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Lot Consistency Clinical Trial of of Recombinant HPV Bivalent Vaccine in 9 to14 Years Old Healthy Female

Primary Purpose

Cervical Intraepithelial Neoplasia, Cervical Cancer, Vaginal Intraepithelial Neoplasia

Status
Completed
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Recombinant Human Papillomavirus Bivalent (Types 16, 18) Vaccine (Escherichia coli) / Cecolin®
Sponsored by
Xiamen Innovax Biotech Co., Ltd
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cervical Intraepithelial Neoplasia focused on measuring Human Papillomavirus Infection, Bivalent HPV Vaccine, Immunogenicity

Eligibility Criteria

9 Years - 14 Years (Child)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • 1. Aged over 9 years old to 14 years old Female at the time of the first vaccine injection;
  • 2. Statutory guardian of the subjects able to provide legal identification or the trustee able to provide the authorization certificate;
  • 3. Judged as healthy and eligible for vaccination by the investigators through a selfreported medical history and some physical examinations;
  • 4.Axillary temperature is below than 37.0 ℃;
  • 5.Negative for urine pregnancy test.
  • 6.The statutory guardian and trustee able to understand this study information and willing to comply with all study requirements(the statutory guardian or subject able to fill in the diary card and attend the follow-up on schedule).
  • 7.Willing to participate in this study and sign informed consent form.

Exclusion Criteria:

Exclusion criteria for the first vaccination:

  1. Administration of HPV Vaccine before the study;
  2. Use of any investigational product or non-registered product (drug or vaccine)within 30 days preceding the first dose of the study vaccine or plan to use during the study period;
  3. Received immunosuppressed, immunoregulation therapy or corticosteroid systemic therapy for more than 14 days in the 6 months before entry, except local treatment(such as ointment, eyedrops, inhalants or nasal sprays);
  4. Administration of any immunoglobulin or blood products within 3 months preceding the first dose of the study vaccine,or plan to use during the study period;
  5. Administration of any inactivated vaccines within 14 days preceding the first dose of the study or attenuated live vaccines within 21 days preceding the first dose of the study;
  6. Had a fever (axillary temperature over 38°C) within 3 days or acute illness, or use systemic antibiotics or antiviral treatment within 5 days before vaccination;
  7. Participate in any other clinical trial during the study period;
  8. Immunodeficiency (such as HIV carriers), primary disease of important organs, malignant tumor, or any immune disease (such as systemic lupus erythematosus, rheumatoid arthritis, splenectomy or functional asplenia or other disease which might affect immune response), or other chronic diseases requiring treatment;
  9. History of allergic disease or history of serious adverse events occurring after vaccination, such as allergy,urticaria, dyspnea, angioneurotic edema or abdominal pain;
  10. Asthma that needed emergency treatment, hospitalization, oral or intravenous corticosteroid to keep stable in the past two years;
  11. Combining another severe internal medicine disease(such as hypertension, cardiopathy,diabetes and hyperthyroidism);
  12. Anormal coagulation function or coagulopathy diagnosed by doctor;
  13. Epilepsy(not including febrile seizures under 2 years old, alcohol epilepsy within 3 years prior to abstinence and simple epilepsy that have not required treatment within 3 years prior to the study) ;
  14. Anormal psychology or mind affecting the individual ability to obey the study requirements. Psychiatric disorders, not controlled in the past two years, required medication, or suicidal tendency in the past five years;
  15. Other medical, psychological, social or occupational factors that, according to the investigators' judgment, might affect the individual ability to obey the protocol or sign the informed consent.

Exclusion criteria for second vaccination:

  1. History of serious allergic reaction occurring after the first HPV vaccination;
  2. History of serious adverse events following immunization caused by the first HPV vaccination;
  3. Subject with new discovery or occurrence that does not meet the inclusion criteria, or conform to the exclusion criteria after the first HPV vaccination;
  4. According to the judgment of the investigator, subject has newly discovered or emerging severe internal medicine disease, anormal coagulation function or coagulopathy that is not suitable for participating after the first HPV vaccination.

Sites / Locations

  • Dongtai City Center for Disease Control and Prevention Dongtai, Jiangsu

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Bivalent HPV Vaccine Consistency Lot 1

Bivalent HPV Vaccine Consistency Lot 2

Bivalent HPV Vaccine Consistency Lot 3

Arm Description

Biological/Vaccine: Participants would receive 2 doses of Recombinant Human Papillomavirus Bivalent (Types 16, 18) Vaccine (Escherichia coli) intramuscularly at 0, 6 month.

Biological/Vaccine: Participants would receive 2 doses of Recombinant Human Papillomavirus Bivalent (Types 16, 18) Vaccine (Escherichia coli) intramuscularly at 0, 6 month.

Biological/Vaccine: Participants would receive 2 doses of Recombinant Human Papillomavirus Bivalent (Types 16, 18) Vaccine (Escherichia coli) intramuscularly at 0, 6 month.

