发明名称 Formulations of viloxazine
摘要 Modified release formulations of viloxazine and methods of administering the same are disclosed. High-drug load formulations of viloxazine are further disclosed.
申请公布号 US9603853(B2) 申请公布日期 2017.03.28
申请号 US201615157549 申请日期 2016.05.18
申请人 Supernus Pharmaceuticals, Inc. 发明人 Vieira Michael L.;Huang Austin B.;Bhatt Padmanabh P.
分类号 A61K31/5375;A61K9/50;A61K9/14;A61K9/20;A61K9/48;A61K9/00 主分类号 A61K31/5375
代理机构 Foley & Lardner LLP 代理人 Foley & Lardner LLP ;Talapatra Sunit
主权项 1. A method of treating ADHD or major depressive disorder in a mammalian subject in need thereof, the method comprising administration to the subject of a formulation comprising: (a) an immediate release (IR) component comprising an inert core and a layer comprising viloxazine and, optionally, a pharmaceutically acceptable excipient, surrounding the core, and (b) an extended release (XR) component comprising: (i) an inert core, (ii) a first layer comprising viloxazine and, optionally, a pharmaceutically acceptable excipient, surrounding the core, and (iii) a second layer comprising a release rate controlling compound and a pore former in a weight ratio of 19:1 to 8.5:1.5, respectively, surrounding the first layer, wherein the pore former is selected from the group consisting of povidone, hypromellose, hydroxyethyl cellulose, hydroxypropyl cellulose, and organic acids, wherein the release rate controlling compound is selected from the group consisting of ethylcellulose; cellulose acetate; cellulose acetate butyrate; waxes; hydrogenated vegetable oils; glyceryl behenate; glyceryl palmitostearate; PEG glyceryl esters; poly(ethyl acrylate-co-methyl methacrylate) ethyl acrylate methyl methacrylate copolymer; poly (ethyl acrylate-co-methyl methacrylate-cotrimethylammonioethyl methacrylate chloride); polyvinyl acetate; cellulose acetate propionate, and combinations thereof, and is present in an amount of from 5% (w/w) to 65% (w/w) of the XR component, wherein the formulation comprises, as a percentage of the total formulation, 25% (w/w) to 75% (w/w) viloxazine, wherein the viloxazine is released immediately and continuously upon administration, and wherein at least 80% of the viloxazine or salt thereof in the formulation is released from the formulation over a period of time of at least 2 hours in vitro.
地址 Rockville MD US