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CompletedNCT00641082Updated Apr 25, 2012

A Double-Blind Randomized Clinical Trial Comparing the Safety and Antiviral Activity of 48-week Clevudine and Adefovir Dipivoxil in HBeAg(-) Chronic Hepatitis B With Compensated Liver Function

A Phase 4 interventional study of Clevudine and Adefovir dipivoxil in HBeAg(-) Chronic Hepatitis B With Compensated Liver Function, sponsored by Bukwang Pharmaceutical. Completed at 2 sites in Korea, Republic of. Open to participants aged 18 Years to 60 Years. Per ClinicalTrials.gov, last updated 2012-04-25.

Sponsored by Bukwang Pharmaceutical · Phase 4, Interventional, and Treatment

Phase
Phase 4
Study type
Interventional
Enrollment
43
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
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Study summary

A double-blind randomized, parallel, multicenter with 48 weeks of treatment period. The purpose of this study is to compare the safety and antiviral activity of 48-week Clevudine and Adefovir dipivoxil in HBeAg(-) Chronic Hepatitis B with compensated liver function.

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Conditions studied

  • HBeAg(-) Chronic Hepatitis B With Compensated Liver Function
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In context

Hepatitis A

2,709 studies on the registry are indexed under Hepatitis A; 142 are open to participants now.

This study's enrollment of 43 is below the median of 100 across 1,886 interventional studies indexed under Hepatitis A.

Browse Hepatitis A studies →

Lead sponsor

Bukwang Pharmaceutical is the lead sponsor of 34 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patient is between 18 and 60
  • Patient is documented to be HBsAg positive for > 6 months.
  • Patient with compensated hepatic function.
  • Nucleoside treatment-naÃ-ve subjects of either gender
  • Patient is HBeAg negative. Patient is HBV DNA positive with DNA levels ≥ 1 x 10(5) copies/mL within 30 days of baseline.
  • Patient has ALT levels which are in the range of 2 x ULN and \< 10 X ULN
  • Patient who has not a history of ascites, variceal hemorrhage or hepatic encephalopathy.

Exclusion criteria

Exclusion Criteria

  • Patient is currently receiving antiviral or corticosteroid therapy.
  • Patients previously treated with lamivudine, adefovir, entecavir, telbivudine, clevudine, lobucavir, famciclovir or any other investigational nucleoside for HBV infection.
  • Previous treatment with interferon must have ended at least 6 months prior to the screening visit.
  • Treatment with nephrotoxic drugs, competitors of renal excretion, and/or hepatotoxic drugs within 2 months before study screening or during the study period
  • Subjects who are currently participating in another investigational study or has been taking any investigational drug within the last 4 weeks prior to screening visit.
  • Patient is coinfected with HCV, HDV or HIV.
  • Patient with following clinical evidence

    • Decompensated liver cirrhosis (Child class B,C: CPT score 7) or hepatocellular carcinoma
    • Significant gastrointestinal, renal, bronchopulmonary, neurological, cardiovascular, oncologic or allergic disease
  • Previous organ transplantation
  • Patient has a clinically relevant history of abuse of alcohol or drugs.
  • 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 α-Fetoprotein more than 100ng/mL
  • Patient has Hemoglobin \<11g/dL (Male), 10g/dL (Female) or WBC count \< 3,500/mm3 (PMN\<1,500/mm3) or Platelet count \<50,000/mm3
  • 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]
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Study design

Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
43 participants (actual)

Study arms

  • Experimental
    1

    Clevudine

    Drug: Clevudine

  • Active comparator
    2

    Adefovir

    Drug: Adefovir dipivoxil

Interventions

  • DrugClevudine

    30mg for 48 weeks

    Also known as: Levovir

  • DrugAdefovir dipivoxil

    10mg for 48 weeks

    Also known as: Hepsera

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What researchers measure

Primary outcomes

  1. Proportion of patients with HBV DNA below 300copies/mL

    Time frame: at week 48

Secondary outcomes

  1. The change of HBV DNA from the baseline

    Time frame: at week 24, 48

  2. Proportion of patients with HBV DNA below LOD of RT-PCR

    Time frame: at week 24, 48

  3. ALT normalization rate

    Time frame: at week 24, 48

  4. Proportion of patients with viral breakthrough during 48-week treatment period

    Time frame: at week 24, 48

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Study locations

2 sites
  • Seoul National University Bundang Hospital
    Bundang, Korea, Republic of
  • Seoul National University Hospital
    Seoul, Korea, Republic of
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 25, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00641082
Lead sponsor
Bukwang Pharmaceutical
First posted
Mar 21, 2008
Start date
Feb 2008
Primary completion
Mar 2012
Last update
Apr 25, 2012
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Apr 2012. You cannot join it, but the record below documents what was studied.

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