Outcomes

Primary Outcome Measures

The Geometric Mean concentration (GMC) of anti-HPV16/18 IgG at at one month after the 2nd dose.
Measure anti-HPV16/18 IgG in serum samples at 7 month to evaluate the immunogenicity of the HPV vaccine.

Secondary Outcome Measures

Seroconversion rate of anti-HPV16/18 IgG at one month after the 2nd dose.
Describe seroconversion rate of anti-HPV16/18 IgG one month after the last dose.
Measure solicited local adverse reactions within 7 days after each vaccination.
Measure solicited systematic adverse reactions within 7 days after each vaccination.
Measure unsolicited adverse reactions within 30 days after vaccination.
Measure serious adverse events occurred throughout the study.
Measure Potential Immune Mediated Diseases occurred throughout the study.
The Potential Immune Mediated Diseases refers to a disease of immune hyperfunction or immune deficiency caused by immune regulation disorder due to insufficient transmission of certain immune mediates, such as Guillain-Barre syndrome and thrombocytopenic purpura.

Full Information

First Posted
June 15, 2022
Last Updated
June 22, 2022
Sponsor
Xiamen Innovax Biotech Co., Ltd
Collaborators
Jiangsu Province Centers for Disease Control and Prevention, Dongtai City Centers for Disease Control and Prevention
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1. Study Identification

Unique Protocol Identification Number
NCT05426148
Brief Title
Lot Consistency Clinical Trial of of Recombinant HPV Bivalent Vaccine in 9 to14 Years Old Healthy Female
Official Title
A Study to Assess the Immunogenicity Consistency of Three Consecutive Batches of Commercial-scale of Recombinant Human Papillomavirus(HPV) Bivalent Vaccine (Escherichia Coli) in Healthy Female Subjects Aged 9-14 Years
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Completed
Study Start Date
May 1, 2020 (Actual)
Primary Completion Date
August 1, 2020 (Actual)
Study Completion Date
April 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Xiamen Innovax Biotech Co., Ltd
Collaborators
Jiangsu Province Centers for Disease Control and Prevention, Dongtai City Centers for Disease Control and Prevention

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This study is to evaluate lot-lot consistency of Recombinant Human Papillomavirus Bivalent (Types 16, 18) Vaccine (Escherichia coli) .
Detailed Description
This study is a mono-center, randomization, double-blind clinical trial in healthy Female subjects between 9 to 14. Under the premise of full informed consent, 540 subjects that meet the requirement of clinical trial in the age of 9-14 will be randomly divided into 3 groups in a ratio of 1:1:1 and injected 2 consecutive batches of Recombinant Human Papillomavirus Bivalent (Types 16, 18) Vaccine (Escherichia coli) Cecolin® separately. The main outcome measures are the immunogenicity consistency and safety surveillance after inoculation according to prescribed immunization procedure.The total number of subjects should be ≥540 and ≤570.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cervical Intraepithelial Neoplasia, Cervical Cancer, Vaginal Intraepithelial Neoplasia, Vulvar Intraepithelial Neoplasia, Persistent Infection
Keywords
Human Papillomavirus Infection, Bivalent HPV Vaccine, Immunogenicity

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
540 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Bivalent HPV Vaccine Consistency Lot 1
Arm Type
Experimental
Arm Description
Biological/Vaccine: Participants would receive 2 doses of Recombinant Human Papillomavirus Bivalent (Types 16, 18) Vaccine (Escherichia coli) intramuscularly at 0, 6 month.
Arm Title
Bivalent HPV Vaccine Consistency Lot 2
Arm Type
Experimental
Arm Description
Biological/Vaccine: Participants would receive 2 doses of Recombinant Human Papillomavirus Bivalent (Types 16, 18) Vaccine (Escherichia coli) intramuscularly at 0, 6 month.
Arm Title
Bivalent HPV Vaccine Consistency Lot 3
Arm Type
Experimental
Arm Description
Biological/Vaccine: Participants would receive 2 doses of Recombinant Human Papillomavirus Bivalent (Types 16, 18) Vaccine (Escherichia coli) intramuscularly at 0, 6 month.
Intervention Type
Biological
Intervention Name(s)
Recombinant Human Papillomavirus Bivalent (Types 16, 18) Vaccine (Escherichia coli) / Cecolin®
Other Intervention Name(s)
There is no other Intervention in this study
Intervention Description
The bivalent HPV 16/18 vaccine was a mixture of two aluminum hydroxide adjuvant-absorbed recombinant L1 VLPs of HPV-16 and HPV-18 expressed in E. coli. A 0.5 ml dose of the bivalent HPV test vaccine comprised 40 μg of HPV-16 and 20 μg of HPV-18 L1 VLPs absorbed with aluminum adjuvant.
Primary Outcome Measure Information:
Title
The Geometric Mean concentration (GMC) of anti-HPV16/18 IgG at at one month after the 2nd dose.
Description
Measure anti-HPV16/18 IgG in serum samples at 7 month to evaluate the immunogenicity of the HPV vaccine.
Time Frame
7 months
Secondary Outcome Measure Information:
Title
Seroconversion rate of anti-HPV16/18 IgG at one month after the 2nd dose.
Description
Describe seroconversion rate of anti-HPV16/18 IgG one month after the last dose.
Time Frame
7 months
Title
Measure solicited local adverse reactions within 7 days after each vaccination.
Time Frame
7 days
Title
Measure solicited systematic adverse reactions within 7 days after each vaccination.
Time Frame
7 days
Title
Measure unsolicited adverse reactions within 30 days after vaccination.
Time Frame
30 days
Title
Measure serious adverse events occurred throughout the study.
Time Frame
up to 7 months
Title
Measure Potential Immune Mediated Diseases occurred throughout the study.
Description
The Potential Immune Mediated Diseases refers to a disease of immune hyperfunction or immune deficiency caused by immune regulation disorder due to insufficient transmission of certain immune mediates, such as Guillain-Barre syndrome and thrombocytopenic purpura.
Time Frame
up to 7 months

