drugset / Trial / NCT02603952

A Phase 2a to Evaluate the Safety of MEDI8852 in Adults With Uncomplicated Influenza

NCT02603952

Phase 1/2 Completed 126 enrolled MedImmune LLC
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to evaluate safety and tolerability of a single dose of MEDI8852 when given with oseltamivir, the safety and tolerability of oseltamivir alone, and the safety and tolerability of a single dose of MEDI8852 alone in adult participants with acute, uncomplicated influenza caused by Type A strains.

Timeline

Start
2015-12-07
Primary completion
2016-12-09
Completion
2016-12-09

Drugs

EvaluationDrugModalityDoseRoute
Subject MEDI8852 Monoclonal antibody 750 mg Intravenous
Subject MEDI8852 Monoclonal antibody 3000 mg Intravenous
Subject Oseltamivir Small molecule 75 mg Oral

Indications