发明名称 Intraventricular drug delivery system for improving outcome after a brain injury affecting cerebral blood flow
摘要 Disclosed is a flowable sustained release microparticulate composition, a kit for treating at least one cerebral artery in a subarachnoid space at risk of interruption due to a brain injury, a method of preparing the composition, and a method for treating an interruption of a cerebral artery in a subarachnoid space at risk of interruption caused by brain injury in a mammal, which reduces signs or symptoms of at least one delayed complication associated with brain injury. The microparticulate composition comprises therapeutic agents, such as endothelin antagonists, transient receptor potential (TRP) protein antagonists, or dihydropyridine L-type voltage dependent calcium channel inhibitors selected from the group consisting of amlodipine, aranidipine, azelnidipine, bamidipine, benidipine, cinaldipine, efonidipine, felodipine, isradipine, lacidipine, lemildipine, lercanidipine, nicardipine, nifedipine, nilvadipine, nimodipine, nisoldipine, nitrendipine, manidipine, and pranidipine. The microparticulate composition further comprises slow release biodegradable polymers such as polylactide-polyglycolide, poly(orthoester), and poly(anhydride).
申请公布号 NZ616458(A) 申请公布日期 2016.01.29
申请号 NZ20120616458 申请日期 2012.04.05
申请人 EDGE THERAPEUTICS INC. 发明人 LEUTHNER BRIAN A.;MACDONALD R. LOCH
分类号 A61M5/00;A61K9/00;A61K9/10;A61K9/16;A61K31/4422;A61K31/4439;A61K31/4545;A61K31/496;A61K47/34 主分类号 A61M5/00
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