Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT02989194Phase 2Completed
Phase 2, randomised, double-blind trial of VIS410 in Influenza A infection (3 arms), sponsored by Visterra. Primary endpoints: Assess the Safety and Tolerability of a Single IV Dose of VIS410 in Participants With Uncomplicated Influenza Infection at 100 days and Percentage of Participants With Any Treatment-emergent Adverse Event (TEAE) and TEAEs of Special Interest at 100 days. Started Jan 2017; 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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