Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
2007-003852-13Phase 2Completed
Phase 2, randomised, double-blind trial of V505 in human papillomavirus infection, Cervical Cancer (CC), Vulval carcinoma and 4 more, sponsored by Merck & Co. Primary endpoints: Safety and tolerability: severe injection-site reactions, Safety and tolerability: vaccine-related serious adverse experiences and 1 more. Started Sep 2007; 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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