发明名称 Pharmaceutical composition for treating cancer comprising trypsinogen and/or chymotrypsinogen and an active agent selected from a selenium compound, a vanilloid compound and a cytoplasmic glycolysis reduction agent
摘要 The present invention generally relates to pharmaceutical compositions containing a protease proenzyme and use thereof for treating cancer. The pharmaceutical compositions are directed to compositions comprising a protease proenzyme and an active agent, the composition being capable of providing a multi-functional approach for treating cancer. The pharmaceutical compositions are also directed to compositions comprising a first and a second protease proenzyme capable of activation at or near a surface of a tumor cell to enhance cell-to-cell adhesion of tumor cells, effect proteolysis of tumor cells, or induce tumor cell apoptosis, differentiation or immunorecognition, wherein the first protease proenzyme is chymotrypsinogen and the second protease proenzyme is trypsinogen. The pharmaceutical compositions are also directed to compositions comprising a first and second active agent each capable of inducing intracellular activity in tumor cells.
申请公布号 US9636359(B2) 申请公布日期 2017.05.02
申请号 US201013502917 申请日期 2010.10.22
申请人 The University of Sydney 发明人 Kenyon Julian Norman;Clayton Paul Rodney;Tosh David;Felquer Fernando;Brandt Ralf
分类号 A61K33/04;A61K31/095;A61K31/21;A61K38/48;A61K45/06;A61K38/47 主分类号 A61K33/04
代理机构 Bozicevic, Field & Francis LLP 代理人 Francis Carol L.;Chin Khin K.;Bozicevic, Field & Francis LLP
主权项 1. A method of treating a solid tumor comprising administering to a subject a pharmaceutical composition comprising a therapeutically effective amount of trypsinogen and chymotrypsinogen, wherein the composition does not contain amylase, and wherein the weight ratio of chymotrypsinogen:trypsinogen is in the range of between 4:1 to 8:1.
地址 New South Wales AU