Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02982889Phase 1Completed
Phase 1, randomised, double-blind trial of LIQ865 in postoperative pain (4 arms), sponsored by Liquidia Corporation. Primary endpoint: Incidence of Treatment Emergent Adverse Events at 30 days. Started Dec 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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