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Trial record 13 of 32 for:    sinovac | China

An Immunogenicity and Safety Study of Sabin Inactivated Poliovirus Vaccine (Vero Cell) in 2-month-old Infants

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ClinicalTrials.gov Identifier: NCT03526978
Recruitment Status : Recruiting
First Posted : May 16, 2018
Last Update Posted : May 16, 2018
Sponsor:
Information provided by (Responsible Party):
Sinovac Biotech Co., Ltd

May 4, 2018
May 16, 2018
May 16, 2018
August 8, 2017
October 18, 2017   (Final data collection date for primary outcome measure)
The seroconversion rates (SCRs) of each group after primary immunization. [ Time Frame: 90 days ]
Subjects whose pre-immune antibody level < 1:8 and post-immune antibody level ≥ 1:8, or those whose pre-immune antibody level ≥ 1:8 and the increase of post-immune antibody level ≥ 4 folds are considered seroconverted. Primary vaccination schedule: 3 doses with one month interval between doses (i.e., month 0, 1, 2).
Same as current
No Changes Posted
  • The incidences of solicited adverse events (AEs) of each group. [ Time Frame: 7 days ]
    Solicited AEs occurred within 7 days after each injection will be collected.
  • The incidences of unsolicited adverse events (AEs) of each group. [ Time Frame: 30 days ]
    Unsolicited AEs occurred within 30 days after each injection will be collected.
  • The incidence of serious adverse events (SAEs) during the period of safety monitoring of each group. [ Time Frame: 90-420 days. ]
    SAEs during the period of safety monitoring will be collected.
  • The post-immune antibody positive rate of each group after primary immunization. [ Time Frame: 90 days ]
    Subjects whose post-immune antibody level ≥ 1:8 are considered antibody positive. Primary vaccination schedule: 3 doses with one month interval between doses (i.e., month 0, 1, 2).
  • The post-immune geometric mean titer (GMT) of each group after primary immunization. [ Time Frame: 90 days. ]
    GMT of each group after primary immunization which lasts 60 days.
  • The geometric mean fold increase (GMI) of each group after primary immunization. [ Time Frame: 90 days ]
    The GMI is the increase of post-immune GMT from pre-immune GMT.
  • The percentage of subjecs with antibody ≥ 1:64 of each group after primary immunization. [ Time Frame: 90 days ]
    Percentage of subjecs with antibody ≥ 1:64 of each group after three-dose
  • The antibody positive rate of each group before booster dose. [ Time Frame: 420 days ]
    Subjects whose post-immune antibody level ≥ 1:8 are considered antibody positive. A booster dose at the age of 18months.
  • The geometric mean titer (GMT) of each group before booster dose. [ Time Frame: 420 days. ]
    GMT of each group before booster dose which occurred at the age of 18months.
  • The geometric mean fold increase (GMI) of each group before booster dose. [ Time Frame: 420 days ]
    The GMI is the increase of post-immune GMT from pre-i mmune GMT.
  • The percentage of subjecs with antibody ≥ 1:64 of each group before booster dose. [ Time Frame: 420 days ]
    Percentage of subjecs with antibody ≥ 1:64 of each group before booster dose which occurred at the age of 18months.
  • The post-immune antibody positive rate of each group after booster dose. [ Time Frame: 570 days ]

    Subjects whose post-immune antibody level ≥ 1:8 are co

    nsidered antibody positive

  • The post-immune geometric mean titer (GMT) of each group after booster dose. [ Time Frame: 570 days ]
    GMT of each group after booster dose. The booster dose at the age of 18months
  • The geometric mean fold increase (GMI) of each group after booster dose. [ Time Frame: 570 days ]
    The GMI is the increase of post-immune GMT from pre-immune GMT.
  • The percentage of subjecs with antibody ≥ 1:64 of each group after booster dose. [ Time Frame: 570 days ]
    Percentage of subjecs with antibody ≥ 1:64 of each group after booster dose which occurred at the age of 18months.
Same as current
Not Provided
Not Provided
 
An Immunogenicity and Safety Study of Sabin Inactivated Poliovirus Vaccine (Vero Cell) in 2-month-old Infants
A Randomized, Double-blind, Controlled Clinical Trial to Evaluate the Immunogenicity and Safety of Sabin Inactivated Poliovirus Vaccine (Vero Cell) in 2-month-old Infants
The purpose of this phase III study is to evaluate the immunogenicity and safety of Sabin Inactivated Poliovirus Vaccine (Vero cell) in 2-month-old infants.
The study is a randomized, double-blind, controlled randomized, double-blind, controlled clinical trial clinical trial. The purpose of this study is to evaluate the immunogenicity and safety of Sabin Inactivated Poliovirus Vaccine (Vero cell) manufactured by Sinovac Vaccine Technology Co., Ltd in 2-month-old infants. The control vaccine is a commercialized Inactivated Poliovirus Vaccine manufactured by Sanofi Pasteur company. 1200 healthy infants between 60-90 days will be randomly assigned into experimental group or control group in the ratio 1:1.
Interventional
Phase 3
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Investigator)
Primary Purpose: Prevention
Poliomyelitis
  • Biological: Investigational sIPV
    Three intramuscular injections of the investigational vaccine (0.5 ml) on Day 0, Day 30 and Day 60 respectively; Single intramuscular injection of the investigational vaccine (0.5 ml) at 18 months; Intervention: investigational sIPV
  • Biological: Control IPV
    Three intramuscular injections of the control vaccine (0.5 ml) on Day 0, Day 30 and Day 60 respectively; Single intramuscular injection of the control vaccine (0.5 ml) at 18 months; Intervention:control IPV
  • Experimental: Experimental Group

    The investigational vaccine was manufactured by Sinovac Vaccine Technology Co., Ltd.

    Intervention: investigational sIPV

    Intervention: Biological: Investigational sIPV
  • Active Comparator: Control Group
    The control vaccine was manufactured by Sanofi Pasteur Company. Intervention: control IPV
    Intervention: Biological: Control IPV
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
1200
Same as current
April 18, 2019
October 18, 2017   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • Healthy volunteer between 60-90 days old;
  • Healthy volunteers who fulfill all the required conditions for receiving the investigational vaccine as established by medical history and clinical examination and determined by investigators;
  • 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;
  • Complying with the requirement of the study protocol;

Exclusion Criteria:

  • Prior vaccination with Poliovirus Vaccine;
  • History of allergy to any vaccine, or any ingredient of the vaccine, or serious adverse reaction(s) 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 nervous system disease (epilepsy, seizures or convulsions) or mental illness;
  • Diagnosed coagulation function abnormal (e.g., coagulation factor deficiency, coagulation disorder, or platelet abnormalities) , or obvious bruising or coagulation disorders;
  • 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) prior to study entry;
  • Blood product prior to study entry;
  • Any other investigational medicine(s) within 30 days prior to study entry;
  • Any live attenuated vaccine within 14 days prior to study entry;
  • 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;
Sexes Eligible for Study: All
60 Days to 90 Days   (Child)
Yes
Contact: Yuemei Hu 86-18915999220 993832717@qq.com
China
 
 
NCT03526978
PRO-sIPV-3001
Not Provided
Studies a U.S. FDA-regulated Drug Product: No
Studies a U.S. FDA-regulated Device Product: No
Not Provided
Sinovac Biotech Co., Ltd
Sinovac Biotech Co., Ltd
Not Provided
Principal Investigator: Yuemei Hu Jiangsu Provincial Center for Disease Control and Prevention
Sinovac Biotech Co., Ltd
April 2018

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP