Safety and Immunogenicity of a Split-Virion Pandemic Influenza A (H5N1) Vaccine in Children

A single center, stratified, randomized and double-blind phase II clinical trial was conducted in children to evaluate the safety and immunogenicity of an split-virion pandemic influenza A vaccine (H5N1).

Study Overview

• Status: Completed
• Conditions: Influenza
• Intervention / Treatment: Biological: split-virion pandemic influenza vaccine (H5N1 strain NIBRG-14)

• Study Type: Interventional
• Phase: Phase 2

Contacts and Locations

Study Locations

• China
  • Beijing, China, 100013
    • Beijing Centers for Diseases Control and Prevention

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 3 years to 11 years (Child)
• Accepts Healthy Volunteers: No
• Genders Eligible for Study: All

Description

Inclusion Criteria:

• Healthy children aged 3-11 years old
• Be able to show legal identity card for the sake of recruitment
• Volunteers or their parents are able to understand and sign the informed consent
• Do not participate in other clinical trial

Exclusion Criteria:

• Any history of allergic reactions
• Autoimmune disease or immunodeficiency
• Asthma that is unstable or required emergent care, hospitalization or intubation during the past two years or that required the use of oral or intravenous corticosteroids
• Diabetes mellitus (type I or II), with the exception of gestational diabetes
• History of thyroidectomy or thyroid disease that required medication within the past 12 months
• Serious angioedema episodes within the previous 3 years or requiring medication in the previous two years
• Hypertension that was not well controlled by medication or the blood pressure is more than 145/95 mmHg at enrollment
• Bleeding disorder diagnosed by a doctor (e.g., factor deficiency, coagulopathy, or platelet disorder requiring special precautions) or significant bruising or bleeding difficulties with IM injections or blood draws
• Active malignancy or treated malignancy for which there is not reasonable assurance of sustained cure or malignancy that is likely to recur during the period of study

• Seizure disorder other than:

  1. Febrile seizures under the age of two years old
  2. Seizures secondary to alcohol withdrawal more than 3 years ago, or
  3. A singular seizure not requiring treatment within the last 3 years
• Asplenia, functional asplenia or any condition resulting in the absence or removal of the spleen
• Guillain-Barre Syndrome
• Any history of immunosuppressive medications or cytotoxic medications or inhaled corticosteroids within the past six months (with the exception of corticosteroid nasal spray for allergic rhinitis or topical corticosteroids for an acute uncomplicated dermatitis)
• History of any blood products administration within 3 months before the dosing
• Administration of any other investigational research agents within 30 days before the dosing
• Administration of any live attenuated vaccine within 30 days before the dosing
• Administration of subunit or inactivated vaccines, e.g. pneumococcal vaccine, or allergy treatment with antigen injections, within 14 days before the dosing
• Be receiving anti-TB prophylaxis or therapy currently
• Axillary temperature > 37.0 centigrade at the time of dosing

• Psychiatric condition that precludes compliance with the protocol:

  1. Past or present psychoses
  2. Past or present bipolar disorder requiring therapy that has not been well controlled on medication for the past two years
  3. Disorder requiring lithium
  4. Suicidal ideation occurring within five years prior to enrollment
• Any medical, psychiatric, social condition, occupational reason or other responsibility that, in the judgment of the investigator, is a contraindication to protocol participation or impairs a volunteer's ability to give informed consent

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Quadruple

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: 10 ug; 10 microgram per dose	Biological: split-virion pandemic influenza vaccine (H5N1 strain NIBRG-14)
Experimental: 15 ug; 15 microgram per dose	Biological: split-virion pandemic influenza vaccine (H5N1 strain NIBRG-14)

What is the study measuring?

Primary Outcome Measures

Outcome Measure
HI antibody and Neutralization antibody

Secondary Outcome Measures

Outcome Measure
Adverse reactions

Collaborators and Investigators

• Sponsor: Sinovac Biotech Co., Ltd
• Collaborators: Centers for Disease Control and Prevention, China

Study record dates

Study Major Dates

• Study Start: December 7, 2022
• Primary Completion: December 7, 2022
• Study Completion: December 7, 2022

Study Registration Dates

• First Submitted: May 12, 2009
• First Submitted That Met QC Criteria: May 12, 2009
• First Posted (Estimate): May 13, 2009

Study Record Updates

• Last Update Posted (Estimate): May 14, 2009
• Last Update Submitted That Met QC Criteria: May 13, 2009
• Last Verified: May 1, 2009

More Information

Terms related to this study

• Keywords: Safety; Pandemic Influenza A Vaccine; Immunogenictiy
• Additional Relevant MeSH Terms: RNA Virus Infections; Virus Diseases; Infections; Respiratory Tract Infections; Respiratory Tract Diseases; Orthomyxoviridae Infections; Influenza, Human
• Other Study ID Numbers: PRO-sPanFlu-2002

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No
• product manufactured in and exported from the U.S.: No