Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03333694Phase 1Terminated
Phase 1, randomised, double-blind trial in cutaneous squamous cell carcinoma in situ (SCCIS) comparing CLL442 with Placebo (2 arms). Primary endpoints: Incidence of adverse events (AE), serious adverse events (SAEs) of CLL442 on lesion free skin at Day 7, Change in the size of One SCCis lesion area at Day 84 and 2 more. Started Dec 2017; status: terminated.
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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