JPWO2019136168A5 - - Google Patents

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JPWO2019136168A5
JPWO2019136168A5 JP2020537006A JP2020537006A JPWO2019136168A5 JP WO2019136168 A5 JPWO2019136168 A5 JP WO2019136168A5 JP 2020537006 A JP2020537006 A JP 2020537006A JP 2020537006 A JP2020537006 A JP 2020537006A JP WO2019136168 A5 JPWO2019136168 A5 JP WO2019136168A5
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JP
Japan
Prior art keywords
glucose
newborn
pharmaceutical composition
clc
oral pharmaceutical
Prior art date
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JP2020537006A
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Japanese (ja)
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JP7381469B2 (en
JP2021509671A (en
Publication date
Priority claimed from US15/860,966 external-priority patent/US10213491B2/en
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Priority claimed from PCT/US2019/012208 external-priority patent/WO2019136168A1/en
Publication of JP2021509671A publication Critical patent/JP2021509671A/en
Publication of JPWO2019136168A5 publication Critical patent/JPWO2019136168A5/ja
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Description

本特許のファイルは、カラーで実行される少なくとも1つの図面を含む。カラー図面を有する本特許のコピーは、要求および必要な手数料の納付により、特許商標庁によって提供される。
特定の実施形態では、例えば以下の項目が提供される。
(項目1)
a)
i)グルコースを含み痙攣を示す新生仔患者;および
ii)グルコースオキシダーゼを含む組成物
を用意するステップ;ならびに
b)前記痙攣が低減されるような条件下で、前記組成物を前記患者に投与するステップを含む、方法。
(項目2)
前記条件が、前記グルコースのグルコネートへの変換を含む、項目1に記載の方法。
(項目3)
前記組成物が、薬学的に許容される組成物である、項目1に記載の方法。
(項目4)
前記投与するステップが、有効量の前記組成物をさらに含む、項目1に記載の方法。
The file of this patent contains at least one drawing performed in color. A copy of this patent with color drawings is provided by the Patent and Trademark Office upon request and payment of the required fees.
In certain embodiments, for example, the following items are provided.
(Item 1)
a)
i) Neonatal patients with glucose and convulsions; and
ii) Composition containing glucose oxidase
Steps to prepare;
b) A method comprising administering the composition to the patient under conditions such that the spasm is reduced.
(Item 2)
The method of item 1, wherein the conditions include the conversion of glucose to gluconate.
(Item 3)
The method of item 1, wherein the composition is a pharmaceutically acceptable composition.
(Item 4)
The method of item 1, wherein the administration step further comprises an effective amount of the composition.

Claims (19)

新生児痙攣の処置を必要とする対象における、新生児痙攣を処置するための医薬品の製造のための、グルコースオキシダーゼを含む組成物の使用。 Use of a composition comprising glucose oxidase for the manufacture of a pharmaceutical product for treating neonatal seizures in a subject requiring treatment of neonatal seizures. 前記組成物が、新生児痙攣の処置を必要とする前記対象において、グルコースをグルコネートへと変換する、請求項1に記載の使用。 The use according to claim 1, wherein the composition converts glucose to gluconate in the subject in need of treatment of neonatal seizures. グルコースオキシダーゼおよび補足的グルコースを含む経口医薬組成物であって、非新生児と比較して上方調節されたCLC-3 Cl An oral pharmaceutical composition comprising glucose oxidase and supplemental glucose, CLC-3 Cl upregulated compared to non-neonatal babies. - チャネルを有する新生児における痙攣活性を低減させるように作用する、経口医薬組成物。An oral pharmaceutical composition that acts to reduce convulsive activity in neonates with channels. 前記新生児が、循環グルコースを有する、請求項3に記載の経口医薬組成物。 The oral pharmaceutical composition of claim 3, wherein the newborn has circulating glucose. 前記グルコースオキシダーゼが、前記循環グルコースをグルコネートへと変換する、請求項4に記載の経口医薬組成物。 The oral pharmaceutical composition according to claim 4, wherein the glucose oxidase converts the circulating glucose into gluconate. 前記グルコネートが、前記CLC-3 Cl The gluconate is the CLC-3 Cl - チャネルを阻害する、請求項5に記載の経口医薬組成物。The oral pharmaceutical composition of claim 5, which inhibits the channel. 前記CLC-3 Cl The CLC-3 Cl - チャネルの阻害が、前記新生児における前記痙攣活性を低減させる、請求項6に記載の経口医薬組成物。The oral pharmaceutical composition of claim 6, wherein inhibition of the channel reduces the convulsive activity in the newborn. 前記新生児が、新生仔てんかんと診断されている、請求項3に記載の経口医薬組成物。 The oral pharmaceutical composition according to claim 3, wherein the newborn is diagnosed with neonatal epilepsy. 前記新生児が、1月齢未満である、請求項3に記載の経口医薬組成物。 The oral pharmaceutical composition of claim 3, wherein the newborn is less than 1 month old. 薬学的に許容される担体をさらに含む、請求項3に記載の経口医薬組成物。 The oral pharmaceutical composition of claim 3, further comprising a pharmaceutically acceptable carrier. 新生児における痙攣活性の処置における医薬品として使用するための医薬製剤であって、固定用量のCLC-3 Cl A pharmaceutical formulation for use as a drug in the treatment of convulsive activity in newborns, a fixed dose of CLC-3 Cl - チャネル阻害剤、補足的グルコースおよび不活性担体を含む、医薬製剤。A pharmaceutical formulation comprising a channel inhibitor, supplemental glucose and an inert carrier. 前記CLC-3 Cl The CLC-3 Cl - チャネル阻害剤が、グルコースオキシダーゼである、請求項11に記載の医薬製剤。The pharmaceutical preparation according to claim 11, wherein the channel inhibitor is glucose oxidase. 前記不活性担体が、食塩水である、請求項11に記載の医薬製剤。 The pharmaceutical preparation according to claim 11, wherein the inert carrier is a saline solution. 前記新生児が循環グルコースを有し、前記グルコースオキシダーゼが、前記循環グルコースをグルコネートへと変換する、請求項12に記載の医薬製剤。 The pharmaceutical preparation according to claim 12, wherein the newborn baby has circulating glucose, and the glucose oxidase converts the circulating glucose into gluconate. 前記補足的グルコースおよび前記グルコースオキシダーゼが、7.3mg/kg/分のグルコース注入速度の前記固定用量で前記新生児に投与されるものである、請求項12に記載の医薬製剤。 12. The pharmaceutical formulation of claim 12, wherein the supplemental glucose and the glucose oxidase are administered to the newborn at the fixed dose of a glucose infusion rate of 7.3 mg / kg / min. 前記投与が、静脈内注射によるものである、請求項15に記載の医薬製剤。 The pharmaceutical preparation according to claim 15, wherein the administration is by intravenous injection. 前記新生児が、新生仔てんかんと診断されている、または前記新生児が、非新生児と比較して上方調節されたCLC-3 Cl The newborn has been diagnosed with neonatal epilepsy, or the newborn has been upregulated compared to a non-newborn CLC-3 Cl. - チャネルを有する、請求項11に記載の医薬製剤。The pharmaceutical preparation according to claim 11, which has a channel. 経皮パッチ剤によって前記新生児に投与されるものである、請求項11に記載の医薬製剤。 The pharmaceutical preparation according to claim 11, which is administered to the newborn baby by a transdermal patch. 新生児痙攣の処置を必要とする対象における、新生児痙攣の処置のための、グルコースオキシダーゼを含む組成物。 A composition comprising glucose oxidase for the treatment of neonatal seizures in a subject in need of treatment of neonatal seizures.
JP2020537006A 2018-01-03 2019-01-03 Glucose oxidase composition as a neonatal anticonvulsant Active JP7381469B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US15/860,966 2018-01-03
US15/860,966 US10213491B2 (en) 2015-05-19 2018-01-03 Glucose oxidase compositions as a neonate anticonvulsant
PCT/US2019/012208 WO2019136168A1 (en) 2018-01-03 2019-01-03 Glucose oxidase compositions as a neonate anticonvulsant

