Efficacy and Safety of Switching to Vemliver From Entecavir in Chronic Hepatitis B Patients Previously Treated With Entecavir

NCT ID: NCT06000657

Last Updated: 2025-03-18

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE4
• Total Enrollment: 196 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-08-28
• Study Completion Date: 2025-02-03

Brief Summary

Enroll patients who are pre-treated with Entecavir at least 24 weeks and confirmed HBV antiviral (HBV DNA <69 IU/mL) effects.

Subjects are given one test drug or comparator once a day for 48 weeks according to the results of random assignments, and their HBV antiviral inhibitory effect and safety are evaluated at 24 and 48 weeks visits.

Detailed Description

Enroll patients who are pre-treated with Entecavir at least 24 weeks and confirmed HBV antiviral (HBV DNA <69 IU/mL) effects.

At the time of screening, potential test subjects of this test are selected by retrospectively collecting information on disease status and prognosis-related factors, including ETV administration information, among those who voluntarily agreed to participate in this clinical trial.

HBeAg status (positive vs. positive) through Visit 1's Heptatis B Serology test before administering clinical trial drugs to test subjects who finally qualify for selection/exclusion criteria at the baseline. Voice) is set as a stratification factor and is randomly assigned to each test institution.

Subjects are given one test drug or comparator once a day for 48 weeks according to the results of random assignments, and their HBV antiviral inhibitory effect and safety are evaluated at 24 and 48 weeks visits.

Conditions

Hepatitis B, Chronic

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Treatment group

Chronic Hepatitis B patients who pretreated with Entecavir

Group Type: EXPERIMENTAL

Vemliver tablet

Intervention Type: DRUG

Chronic Hepatitis B Patients Who Pretreated with Entecavir switching to Vemliver tab (Tenofovir Alafenamide Hemitartrate)

Comparator group

Chronic Hepatitis B patients who pretreated with Entecavir

Group Type: ACTIVE_COMPARATOR

Baracross Tablet

Intervention Type: DRUG

Chronic Hepatitis B Patients Who Pretreated with Entecavir continuting treatement with Baracross Tablet

Interventions

Vemliver tablet

Chronic Hepatitis B Patients Who Pretreated with Entecavir switching to Vemliver tab (Tenofovir Alafenamide Hemitartrate)

Intervention Type: DRUG

Baracross Tablet

Chronic Hepatitis B Patients Who Pretreated with Entecavir continuting treatement with Baracross Tablet

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Participants aged 19 years and older as of the date of written consent.

2. Individuals with a positive HBsAg for at least 24 weeks prior to screening or a history of chronic hepatitis B.

3. Individuals with chronic hepatitis B who have been receiving ETV 0.5 mg as monotherapy for at least 24 weeks and have expressed the intention to switch to Barakros tablets or Bemeliver tablets.

4. Participants with good adherence to ETV 0.5 mg monotherapy confirmed through questionnaire (≥80%).

5. Participants who have demonstrated viral suppression efficacy (HBV DNA <69 IU/mL) and are deemed to require monotherapy with Tenofovir alafenamide or ETV for at least 48 weeks.

6. Individuals who voluntarily agree to participate in the clinical trial and have signed the informed consent form.

Exclusion Criteria

Medical history or surgical (treatment) history at the time of screening visit:

① Individuals diagnosed with substance abuse or alcohol addiction within the past year of screening.

• Confirmed diagnosis of malignant tumors, including liver cancer, within the past 5 years.

• Organ or bone marrow transplant recipients.

Coexisting conditions at the time of screening visit:

① Non-selective clinical signs/symptoms in non-selective liver disease.

• Galactose intolerance, lactase deficiency, or glucose-galactose malabsorption.

• Kidney disease patients requiring hemodialysis or peritoneal dialysis. ④ Other clinically significant cardiovascular, respiratory, neurological, or psychiatric conditions considered inappropriate for participation in the clinical trial according to the participant's judgment.

Laboratory test results at the time of screening visit:

① Co-infection with HCV and HIV.

• Hemoglobin <8 g/dL.

• Impaired renal function. ④ ALT >3 × ULN.

Anticipated use of the following drugs during the specified period:

During the clinical trial period:

• Immunosuppressants.

• Systemic corticosteroids administered at a dose equal to or greater than a restricted dose for more than 2 weeks.

• Drugs affecting renal excretion, drugs with renal or hepatic toxicity. ④ Anti-HBV drugs other than investigational medicinal products. ⑤ Hepatotonics.

• Minimum Eligible Age: 19 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Daewoong Pharmaceutical Co. LTD.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Yoon Jun Kim

Role: PRINCIPAL_INVESTIGATOR

Seoul National University Hospital

Locations

Seoul National University Hospital

Seoul, , South Korea

Countries

South Korea

Other Identifiers

DWVMLV_P401

Identifier Type: -

Identifier Source: org_study_id