发明名称 Drug depots having different release profiles for reducing, preventing or treating pain and inflammation
摘要 Effective treatments of pain and/or inflammation are provided. Through the administration of an effective amount of at least analgesic and/or at least one anti-inflammatory agent at or near a target site, one can reduce, prevent or treat inflammation and pain.
申请公布号 US8968767(B2) 申请公布日期 2015.03.03
申请号 US201313891225 申请日期 2013.05.10
申请人 Warsaw Orthopedic, Inc. 发明人 McKay William F.
分类号 A61K9/00;A61F2/00;A61K9/70;A61K31/485;A61K31/135;A61K31/192;A61K31/366;A61K31/4168;A61K31/573;A61K31/58;A61K31/655 主分类号 A61K9/00
代理机构 Sorell Lenna & Schmidt LLP 代理人 Sorell Lenna & Schmidt LLP
主权项 1. A plurality of implantable drug depots useful for reducing, preventing or treating pain and/or inflammation in a patient in need of such treatment, the plurality of drug depots comprising a first set of one or more drug depots capable of releasing a therapeutically effective bolus dose of an analgesic and/or an anti-inflammatory agent or pharmaceutically acceptable salts thereof at a site beneath the skin and a second set of one or more drug depots capable of releasing a therapeutically effective amount of the analgesic and/or the anti-inflammatory agent or pharmaceutically acceptable salts thereof over a period of at least three days, the first set of one or more drug depots and the second set of one or more drug depots being solid and separate from each other and the second set of one or more drug depots comprises a polymer having an average molecular weight of between about 10,000 to 100,000, wherein the analgesic comprises alfentanil, butorphanol, codeine, fentanyl, hydromorphone, levorphanol, meperidine, morphine, sufentanil, tramadol or a combination thereof, and the anti-inflammatory agent comprises clonidine, fluocinolone, dexamethasone, sulindac, sulfasalazine or a combination thereof, and each depot of the first and second set comprises a pore forming agent, wherein the pore forming agent is polyethylene glycol or N-methyl-2-pyrrolidone, and each depot of the first and second set comprises an inherent viscosity from about 0.10 dL/g and 1.2 dL/g, and each depot of the first and second set comprises an adherent gel, wherein the gel stiffens after delivery to a target site having a pre-dosed modulus of elasticity of about 1×104 to about 3×105 dynes/cm2 and a post-dosed modulus of elasticity of about 1×105 to about 7×105 dynes/cm2.
地址 Warsaw IN US