 | 1991-04-24 | Farmos Oy | Optical isomers of an imidazole derivative |
| US5344840A (en) | 1988-02-29 | 1994-09-06 | Orion-Yhtyma Oy | 4-substituted imidazole derivatives useful in perioperative care |
| US5124157A (en) | 1989-08-18 | 1992-06-23 | Cygnus Therapeutic Systems | Method and device for administering dexmedetomidine transdermally |
| US5217718A (en) | 1989-08-18 | 1993-06-08 | Cygnus Therapeutic Systems | Method and device for administering dexmedetomidine transdermally |
| FI894911A0 (fi) | 1989-10-17 | 1989-10-17 | Farmos Oy | En terapeutiskt vaerdefull foerening. |
| US5304569A (en) | 1989-11-13 | 1994-04-19 | Orion-Yhtyma Oy | Compositions and their use in lowering intraocular pressure |
| EP0585368B1 (en) | 1991-04-25 | 1997-08-06 | Brown University Research Foundation | Implantable biocompatible immunoisolatory vehicle for delivery of selected therapeutic products |
| US5383851A (en) | 1992-07-24 | 1995-01-24 | Bioject Inc. | Needleless hypodermic injection device |
| US5569189A (en) | 1992-09-28 | 1996-10-29 | Equidyne Systems, Inc. | hypodermic jet injector |
| KR100291620B1 (ko) | 1992-09-29 | 2001-10-24 | 추후제출 | 부갑상선호르몬의활성단편의폐를통한전달방법 |
| GB2281206A (en) | 1993-08-25 | 1995-03-01 | Orion Yhtymae Oy | Use of dexmedetomidine |
| FR2718357B1 (fr) | 1994-04-06 | 1997-10-03 | Defarges Alain Moreau | Perfectionnements apportés à un dispositif d'injection par jet sans aiguille. |
| CZ286714B6 (en) | 1994-08-08 | 2000-06-14 | Debiopharm Sa | Pharmaceutically stable preparation based on oxaliplatinum |
| US5599302A (en) | 1995-01-09 | 1997-02-04 | Medi-Ject Corporation | Medical injection system and method, gas spring thereof and launching device using gas spring |
| US5780014A (en) | 1995-04-14 | 1998-07-14 | Inhale Therapeutic Systems | Method and apparatus for pulmonary administration of dry powder alpha 1-antitrypsin |
| US5654007A (en) | 1995-06-07 | 1997-08-05 | Inhale Therapeutic Systems | Methods and system for processing dispersible fine powders |
| DE19758564A1 (de) | 1997-11-11 | 1999-08-26 | Gruenenthal Gmbh | Formulierung einer Kombination aus Morphin und einem alpha¶2¶-adrenergem Agonisten und deren Verwendung |
| AR015744A1 (es) * | 1998-04-01 | 2001-05-16 | Orion Corp | Uso de dexmedetomidina para sedacion en terapia intensiva |
| US6716867B1 (en) * | 1998-04-01 | 2004-04-06 | Orion Corporation | Use of dexmedetomidine for ICU sedation |
| PE20001396A1 (es) | 1999-01-18 | 2000-12-23 | Gruenenthal Chemie | Formulaciones medicamentosas retardadas que contienen una combinacion de un opioide o una sal fisiologicamente tolerables del mismo, un o-agonista |
| GB9913677D0 (en) | 1999-06-11 | 1999-08-11 | Imperial College | Formulation |
| US6806291B1 (en) | 2003-10-09 | 2004-10-19 | The Foundation For The Lsu Health Sciences Center | Analgesic compounds, their synthesis and pharmaceutical compositions containing them |
| US20080308444A1 (en) | 2007-06-13 | 2008-12-18 | Baxter International Inc. | Packaging system and method of alerting a practitioner |
| US20100197694A1 (en) | 2008-08-01 | 2010-08-05 | Gerald Horn | Compositions and methods for treatment of diseases and conditions with increased vascular permeability |
| EP2165706A1 (en) | 2008-09-18 | 2010-03-24 | BioAlliance Pharma | Treating Inflammatory Pain in Mucosa of the Oral Cavity Using Mucosal Prolonged Release Bioadhesive Therapeutic Carriers. |
| US8100890B2 (en) * | 2008-10-15 | 2012-01-24 | Bioquiddity, Inc. | Special purpose fluid dispenser with pre-filled reservoir |
| US7896843B2 (en) * | 2008-10-15 | 2011-03-01 | Bioquiddity, Inc. | Special purpose fluid dispenser |
| US8603497B2 (en) | 2008-10-30 | 2013-12-10 | National University Corporation Okayama University | Composition for local anesthesia |
| KR101859486B1 (ko) | 2009-05-15 | 2018-06-28 | 레크로파마, 인코포레이티드 | 설하용 덱스메데토미딘 조성물과 그의 사용 방법 |
| US8410140B2 (en) | 2009-06-01 | 2013-04-02 | The Regents Of The University Of Michigan | Anesthetic methods and compositions |
| WO2011075621A1 (en) | 2009-12-17 | 2011-06-23 | Alpha Synergy Development, Inc. | Compositions and methods for ophthalmic delivery of nasal decongestants |
| FR2959414B1 (fr) | 2010-04-30 | 2016-01-08 | Luc Quintin | Combinaison de molecules aux fins de traitement d'hypotension survenant au cours du choc septique, cardiogenique, ou anaphylactique refractaire, ou hemorragique terminal, apres correction de la volemie et de l'etat de mal asthmatique refractaire |
| US20130096170A1 (en) | 2011-10-14 | 2013-04-18 | Hospira, Inc. | Methods of treating pediatric patients using dexmedetomidine |
| US8242158B1 (en) | 2012-01-04 | 2012-08-14 | Hospira, Inc. | Dexmedetomidine premix formulation |
-
2012
- 2012-01-04 US US13/343,693 patent/US20130096170A1/en not_active Abandoned
- 2012-05-14 US US13/471,403 patent/US8324260B1/en active Active
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- 2012-09-27 PT PT12840033T patent/PT2766014T/pt unknown
- 2012-09-27 WO PCT/US2012/057652 patent/WO2013055528A1/en not_active Ceased
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- 2012-09-27 KR KR1020197007143A patent/KR20190029775A/ko not_active Ceased
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- 2012-09-27 EP EP12840033.0A patent/EP2766014B1/en not_active Revoked
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- 2012-09-27 IN IN996KON2014 patent/IN2014KN00996A/en unknown
- 2012-09-27 PL PL12840033T patent/PL2766014T3/pl unknown
- 2012-09-27 KR KR1020207004550A patent/KR20200019791A/ko not_active Ceased
- 2012-09-27 CN CN201280058634.1A patent/CN103957906A/zh active Pending
- 2012-09-27 HR HRP20181378TT patent/HRP20181378T1/hr unknown
- 2012-09-27 LT LTEP12840033.0T patent/LT2766014T/lt unknown
- 2012-12-24 US US13/726,496 patent/US9314449B2/en active Active
- 2012-12-24 US US13/726,479 patent/US8507542B2/en active Active
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2013
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2014
- 2014-04-10 IL IL232070A patent/IL232070A0/en unknown
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2015
- 2015-11-16 US US14/942,880 patent/US20160067220A1/en not_active Abandoned
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2017
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2018
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2019
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2020
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2021
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2023
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