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NCT00959049 · ClinicalTrials.gov registry record · Phase 3

A Study to Determine the Immunogenicity and Safety Profile of CSL Limited's Influenza Virus Vaccine Compared to a US Licensed Comparator Influenza Virus Vaccine in a Pediatric Population

A Phase 3 study, sponsored by Seqirus.

Completed
Registry status
Phase 3
Development phase
1,474
Enrollment target

NCT00959049 is a Phase 3 study that has completed, run by Seqirus. The registered enrollment target is 1,474 participants.

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The verdict

NCT00959049, a Phase 3 study, has completed, sponsored by Seqirus.

COMPLETED
Registry status
Phase 3
Development phase
1,474 participants
Enrollment target

Study Summary

The purpose of this study is to determine the immunogenicity and safety profile of CSL Limited's Influenza Virus Vaccine compared to a US licensed comparator Influenza Virus Vaccine in a pediatric population aged greater than or equal to 6 months to less than 18 years.

Interventions

  • BIOLOGICAL CSL's Influenza Virus Vaccine (Afluria)
  • BIOLOGICAL Influenza Virus Vaccine (Fluzone)

Trial Details

FieldValue
Enrollment Target 1,474 participants
Start Date 2009-09
Est. Completion 2010-05
Phase Phase 3

Sponsor

Seqirus

25 total trials

What the Registry Record Tells You About NCT00959049

The ClinicalTrials.gov registry entry for NCT00959049 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 1,474 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Seqirus, which has 25 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which CSL's Influenza Virus Vaccine (Afluria) is the first listed.

NCT00959049 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00959049 about?

NCT00959049 is a clinical study titled "A Study to Determine the Immunogenicity and Safety Profile of CSL Limited's Influenza Virus Vaccine Compared to a US Licensed Comparator Influenza Virus Vaccine in a Pediatric Population". The purpose of this study is to determine the immunogenicity and safety profile of CSL Limited's Influenza Virus Vaccine compared to a US licensed comparator Influenza Virus Vaccine in a pediatric population aged greater than or equal to 6 months to less than 18 years.

What is the current status of trial NCT00959049?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,474 participants. The study started on 2009-09. Estimated completion is 2010-05.

What interventions are being tested in trial NCT00959049?

The interventions under investigation include: CSL's Influenza Virus Vaccine (Afluria) (BIOLOGICAL), Influenza Virus Vaccine (Fluzone) (BIOLOGICAL).

Who is sponsoring clinical trial NCT00959049?

This trial is sponsored by Seqirus, which has 25 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.