Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2024-519779-24-00Phase 2Authorised
Phase 2, open-label, single-arm trial of mivavotinib in VEXAS syndrome (VEXAS) and myelodysplastic syndrome (MDS), sponsored by Groupe Français des Myélodysplasies. Primary endpoints: Dose-limiting toxicities and maximal tolerated dose and Overall clinical response rate. Planned start Nov 2025; status: authorised.
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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