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COMPLETED Phase 3

Safety, PK and Effectiveness of IV Peramivir Versus Oseltamivir in Pediatric Subjects With Uncomplicated Influenza

NCT02369159 · View on ClinicalTrials.gov ↗

Study Summary

This study will evaluate the safety, pharmacokinetics and effectiveness of a single dose of IV peramivir compared to a standard 5 day course of oral oseltamivir in the treatment of pediatric subjects with acute uncomplicated influenza.

Conditions Studied

Interventions

  • DRUG Oseltamivir
  • DRUG Peramivir

Study Locations (10)

Texas

  • Peramivir Investigative Site — Houston
  • Peramivir investigative site — San Antonio
  • Peramivir investigative site — Splendora

Utah

  • Peramivir investigative site — Draper
  • Peramivir investigative site — Salt Lake City
  • Peramivir investigative site — South Jordan

Louisiana

  • Peramivir Investigative Site — Shreveport

Ohio

  • Peramivir investigative site — Dayton

Pennsylvania

  • Peramivir investigative site — Smithfield

Other

  • Peramivir Investigative Site — Pretoria

Trial Details

FieldValue
Enrollment Target 137 participants
Start Date 2015-03-11
Est. Completion 2020-05-14
Phase Phase 3

Sponsor

BioCryst Pharmaceuticals

7 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT02369159

The ClinicalTrials.gov registry entry for NCT02369159 describes a study currently listed as completed. It is categorized as Phase 3, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 137 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BioCryst Pharmaceuticals, which has 7 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Influenza appearing as the primary indexed condition, and to 2 interventions — of which Oseltamivir is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT02369159 reports 10 study locations spanning 6 distinct geographic areas — top geographies include Texas, Utah, Louisiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT02369159 about?

NCT02369159 is a clinical study titled "Safety, PK and Effectiveness of IV Peramivir Versus Oseltamivir in Pediatric Subjects With Uncomplicated Influenza". This study will evaluate the safety, pharmacokinetics and effectiveness of a single dose of IV peramivir compared to a standard 5 day course of oral oseltamivir in the treatment of pediatric subjects with acute uncomplicated influenza.

What is the current status of trial NCT02369159?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 137 participants. The study started on 2015-03-11. Estimated completion is 2020-05-14.

What conditions does trial NCT02369159 study?

This clinical trial studies the following conditions: Influenza. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT02369159?

The interventions under investigation include: Oseltamivir (DRUG), Peramivir (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT02369159?

This trial is sponsored by BioCryst Pharmaceuticals, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT02369159 being conducted?

This trial has 10 study locations across Louisiana, Ohio, Pennsylvania, Texas, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial