Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03291002Phase 1Unknown
Phase 1, open-label trial of CV8102 in melanoma, cutaneous squamous cell carcinoma (cSCC), head and neck squamous cell carcinoma (HNSCC) and 1 more (4 cohorts), sponsored by CureVac. Primary endpoints: Dose determination for dose escalation cohorts at 2 weeks and Incidence of treatment related (Serious) Adverse Events up to 12 months. Status: unknown.
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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