发明名称 ANTAGONISTS OF A NON-SELECTIVE CATION CHANNEL IN NEURAL CELLS
摘要 The present invention is directed to a combination of therapeutic compounds and treatment methods and kits using the combination. In particular, one of the combination affects the NCca-ATP channel of neural tissue, including neurons, glia and blood vessels within the nervous system. Exemplary SUR1 and/or TRPM4 antagonists that inhibit the NCca-ATP channel may be employed in the combination. The combination therapy also employs one or more of a non-selective cation channel blocker and/or an antagonist of VEFG, NOS, MMP, or thrombin. Exemplary indications for the combination therapy includes the prevention, diminution, and/or treatment of injured or diseased neural tissue, including astrocytes, neurons and capillary endothelial cells, that is due to ischemia, tissue trauma, brain swelling and increased tissue pressure, or other forms of brain or spinal cord disease or injury, for example. In other embodiments, there are methods and compositions directed to antagonists of TRPM4, including at least for therapeutic treatment of traumatic brain injury, cerebral ischemia, central nervous system (CNS) damage, peripheral nervous system (PNS) damage, cerebral hypoxia, or edema, for example.
申请公布号 EP2114160(B1) 申请公布日期 2016.11.16
申请号 EP20080729376 申请日期 2008.02.08
申请人 UNIVERSITY OF MARYLAND, BALTIMORE;THE UNITED STATES OF AMERICA, AS REPRESENTED BY THE DEPARTMENT OF VETERANS AFFAIRS 发明人 SIMARD, J., MARC;GERZANICH, VLADIMIR
分类号 A61K31/56;A01N45/00;A61K45/06;A61P25/00 主分类号 A61K31/56
代理机构 代理人
主权项
地址