Study of Therapeutic Vaccination With Intensified Schedule Plus Pegasys Dual Therapy on Chronic Hepatitis B Infection

Hepatitis B, Chronic Clinical Trial

— E+VIP  

Official title:

Phase4, to Compare Efficacy and Safety of Therapeutic Vaccination With Intensified Schedule Plus Pegylated Interferon Dual Therapy on Seroclearance of HBS Antigen in Patients With Complete Virological Response Induced by Entecavir

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02097004
• Other study ID #: E+VIP
• Status: Completed
• Phase: Phase 4
• Start date: April 2014
• Est. completion date: March 13, 2018

Study information

• Verified date: May 2018
• Source: Seoul National University Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

A randomized, Open label, Single center, Prospective study to compare efficacy and safety of Therapeutic Vaccination with Intensified schedule plus Pegylated Interferon dual Therapy on Seroclearance of Hepatitis B virus Surface Antigen in Patients with Complete Virological Response Induced by Entecavir

Description:

A randomized, Open label, Single center, Prospective study to compare efficacy and safety of Therapeutic Vaccination with Intensified schedule plus Pegylated Interferon dual Therapy on Seroclearance of Hepatitis B virus Surface Antigen in Patients with Complete Virological Response Induced by Entecavir (E + VIP)

Recruitment information / eligibility

• Status: Completed
• Enrollment: 111
• Est. completion date: March 13, 2018
• Est. primary completion date: January 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 75 Years

Eligibility

Inclusion Criteria:

1. Age between 20 and 75 year-old

2. HBsAg-positive for > 6 months apart (medical history can be alternative)

3. Currently being treated with entecavir 0.5 mg/day for more than 18 months

4. Undetectable HBV DNA in serum (<20IU/mL) and HBeAg-negative or positive for > 1year

5. HBsAg titer < 3,000 IU/mL

6. ALT<300 IU/L

7. Signed written informed consent after being instructed about the objective and procedure of the clinical study

Exclusion Criteria:

1. Patients with decompensated liver cirrhosis, any one of the following ? Serum bilirubin > 3 mg/dL

? Prothrombin time > 6 seconds prolonged or INR >2.3

? Serum albumin < 2.8 g/dL

? History of ascites, variceal hemorrhage, or hepatic encephalopathy

? Child-Pugh score =7 (Child-Pugh class B or C)

2. Patients who have evidence of renal insufficiency defined as serum creatinine>1.5 mg/dL

3. Patients with psychological problem including depression

4. Patients who have previous/current significant co-morbidities including congestive heart failure, chronic kidney disease, hematologic disease and malignancy including hepatocellular carcinoma(patients with malignancy cured 5 years before screening can be enrolled)

5. Patients with seropositivity for anti-HCV, anti-HDV or anti-HIV

6. Patients who have excessive alcohol consumption (> 30 g/day)

7. Patients who have evidence of autoimmune hepatitis, hemochromatosis or Wilson's disease

8. Pregnant or breast feeding females or plan for pregnancy or no contraception

9. Patients with disease may deteriorate with interferon therapy(eg, autoimmune thyroiditis)

10. Patients who have an psoriasis

11. Patients who have history of antiviral-resistant HBV after previous treatment with oral antiviral agents

12. Previous diagnosis with immunodeficiency or concomitant treatment of immune suppressive agent or previous organ transplantation Recipients

13. Patients who have a history of hypersensitivity to study drug

14. Uncontrollable seizure, convulsion and/or central nervous system disorders

15. Patients with severe bone marrow disorder or with history of hypersensitivity to biologic agent such as vaccine.

16. Neutrophil count < 1,500/mm3 or platelet count < 75,000/mm3 or hemoglobin < 10 g/dl

17. Patients with Pulmonary disease (in case of history of pulmonary disease with complete recovery, enrollment is on investigator's discretion)

18. Patients who have a fever = 38 °C at the baseline

19. Patients who have a risk of febrile response or systemic reaction

20. Patients who the investigator deems inappropriate to participate in this study

Related Conditions & MeSH terms

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

Intervention

Biological:
• Peginterferon alfa-2a
once weekly 180 µg subcutaneous injection for 48 weeks
• HBV vaccination
1.0 mL (20 µg) intramuscular injection at 4, 8, 12 and 28 weeks

Drug:
• Entecavir
Continue Entecavir(0.5mg) for 100 weeks

Locations

Country	Name	City	State
Korea, Republic of	Seoul National University	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The rate of HBsAg-seroclearance	The rate of HBsAg-seroclearance at the time point of at weeks 100 in the sequential treatment group (24 weeks after termination of treatment) versus control group(ETV monotherapy) at weeks 100.	The rate of HBsAg-seroclearance at the time point of at weeks 100
Secondary	The rate of HBsAg-seroconversion	The rate of HBsAg-seroconversion at weeks 100 in the sequential treatment group versus control group(ETV monotherapy) at weeks 100.	The rate of HBsAg-seroconversion at weeks 100
Secondary	The change of HBsAg level from baseline	The change of HBsAg level from baseline at weeks 100 in the sequential treatment group versus control group(ETV monotherapy) at weeks 100.	The change of HBsAg level from baseline at weeks 100
Secondary	The change of HBsAg-seroclearance	The change of HBsAg-seroclearance in the concomitant treatment group versus control group(ETV monotherapy) for exploratory assessment.	The change of HBsAg-seroclearance at weeks 4, weeks 12, weeks 24, weeks 36, weeks 48, weeks 60, weeks 72, weeks 96, weeks 100, weeks 148
Secondary	The change of HBsAg-seroconversion	The change of HBsAg-seroconversion in the concomitant treatment group versus control group(ETV monotherapy) for exploratory assessment.	The change of HBsAg-seroconversion at weeks 4, weeks 12, weeks 24, weeks 36, weeks 48, weeks 60, weeks 72, weeks 96, weeks 100, weeks 148
Secondary	The change of HBsAg level	The change of HBsAg level in the concomitant treatment group versus control group(ETV monotherapy) for exploratory assessment.	The change of HBsAg level at weeks 4, weeks 12, weeks 24, weeks 36, weeks 48, weeks 60, weeks 72, weeks 96, weeks 100, weeks 148