drugset / Trial / NCT02635724

Safety, PK and Effectiveness of IV Peramivir in Elderly and Higher Risk Subjects With Uncomplicated Influenza

NCT02635724

Phase 3 Completed 74 enrolled BioCryst Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This study will evaluate the safety, pharmacokinetics and effectiveness of a single dose of 600 mg IV peramivir in the treatment of elderly subjects with acute uncomplicated influenza infection and in subjects with acute uncomplicated influenza infection at higher risk for influenza complications. All subjects will receive IV peramivir.

Timeline

Start
2015-12
Primary completion
2018-04
Completion
2018-09

Drugs

EvaluationDrugModalityDoseRoute
Subject PERAMIVIR ANHYDROUS Small molecule 600 mg Intravenous

Indications