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公开(公告)号:WO2022204562A1
公开(公告)日:2022-09-29
申请号:PCT/US2022/022027
申请日:2022-03-25
申请人: BRAIN LUXURY INC.
IPC分类号: A23L2/52 , A23L2/44 , A23L2/06 , A23L33/12 , A23L33/155 , A23L33/175 , C11B5/00 , A61K45/06 , A61P25/26 , A61P39/06
摘要: The disclosure is in part directed to shelf-stable, emulsion-forming liquid compositions, liquid beverage compositions, and fatty acid vesicle-forming liquid compositions for increased neurosystem uptake of amino acids present in the compositions when consumed by a subject.
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公开(公告)号:WO2022191092A1
公开(公告)日:2022-09-15
申请号:PCT/JP2022/009571
申请日:2022-03-04
申请人: 国立大学法人東北大学
IPC分类号: C07D215/42 , A61K31/4706 , A61K31/473 , A61K31/565 , A61K31/57 , A61P25/00 , A61P25/20 , A61P25/26 , A61P25/28 , A61P43/00 , C07D219/10 , C07J43/00
摘要: 本発明は、脳内ヒスタミン濃度を上昇させる新たな方法を提供することを課題とする。本発明は、下記一般式(I)で表される化合物又はその塩を提供する: [式中、各基の構造は明細書に記載の通り]
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公开(公告)号:WO2022181625A1
公开(公告)日:2022-09-01
申请号:PCT/JP2022/007314
申请日:2022-02-22
发明人: MATEEN, Syed Asfar , MIDIDODDI, Praveen Kumar , MEHROTRA, Shailly , SHOAF, Susan Elizabeth , GUPTA, Salin , SUZUKI, Kai , HASEGAWA, Masahiro
IPC分类号: A61K9/50 , A61K31/403 , A61P25/26
摘要: Pharmaceutical formulation comprising centanafadine (CTN) or a pharmaceutically acceptable salt thereof and an excipient, and related methods of manufacture and use, are disclosed.
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公开(公告)号:WO2021106975A1
公开(公告)日:2021-06-03
申请号:PCT/JP2020/043924
申请日:2020-11-26
申请人: 武田薬品工業株式会社
发明人: 伊藤 吉輝 , 宮野鼻 悠平 , 梶田 雄一 , 帆足 保孝 , 服部 靖志 , 小池 竜樹 , ▲徳▼永 礼仁 , 木村 英司 , パブリチェック アレキサンダー マーティン , ピラ マリレナ , ミゲレス-ラモス ハビエル
IPC分类号: A61P3/04 , A61P5/50 , A61P9/04 , A61P19/08 , A61P23/00 , A61P25/16 , A61P25/20 , A61P25/26 , A61P25/28 , A61P43/00 , C07D455/02 , C07D471/04 , A61K31/4375 , A61K31/444
摘要: 本発明は、オレキシン2型受容体作動活性を有する複素環化合物を提供する。 式(I): [式中、各記号は明細書記載のとおりである。] で表される化合物またはその塩は、オレキシン2型受容体作動活性を有し、ナルコレプシーの予防または治療剤として有用である。
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公开(公告)号:WO2020214841A1
公开(公告)日:2020-10-22
申请号:PCT/US2020/028566
申请日:2020-04-16
IPC分类号: C07C211/62 , C07C211/06 , C07C209/68 , C07C51/41 , C07C55/10 , C07C59/265 , C07C53/10 , C07C57/145 , C07C57/15 , C07C59/245 , A61K31/131 , A61K31/205 , A61P25/00 , A61P25/26 , A61P25/28 , A61P3/00
摘要: Salts of hexylamine, for example, hexylamine succinate and tri-hexylamine citrate and their method of production are described. The disclosure also relates to compositions comprises hexyalmine and the use of hexylamine for for reducing appetite in a human subject, treating obesity in a human subject, preventing obesity in a human subject, preventing weight gain in a human subject, increasing fat loss in a human subject, treating an overweight human subject, increasing athletic performance in a human subject, increasing endurance in a human subject, increasing muscle strength in a human subject, improving cognitive function in a human subject, treating ADHD in a human subject, increasing sweating in a human subject, reducing reaction time of a human subject, increasing psychomotor vigilance of a human subject, enhancing memory in a human subject, increasing central nervous system activity in a human subject, and enhancing alertness, attention, concentration, and/or memory in a human subject.
