Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02538185Phase 1Completed
Phase 1, randomised, double-blind trial (3 arms), sponsored by Lausanne University Hospital. Primary endpoints: Number of Adverse Events as a Measure of Safety and Tolerability at Day 56, Pain Scores at needle insertion and at product injection at Day 28 and 3 more. Started Aug 2013; 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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