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PF-06305591 is a potent and highly selective small molecule blocker of the voltage-gated sodium channel NaV1.8 (encoded by SCN10A), with an IC50 of approximately 15 nM[2][3][8]. It was developed by Pfizer for the potential treatment of pain conditions, particularly those involving inflammatory and neuropathic pain[5][8]. The compound demonstrates high selectivity for NaV1.8 over other sodium channel subtypes and has shown favorable preclinical ADME properties as well as safety in early clinical studies[3][5][8]. Clinical trials have included Phase 1 studies assessing safety and tolerability in healthy volunteers[4].
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