Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06089837Phase 1Completed
Phase 1, randomised, double-blind trial in pain and neuropathic pain comparing EC5026 with Placebo (2 arms). Primary endpoints: Incidence of Adverse Events (AEs) and Serious Adverse Events (SAE) at 30 days, Dose-related effects on electrocardiographic QTc interval at 7 days and 11 more. Started Nov 2023; status: completed.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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