An Immunity Persistence Study of Live Attenuated Varicella Vaccine

Sponsor
Sinovac (Dalian) Vaccine Technology Co., Ltd. (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05095701
Collaborator
(none)
703
2
2
8
351.5
44.2

Study Details

Study Description

Brief Summary

This an open phase Ⅳ clinical trial of live attenuated varicella vaccines manufactured by Sinovac (Dalian) Vaccine Technology Co., Ltd .The purpose of this study is to evaluate the immunity persistence of live attenuated varicella vaccine at 5 and 8 years after primary immunization with live attenuated varicella vaccine.

Condition or Disease Intervention/Treatment Phase
  • Biological: Investigational Live Attenuated Varicella Vaccine
  • Biological: Placebo (Freeze Dired Dilution)
Phase 4

Detailed Description

This study is an open phase Ⅳ clinical trial in subjects who enrolled in the clinical trial and included in the immunogenicity subgroup PPS set from August to September 2016 .The experimental vaccine and placebo (Freeze Dired Dilution) were manufactured by Sinovac (Dalian) Vaccine Technology Co., Ltd.A total of 703 subjects will be enrolled including 349 subjects in experimental group and 354 subjects in control group .And 3.0-3.5ml of venous blood was collected from all subjects at 5 and 8 years after primary immunization, and the serum was separated for varicella antibody detection. The window period of blood collection was six months.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
703 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
An Open Clinical Trial to Evaluate the Immunity Persistence of Live Attenuated Varicella Vaccine at 5 and 8 Years After Primary Immunization With Live Attenuated Varicella Vaccine
Anticipated Study Start Date :
Nov 1, 2021
Anticipated Primary Completion Date :
Dec 1, 2021
Anticipated Study Completion Date :
Jul 1, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental Group

349 subjects who enrolled in the experimental group of clinical trial and included in the immunogenicity subgroup PPS set from August to September 2016 will be collected venous blood 3.0~3.5ml at 5 and 8 years after primary immunization.

Biological: Investigational Live Attenuated Varicella Vaccine
The live attenuated varicella vaccine was manufactured by Sinovac (Dalian) Vaccine Technology Co., Ltd. Live attenuated varicella-virus in 0·5 mL injection water with sucrose,sodium glutamate,sodium chloride,potassium chloride, sodium dihydrogen phosphate, potassium dihydrogen phosphate per injection.

Placebo Comparator: Control Group

354 subjects who enrolled in the control group of clinical trial and included in the immunogenicity subgroup PPS set from August to September 2016 will be collected venous blood 3.0~3.5ml at 5 and 8 years after primary immunization.

Biological: Placebo (Freeze Dired Dilution)
The placebo (freeze dired dilution) was manufactured by Sinovac (Dalian) Vaccine Technology Co., Ltd. and contained no active ingredient.It was 0·5 mL injection water with sucrose,sodium glutamate,sodium chloride,potassium chloride and phosphate.

Outcome Measures

Primary Outcome Measures

  1. Immunogenicity index-seropositive rates of varicella antibody [5 years after primary immunization]

    The seropositive rates of varicella antibody in 5 years after primary immunization with varicella vaccine

  2. Immunogenicity index-GMT of varicella antibody [5 years after primary immunization]

    GMT of varicella antibody in 5 years after primary immunization with varicella vaccine

  3. Immunogenicity index-the seropositive rates of varicella antibody [8 years after primary immunization]

    The seropositive rates of varicella antibody in 8 years after primary immunization with varicella vaccine

  4. Immunogenicity index-the GMT of varicella antibody [8 years after primary immunization]

    GMT of varicella antibody in 8 years after primary immunization with varicella

Eligibility Criteria

Criteria

Ages Eligible for Study:
1 Year to 17 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Subjects in PPS immunogenicity subgroup of phase Ⅲ clinical trial of protective effect of varicella vaccine;

  • The subject and/or guardian can understand and voluntarily sign the informed consent form;

  • Proven legal identity.

Exclusion Criteria:
  • History of chickenpox or shingles;

  • History of varicella vaccination since phase Ⅲ clinical trial;

  • Autoimmune disease or immunodeficiency / immunosuppression;

  • History of immunosuppressive therapy since phase Ⅲ clinical trial;

  • According to the investigator's judgment, the subject has any other factors that are not suitable for participating in the clinical trial.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Xiangcheng County Center for Disease Control and Prevention Xuchang Henan China 461700
2 Biyang County Center for Disease Control and Prevention Zhumadian Henan China 463700

Sponsors and Collaborators

  • Sinovac (Dalian) Vaccine Technology Co., Ltd.

Investigators

  • Principal Investigator: Lili Huang, Bachelor, Henan Provincial Center for Disease Prevention and Control

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Sinovac (Dalian) Vaccine Technology Co., Ltd.
ClinicalTrials.gov Identifier:
NCT05095701
Other Study ID Numbers:
  • PRO-VZV-4004
First Posted:
Oct 27, 2021
Last Update Posted:
Oct 27, 2021
Last Verified:
Oct 1, 2021
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 27, 2021