发明名称 Corticosteroids for the Treatment of Joint Pain
摘要 Corticosteroid microparticle formulations are provided for use for treating pain, including pain caused by inflammatory diseases such as osteoarthritis or rheumatoid arthritis, and for slowing, arresting or reversing structural damage to tissues caused by an inflammatory disease, for example damage to articular and/or peri-articular tissues caused by osteoarthritis or rheumatoid arthritis. Corticosteroid microparticle formulations are administered locally as a sustained release dosage form (with or without an immediate release component) that results in efficacy accompanied by clinically insignificant or no measurable effect on endogenous cortisol production.
申请公布号 US2014356437(A1) 申请公布日期 2014.12.04
申请号 US201414461884 申请日期 2014.08.18
申请人 Flexion Therapeutics, Inc. 发明人 Bodick Neil;Blanks Robert C.;Kumar Anjali;Clayman Michael D.;Moran Mark
分类号 A61K31/58;A61K31/573;A61K9/14 主分类号 A61K31/58
代理机构 代理人
主权项 1. A method of treating pain or inflammation in a patient comprising administering to said patient a therapeutically effective amount of a formulation comprising controlled- or sustained-release microparticles comprising triamcinolone acetonide (TCA) or a pharmaceutically-acceptable salt thereof and a poly(lactic-co-glycolic) acid copolymer (PLGA) matrix, wherein the TCA comprises between 22% to 28% of the microparticles and wherein the PLGA has the following characteristics: (i) a molecular weight in the range of about 40 to 70 kDa; and (ii) a lactic acid:glycolic acid molar ratio of 80:20 to 60:40.
地址 Burlington MA US