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NCT00240968 · ClinicalTrials.gov registry record · Phase 2

H5 Booster After a Two Dose Schedule

A Phase 2 study of Influenza, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

Completed
Registry status
Phase 2
Development phase
337
Enrollment target
3
Study locations

NCT00240968 is a Phase 2 study of Influenza that has completed, run by National Institute of Allergy and Infectious Diseases (NIAID). The registered enrollment target is 337 participants, below the 36,802-participant average among 156 other Influenza trials with a reported enrollment target (99% lower). The trial reports 3 study locations across 3 states.

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The verdict

NCT00240968, a Phase 2 study of Influenza, has completed, sponsored by National Institute of Allergy and Infectious Diseases (NIAID).

COMPLETED
Registry status
Phase 2
Development phase
337 participants
Enrollment target
3
Study locations

Study Summary

The purpose of this study is to determine whether a third dose of vaccines containing A/Vietnam/1203/04 provides more immunity than two doses. Subjects who participate in this study will have participated in DMID protocol 04-063 involving the A/Vietnam/1203/04. In this study, each subject will be asked to receive a third dose of the H5 vaccine at the same level administered in protocol 04-063. Subjects will be asked to record oral temperature and any experienced side effects for 7 days following the vaccine. Study procedures will include up to 3 blood sample collections. Participants will be involved in study related procedures for up to 6 months.

Conditions Studied

Interventions

  • BIOLOGICAL Inactivated Influenza A/H5N1 Vaccine (sanofi pasteur)

Study Locations (3)

California

  • UCLA Center For Vaccine Research - Torrance

Maryland

  • University of Maryland Baltimore - Baltimore

New York

  • University of Rochester Medical Center - Strong Memorial Hospital - Infectious Diseases - Rochester

Trial Details

FieldValue
Enrollment Target 337 participants
Start Date 2005-10
Est. Completion 2006-07
Phase Phase 2

What the Registry Record Tells You About NCT00240968

The ClinicalTrials.gov registry entry for NCT00240968 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 337 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 36,802-participant average among 156 other Influenza trials with a reported enrollment target (99% lower). The listed sponsor is National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Influenza appearing as the primary indexed condition, and to 1 intervention - of which Inactivated Influenza A/H5N1 Vaccine (sanofi pasteur) is the first listed.

NCT00240968 reports 3 study locations spanning 3 distinct geographic areas - top geographies include California, Maryland, New York.

Frequently Asked Questions

What is clinical trial NCT00240968 about?

NCT00240968 is a clinical study titled "H5 Booster After a Two Dose Schedule". The purpose of this study is to determine whether a third dose of vaccines containing A/Vietnam/1203/04 provides more immunity than two doses. Subjects who participate in this study will have participated in DMID protocol 04-063 involving the A/Vietnam/1203/04. In this study, each subject will be as...

What is the current status of trial NCT00240968?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 337 participants. The study started on 2005-10. Estimated completion is 2006-07.

What conditions does trial NCT00240968 study?

This clinical trial studies the following conditions: Influenza.

What interventions are being tested in trial NCT00240968?

The interventions under investigation include: Inactivated Influenza A/H5N1 Vaccine (sanofi pasteur) (BIOLOGICAL).

Who is sponsoring clinical trial NCT00240968?

This trial is sponsored by National Institute of Allergy and Infectious Diseases (NIAID), which has 2,006 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00240968 being conducted?

This trial has 3 study locations across California, Maryland, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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