A Phase 4 interventional study of Lamivudine in Chronic Hepatitis B, sponsored by Kaohsiung Medical University Chung-Ho Memorial Hospital. Status unknown at 1 site in Taiwan. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-01-13.
Sponsored by Kaohsiung Medical University Chung-Ho Memorial Hospital · Phase 4, Interventional, and Treatment
Current treatment guidelines indicate that oral antiviral agents for HBeAg-positive chronic hepatitis B virus infection (CHB) can be stopped if the patient has undergone HBeAg seroconversion with HBV-DNA loss measured at two consecutive occasions at least 6 months apart (primary treatment endpoint). Stopping treatment can be considered if undetectable HBV-DNA has been documented on three separate occasions 6 months apart in HBeAg-negative patients. However, oral antiviral drugs currently approved for the treatment of CHB have relatively limited sustained long-term efficacy and a large proportion of patients will suffer from HBV recurrence after stopping treatment.
The purposes of this study are:
A prospective, open-label, multicenter study will enroll 500 treatment-naïve CHB patients who received at least 3-year of oral antiviral agents. With their voluntary decision after consultation, 250 patients will receive Lamivudine extending therapy for 5 years and the other 250 patients will receive follow-up and serve as controls. The primary outcome measurement is HBV DNA recurrence, whilst the secondary outcome measurement is liver-related outcomes and associated predictive factors
2,709 studies on the registry are indexed under Hepatitis A; 142 are open to participants now.
This study's planned enrollment of 500 is above the median of 100 across 1,886 interventional studies indexed under Hepatitis A.
Browse Hepatitis A studies →Kaohsiung Medical University Chung-Ho Memorial Hospital is the lead sponsor of 281 studies on the registry; 57 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
250 treatment-naïve CHB patients who received at least 3-year of oral antiviral agents will receive Lamivudine extending therapy for 5 years.
Drug: Lamivudine
250 treatment-naïve CHB patients who received at least 3-year of oral antiviral agents will receive follow-up.
Lamivudine, 100mg/day, per os
Also known as: Zeffix
Rate of HBV DNA recurrence
Time frame: up to 12 months
Associated predictive factors of HBV DNA recurrence
Time frame: up to 12 months
Rate of drug resistant mutation
Time frame: up to 12 months
Rate of clinical relapse in Group B (non-intervention)
clinical relapse means HBV DNA\>2000 IU/mL plus ALT \> 2 fold upper limit of normal (ULN) in end of entecavir (ETV) normal alanine aminotransferase (ALT) or 2 fold elevation in end of ETV abnormal ALT patients
Time frame: up to 12 months
Rate of severe reactivation or death
severe reactivation means alanine aminotransferase (ALT) \> 10 fold upper limit of normal plus either total bilirubin \> 2 mg/dL or prothrombin time prolong \> 3 seconds
Time frame: up to 12 months
This study is status unknown, as verified in Jan 2015. You cannot join it, but the record below documents what was studied.
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Kaohsiung Medical University Chung-Ho Memorial Hospital