Abstract

CIPN is a common side-effect of anti-neoplastic drugs with no level 1 supportive treatment (Tx) approvals. Management of the adverse event (AE) is restricted to dose reductions and Tx interruptions. GTX is a PSP phycotoxin that reversibly binds voltage-gated sodium channel receptor sites on excitable cells, inhibiting membrane depolarization and nerve impulse conduction. Initial data indicates that GTX (topical formulation) improves PN-symptoms related to anti-HIV drugs. The aim of this study is to evaluate the effect of GTX on sensory symptoms of pts with grade 2 or higher (G≥2) CIPN.

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