A FORMULATION FOR IMPROVING SEIZURE CONTROL
    2.
    发明申请

    公开(公告)号:WO2020176276A1

    公开(公告)日:2020-09-03

    申请号:PCT/US2020/018359

    申请日:2020-02-14

    Abstract: Described herein is a method of improving seizure control in a patient experiencing uncontrolled seizures persisting 10 minutes or more, comprising administering fenfluramine or a pharmaceutically acceptable salt, base, acid or amine thereof, at a dose of from 0.2 to 1.2 m/kg/day for a period of about 12 hours to about 7 days to a patient having been put into a therapeutic, medically-induced coma via a general anesthetic; and after about 12 hours to about 7 days, weaning the patient from the general anesthetic and assessing whether the seizure control has improved as compared to a pre-treatment time point. The patient experiencing seizures may have epilepsy or epileptic encephalopathy that has led to established status epilepticus (SE), refractory status epilepticus (RSE) or super-refractory status epilepticus (SRSE).

    HYDROXYCITRIC ACID COMPOUNDS AND CAPSULE LIQUID DELIVERY
    4.
    发明申请
    HYDROXYCITRIC ACID COMPOUNDS AND CAPSULE LIQUID DELIVERY 审中-公开
    羟基酸化合物和胶囊液体递送

    公开(公告)号:WO2018080795A1

    公开(公告)日:2018-05-03

    申请号:PCT/US2017/056111

    申请日:2017-10-11

    Abstract: A capsule oral delivery system is disclosed. The system includes an outer capsule completely enclosing an inner content, or a hard shell comprised of hydroxypropyl methylcellulose (HPMC) enclosing the content. A liquid formulation forming the inner content of the outer capsule is comprised of a hydroxycitric acid (HCA) salt, water, and glycerol, with the HCA being completely dissolved in the water and glycerol which may be the only components present in the capsule, which may be administered to a patient in a method of treatment to cause weight loss when repeatedly administered.

    Abstract translation: 公开了一种胶囊口服递送系统。 该系统包括完全封闭内容物的外胶囊或包封内容物的由羟丙基甲基纤维素(HPMC)组成的硬壳。 形成外胶囊内含量的液体制剂由羟基柠檬酸(HCA)盐,水和甘油组成,其中HCA完全溶于水和甘油中,甘油可以是胶囊中存在的唯一组分,其中 可以在治疗方法中给患者施用以在重复施用时引起体重减轻。

    INHALED SURFACTANT-MODIFIED LIPOSOMAL FORMULATIONS PROVIDING BOTH AN IMMEDIATE AND SUSTAINED RELEASE PROFILE
    6.
    发明申请
    INHALED SURFACTANT-MODIFIED LIPOSOMAL FORMULATIONS PROVIDING BOTH AN IMMEDIATE AND SUSTAINED RELEASE PROFILE 审中-公开
    补充的表面活性剂修饰的脂质体制剂提供立即和持续的释放特征

    公开(公告)号:WO2015061025A1

    公开(公告)日:2015-04-30

    申请号:PCT/US2014/059092

    申请日:2014-10-03

    CPC classification number: A61K9/127 A61K9/0078 A61K31/496 A61K47/10 A61K47/26

    Abstract: Methods for formulating and compositions of immediate and sustained release liposomal products which comprise a surfactant that interacts with liposomes to effect drug release therefrom, and delivery of such for treatment of respiratory tract infections and other medical conditions, and devices and formulations used in connection with such are described.

    Abstract translation: 用于配制和立即和持续释放的脂质体产品的组合物的方法,其包含与脂质体相互作用以实现药物释放的表面活性剂,以及用于治疗呼吸道感染和其它医学病症的递送剂,以及与其结合使用的装置和制剂 被描述。

    CONTROLLED RELEASE VAGINAL GEL WITH ANTIVIRAL PARTICLES
    7.
    发明申请
    CONTROLLED RELEASE VAGINAL GEL WITH ANTIVIRAL PARTICLES 审中-公开
    控制释放阴道凝胶与抗菌颗粒

    公开(公告)号:WO2014159169A1

    公开(公告)日:2014-10-02

    申请号:PCT/US2014/022338

    申请日:2014-03-10

    CPC classification number: A61K9/146 A61K9/06 A61K9/4808 A61K9/5084 A61K31/675

    Abstract: Formulations are disclosed which are comprised of tenofovir particles, and a biocompatible gel having the particles dispersed therein. The gel may be comprised of a flavoring agent and one or more compounds which generate heat. The particles may be provided in a plurality of groups (2, 3 or more) of different size spheres. The spheres may be comprised of tenofovir alone or in combination with emtricitabine and a controlled release polymer such as poly lactic glycolic acid (PLGA) or other suitable, biocompatible material.

    Abstract translation: 公开了由替诺福韦颗粒和分散有颗粒的生物相容性凝胶组成的制剂。 凝胶可以由调味剂和一种或多种产生热的化合物组成。 颗粒可以以不同大小的球体的多个组(2,3个或更多个)提供。 球体可以单独使用替诺福韦或与恩曲他滨组合和控释聚合物如聚乳酸乙醇酸(PLGA)或其它合适的生物相容性材料组合。

    TREATING PAIN IN PATIENTS WITH HEPATIC IMPAIRMENT
    8.
    发明申请
    TREATING PAIN IN PATIENTS WITH HEPATIC IMPAIRMENT 审中-公开
    治疗患有疼痛的患者的疼痛

    公开(公告)号:WO2014022570A1

    公开(公告)日:2014-02-06

    申请号:PCT/US2013/053043

    申请日:2013-07-31

    Applicant: ZOGENIX, INC.

    Abstract: An extended release composition for an analgesic active pharmaceutical ingredient which may be an opioid, preferably hydrocodone as the only active ingredient. The extended release composition comprises a multiparticulate modified release composition which may be in the form of beads contained in an oral dosage form such as gelatin capsules as the primary package. The oral dosage units are supplied as part of a kit, which also includes a package insert all sold as a commercially marketed product. The primary package and package insert are contained in an optional secondary package and the package insert does not contain a warning, a dosing instruction, or a dosing table specifically directed to patients suffering from mild, moderate or severe hepatic impairment.

    Abstract translation: 用于止痛活性药物成分的延长释放组合物,其可以是阿片样物质,优选为氢可酮作为唯一活性成分。 延长释放组合物包含多颗粒改性释放组合物,其可以是口服剂型中包含的珠粒形式,例如明胶胶囊作为主要包装。 口服剂量单位作为试剂盒的一部分提供,其还包括作为市售产品销售的包装。 主包装和包装插入物包含在可选的二次包装中,包装插页不包含警告,剂量说明或专门针对患有轻度,中度或重度肝损伤的患者的剂量表。

    CAGED QUANTUM DOTS
    9.
    发明申请
    CAGED QUANTUM DOTS 审中-公开

    公开(公告)号:WO2010005550A1

    公开(公告)日:2010-01-14

    申请号:PCT/US2009/003965

    申请日:2009-07-06

    Inventor: COHEN, Bruce

    Abstract: Semiconductor nanocrystals known as quantum dots (QD) are caged by being associated with a molecule such as an orth-Nitrobenzyl (ONB) group. The luminescence of the QD is suppressed until activated by violet or ultra violet light.

    Abstract translation: 称为量子点(QD)的半导体纳米晶体通过与诸如邻硝基苄基(ONB)基团的分子相关而笼罩。 QD的发光被抑制直到由紫罗兰或紫外线激发。

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