Safety and Antiviral Activity of Clevudine in Patients Infected With Hepatitis B Virus

Bukwang Pharmaceutical

Status and phase: Terminated; Phase 2

Conditions: Hepatitis B

Treatments: Drug: clevudine

Study type: Interventional

Funder types: Industry

Identifiers

NCT00305019

L-FMAU-201

Details and patient eligibility

About

The purpose of this study is to determine the antiviral effects and safety of clevudine 30 mg once a day (QD) and 50 mg QD in patients infected with hepatitis B virus (HBV).

Sex: All

Ages: 18 to 60 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Patient who is between 18 and 60 years of age, inclusive

2. Patient who is HBV DNA positive with DNA levels at screening more than 3 x 10^6 copies/mL.

3. Patient who is documented to be hepatitis B surface antigen (HBsAg) positive for > 6 months. Patient is HBeAg positive and anti-HBe negative.

   Evidence of HBsAg (+) for the previous 6 months may include the following:

   • documentation of HBsAg (+) for the previous 6 months
   • documentation of HBsAg (+) for the previous 3 months and IgM anti-HBc negative at screening
   • IgM anti-HBc negative and IgG anti-HBc positive at screening

4. Patient who has ALT levels which are in the range of more than 2 to less than 10 times the upper limit of normal (x ULN) and bilirubin levels < 1.5 x ULN.

5. Female patient with a negative serum (HCG) pregnancy test taken within 14 days of starting therapy.

6. Patient who is able to give written informed consent prior to study start and to comply with the study requirements.

7. Patients who continue to meet the following criteria after completion of the Week 36 visit will have additional follow-up visits at Week 40, 44, 48:

   • have received no additional therapy since completion of 12 weeks of treatment of L-FMAU and
   • continue with period 1 log10 decrease in HBV DNA from baseline.

Exclusion criteria

1. Patient who is currently receiving antiviral, immunomodulatory or corticosteroid therapy.
2. Patients previously treated with lamivudine, lobucavir, adefovir or any other investigational nucleoside for HBV infection.
3. Patients with previous treatment with interferon that have ended less than 6 months prior to the screening visit.
4. Patient who has a history of ascites, variceal hemorrhage or hepatic encephalopathy.
5. Patient who is coinfected with hepatitis C virus (HCV), hepatitis D virus (HDV) or HIV.
6. Patient with clinical evidence of cirrhosis or hepatocellular carcinoma
7. Patient who is pregnant or breast-feeding.
8. Patient who is unwilling to use an "effective" method of contraception during the study and for up to 30 days after the use of study drug ceases. For males, condoms should be used. Females must be surgically sterile (via hysterectomy or bilateral tubal ligation), post-menopausal or using at least a medically acceptable barrier method of contraception (i.e., intrauterine device [IUD], barrier methods with spermicide or abstinence)
9. Patient who has a clinically relevant history of abuse of alcohol or drugs.
10. Patient who has a significant gastrointestinal, renal, hepatic (decompensated), bronchopulmonary, neurological, cardiovascular, oncologic or allergic disease.
11. Patient who has creatinine clearance less than 60 mL/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]

Patients found to have tyrosine, methionine, aspartate, aspartate (YMDD) HBV DNA polymerase mutation after the enrollment will be excluded from the efficacy evaluation but included in the safety evaluation.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind