Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07141199Phase 1Completed
Phase 1, randomised, double-blind trial of ABBV-8736 (4 arms), sponsored by AbbVie Inc. Primary endpoints: Number of Participants with Adverse Events at 113 days, Maximum Observed Concentration of ABBV-8736 at 113 days and 7 more. Started Sep 2025; 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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