Publications (3)

Publication Number Publication Date
JP2021509671A JP2021509671A (en) 2021-04-01
JPWO2019136168A5 true JPWO2019136168A5 (en) 2022-01-14
JP7381469B2 JP7381469B2 (en) 2023-11-15

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US (1) US11666640B2 (en)
EP (1) EP3735262A4 (en)
JP (1) JP7381469B2 (en)
CN (1) CN112105378A (en)
WO (1) WO2019136168A1 (en)

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CN111440771A (en) * 2020-03-17 2020-07-24 中山大学附属第三医院 C L CN2 homozygous mutation-containing white matter encephalopathy patient specific induced pluripotent stem cell line

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5364634A (en) 1991-11-08 1994-11-15 Southwest Research Institute Controlled-release PH sensitive capsule and adhesive system and method
DE69422163T2 (en) 1993-02-19 2000-06-15 Nippon Shinyaku Co., Ltd. GLYCEROL DERIVATIVE, DEVICE AND PHARMACEUTICAL COMPOSITION
AU7166200A (en) * 1995-12-27 2001-03-08 Genencor International, Inc. Process for the preparation of gluconic acid and gluconic acid produced thereby
US5994316A (en) 1996-02-21 1999-11-30 The Immune Response Corporation Method of preparing polynucleotide-carrier complexes for delivery to cells
WO1997044015A1 (en) 1996-05-17 1997-11-27 Andaris Limited Microparticles and their use in wound therapy
US20100029613A1 (en) 2004-11-15 2010-02-04 University Of Rochester Treatment and prevention of epilepsy
GB0619786D0 (en) * 2006-10-06 2006-11-15 Inst Of Technology Sligo An antimicrobial and immunostimulatory system
AU2007347990B2 (en) * 2007-02-28 2011-04-28 Morinaga Milk Industry Co., Ltd. Oral disinfectant and food additive comprising the disinfectant
PL2276505T3 (en) 2008-03-20 2014-01-31 Karobio Ab Nasal spray or nasal drops for treatment of common cold
WO2012050895A1 (en) 2010-09-28 2012-04-19 Lisa Geng Methods for treating neurological disorders using nutrient compositions
WO2014165566A1 (en) * 2013-04-03 2014-10-09 Emory University Hydrophilic particle compositions, processes of production, and uses in dietary management and digestive disorders
RU2015151135A (en) * 2013-04-30 2017-06-02 Массачусетс Инститьют Оф Текнолоджи INJECTION GEL NANO-FRAMES FOR TREATING DIABETES
US20170065728A1 (en) 2014-03-03 2017-03-09 The Penn State Research Foundation Self-powered enzyme micropumps
CN104450806B (en) * 2014-11-27 2018-01-16 江南大学 A kind of method that enzyme process prepares sodium gluconate
US9861597B2 (en) 2015-05-19 2018-01-09 Penn State Research Foundation Gluconate-based compositions as a neonate anticonvulsant
US10213491B2 (en) * 2015-05-19 2019-02-26 The Penn State Research Foundation Glucose oxidase compositions as a neonate anticonvulsant
CN106978451B (en) * 2017-03-29 2020-04-28 华南理工大学 Method for preparing sodium gluconate by immobilized glucose oxidase
CN106929500A (en) * 2017-04-27 2017-07-07 南京工业大学 Preparation method and application of glucose oxidase/catalase cross-linked enzyme polymer

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