Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03655756Phase 1Completed
Phase 1, open-label, single-arm trial of IFx-Hu2.0 in cutaneous melanoma (CM), sponsored by TuHURA Biosciences, Inc. Primary endpoint: Number of Participants With Serious Adverse Events (SAEs) and/or Dose Limiting Toxicities (DLTs) at 28 days. Started Nov 2018; status: completed.
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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