Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04354246Phase 1Completed
Phase 1, open-label trial of COM902 in cancer, ovarian cancer, lung cancer and 5 more (6 arms), sponsored by Compugen Ltd. Primary endpoints: Safety and tolerability of COM902 monotherapy and in combination with COM701 at 21 days, Maximum tolerated dose (MTD) and/or recommended dose for expansion at 18 months and 3 more. Started Mar 2020; 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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