Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02609126Phase 1Completed
Phase 1, randomised, double-blind trial in osteoarthritis (OA) comparing EP-104IAR with Vehicle (2 arms). Primary endpoints: Peak Plasma Concentration of fluticasone propionate up to 42 weeks, Fluticasone propionate concentrations in synovial fluid up to 30 weeks and 3 more. Started Apr 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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