Safety and Efficacy Study of Clevudine Compared With Clevudine and Vaccine in Patient With HBeAg(+) Chronic HBV
This study has been completed.
Sponsor:
Bukwang Pharmaceutical
Information provided by:
Bukwang Pharmaceutical
ClinicalTrials.gov Identifier:
NCT00501124
First received: July 12, 2007
Last updated: December 21, 2010
Last verified: August 2009
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Purpose
A randomized, parallel, multicenter, active-controlled with 48 weeks of treatment period. Patients will be randomized to receive clevudine alone for 48 weeks or clevudine for 24 weeks followed by 24 weeks of clevudine in addition to monthly HBV vaccination.The purpose of this study is to investigate efficacy of combination of clevudine and HBV vaccine over clevudine alone in patients with chronic hepatitis B infection.
| Condition | Intervention | Phase |
|---|---|---|
|
Hepatitis B |
Drug: Clevudine Biological: Purified hepatitis B surface antigen |
Phase 4 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Phase IV Study to Evaluate the Safety and Efficacy of Clevudine Compared With Clevudine and Vaccine in Patients Chronically Infected With HBV, HBeAg(+) |
Resource links provided by NLM:
Further study details as provided by Bukwang Pharmaceutical:
Primary Outcome Measures:
- Antiviral Activity: Proportion of patients with HBeAg loss [ Time Frame: Screening, Day1(predose), every 4 weeks during treatment period(48weeks) ]
- Safety Endpoints:Laboratory tests, Adverse Events, Vital signs, ECG [ Time Frame: Screening, Day1(predose), every 4 weeks during treatment period(48weeks), ECG: screening, Week48 ]
Secondary Outcome Measures:
- Proportion of patients with HBV DNA below LOD, Biochemical improvement, Proportion of patients with seroconversion [ Time Frame: Screening, Day1(predose), every 4 weeks during treatment period(48weeks) ]
- Immunological endpoints: Alterations in immunological parameters before, after therapy, particularly with regards to the proliferative a [ Time Frame: Day1(predose), Week 8, 16, 24, 28, 32, 40 and 48 ]
| Estimated Enrollment: | 70 |
| Study Start Date: | May 2007 |
| Primary Completion Date: | July 2010 (Final data collection date for primary outcome measure) |
Eligibility| Ages Eligible for Study: | 18 Years to 60 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
Inclusion Criteria:
- Patient is between 18 and 60
- Patient is HBV DNA positive with DNA levels ≥ 5 x 10(6) copies/mL within 30 days of baseline.
- Patient is documented to be HBsAg positive for > 6 months. Patient is HBeAg positive.
- Patient has ALT levels which are in the range of ≥2 x ULN/L at least 2 consecutive visits, at least one month apart and bilirubin levels less than 2.0 mg/dL, prothrombin time of less than 1.7 (INR), a serum albumin level of at least 3.5 g/dL.
- Women of childbearing potential must have a negative urine (β-HCG) pregnancy test 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, lamivudine, adefovir, entecavir, telbivudine or any other investigational nucleoside for HBV infection.
- Patient has a history of ascites, variceal hemorrhage or hepatic encephalopathy.
- Patient is coinfected with HCV, HDV or HIV.
- Patient with clinical evidence of decompensated liver disease or HCC
- ANA > 1:160 and positive anti-smooth muscle antibody as evidence 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]
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00501124
Locations
| Korea, Republic of | |
| Chungbuk National University Hospital | |
| Gaesin-dong, Cheongju Si Heungdeok-gu, Chungcheongbuk-Do, Korea, Republic of | |
| Dankook University Hospital | |
| Anseo-dong, Cheonan Si, Chungcheongnam-Do, Korea, Republic of | |
| Soon Chun Hyang University Cheonan Hospital | |
| Bongmyeong-dong, Cheonan Si, Chungcheongnam-Do, Korea, Republic of | |
| The Catholic University of Korea, Daejeon St. Mary's Hospital | |
| Daeheung-dong, Jung-gu, Daejeon, Korea, Republic of | |
| Chungnam National University Hospital | |
| Daesa-dong, Jung-gu, Daejeon, Korea, Republic of | |
| Eulji University Hospital | |
| Dunsan 2-dong, Seo-gu, Daejeon, Korea, Republic of | |
| Konyang University Hospital | |
| Gasuwon-dong, Seo-gu,, Daejeon, Korea, Republic of | |
Sponsors and Collaborators
Bukwang Pharmaceutical
Investigators
| Principal Investigator: | Heon Young Lee, MD. PhD. | Chungnam National University Hospital |
| Principal Investigator: | Hyeon Woong Yang, MD. PhD. | Eulji University Hospital |
More Information
No publications provided
| Responsible Party: | HY Lee, Chungnam University Hospital |
| ClinicalTrials.gov Identifier: | NCT00501124 History of Changes |
| Other Study ID Numbers: | L-FMAU-402 |
| Study First Received: | July 12, 2007 |
| Last Updated: | December 21, 2010 |
| Health Authority: | South Korea: Korea Food and Drug Administration (KFDA) |
Additional relevant MeSH terms:
|
Hepatitis Hepatitis A Hepatitis B Liver Diseases Digestive System Diseases Hepatitis, Viral, Human Virus Diseases Enterovirus Infections Picornaviridae Infections |
RNA Virus Infections Hepadnaviridae Infections DNA Virus Infections 2'-fluoro-5-methylarabinosyluracil Antiviral Agents Anti-Infective Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 16, 2013