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Status unknownNCT02337127Updated Jan 13, 2015

Lamivudine Extending Therapy in Chronic Hepatitis B Patients After 3-year of Oral Antiviral Agents

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

The sponsor has not verified this record recently (last verified Jan 2015), so the status shown — last known as Recruiting — may be out of date.
Phase
Phase 4
Study type
Interventional
Enrollment
500
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
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Study summary

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.

Read the detailed description

The purposes of this study are:

  1. To evaluate the long-term efficacy of Lamivudine extending therapy in CHB patients who received at least 3-year of oral antiviral agents.
  2. To evaluate the long-term outcomes and predictive factors of Lamivudine extending therapy in CHB patients who received at least 3-year of oral antiviral agents.

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

02

Conditions studied

03

In context

Hepatitis A

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 →

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Male and female patients >=18 years of age
  2. Negative serum HBV DNA within 3 months prior to entry
  3. ALT \<1.5 ULN within 3 months prior to entry
  4. Negative urine or serum pregnancy test (for women of childbearing potential) documented within the 24-hour period prior to the first dose of test drug. Additionally, all fertile males with partners of childbearing age and females of the Lamivudine treatment arm must be using reliable contraception during the study and for 6 months after treatment completion.

Exclusion criteria

Exclusion Criteria:

  1. Women with ongoing pregnancy or breast feeding
  2. Therapy with any systemic anti-neoplastic or immunomodulatory treatment (including supraphysiologic doses of steroids and radiation) *6 months prior to the first dose of study drug
  3. Any investigational drug *6 weeks prior to the first dose of study drug
  4. Co-infection with active hepatitis A, hepatitis C and/or human immunodeficiency virus (HIV)
  5. Patients who have virological evidence of Lamivudine-associated YMDD mutants.
  6. Patients who have clinical evidence of liver cirrhosis or hepatocellular carcinoma.
  7. History or other evidence of a medical condition associated with chronic liver disease other than HCV (e.g., hemochromatosis, autoimmune hepatitis, metabolic liver disease, alcoholic liver disease, toxin exposures)
  8. Signs or symptoms of hepatocellular carcinoma
  9. History or other evidence of bleeding from esophageal varices or other conditions consistent with decompensated liver disease
  10. Neutrophil count \<1500 cells/mm3 or platelet count \<90,000 cells/mm3 at screening
  11. Serum creatinine level >1.5 times the upper limit of normal at screening
  12. History of severe psychiatric disease, especially depression. Severe psychiatric disease is defined as treatment with an antidepressant medication or a major tranquilizer at therapeutic doses for major depression or psychosis, respectively, for at least 3 months at any previous time or any history of the following: a suicidal attempt, hospitalization for psychiatric disease, or a period of disability due to a psychiatric disease
  13. History of a severe seizure disorder or current anticonvulsant use
  14. History of immunologically mediated disease, chronic pulmonary disease associated with functional limitation, severe cardiac disease, major organ transplantation or other evidence of severe illness, malignancy, or any other conditions which would make the patient, in the opinion of the investigator, unsuitable for the study
  15. Evidence of drug abuse (including excessive alcohol consumption) within one year of study entry
  16. Inability or unwillingness to provide informed consent or abide by the requirements of the study
05

Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
500 participants (estimated)

Study arms

  • Active comparator
    Arm A

    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

  • No intervention
    Arm B

    250 treatment-naïve CHB patients who received at least 3-year of oral antiviral agents will receive follow-up.

Interventions

  • DrugLamivudine

    Lamivudine, 100mg/day, per os

    Also known as: Zeffix

06

What researchers measure

Primary outcomes

  1. Rate of HBV DNA recurrence

    Time frame: up to 12 months

Secondary outcomes

  1. Associated predictive factors of HBV DNA recurrence

    Time frame: up to 12 months

  2. Rate of drug resistant mutation

    Time frame: up to 12 months

  3. 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

Other outcomes

  1. 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

07

Study locations

1 of 1 sites recruiting
  • Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital
    Kaohsiung, NRW, Taiwan
    • Wan-Long Chuang · Contact
    Recruiting
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jan 13, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02337127
Lead sponsor
Kaohsiung Medical University Chung-Ho Memorial Hospital
Responsible party
Sponsor
First posted
Jan 13, 2015
Start date
Jun 2011
Primary completion
May 2015 (estimated)
Completion
May 2016 (estimated)
Last update
Jan 13, 2015

Study contacts

Wan-Long Chuang
Contact
waloch@kmu.edu.tw
Wan-Long Chuang
principal investigator · Kaohsiung Medical University Hospital, Internal Medicine

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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