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Parion’s dry mouth treatment well tolerated in Phase I study

Parion Sciences has presented preliminary results from a Phase I clinical safety study of a novel sodium channel blocker, P-552-02, as a topical therapy for dry mouth associated with primary Sjogren's syndrome.

The preliminary results of the 28-day, 30-patient, randomized, double-blind, placebo-controlled, crossover study showed that P-552-02 was safe and well tolerated, both locally in the oral cavity and systemically. No side effects or other safety issues were reported in the study.

Ross Johnson, Parion’s CEO, said: “Based on these results, we plan to proceed with a Phase I/IIA study designed to test the efficacy of higher concentrations of P-552-02 delivered in a spray formulation and dosing at different intervals, and to pursue other potential indications.”