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Study of an Investigational Monoclonal Antibody, VIS410, in Subjects With Uncomplicated Influenza A

Influenza Clinical Trial

Official title:
A Phase 2a Double-blind, Placebo-controlled Study to Assess the Safety and Tolerability of a Single Intravenous Dose of an Investigational Monoclonal Antibody With Code Name VIS410 in Subjects With Uncomplicated Influenza A Infection

Clinical Trial Summary

This is a Phase 2a randomized, double-blind, placebo-controlled study designed to assess the safety and tolerability of an investigational monoclonal antibody, VIS410, in subjects with uncomplicated influenza.

Clinical Trial Description

Subjects will be admitted to an infusion unit for drug administration and observation following infusion. The study is designed to compare an infusion of a single high or low IV dose of VIS410 against placebo. Subjects will be followed for 100 (±7 days). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02989194
Study type Interventional
Source Visterra, Inc.
Contact
Status Completed
Phase Phase 2
Start date January 6, 2017
Completion date October 27, 2017
View Details
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