Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06204614Phase 1Enrolling by invitation
Phase 1, open-label, single-arm trial, sponsored by Brigham and Women's Hospital. Primary endpoints: Safety of microdevice placement and removal based on assessment of adverse events at 6 weeks and Feasibility of microdevice placement at 48 hours. Started Jun 2024; status: enrolling by invitation.
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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