Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06602193Phase 2Active, not recruiting
Phase 2, randomised, double-blind trial in Parkinson's disease (PD) comparing BIIB122 225 mg with BIIB122 Matching Placebo (2 arms). Primary endpoint: Incidence of treatment-emergent adverse events (TEAEs) and serious adverse events (SAEs) at 12 weeks. Started Oct 2024; 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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