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A Study to Evaluate the Efficacy and Safety of Clevudine and Peg-interferon in Sequence Compared With Clevudine Alone in the Patients With HBeAg(+) Chronic Hepatitis B or Clevudine and Peg-interferon Sequential Treatment in Patients With Chronic Hepatitis B Who Have HBeAg(+)

Primary Purpose

HBeAg(+) Chronic Hepatitis B

Status
Completed
Phase
Phase 4
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Clevudine
Clevudine + Peg-interferon
Sponsored by
Bukwang Pharmaceutical
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HBeAg(+) Chronic Hepatitis B

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Patient is between 18~60 years
  2. Patient is HBV DNA positive with DNA levels ≥ 5 x 10^5 copies/mL within 30 days of baseline.
  3. Patient is documented to be HBsAg positive for > 6 months and Patient is HBeAg positive.
  4. Patient has ALT levels >=80IU/L, prothrombin time(INR)<1.7 and a serum albumin level of at least 3.5 g/dL.
  5. Patient has hemoglobin levels >=11.5g/dl(if woman) or >=12.5g/dl(if man)
  6. Women of childbearing potential must have a negative urine pregnancy test(β-HCG) taken within 14 days of starting therapy.
  7. Patient 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, immunomodulatory, cytotoxic or corticosteroid therapy.
  2. Patients previously treated with interferon, peg-interferon, clevudine, lamivudine, adefovir, entecavir, telbivudine, tenofovir or any other investigational nucleoside for HBV infection.
  3. Patient is coinfected with HCV or HIV.
  4. Patient with clinical evidence of decompensated liver disease or HCC
  5. Patient has WBC levels < 3.0x10^9/L
  6. Patient has Platelets levels < 90x10^9/L
  7. Patient has alpha fetoprotein levels > 100ng/mL
  8. Patient has a history of Thyroid disease.
  9. Patient has a history of autoimmune hepatitis.
  10. Patient is pregnant or breast-feeding.
  11. Patient is unwilling to use an "effective" method of contraception during the study and for up to 3 months after the use of study drug ceases.
  12. Patient has a clinically relevant history of abuse of alcohol or drugs.
  13. Patient has a significant immunocompromised, gastrointestinal, renal, hematological, psychiatric, bronchopulmonary, biliary diseases excluding asymptomatic GB stone, neurological, cardiac, oncologic or allergic disease or medical illness that in the investigator's opinion might interfere with therapy. The patient with a benign tumor, excluded if judged by an investigator that the continuation of study would be interfered by the tumor.
  14. 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

  • Uijeongbu St.Mary's Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

1

2

Arm Description

Clevudine 30mg

Clevudine 30mg + peg-interferon 180mcg

Outcomes

Primary Outcome Measures

antiviral activity;Proportion of patients with HBV DNA below LOD(HBV DAN levels < 300 copies/mL) by real time PCR

Secondary Outcome Measures

antiviral activity;Proportion of patients with HBV DNA below LOD(HBV DAN levels < 300 copies/mL) by real time PCR
antiviral activity: The change of HBV DNA from the baseline
ALT normalization rate
Proportion sustained complete response of patients with complete response
Immunological endpoints
Proportion of patients with HBeAg loss/ HBeAg seroconversion

Full Information

First Posted
December 19, 2010
Last Updated
December 17, 2014
Sponsor
Bukwang Pharmaceutical
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1. Study Identification

Unique Protocol Identification Number
NCT01264367
Brief Title
A Study to Evaluate the Efficacy and Safety of Clevudine and Peg-interferon in Sequence Compared With Clevudine Alone in the Patients With HBeAg(+) Chronic Hepatitis B or Clevudine and Peg-interferon Sequential Treatment in Patients With Chronic Hepatitis B Who Have HBeAg(+)
Official Title
A Study to Evaluate the Efficacy and Safety of Clevudine and Peg-interferon in Sequence Compared With Clevudine Alone in the Patients With HBeAg(+) Chronic Hepatitis B or Clevudine and Peg-interferon Sequential Treatment in Patients With Chronic Hepatitis B Who Have HBeAg(+)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Completed
Study Start Date
December 2008 (undefined)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Bukwang Pharmaceutical