10. Eligibility

Sex
Female
Gender Based
Yes
Gender Eligibility Description
Cecolin® is indicated for women to prevent the diseases caused by human papillomavirus (HPV) types 16 and/or 18, such as cervical cancer, cervical intraepithelial neoplasia Grade 2 or 3 (CIN2/3) and adenocarcinoma in-situ (AIS).
Minimum Age & Unit of Time
9 Years
Maximum Age & Unit of Time
14 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: 1. Aged over 9 years old to 14 years old Female at the time of the first vaccine injection; 2. Statutory guardian of the subjects able to provide legal identification or the trustee able to provide the authorization certificate; 3. Judged as healthy and eligible for vaccination by the investigators through a selfreported medical history and some physical examinations; 4.Axillary temperature is below than 37.0 ℃; 5.Negative for urine pregnancy test. 6.The statutory guardian and trustee able to understand this study information and willing to comply with all study requirements(the statutory guardian or subject able to fill in the diary card and attend the follow-up on schedule). 7.Willing to participate in this study and sign informed consent form. Exclusion Criteria: Exclusion criteria for the first vaccination: Administration of HPV Vaccine before the study; Use of any investigational product or non-registered product (drug or vaccine)within 30 days preceding the first dose of the study vaccine or plan to use during the study period; Received immunosuppressed, immunoregulation therapy or corticosteroid systemic therapy for more than 14 days in the 6 months before entry, except local treatment(such as ointment, eyedrops, inhalants or nasal sprays); Administration of any immunoglobulin or blood products within 3 months preceding the first dose of the study vaccine,or plan to use during the study period; Administration of any inactivated vaccines within 14 days preceding the first dose of the study or attenuated live vaccines within 21 days preceding the first dose of the study; Had a fever (axillary temperature over 38°C) within 3 days or acute illness, or use systemic antibiotics or antiviral treatment within 5 days before vaccination; Participate in any other clinical trial during the study period; Immunodeficiency (such as HIV carriers), primary disease of important organs, malignant tumor, or any immune disease (such as systemic lupus erythematosus, rheumatoid arthritis, splenectomy or functional asplenia or other disease which might affect immune response), or other chronic diseases requiring treatment; History of allergic disease or history of serious adverse events occurring after vaccination, such as allergy,urticaria, dyspnea, angioneurotic edema or abdominal pain; Asthma that needed emergency treatment, hospitalization, oral or intravenous corticosteroid to keep stable in the past two years; Combining another severe internal medicine disease(such as hypertension, cardiopathy,diabetes and hyperthyroidism); Anormal coagulation function or coagulopathy diagnosed by doctor; Epilepsy(not including febrile seizures under 2 years old, alcohol epilepsy within 3 years prior to abstinence and simple epilepsy that have not required treatment within 3 years prior to the study) ; Anormal psychology or mind affecting the individual ability to obey the study requirements. Psychiatric disorders, not controlled in the past two years, required medication, or suicidal tendency in the past five years; Other medical, psychological, social or occupational factors that, according to the investigators' judgment, might affect the individual ability to obey the protocol or sign the informed consent. Exclusion criteria for second vaccination: History of serious allergic reaction occurring after the first HPV vaccination; History of serious adverse events following immunization caused by the first HPV vaccination; Subject with new discovery or occurrence that does not meet the inclusion criteria, or conform to the exclusion criteria after the first HPV vaccination; According to the judgment of the investigator, subject has newly discovered or emerging severe internal medicine disease, anormal coagulation function or coagulopathy that is not suitable for participating after the first HPV vaccination.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yuemei Hu
Organizational Affiliation
Jiangsu Provincial Center for Disease Prevention and Control
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dongtai City Center for Disease Control and Prevention Dongtai, Jiangsu
City
Dongtai
State/Province
Jiangsu
ZIP/Postal Code
224200
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No

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Lot Consistency Clinical Trial of of Recombinant HPV Bivalent Vaccine in 9 to14 Years Old Healthy Female

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