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NCT00903552 · ClinicalTrials.gov registry record · Phase 2

Trial to Evaluate Safety and Immunogenicity of Trivalent Seasonal Influenza Virus-Like Particle (VLP) Vaccine (Recombinant)

A Phase 2 study, sponsored by Novavax.

Completed
Registry status
Phase 2
Development phase
221
Enrollment target

NCT00903552: Completed Phase 2 study, sponsored by Novavax.

NCT00903552 is a Phase 2 study that has completed, run by Novavax. The registered enrollment target is 221 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (66% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00903552, a Phase 2 study, has completed, sponsored by Novavax.

COMPLETED
Registry status
Phase 2
Development phase
221 participants
Enrollment target

Study Summary

This is a phase 2A randomized, double blind, placebo controlled trial to evaluate the safety and immunogenicity of a trivalent seasonal influenza virus-like particle (VLP) vaccine (recombinant) in healthy adults.

Interventions

  • BIOLOGICAL Placebo
  • BIOLOGICAL Influenza VLP Vaccine

Trial Details

FieldValue
Enrollment Target 221 participants
Start Date 2009-05
Est. Completion 2009-10
Phase Phase 2
Novavax

31 total trials

What the finished NCT00903552 record still lists

NCT00903552 is an interventional study that assigns participants to a tested intervention. The registered 221 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (66% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00903552 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00903552 about?

NCT00903552 is a clinical study titled "Trial to Evaluate Safety and Immunogenicity of Trivalent Seasonal Influenza Virus-Like Particle (VLP) Vaccine (Recombinant)". This is a phase 2A randomized, double blind, placebo controlled trial to evaluate the safety and immunogenicity of a trivalent seasonal influenza virus-like particle (VLP) vaccine (recombinant) in healthy adults.

What is the current status of trial NCT00903552?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 221 participants. The study started on 2009-05. Estimated completion is 2009-10.

What interventions are being tested in trial NCT00903552?

The interventions under investigation include: Placebo (BIOLOGICAL), Influenza VLP Vaccine (BIOLOGICAL).

Who is sponsoring clinical trial NCT00903552?

This trial is sponsored by Novavax, which has 31 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00903552's enrollment target sits among peer trials

221 275th of 2000 higher than 1,726 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00903552, the US trial registry maintained by the National Library of Medicine. NCT00903552 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.