Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT06538181Phase 1Recruiting
Phase 1, open-label trial of pacritinib in VEXAS syndrome (VEXAS) (2 arms), sponsored by Washington University School of Medicine. Primary endpoints: Dose-limiting toxicities at 28 days and Recommended phase II dose at 28 days. Started Feb 2025; 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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