Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06690996Phase 1Completed
Phase 1, randomised, double-blind trial of LY4005130 (12 arms), sponsored by Eli Lilly and Company. Primary endpoint: Number of Participants with One or More Treatment Emergent Adverse Events (TEAEs) and Serious Adverse Event(s) (SAEs) Considered by the Investigator to be Related to Study Drug Administration up to 26 Weeks. Started Nov 2024; 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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