A Phase Ⅳ Clinical Trial of the Recombinant Hepatitis E Vaccine (Escherichia Coli)(the Chronic Hepatitis B Patients )

Hepatitis E Clinical Trial

Official title:

An Open, Pared Trial of Recombinant Hepatitis E Vaccine (Escherichia Coli) Hecolin® in the Chronic Hepatitis B Patients on the Clinical Stability .( Aged 30 Years or Over)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02964910
• Other study ID #: PRO-HE-009
• Status: Completed
• Phase: Phase 4
• Start date: August 2016
• Est. completion date: December 2017

Study information

• Verified date: July 2019
• Source: Xiamen Innovax Biotech Co., Ltd
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This phase IV clinical study was designed to evaluate the immunogenicity and safety of Hecolin® in the chronic Hepatitis B patients on the clinical stability.

Description:

This phase IV clinical study was designed to evaluate the immunogenicity and safety of the recombinant Hepatitis E vaccine(Hecolin®), manufactured by Xiamen Innovax Biotech CO., LTD., in the chronic Hepatitis B patients on the clinical stability and aged over 30 years of age at enrollment. The study volunteers will receive the 3 doses of Hecolin® administered intramuscularly according to a 0-1-6 month schedule.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 475
• Est. completion date: December 2017
• Est. primary completion date: August 2017
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 30 Years and older

Eligibility

Inclusion Criteria(all volunteers):

1. Aged over 30 years old on the day of enrollment

2. Axillary temperature is below than 37.0 ?.

3. No administration of HEV vaccine before the study

4. Judged as healthy and eligible for vaccination by the investigators through a selfreported medical history and some physical examinations.

5. Able to understand this study information and willing to comply with all study requirements.

6. Willing to participate in this study and sign informed consent form.

7. Negative serological markers for hepatitis E

Inclusion Criteria(experiment group):

1. ALT < 1.5×ULN

2. No spleen swelling,no cirrhosis and no hepatocellular carcinoma

Inclusion Criteria(control group):

1. HBsAg(-)

Exclusion Criteria:

1. With clinical evidence of malignant tumor

2. History of severe cardio-cerebrovascular disease

3. Administration of hepatotoxicity drugs before or during the study

4. Pregnancy,breast-feeding or plan to be pregnant in 7 months later

5. Participated in any other clinical trial during the study period.

6. 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.

7. Received immunosuppressed, immunoregulation therapy or corticosteroid systemic therapy for more than 14 days in the 6 months before entry, except local treatment.

8. 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.

9. 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.

10. Had a fever (axillary temperature over 38°C) within 3 days or acute illness requiring systemic antibiotics or antiviral treatment within 5 days before vaccination.

11. Immunodeficiency (such as HIV carriers), primary disease of important organs, malignant tumor, or any immune disease (such as systemic lupus erythematosus, arthritis pauperum, splenectomy or functional asplenia or other disease which might affect immune response).

12. History of allergic disease or history of serious adverse events occurring after vaccination, i.e., allergy,urticaria, dyspnea, angioneurotic edema or abdominal pain.

13. Allergic history to any component of this vaccine.

14. Asthma that needed emergency treatment, hospitalization, oral or intravenous corticosteroid to keep stable in the past two years.

15. Combining another severe internal medicine disease(such as severe hypertension, cardiopathy,diabetes and hyperthyroidism)

16. Anomal coagulation function or coagulopathy diagnosed by doctor

17. Epilepsy(not including alcohol epilepsy within 3 years prior to abstinence and simple epilepsy that do without curing within 3 years prior to the study )

18. Anomal psychology or mind affecting the individual's ability to obey the study requie

19. Other medical, psychological, social or occupational factors that, according to the investigators' judgment,might affect the individual's ability to obey the protocol or sign the informed consent.

Related Conditions & MeSH terms

• Hepatitis
• Hepatitis A
• Hepatitis B
• Hepatitis B, Chronic
• Hepatitis E
• Hepatitis, Chronic

Intervention

Biological:
• Recombinant Hepatitis E Vaccine (Escherichia Coli)
Participants would receive 3 doses of Recombinant Hepatitis E Vaccine (Escherichia Coli) intramuscularly at 0, 1, 6 month.

Locations

Country	Name	City	State
China	Rushan Center for Disease Control and Prevention	Weihai	Shandong

Sponsors (1)

Lead Sponsor	Collaborator
Xiamen Innovax Biotech Co., Ltd

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of Participants Whose Anti-HEV Antibody Seroconverted at One Month After The Third Dose	Measure the number of participants whose anti-HEV antibody seroconverted at month 7 to evaluate the immunogenicity of the Hepatitis E vaccine.	Month 7
Primary	Geometric Mean Concentrations of Anti-HEV Antibody at One Month After The Third Dose	Measure the level of anti-HEV antibody in serum samples at month 7 to evaluate the immunogenicity of the Hepatitis E vaccine.; Wu/ml:World Health Organization (WHO) units per ml. The WHO standard was used to calibrate the antibody quantitative reference.	Month 7
Secondary	Number of Participants With Changes in Liver Function Index Before and One Month After the First Dose	ALT, AST and TBIL were detected in both groups to determine the liver function of participants. The grade of ALT, AST and TBIL was determined according to the rules issued by CFDA. The fluctuations were classified into three categories: "no change" indicated no grade change; "processed" indicated a change from normal to abnormal or an increase in grade; and "improved" indicated a change from abnormal to normal or a decrease in grade or the change from abnormal to normal.	Day 0-Month 1
Secondary	Number of Participants With Changes in Liver Function Index Before and One Month After the Third Dose	ALT, AST and TBIL were detected in both groups to determine the liver function of participants. The grade of ALT, AST and TBIL was determined according to the rules issued by CFDA. The fluctuations were classified into three categories: "no change" indicated no grade change; "processed" indicated a change from normal to abnormal or an increase in grade; and "improved" indicated a change from abnormal to normal or a decrease in grade or the change from abnormal to normal.	Month 6-Month 7
Secondary	Number of Participants With Changes in Liver Function Index Before The First Dose and One Month After the Third Dose	ALT, AST and TBIL were detected in both groups to determine the liver function of participants. The grade of ALT, AST and TBIL was determined according to the rules issued by CFDA. The fluctuations were classified into three categories: "no change" indicated no grade change; "processed" indicated a change from normal to abnormal or an increase in grade; and "improved" indicated a change from abnormal to normal or a decrease in grade or the change from abnormal to normal.	Day0-Month 7
Secondary	Number of Participants Who Experienced Any Adverse Reactions/Events	Any adverse reactions/events contains solicited and unsolicited adverse reactions/events during the whole period of observation.	Day 0-Month 7
Secondary	Number of Participants Who Experienced Solicited Adverse Reactions/Events	Number of participants who experienced local, system adverse reactions/events within 7 days after each vaccination.	Day 0-Day 7
Secondary	Number of Participants Who Experienced Solicited Local Adverse Reactions/Events	Number of participants who experienced solicited local adverse reactions/events within 7 days after each vaccination.	Day 0-Day 7
Secondary	Number of Participants Who Experienced Solicited System Adverse Reactions/Events	Number of participants who experienced solicited system adverse reactions/events within 7 days after each vaccination.	Day 0-Day 7
Secondary	Number of Participants Who Experienced Unsolicited Adverse Reactions/Events	Number of participants who experienced unsolicited adverse reactions/events during the whole period of observation.	Day 0-Month 7