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Replacement of Lamivudine by Telbivudine to Improve Renal Function

Primary Purpose

Disorder Related to Transplantation, Virus Diseases, Injury Due to Exposure to External Cause

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
telbivudine
Sponsored by
Chang Gung Memorial Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Disorder Related to Transplantation

Eligibility Criteria

16 Years - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  1. Sign inform consent
  2. Age is not less than 16 years old.
  3. Post liver transplantation patient for HBV-related indication.
  4. Chronic hepatitis B transplant patients who are treated by lamivudine for not less than 6 months.
  5. eGRF stage 2-4 patients (15<eGFR<90ml)
  6. Stable liver function, ALT not more than 2 folds of upper limit.

Exclusion Criteria:

  1. Acute rejection with increase CNI dose within a month.
  2. Pregnant or nursing.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    No Intervention

    Experimental

    Arm Label

    Lamivudine group

    Telbivudine group

    Arm Description

    continue Lamivudine

    Telbivudine replaces Lamivudine

    Outcomes

    Primary Outcome Measures

    Renal function measurement
    Measure eGFR when the patients were enrolled, every 2 months and up to 12 months. The most important time point will be to compare eGRF at 6 month and 12 months after medication conversion to the beginning levels. Renal function is improved if eGRF is better after medication conversion.

    Secondary Outcome Measures

    hepatitis B recurrence
    Measure hepatitis B surface antigen every 6 months. If HBs AG appears, hepatitis B recurrence is diagnosed.

    Full Information

    First Posted
    June 3, 2013
    Last Updated
    February 5, 2017
    Sponsor
    Chang Gung Memorial Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02447705
    Brief Title
    Replacement of Lamivudine by Telbivudine to Improve Renal Function
    Official Title
    Replacement of Lamivudine by Telbivudine to Improve Renal Function for Post-transplant Hepatitis B Patients - a Randomized Clinical Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2013
    Overall Recruitment Status
    Completed
    Study Start Date
    June 2013 (undefined)
    Primary Completion Date
    December 31, 2016 (Actual)
    Study Completion Date
    January 31, 2017 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Chang Gung Memorial Hospital

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Nephrotoxicity is one of the adverse effects of lamivudine and dosage of lamivudine has to be reduced if patients' renal function is insufficiency. Telbivudine may improve glomerular filtration rate. This study is to see whether renal function is improved when Lamivudine is replaced by telbivudine in liver transplantation patients.
    Detailed Description
    Liver transplantation is the only effective treatment for the patients with liver failure. Hepatitis B-related liver cirrhosis is the major indication to have liver transplantation in Taiwan. After liver transplantation, prophylaxis of hepatitis B recurrence will be performed by anti-hepatitis B immunoglobulin and anti-viral agents. Currently, lamivudine is the drug the investigators choose to prevent HBV recurrence for many years because it is safe for long-term use. However, nephrotoxicity is one of the adverse effects of lamivudine and dosage of lamivudine has to be reduced if patients' renal function is insufficiency. Recently, the studies on chronic hepatitis B patients showed improvement of glomerular filtration rate for those receiving telbivudine treatment. In this study, the investigators will include our post-transplant HBV patients who have stable liver function, receive lamivudine for prophylaxis of recurrent hepatitis B, and have renal dysfunction in stage II-IV. The patients will be randomized to receive telbivudine or lamivudine continuously at 1:1 ratio. Renal function will be examined at 6 months interval to determine whether renal function is improved. The achievement will determine whether telbivudine is better than lamivudine for the HBV patients with renal dysfunction.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Disorder Related to Transplantation, Virus Diseases, Injury Due to Exposure to External Cause

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2, Phase 3
    Interventional Study Model
    Parallel Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    120 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Lamivudine group
    Arm Type
    No Intervention
    Arm Description
    continue Lamivudine
    Arm Title
    Telbivudine group
    Arm Type
    Experimental
    Arm Description
    Telbivudine replaces Lamivudine
    Intervention Type
    Drug
    Intervention Name(s)
    telbivudine
    Other Intervention Name(s)
    sobivo
    Intervention Description
    telbivudine replace Lamivudine
    Primary Outcome Measure Information:
    Title
    Renal function measurement
    Description
    Measure eGFR when the patients were enrolled, every 2 months and up to 12 months. The most important time point will be to compare eGRF at 6 month and 12 months after medication conversion to the beginning levels. Renal function is improved if eGRF is better after medication conversion.
    Time Frame
    every 2 months, up to 12 months
    Secondary Outcome Measure Information:
    Title
    hepatitis B recurrence
    Description
    Measure hepatitis B surface antigen every 6 months. If HBs AG appears, hepatitis B recurrence is diagnosed.
    Time Frame
    every 6 months, up to 12 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    16 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Sign inform consent Age is not less than 16 years old. Post liver transplantation patient for HBV-related indication. Chronic hepatitis B transplant patients who are treated by lamivudine for not less than 6 months. eGRF stage 2-4 patients (15<eGFR<90ml) Stable liver function, ALT not more than 2 folds of upper limit. Exclusion Criteria: Acute rejection with increase CNI dose within a month. Pregnant or nursing.

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    28884132
    Citation
    Lee WC, Wu TH, Wang YC, Cheng CH, Lee CF, Wu TJ, Chou HS, Chan KM, Lee CS. Renal Function Improvement by Telbivudine in Liver Transplant Recipients with Chronic Kidney Disease. Biomed Res Int. 2017;2017:9324310. doi: 10.1155/2017/9324310. Epub 2017 Aug 13.
    Results Reference
    derived

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    Replacement of Lamivudine by Telbivudine to Improve Renal Function

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