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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT02635724

Public ClinicalTrials.gov record NCT02635724. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 28, 2026, 11:42 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Multicenter, Single-arm, Open-label, Study to Evaluate the Safety, Pharmacokinetics and Effectiveness of Intravenous Peramivir in Elderly Subjects With Acute Uncomplicated Influenza Infection and in Subjects With Acute Uncomplicated Influenza Infection at Higher Risk for Influenza Complications

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT02635724
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
BioCryst Pharmaceuticals
Industry
Enrollment
74 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 30, 2015
Primary completion
Mar 31, 2018
Completion
Aug 31, 2018
Last update posted
Mar 22, 2021

2015 – 2018

United States locations

U.S. sites
15
U.S. states
7
U.S. cities
15
Facility City State ZIP Site status
Peramivir Investigational Site Brooksville Florida — —
Peramivir Investigational Site Lakeland Florida — —
Peramivir Investigational Site Miami Florida — —
Peramivir Investigational Site St. Petersburg Florida — —
Peramivir Investigational Site Tampa Florida — —
Peramivir investigative site Indianapolis Indiana — —
Peramivir investigative site Detroit Michigan — —
Peramivir Investigational Site Dayton Ohio — —
Peramivir investigative site Smithfield Pennsylvania — —
Peramivir Investigational Site Houston Texas — —
Peramivir Investigative Site San Antonio Texas — —
Peramivir investigative site Splendora Texas — —
Peramivir Investigational Site Draper Utah — —
Peramivir Investigational Site Salt Lake City Utah — —
Peramivir investigative site South Jordan Utah — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02635724, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 22, 2021 · Synced Sep 28, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02635724 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →