Status:
COMPLETED
Entecavir Plus Adefovir Combination Therapy Versus Entecavir Monotherapy vs Therapy With Adefovir Plus Lamivudine for Chronic Hepatitis B Infected Subjects With Lamivudine-resistant Virus
Lead Sponsor:
Bristol-Myers Squibb
Conditions:
Hepatitis B, Chronic
Eligibility:
All Genders
16+ years
Phase:
PHASE3
Brief Summary
The purpose of this study is to evaluate the effectiveness of entecavir plus adefovir combination therapy versus entecavir monotherapy or therapy with adefovir plus lamivudine
Eligibility Criteria
Inclusion
- Evidence of lamivudine (LVD) resistance
- Subjects must have a history of previous LVD treatment at screening, and must have evidence of at least 1 LVD resistance substitution (valine, isoleucine, or serine) at reverse transcriptase codon 204 (M204V/I/S)
- Nucleoside- and nucleotide-naive, except for LVD, and had chronic hepatitis B (HBV) infection
- Compensated liver function and must have met ALL of the following criteria:International normalization ratio (INR) ≤ 1.5; Serum albumin ≥ 3 g/dL (≥ 30 g/L); Serum total bilirubin ≤ 2.5 mg/dL (≤ 42.75 μmol/L)
- HBV DNA \> 1.72 x 10\*4\* IU/mL (approximately 10\*5\* copies/mL)
- Documentation of hepatitis B e antigen (HBeAg) positive and hepatitis B e antibody (HBeAb) negative status at screening
- alanine aminotransferase (ALT) ≤ 10 \* upper limit of normal (ULN) at screening
- Women of childbearing potential (WOCBP) must be using an adequate method of contraception to avoid pregnancy throughout the study (and for up to 6 weeks after the last dose of investigational product) in such a manner that the risk of pregnancy is minimized
- WOCBP include any female who has experienced menarche and who has not undergone successful surgical sterilization (hysterectomy, bilateral tubal ligation or bilateral oophorectomy) or is not postmenopausal. Post menopausal is defined as:
- Women who are using oral contraceptives, other hormonal contraceptives (vaginal products, skin patches, or implanted or injectable products), or mechanical products such as an intrauterine device or barrier methods (diaphragm, condoms, spermicides) to prevent pregnancy, or are practicing abstinence or where partner is sterile (e.g., vasectomy), should be considered to be of child bearing potential
- WOCBP must have a negative serum or urine pregnancy test (minimum sensitivity 25 IU/L or equivalent units of human chorionic gonadotropin) within 72 hours prior to the start of investigational product
Exclusion
- Evidence of decompensated cirrhosis
- Coinfection with human immunodeficiency virus, hepatitis C virus , or hepatitis D virus
- Women who are pregnant or breastfeeding
- Sexually active fertile men not using effective birth control if their partners were WOCBP
- Laboratory values out of protocol-specified range
Key Trial Info
Start Date :
March 1 2008
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
July 1 2012
Estimated Enrollment :
629 Patients enrolled
Trial Details
Trial ID
NCT00410202
Start Date
March 1 2008
End Date
July 1 2012
Last Update
November 21 2013
Active Locations (67)
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1
University Of Connecticut Health Center
Farmington, Connecticut, United States, 06030
2
Local Institution
Concord, New South Wales, Australia, 2139
3
Local Institution
Randwick, New South Wales, Australia, 2031
4
Local Institution
Porto Alegre Rs, Rio Grande do Sul, Brazil, 90035