DSP-2230
Investigational analgesic drug / From Wikipedia, the free encyclopedia
DSP-2230 is a selective small-molecule Nav1.7 and Nav1.8 voltage-gated sodium channel blocker which is under development by Dainippon Sumitomo Pharma for the treatment of neuropathic pain.[1][2] As of June 2014, it is in phase I/phase II clinical trials.[1][2]
Quick Facts Clinical data, Routes ofadministration ...
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Routes of administration | By mouth |
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Formula | C20H20F3N5O2 |
Molar mass | 419.408 g·mol−1 |
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