Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT03976713Phase 3Unknown
Phase 3, randomised, double-blind trial in chronic obstructive pulmonary disease (COPD) comparing Bufei Yishen granule + Western medicine with Placebo + Western medicine (2 arms). Primary endpoints: Frequency of acute exacerbation at 52 weeks and Duration of acute exacerbation at 52 weeks. Status: unknown.
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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