Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02470871Phase 1Completed
Phase 1, randomised, open-label trial of CSL689 in congenital factor VII deficiency (2 arms), sponsored by CSL Limited. Primary endpoints: Terminal half-life of plasma FVIIa activity up to 48 hours, Maximum observed plasma FVIIa activity up to 48 hours and 1 more. Started Jul 2015; 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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