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公开(公告)号:WO2020075110A1
公开(公告)日:2020-04-16
申请号:PCT/IB2019/058651
申请日:2019-10-10
申请人: NOVARTIS AG
发明人: JOHNS, Donald , SOVAGO, Judit
IPC分类号: A61K31/165 , A61K31/496 , A61K45/06 , A61P25/16 , A61P25/26
摘要: The invention relates to the use of Compound (I), as defined herein, or pharmaceutically acceptable salt thereof, in the treatment of excessive daytime sleepiness associated with Parkinson's disease.
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公开(公告)号:WO2019173384A1
公开(公告)日:2019-09-12
申请号:PCT/US2019/020815
申请日:2019-03-05
申请人: KASHIV PHARMA LLC
摘要: The present disclosure provides programmable osmotic-controlled oral compositions providing delayed release of a therapeutically acceptable amount of a drug, hi certain embodiments, the programmable osmotic-controlled compositions of the disclosure provide a lag time that is independent of the presence or absence of food, type of food, pH, gastric emptying, and volume of gastric fluid. The programmable osmotic-controlled oral compositions of the disclosure comprise a multilayer core comprising a drug for controlled release, wherein the core is coated with a semipermeable membrane comprising an orifice and, optionally, an immediate release coating, comprising a drug for immediate release, over the semipermeable membrane. The multilayered core comprises a pull layer containing the drug and a push layer. The pull layer comprises at least two layers: a placebo layer for providing a desired lag time for the drug release; and an active layer containing the drug and providing a delayed controlled release of the drug. The compositions of the disclosure can be programmed to provide a desired and precise lag time, and release drug, after the lag time, at a rhythm, e.g., that matches the human circadian rhythm of a condition's symptoms and/or of the individual being treated in the application of the therapy to optimize therapeutic outcome and minimize side effects.
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公开(公告)号:WO2019167695A1
公开(公告)日:2019-09-06
申请号:PCT/JP2019/005829
申请日:2019-02-18
申请人: 久光製薬株式会社
IPC分类号: A61K47/02 , A61K9/70 , A61K31/4458 , A61K47/32 , A61P25/26
摘要: 本発明の課題は、物性や濃度に拘らず、包材中あるいは貼付中のコールドフローを抑制し、保管中の貼付剤における薬物の安定維持と長期間に亘る適切な投与形態の維持によって、持続的に十分な薬効を得られる、取り扱いに優れたアクリル系粘着基剤を含む貼付剤を提供することにある。本発明は、支持体層および粘着剤層を備える貼付剤であって、粘着剤層が、薬物、アクリル系粘着基剤およびケイ酸カルシウムを含有する、前記貼付剤、ならびに、その製造方法に関する。
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公开(公告)号:WO2018219650A1
公开(公告)日:2018-12-06
申请号:PCT/EP2018/062749
申请日:2018-05-16
申请人: ENORAMA PHARMA AB
发明人: RUDRARAJU, Varma , RAJESH, Yelchuri
IPC分类号: A61K9/68 , A61K31/465 , A61P25/26
摘要: The present invention relates to nicotine-containing chewing gum compositions and the method of preparing the same. The present invention provides improved and stable nicotine-containing chewing gum compositions for use in nicotine replacement therapy, which provide rapid nicotine release in the oral cavity and effectively satisfy the craving that most smokers experience.
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公开(公告)号:WO2018164192A1
公开(公告)日:2018-09-13
申请号:PCT/JP2018/008813
申请日:2018-03-07
申请人: 武田薬品工業株式会社
IPC分类号: C07D207/09 , A61K31/40 , A61K31/4025 , A61K31/4035 , A61K31/4155 , A61K31/438 , A61K31/4439 , A61K31/454 , A61K31/5377 , A61P3/04 , A61P3/10 , A61P9/04 , A61P11/00 , A61P19/10 , A61P25/00 , A61P25/16 , A61P25/26 , A61P25/28 , A61P31/04 , A61P43/00 , C07D207/12 , C07D207/14 , C07D207/16 , C07D401/06 , C07D401/12 , C07D403/12 , C07D405/12 , C07D409/12 , C07D491/107
摘要: 本発明は、オレキシン2型受容体作動活性を有する置換ピロリジン化合物を提供する。 式(I): [式中、各記号は明細書記載のとおり] で表される化合物またはその塩は、オレキシン2型受容体作動活性を有し、ナルコレプシーの予防または治療剤として有用である。
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