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
A study to evaluate the efficacy and safety of clevudine and peg-interferon in sequence compared with clevudine alone in the patients with HBeAg(+) chronic Hepatitis B or clevudine and peg-interferon sequential treatment in patients with chronic Hepatitis B who have HBeAg(+)

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HBeAg(+) Chronic Hepatitis B

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
Clevudine 30mg
Arm Title
2
Arm Type
Active Comparator
Arm Description
Clevudine 30mg + peg-interferon 180mcg
Intervention Type
Drug
Intervention Name(s)
Clevudine
Other Intervention Name(s)
Levovir
Intervention Description
30mg,QD
Intervention Type
Drug
Intervention Name(s)
Clevudine + Peg-interferon
Other Intervention Name(s)
Levovir + Pagasys
Intervention Description
30mg, QD(for 24 weeks) + 180mcg,QW(for 24 weeks)
Primary Outcome Measure Information:
Title
antiviral activity;Proportion of patients with HBV DNA below LOD(HBV DAN levels < 300 copies/mL) by real time PCR
Time Frame
At week 48
Secondary Outcome Measure Information:
Title
antiviral activity;Proportion of patients with HBV DNA below LOD(HBV DAN levels < 300 copies/mL) by real time PCR
Time Frame
At week 72
Title
antiviral activity: The change of HBV DNA from the baseline
Time Frame
Screening, Day1(predose), at week 12, 24, 36, 48, 60, 72
Title
ALT normalization rate
Time Frame
Screening, Day1(predose), at week 12, 24, 36, 48, 60, 72
Title
Proportion sustained complete response of patients with complete response
Time Frame
At week 72
Title
Immunological endpoints
Time Frame
Day1(predose), at week 24, 48, 72
Title
Proportion of patients with HBeAg loss/ HBeAg seroconversion
Time Frame
At week 48

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient is between 18~60 years Patient is HBV DNA positive with DNA levels ≥ 5 x 10^5 copies/mL within 30 days of baseline. Patient is documented to be HBsAg positive for > 6 months and Patient is HBeAg positive. Patient has ALT levels >=80IU/L, prothrombin time(INR)<1.7 and a serum albumin level of at least 3.5 g/dL. Patient has hemoglobin levels >=11.5g/dl(if woman) or >=12.5g/dl(if man) Women of childbearing potential must have a negative urine pregnancy test(β-HCG) taken within 14 days of starting therapy. Patient 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, immunomodulatory, cytotoxic or corticosteroid therapy. Patients previously treated with interferon, peg-interferon, clevudine, lamivudine, adefovir, entecavir, telbivudine, tenofovir or any other investigational nucleoside for HBV infection. Patient is coinfected with HCV or HIV. Patient with clinical evidence of decompensated liver disease or HCC Patient has WBC levels < 3.0x10^9/L Patient has Platelets levels < 90x10^9/L Patient has alpha fetoprotein levels > 100ng/mL Patient has a history of Thyroid disease. Patient has a history of autoimmune hepatitis. Patient is pregnant or breast-feeding. Patient is unwilling to use an "effective" method of contraception during the study and for up to 3 months after the use of study drug ceases. Patient has a clinically relevant history of abuse of alcohol or drugs. Patient has a significant immunocompromised, gastrointestinal, renal, hematological, psychiatric, bronchopulmonary, biliary diseases excluding asymptomatic GB stone, neurological, cardiac, oncologic or allergic disease or medical illness that in the investigator's opinion might interfere with therapy. The patient with a benign tumor, excluded if judged by an investigator that the continuation of study would be interfered by the tumor. 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]
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lee Chang Don, MD, PhD
Organizational Affiliation
The catholic university of korea, Uijeongbu ST.Mary's hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Uijeongbu St.Mary's Hospital
City
Uijeongbu
Country
Korea, Republic of

12. IPD Sharing Statement

Learn more about this trial

A Study to Evaluate the Efficacy and Safety of Clevudine and Peg-interferon in Sequence Compared With Clevudine Alone in the Patients With HBeAg(+) Chronic Hepatitis B or Clevudine and Peg-interferon Sequential Treatment in Patients With Chronic Hepatitis B Who Have HBeAg(+)

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