Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT05680454Phase 1Completed
Phase 1, randomised, double-blind trial of KLWS-V502 in human papillomavirus infection (6 arms), sponsored by Beijing Health Guard Biotechnology Inc. Primary endpoint: Percentage of adverse reaction(s) within 7 days post any dose. Started Sep 2019; 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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