Trial of Lamivudine Treatment in HBeAg Negative Chronic Hepatitis B Patients (in Asia)

Phase 4

Completed

• Conditions: Chronic Hepatitis B

• Registration Number: NCT00338780
• Lead Sponsor: Chinese University of Hong Kong

Brief Summary

The aim is to investigate whether Lamivudine 100mg daily is effective in the long term treatment of HBeAg negative chronic HBV infected patients with active liver disease in Asia

Detailed Description

Recent studies have proved lamivudine a very potent antiviral drug in suppressing viral replication and improving hepatic necro-inflammation with minimal adverse effects in HBeAg positive chronic hepatitis B patients. The efficacy of lamivudine in HBeAg positivce Asian patients has been weel established. However, the evidence in HBeAg negative patients is limited.

In the absence of HBeAg seroconversion, guidance on the clinical management of HBeAg negative hepatitis B patitents treated with lamivudine and data on the efficacy of lamivudine in controlling pre-core HBV disease long-term is still needed. Existing data in HBeAg negative/ HBV DNA positive HBV demonstrate clear and statisticallysignificant serological benefit of lamivudine over placebo during treatment. Limited sustained response was observed post-treatment following a one year treatment period. Whether these results can be applied to patients in Asia is uncertain. This study is therefore intended to further assess te efficacy profile over an extended treatment period in the Asian population.

Study Timeline

• Study Start: 2000-11
• Study Completion: 2005-01
• Study First Submitted: 2006-06-19
• Study First Submitted QC: 2006-06-19
• Study First Posted: 2006-06-20
• Status Verified: 2006-10
• Last Update Submitted: 2006-10-27
• Last Update Posted: 2006-10-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: Not specified

Inclusion Criteria

• Age=>18 years
• HBsAg positive and HBeAg negative for at least 6 months prior to screening
• Serum HBV-DNA postiviet, HBeAg negative and HBeAb positive at the same timepoint on at least one occasion during the last 6 months
• ALT >1.5 to 10 x upper limit of normal for at least two occasions within the previous 6 months and at screening, or ALT > upper limit normal and with at least one biochemical flare-up (ALT > 200IU/l) in the last 12 months.
• Informed writted consent
• Liver biopsy material/ slides taken within the previous 12 months, and at least 5 months after any previous antiviral treatment which show evidence of active liver disease (ie. evidence of necroinflammatory activity)
• Written informed consent

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Exclusion Criteria

• Hepatocellular carcinoma
• ALT > 10xULN at screening or history of acute exacerbation leading to transient decompensation
• Serum hepatitis C, hepatitis D or HIV
• Decompensated liver desease as indicated by any of the following: serum bilirubin >3mg/dL, prothrombin time >=2 seconds prolonged above upper limit of reference range, serum albumin <28g/L, history of variceal haemorrhage, presence of intractable ascites at the screening assessment.
• Encepalopathy
• Planned for liver transplantation or previous liver transplantation
• Evidence of autoimmune hepatitis
• Amylase and/ or lipase > 2 times upper limit of reference range
• Serum creatinine >1.5 times upper limit of reference range
• Haemoglobin < 11g/dL
• WBC count <3x10^9/L
• Platelets <100x10^9
• Serious concurrent medical illness other than hepatitis B
• Use of immunosuppressive therapy, immunomodylatory therapy or chronic antiviral thgerpay with other agents within the previous 6 months or during the study
• Previous treatment with lamivudine or famciclovir within the last 6 months
• History of hypersensitivity to nucleoside analogues
• Women of childbearing potential not practising adequate contraception
• Pregnancy or lactation
• Receipt of any investigational drug within 30 days of the first dose of study drug
• Child-Pugh class B or C cirrhosis

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Proportion of patients with complete response (normalisation of LAT, ie. <1xULN and disappearance of HBV DNA, lower limit of detection), at MOnth 24

Secondary Outcome Measures

Name	Time	Method
Proportion of patients with partial response
Histological improvement at month 24
Proportion of patients with complete response post-treatment (at Month 30)
Proportion of patinets with partial response post-treatment (at Month 30)
Progression of fibrosis
Progression of fibrosis to cirrhosis
HBsAg seroconversion
Safety of treatment

Trial Locations

Locations (1)

Cheng Suen Man Shook Hepatitis Center, Institute of Digestive Disease, The Chinese University of Hong Kong, Prince of Wales Hospital; 🇨🇳 Hong Kong SAR, China