Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02641340Phase 1Completed
Phase 1, randomised, open-label trial of fentanyl (transdermal patch + oral transmucosal lozenge) in pain (12 cohorts), sponsored by Insys Therapeutics. Primary endpoints: Maximum concentration at 24 hours, Time to reach peak or maximum concentration at 24 hours and 7 more. Started Jan 2016; 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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