Clinical Trial of Enterovirus 71（EV71） Inactivated Vaccine in Children Aged 36-71 Months

Sinovac

Status and phase: Completed; Phase 3

Conditions: Hand, Foot and Mouth Disease

Treatments: Biological: 36-71 months old children-experimental EV71 vaccine.; Biological: 6-35 months old children-experimental EV71 vaccine.; Biological: 36-71 months old children-control EV71 vaccine.

Study type: Interventional

Funder types: Industry

Identifiers

NCT03909074

PRO-EV71-3003

Details and patient eligibility

About

The purpose of this study is to evaluate the non-inferiority of experimental EV71 vaccine compared to the control EV71 vaccine in children aged 36-71 months, to evaluate the non-inferiority of EV71 vaccine used in children aged 36-71 months compared to 6-35 months. The experimental vaccine was manufactured by Sinovac Biotech Co., Ltd, and the control vaccine was manufactured by Institute of Medical Biology Chinese Academy of Medical Sciences.

Full description

This study is a randomized, double-blind, single-center, controlled phase III clinical trial in children aged 36-71 months, and bridging trial between agegroup of 6-35 and 36-71 months. The purpose of this study is to evaluate the immunogenicity and safety of the experimental EV71 vaccine in children aged 36-71 months. The primary objective of this study is to evaluate the non-inferiority of experimental EV71 vaccine compared to the control EV71 vaccine in children aged 36-71 months, and the non-inferiority of EV71 vaccine used in children aged 36-71 months compared to 6-35 months. The secondary objective is to evaluate the safety of the experimental vaccine used in children aged 36-71 months. The experimental vaccine is manufactured by Sinovac Biotech Co., Ltd, and the control vaccine is manufactured by Institute of Medical Biology Chinese Academy of Medical Sciences. 600 children aged 36-71 months will be randomly assigned in to receive the experimental vaccine or control vaccine, and 300 children aged 6-35 months will receive the experimental vaccine.

Enrollment: 900 patients

Sex: All

Ages: 6 to 71 months old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Healthy volunteers ≥ 2 years old;
• Proven legal identity;
• Participants or guardians of the participants should be capable of understanding the written consent form, and such form should be signed prior to enrolment.

Exclusion criteria

• Prior vaccination with EV71 vaccine;

• History of hand, foot and mouth disease;

• History of allergy to any vaccine or vaccine ingredient, asthma, serious adverse reactions to vaccination, such as urticaria, dyspnea, angioneurotic edema, abdominal pain, etc;

• Congenital malformation, developmental disorders, genetic defects, or severe malnutrition;

• Autoimmune disease or immunodeficiency/immunosuppressive;

• Severe/uncontrollable nervous system disease (epilepsy, seizures or convulsions) or mental illness;

• History of thyroidectomy, no spleen and functional spleen;

• Diagnosed coagulation function abnormal (e.g., coagulation factor deficiency, coagulation disorder, or platelet abnormalities) , or obvious bruising or coagulation disorders;

• Receipt of any of the following products:

  1. Any immunosuppressant, cytotoxic medicine, or inhaled corticosteroids (except corticosteroid spray for treatment of allergic rhinitis or corticosteroid treatment on surface for acute non-complicated dermatitis) within 6 month prior to study entry
  2. Blood products within 2 months prior to study entry
  3. Any other investigational products (drug or vaccine）within 30 days prior to study entry
  4. Any live attenuated vaccine within 14 days prior to study entry
  5. Any subunit vaccine or inactivated vaccine within 7 days prior to study entry;

• Acute disease or acute stage of chronic disease within 7 days prior to study entry;

• Axillary temperature > 37.0 °C;

• Any other factor that suggesting the volunteer is unsuitable for this study based on the opinions of investigators.

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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900 participants in 3 patient groups

Experimental group

Experimental group

Description:

36-71 months old children-experimental EV71 vaccine.

Treatment:

Biological: 36-71 months old children-experimental EV71 vaccine.

Vaccine-controlled group

Active Comparator group

Description:

36-71 months old children-control EV71 vaccine.

Treatment:

Biological: 36-71 months old children-control EV71 vaccine.

Age-controlled group

Active Comparator group

Description:

6-35 months old children-experimental EV71 vaccine.

Treatment:

Biological: 6-35 months old children-experimental EV71 vaccine.