CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 1,794 enrolled
Drug / intervention
IL-YANG Quadrivalent Influenza Vaccine +2 morebiological
Likely dose
IL-YANG Quadrivalent Influenza Vaccine 0.5mLfrom 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/NCT02677493
NCT02677493Phase 3Completed

A Multicenter, Randomized, Double-blind, Active-controlled, Parallel Phase III Study to Investigate the Immunogenicity and Safety of 'IL-YANG Quadrivalent Influenza Vaccine Inj.' After Intramuscular Administration in Healthy Adult Subjects

Il-Yang Pharm. Co., Ltd.·interventional·Posted Feb 9, 2016·Updated Sep 28, 2023

In Brief

A Phase 3 clinical trial evaluating IL-YANG Quadrivalent Influenza Vaccine, IL-YANG Flu Vaccine Prefilled Syringe, and 1 other intervention for Influenza. Completed, enrolled 1,794 participants.

Detailed Summary

This study evaluates the immunogenicity and safety of 'IL-YANG Quadrivalent Influenza Vaccine Inj.' in healthy male and female adults at the age of 19 or older.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsInfluenza
Countries--
Collaborators--

Timeline

Phase 3CompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 9, 2016
Enrollment StartOct 1, 2015
Primary CompletionJan 1, 2016
Study CompletionJun 1, 2016
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 10.4 years ago

Interventions

IL-YANG Quadrivalent Influenza Vaccinebiological

A single 0.5mL dose administrated as an intramuscular injection.

IL-YANG Flu Vaccine Prefilled Syringebiological

A single 0.5mL dose administrated as an intramuscular injection.

IL-YANG Trivalent Influenza Vaccinebiological

A single 0.5mL dose administrated as an intramuscular injection.