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NCT00966238 · ClinicalTrials.gov registry record · Phase 2

Safety and Immunogenicity of VAX125 Influenza Vaccine in Community-living Adults >= 65 Years of Age

A Phase 2 study, sponsored by VaxInnate Corporation.

Completed
Registry status
Phase 2
Development phase
120
Enrollment target

NCT00966238: Completed Phase 2 study, sponsored by VaxInnate Corporation.

NCT00966238 is a Phase 2 study that has completed, run by VaxInnate Corporation. The registered enrollment target is 120 participants, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (10% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00966238, a Phase 2 study, has completed, sponsored by VaxInnate Corporation.

COMPLETED
Registry status
Phase 2
Development phase
120 participants
Enrollment target

Study Summary

A multi-center, open-label, escalating dose-ranging study to assess the safety, reactogenicity, and immunogenicity of four different VAX125 vaccine doses; 0.5 µg, 1.0 µg, 2.0 µg, or 3.0 µg, delivered i.m. as a single dose vaccination on Day 0. Hypothesis: VAX125 is safe and immunogenic at one or more of the doses tested.

Interventions

  • BIOLOGICAL VAX125

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2009-09
Est. Completion 2011-03
Phase Phase 2
VaxInnate Corporation

9 total trials

What the finished NCT00966238 record still lists

NCT00966238 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (10% lower).

The record links to 0 conditions, and to 1 intervention - of which VAX125 is the first listed.

NCT00966238 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00966238 about?

NCT00966238 is a clinical study titled "Safety and Immunogenicity of VAX125 Influenza Vaccine in Community-living Adults >= 65 Years of Age". A multi-center, open-label, escalating dose-ranging study to assess the safety, reactogenicity, and immunogenicity of four different VAX125 vaccine doses; 0.5 µg, 1.0 µg, 2.0 µg, or 3.0 µg, delivered i.m. as a single dose vaccination on Day 0. Hypothesis: VAX125 is safe and immunogenic at one or mor...

What is the current status of trial NCT00966238?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 120 participants. The study started on 2009-09. Estimated completion is 2011-03.

What interventions are being tested in trial NCT00966238?

The interventions under investigation include: VAX125 (BIOLOGICAL).

Who is sponsoring clinical trial NCT00966238?

This trial is sponsored by VaxInnate Corporation, which has 9 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00966238's enrollment target sits among peer trials

120 569th of 2000 higher than 1,383 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 NCT00966238, the US trial registry maintained by the National Library of Medicine. NCT00966238 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.