Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06049095Phase 1Active, not recruiting
Phase 1, randomised, double-blind trial in pain comparing LTG-001 with Placebo (2 arms). Primary endpoints: Safety and tolerability of single and multiple ascending oral doses, relative bioavailability and food effect at 10 days, Absolute Bioavailability of LTG-001 Following Oral and Intravenous Administration at 35 days and 1 more. Started Oct 2023; status: active, not recruiting.
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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