CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 413 enrolled
Drug / intervention
FluBlok +3 morebiological
Likely dose
FluBlok 5 mLfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03068949
NCT03068949Phase 4Completed

A Comparison of CD4 T Cell Induction and Antibody Responses Between a Pure Hemagglutinin Influenza Vaccine and Licensed Subvirion Influenza Vaccine Made in Eggs or Cell Culture in Healthy Adults.

University of Rochester·interventional·Posted Mar 3, 2017·Updated Nov 30, 2021

In Brief

A Phase 4 clinical trial evaluating FluBlok, Fluzone, and 2 other interventions for Influenza. Completed, enrolled 413 participants across 1 site.

Detailed Summary

This study will evaluate in detail the way that the immune system responds to three different kinds of flu shots that are licensed in the United States.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsInfluenza
CountriesUnited States

Timeline

Phase 4CompletedFinished
20162017201820192020202120222023202420252026
First PostedMar 3, 2017
Enrollment StartOct 28, 2015
Primary CompletionJun 30, 2020
Study CompletionJun 30, 2021
TodayJul 2, 2026
Enrollment to primary: 4.7 yearsPosted 9.3 years ago

Interventions

FluBlokbiological

FluBlok trivalent Influenza Vaccine .5 mL given Intramuscularly

Fluzonebiological

Fluzone Quadrivalent Influenza Vaccine .5 mL given intramuscularly

FluCelVaxbiological

FluCelVax Quadrivalent Influenza Vaccine .5 mL given intramuscularly

Fluzone HDbiological

Fluzone HD Trivalent High Dose Influenza Vaccine .5 mL given intramuscularly