Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04633213Phase 3Completed
Phase 3, randomised, double-blind trial in dry eye syndrome (DED) comparing HBM9036 0.25% Ophthalmic Solution with Placebo Ophthalmic Solution (2 arms). Primary endpoint: Change from baseline in total corneal staining scores (upper, central and lower cornea) of the study eye at 8 weeks. Started Feb 2021; 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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