Telbivudine Versus Entecavir in Reducing Serum HBsAg Levels in Patients With HBeAg-positive Chronic Hepatitis B

Chronic Viral Hepatitis B Without Delta-agent Clinical Trial

— TERESA  

Official title:

A Randomized, Open-label Trial Comparing Telbivudine vs, Entecavir in Reducing Serum HBsAg Levels in Patients With HBeAg-positive Chronic Hepatitis B Who Have Achieved Serum HBV DNA Undetectability by Preceding Entecavir Treatment

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01595685
• Other study ID #: AMC2012-0201
• Status: Completed
• Phase: Phase 3
• First received: May 8, 2012
• Last updated: January 24, 2017
• Start date: May 2012
• Est. completion date: December 2014

Study information

• Verified date: January 2017
• Source: Asan Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The goal of chronic hepatitis B (CHB) treatment is complete and permanent eradication of hepatitis B virus (HBV) from patient's body, which is best represented by serum HBsAg loss accompanied by undetectable serum HBV DNA level.

While the most recently approved nucleos(t)ide analogues (NA) have marked antiviral potency and can induce HBV DNA undetectability in the majority of patients through prolonged treatment, NA need to be given long term, almost indefinitely, in most cases because they suppress HBV DNA only during therapy. For example, even after HBeAg-loss by a potent NA, suppression of serum HBV DNA to undetectable level is sustained only in about 23%-37% at 24 weeks off treatment. Thus, continuous therapy with NA until HBsAg clearance remains necessary in a majority of cases.

The recent availability of commercial quantitative assays of serum hepatitis B surface antigen (HBsAg) has enabled quantitative HBsAg to be used as a biomarker for prognosis and treatment response in CHB. It has been suggested that HBsAg decline during lamivudine or entecavir therapy is slower and less pronounced compared to interferon treatment, despite a higher effect on HBV DNA suppression. Based on HBsAg kinetics, it has been estimated that the predicted median time to HBsAg loss in patients treated with lamivudine or entecavir is more than 30 years. Thus, treatment that can induce rapid decline of HBsAg would have clear advantage in reducing the treatment duration required to achieve HBsAg-loss.

Interestingly, in a recent preliminary study, 24-weeks of treatment with telbivudine has induced HBsAg decline as comparable to pegylated interferon treatment. Although there has been no head-to-head trial comparing NAs in inducing HBsAg decline, previous studies consistently suggested that the decline of HBsAg is greater during telbivudine treatment compared with lamivudine or entecavir.

Thus, in this clinical trial, the investigators will investigate whether telbivudine is more effective in inducing HBsAg decline compared with entecavir in HBeAg-positive CHB patients who have achieved undetectable serum HBV DNA by preceding entecavir treatment.

Description:

A single-center randomized active-controlled open-label superiority trial

• Patients will be randomly assigned 1:1 to receive telbivudine (600 mg/day) or ongoing entecavir (0.5 mg/day) for 48 weeks.

• Eligible patients will be randomized using blocks of permuted treatment assignments after stratification by HBsAg level (1,000 IU/mL-5,000 IU/mL and ≥5,000 IU/mL IU/mL) and by entecavir treatment duration (1 year-2 year, ≥2 year).

• Because over 98% of Korean patients with CHB have HBV genotype C,9 HBV genotype will not determined or be regarded as a stratification factor.

• There will be no interruption in entecavir therapy before randomization.

• Patients' treatment information will be retrospectively collected during entecavir treatment phase as well (DNA change, HBeAg status, HBsAg titre, ALT, and treatment duration. etc)

• Patients will be screened within 4 weeks before randomization to determine study eligibility.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 98
• Est. completion date: December 2014
• Est. primary completion date: December 2014
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 80 Years

Eligibility

Inclusion Criteria: All of below

• HBsAg titer > 1,000 IU/mL

• HBeAg positive at study entry and at the baseline of ETV treatment

• HBV DNA undetectable (<15 IU/mL) at least 2 occasions of more than 3 months apart

• Treatment with entecavir (0.5 mg/day) for more than 1 year

• Patient is ambulatory.

• Patient is able and willing to give informed consent.

Exclusion Criteria: Any of below

• Prior exposure to oral nucloes(t)ide analogue other than entecavir

• Prior any exposure to interferon or pegylated interferon

• Cirrhosis with Child-Pugh score =8

• Hepatocellular carcinoma Identified or suspected

• Other malignancy

• Prior organ transplantation

• Under immunosuppressive agent

• Renal insufficiency (serum creatinine > 1.4)

• Pregnant woman or willing to be pregnant woman or man

Related Conditions & MeSH terms

• Chronic Viral Hepatitis B Without Delta-agent
• Hepatitis
• Hepatitis A
• Hepatitis B
• Hepatitis B, Chronic
• Hepatitis, Chronic

Intervention

Drug:
• Telbivudine
Telbivudine 600 mg Daily Oral
• Entecavir
Entecavir 0.5 mg Daily Oral

Locations

Country	Name	City	State
Korea, Republic of	Asan Medical Center	Seoul

Sponsors (1)

Lead Sponsor	Collaborator
Asan Medical Center

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	HBsAg titer at 48 weeks		at 48 weeks
Secondary	Proportion of patients with serum HBsAg decline of =0.5 log10 IU/mL and <1.0 log10 IU/mL		at 48 weeks of treatment
Secondary	Proportion of patients with serum HBsAg decline greater than 1.0 log10 IU/mL		at 48 weeks of treatment
Secondary	Proportion of patients with serum HBsAg loss		at 48 weeks of treatment
Secondary	Proportion of patients with serum HBeAg loss or HBeAg seroconversion		at 48 weeks of treatment
Secondary	Proportion of patients with virologic rebound or genotypic resistance		up to 48 weeks of treatment
Secondary	Proportion of patients with normal ALT		at 48 weeks of treatment
Secondary	Adverse events: Creatine kinase level, GFR, Muscle events, Other AEs		up to 48 weeks of treatment