Post-License Safety Evaluation of Influenza Virus Vaccine

NCT02136017 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 400000

Last updated 2014-05-12

No results posted yet for this study

Summary

To evaluate the safety of the post-licensed influenza virus vaccine made of Changchun Institute of Biological Products Co.,Ltd.

Conditions

Sponsors & Collaborators

  • China National Biotec Group Company Limited

    collaborator INDUSTRY
  • Sichuan Center for Disease Control and Prevention

    lead OTHER_GOV

Principal Investigators

  • rui ao, master · Sichuan CDC

Eligibility

Min Age
3 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-01-31
Primary Completion
2013-12-31
Completion
2013-12-31

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Entities

Diseases

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 NCT02136017 on ClinicalTrials.gov