Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT07604272Phase 1Recruiting
Phase 1, randomised, open-label trial in inguinal hernia comparing Fulvestrant 250 mg with Anastrozole 1 mg (2 arms). Primary endpoint: Composite Safety Event Rate at 6 months. Started Oct 2026; status: 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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