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Evaluate Safety of GCFLU® Administered Intramuscularly in Healthy Vietnamese Volunteer Aged From 3 Years Old

NCT02723812 · Status: COMPLETED · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 120

Last updated 2016-03-30

No results posted yet for this study

Summary

An open label, non-comparative bridging study to evaluate the safety of GCFLU® (seasonal influenza vaccine) administered intramuscularly in healthy Vietnamese volunteer aged from 3 years old

Conditions

  • Influenza, Human

Interventions

BIOLOGICAL

GCFLU® Influenza vaccine (Split virion, Inactivated)

Sponsors & Collaborators

  • Green Cross Corporation

    collaborator INDUSTRY

  • Institute of Clinical Research and Clinical Trial Support for Vaccine and Biological Products

    lead OTHER

Principal Investigators

  • Thuong Nguyen Vu, PhD. · Pasteur Institute, Ho Chi Minh City

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
3 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2015-12-31
Completion
2015-12-31

Countries

  • Vietnam

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02723812 on ClinicalTrials.gov