A Study to Evaluate the Efficacy and Safety of Therapeutic Hepatitis B Vaccine

A randomized, double-blinded, placebo-controlled, parallel, multicenter, phase 2b study to evaluate the efficacy and safety of CVI-HBV-002 in patients with chronic hepatitis B taking Tenofovir disoproxil fumarate/Tenofovir disoproxil

Inclusion criteria

• Adult between 19 to 60 years of age
• Those who have been diagnosed as chronic hepatitis B patients (e.g.HBsAg positive detected for 6 months or more)
• Started treatment with Tenofovir Disoproxil Fumarate(TDF) or Tenofovir Diproxil(TD), oral HBV antiviral agent, for 6 months to 5 years.
• HBsAg ≥ 100 IU/mL, HBV DNA ≤ 100 IU/mL at screening
• HBV DNA ≤ 2000 IU/mL at screening
• ALT ≤ Upper Limit of Normal) x 2 at screening
• Ability to understand and sign a written informed consent form, which must be obtained prior to initiation of study procedures

Exclusion criteria

• Patients with other hepatic disease other than chronic hepatitis B(e.g., hemochromatosis, Wilson disease, alcoholic liver disease, nonalcoholic steatohepatitis, alpha-1 antitrypsin deficiency, etc)
• If any of the following laboratory tests were found at screening

• Total bilirubin > Upper Limit of Normal x 2
• Prothrombin time delayed more than 3 seconds than normal
• Serum Albumin < 30 g/L (3 g/dL)
• Hemoglobin < 9.0 g/dL eGFR < 60 mL/min (Cockcroft-Gault)
• Absolute neutrophil count (ANC) < 1.5 x 10^9 /L (1500 /mm3)
• Platelet count < 100 x 10^9 /L (100 x 10^3 /mm3)
• Serum creatinine > 1.5 mg/dL
• Serum amylase > 2 x ULN and Lipase > 2 x ULN
• A history of ascites, jaundice, varicoses vein bleeding, hepatic encephalopathy, or other signs of liver failure
• Treated with oral antiviral agents or interferon therapy other than TDF(or TD)
• In case of receiving nephroxic drugs(Aminoglycosides, Amphotericin B, NSAIDs, etc.) within 14 days prior to screening
• When hepatotoxic drugs(Erythromycin, Ketoconazole, Rifampin, Fluconazole, Dapsone, etc.) are administered within 14 days prior to screening
• Patients with active bacterial, viral or fungal infections requiring systemic treatment
• Patients diagnosed with Alpha-fetoprotein (AFP) >50 ng/mL or with Hepatocellular Carcinoma (HCC) in screening
• Of those who have received immunosuppressive drugs within 6 months prior to screening, patients suspected of having decreased immunity by the judgment of the Investigator
• Patients who have received high dose (prednisone 20mg or more*) systemic corticosteroids for a long period of time(consecutive 14 days or longer) within 3 months before screening (at the discretion of the investigator in case of local corticosteroids)

• Corresponding to 125 mg of cortisone, 100 mg of hydrocortisone, 20 mg of prednisone, 16 mg of methylpreprednisolone, 16 mg of triamsynolone, 3 mg of dexamethasone and 2.4 mg of betametasone.
• Patients who have been diagnosed with malignant tumors within 5 years before screening, or who have recurred malignant tumors(in case of benign tumors, if the Investigator considers that the progress of the clinical trial is not affected during the clinical trial)
• Organ transplantation recipients
• Patients with serious illnesses, such as heart failure, renal failure, and pancreatitis, other than liver disease
• Patients with a history of serious heart disease (NYHA Functional Class III or IV heart failure, myocardial infarction within 6 months, ventricular tachyarrhythmias requiring treatment or unstable angina)
• Patients with seizure disorders who require anticonvulsant therapy
• HbA1c>7.5%
• SBP≥140mmHg or DBP≥90mmHg
• Patients infected with hepatitis C(HCV), hepatitis D(HDV) or human immunodeficiency virus(HIV)
• A hypersensitivity or anaphylactic reaction to the components of the clinical trial drug or HBV vaccine components
• Continued drinking(>21 units/week, 1 unit = 10g of pure alcohol) or alcohol dependence
• Pregnancy or breastfeeding, or cannot agree with the approved method of contraception of the patient and partner during the clinical trial(e.g., infertility surgery, intrauterine contraceptive, oral contraceptive and concomitant use of diaphragm or condom, other hormonal delivery systems and concomitant use of diaphragm or condom)
• Patients who are concerned about the deterioration of daily function due to mental illness or who cannot understand the purpose and method of this trial
• Patient who has potential to severe febrile or systemic reaction
• Patients who are scheduled to participate in other clinical trials after enrolling in this trial, or have participated in other clinical trials within 3 month of enrollment in this trial
• Others those who are considered to be difficult to perform the clinical trial by the judgment of the Investigator