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Efficacy of Clevudine Plus Lamivudine for Lamivudine-resistant Chronic Hepatitis B Patients

I

Inje University

Status and phase

Terminated
Phase 4

Conditions

Chronic Hepatitis B

Treatments

Drug: clevudine
Drug: lamivudine
Drug: adefovir

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00798460
IB-0809-055

Details and patient eligibility

About

The purpose of this study is to determine the optimal antiviral treatment for lamivudine resistant hepatitis B patients.

Full description

Lamivudine with adefovir combination therapy has been known as effective antiviral therapy for lamivudine resistant chronic hepatitis B patients. It is superior to adefovir monotherapy since the incidence of viral breakthrough of combination therapy used to be less than that of adefovir monotherapy in lamivudine resistant chronic hepatitis B patients. Clevudine, which is being marketed in Korea, is a nucleoside analogue of the unnatural beta-L configuration that has potent activity against HBV. It has demonstrated potent antiviral efficacy and significant biochemical improvement after 24 weeks of therapy. We hypothesized that clevudine plus adefovir combination therapy for lamivudine resistant patients might be as effective as the lamivudine plus adefovir combination therapy.

In detail, we designed to perform this clinical study comparing the combination of clevudine and adefovir with lamivudine plus adefovir in lamivudine resistant chronic hepatitis B patient. Total treatment duration of both groups will be 12 months, and compare the efficacy of antiviral effects of these drugs.

Enrollment

30 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • HBsAg positive and anti-HBs negative more than 6 months
  • YMDD mutation (+)during lamivudine therapy
  • Serum ALT more than two times upper normal value

Exclusion criteria

  • HAV IgM Ab + and/or HCV Ab+ and/or HDV Ab and/or HIV Av+
  • The sign of decompensated liver disease
  • Pregnant or lactating woman
  • The history of hemoglobinopathy, autoimmune hepatitis, alcoholic liver disease
  • Hemoglobin less than 8 g/dL (male), 7.5g/dL (female) or neutrophil count less than 1500/mm3 or platelet count less than 50,000/mm3
  • Serum creatinine more than 1.5 times upper normal limit value
  • The sign of malignancy or suggestive of malignancy or the history of malignancy, the recurrence rate within 2 years of which is more than 20%

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

30 participants in 2 patient groups

Lamivudine plus adefovir
Active Comparator group
Treatment:
Drug: lamivudine
Drug: adefovir
Clevudine plus adefovir
Active Comparator group
Treatment:
Drug: adefovir
Drug: clevudine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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