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A Study With Clevudine Monotherapy or Adefovir and Clevudine Combination in Proportion to Roadmap Concept in Patients With HBV Associated-HCC

Primary Purpose

Hepatitis B Associated Hepatocellular Carcinoma

Status
Completed
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
clevudine, Adefovir
Sponsored by
Bukwang Pharmaceutical
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hepatitis B Associated Hepatocellular Carcinoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria

  1. Patient with chronic HBV DNA and/or with symptoms of liver cirrhosis
  2. Patient with Hepatocellular carcinoma evidenced by sonography, CT scan, or MRI scan)
  3. Patient is 18 years and older.
  4. Patient is documented to be HBsAg positive for > 6 months.

    • Laboratory report proving HBsAg positive or HBeAg positive for at least six months
    • IgM anti-HBc negative, IgG anti-HBc positive at screening
  5. Patient is HBV DNA positive with DNA levels ≥ 2,000 IU/mL within 30 days of baseline.
  6. Patient has ALT or AST levels >=40 IU/L
  7. Cell carcinoma/hepatocellular carcinoma patient who is anticipated to live at least 1 year.
  8. Patient who is fully active, able to carry on all pre-disease performance without restriction or restricted in physically strenuous activity but ambulatory and able to carry out work of a light or sedentary nature, e.g., light house work, office work.
  9. Patient who is classified as NYHA functional classification grade 1-2. (NYHA;New York Heart Association)
  10. Patient who is able to give written informed consent prior to study start and to comply with the study requirements.

Exclusion Criteria

  1. Patient is currently receiving antiviral therapy.
  2. Patients previously treated with interferon, peg-interferon or other immunomodulatory within the previous 6 months.
  3. Patients previously treated with clevudine, lamivudine, adefovir, entecavir, telbivudine, tenofovir or any other investigational nucleoside for HBV infection.
  4. Patient is coinfected with HCV, HDV or HIV.
  5. Patient with metastatic malignancy.
  6. Patient with previous liver transplantation
  7. Patient is pregnant or breast-feeding.
  8. Patient has a clinically relevant history of abuse of alcohol or drugs.
  9. Patient use oriental medicine within the previous 2 weeks.
  10. Patient has a significant immunocompromised, gastrointestinal, renal, hematological, psychiatric, bronchopulmonary, biliary diseases excluding asymptomatic GB stone, neurological, cardiac, oncologic(except HCC)or allergic disease or medical illness that in the investigator's opinion might interfere with therapy.
  11. Patient has creatinine clearance less than 60mL/min as estimated by the following formula: (140-age in years) (body weight [kg])/(72) (serum creatinine [mg/dL]) [Note: multiply estimates by 0.85 for women]

Sites / Locations

  • Seoul National University Hospital

Outcomes

Primary Outcome Measures

Proportion of patients with HBV DNA levels < 60 IU/mL

Secondary Outcome Measures

Full Information

First Posted
December 17, 2010
Last Updated
December 16, 2014
Sponsor
Bukwang Pharmaceutical
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1. Study Identification

Unique Protocol Identification Number
NCT01263002
Brief Title
A Study With Clevudine Monotherapy or Adefovir and Clevudine Combination in Proportion to Roadmap Concept in Patients With HBV Associated-HCC
Official Title
An Open Study to Evaluate the Efficacy, Safety and Sustained Effect of Clevudine Monotherapy or Adefovir and Clevudine Combination in Proportion to Roadmap Concept in Patients With Chronic Hepatitis B Associated Hepatocellular Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
June 2010 (undefined)
Primary Completion Date
January 2013 (Actual)
Study Completion Date
September 2013 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Bukwang Pharmaceutical

4. Oversight

5. Study Description

Brief Summary
An open study to evaluate the Efficacy, Safety of Clevudine monotherapy or Adefovir and Clevudine combination in Proportion to Roadmap Concept in patients with chronic hepatitis B Associated Hepatocellular Carcinoma

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hepatitis B Associated Hepatocellular Carcinoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
33 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
clevudine, Adefovir
Intervention Description
Nucleoside-analogue naive patient : Clevudine 30mg qd Assess the complete virological response(HBV DNA < 60 IU/ml) at 24 weeks: Only Clevudine 30mg qd Assess not the complete virological response at 24 weeks : Add Adefovir 10mg qd During medication of Clevudine, virological breakthrough : add adefovir 10mg qd During treatment period, composite virological response : stop the medication and F/U for 2 years Recurrence after stopping treatment(HBV DNA > 2,000IU/ml) retreat medication at composite virological response. complete virological response: HBV DNA < 60 IU/ml virological breakthrough : During antiviral treatment, HBV DNA increased from nadir to 1 log10IU/ml continuously.
Primary Outcome Measure Information:
Title
Proportion of patients with HBV DNA levels < 60 IU/mL
Time Frame
48 week

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria Patient with chronic HBV DNA and/or with symptoms of liver cirrhosis Patient with Hepatocellular carcinoma evidenced by sonography, CT scan, or MRI scan) Patient is 18 years and older. Patient is documented to be HBsAg positive for > 6 months. Laboratory report proving HBsAg positive or HBeAg positive for at least six months IgM anti-HBc negative, IgG anti-HBc positive at screening Patient is HBV DNA positive with DNA levels ≥ 2,000 IU/mL within 30 days of baseline. Patient has ALT or AST levels >=40 IU/L Cell carcinoma/hepatocellular carcinoma patient who is anticipated to live at least 1 year. Patient who is fully active, able to carry on all pre-disease performance without restriction or restricted in physically strenuous activity but ambulatory and able to carry out work of a light or sedentary nature, e.g., light house work, office work. Patient who is classified as NYHA functional classification grade 1-2. (NYHA;New York Heart Association) Patient who is able to give written informed consent prior to study start and to comply with the study requirements. Exclusion Criteria Patient is currently receiving antiviral therapy. Patients previously treated with interferon, peg-interferon or other immunomodulatory within the previous 6 months. Patients previously treated with clevudine, lamivudine, adefovir, entecavir, telbivudine, tenofovir or any other investigational nucleoside for HBV infection. Patient is coinfected with HCV, HDV or HIV. Patient with metastatic malignancy. Patient with previous liver transplantation Patient is pregnant or breast-feeding. Patient has a clinically relevant history of abuse of alcohol or drugs. Patient use oriental medicine within the previous 2 weeks. Patient has a significant immunocompromised, gastrointestinal, renal, hematological, psychiatric, bronchopulmonary, biliary diseases excluding asymptomatic GB stone, neurological, cardiac, oncologic(except HCC)or allergic disease or medical illness that in the investigator's opinion might interfere with therapy. Patient has creatinine clearance less than 60mL/min as estimated by the following formula: (140-age in years) (body weight [kg])/(72) (serum creatinine [mg/dL]) [Note: multiply estimates by 0.85 for women]
Facility Information:
Facility Name
Seoul National University Hospital
City
Seoul
Country
Korea, Republic of

12. IPD Sharing Statement

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A Study With Clevudine Monotherapy or Adefovir and Clevudine Combination in Proportion to Roadmap Concept in Patients With HBV Associated-HCC

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