drugset / Trial / NCT02468115

Influenza Challenge Study of VIS410 in Healthy Volunteers

NCT02468115 ↗

Phase 2 Completed 46 enrolled Visterra, Inc.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A phase 2 a study to assess the safety profile and the effect of VIS410 in healthy subjects after inoculation with influenza A virus (H1N1).

Timeline

Start
2015-05
Primary completion
2016-02
Completion
2016-02

Outcome

Met primary endpoint

paper VIS410 treatment was associated with a 76% reduction in median VL AUC as measured by qRT-PCR (p = 0.024). PMID 32151645 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject VIS410 Monoclonal antibody — Intravenous

Indications