Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
ISRCTN15169433Phase 2Active, not recruiting
Phase 2, randomised, double-blind trial in achondroplasia (ACH) comparing TransCon CNP with Placebo then open-label TransCon CNP (2 arms). Primary endpoints: Incidence of treatment-emergent adverse events over 52 weeks and Change from baseline to 52 weeks in length/height Z-score. Started Jan 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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