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Clinical Trials/NCT01079806
NCT01079806
Completed
Phase 3

A Comparative Study of the Antiviral Efficacy and Safety of Entecavir (ETV) Versus Placebo in Pediatric Subjects With Chronic Hepatitis B Virus (HBV) Infection Who Are HBeAg-Positive

Bristol-Myers Squibb16 sites in 2 countries180 target enrollmentJune 30, 2010

Overview

Phase
Phase 3
Intervention
Entecavir
Conditions
Chronic Hepatitis B Virus, Pediatric
Sponsor
Bristol-Myers Squibb
Enrollment
180
Locations
16
Primary Endpoint
Percentage of Participants Who Achieved a Combination of Hepatitis B Virus (HBV) DNA Suppression and Hepatitis B e Antigen (HBeAg) Seroconversion at Week 48
Status
Completed
Last Updated
6 years ago

Overview

Brief Summary

The purpose of this study was to evaluate the safety and efficacy of entecavir in pediatric patients with chronic hepatitis B virus infection

Registry
clinicaltrials.gov
Start Date
June 30, 2010
End Date
March 31, 2018
Last Updated
6 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Arms & Interventions

Entecavir

Participants received entecavir, 0.015 mg/kg up to 0.5 mg, once daily, for 96 to 144 weeks, depending on response

Intervention: Entecavir

Placebo

Participants received placebo, 0 mg, once daily, for 48 to 96 weeks, depending on response

Intervention: Placebo

Outcomes

Primary Outcomes

Percentage of Participants Who Achieved a Combination of Hepatitis B Virus (HBV) DNA Suppression and Hepatitis B e Antigen (HBeAg) Seroconversion at Week 48

Time Frame: At Week 48

Suppression=HBV DNA\<50 IU/mL (approximately 300 copies/mL) using the Roche COBAS TaqMan HBV Test for use with the High Pure System assay; seroconversion=undetectable HBeAg and detectable anti-hepatitis B e antibodies. While the analysis of the primary endpoint was based on a randomized sample size of 123 participants (the Primary Cohort), the size of the overall study population was augmented to 180 randomized participants to meet global regulatory requirements.

Secondary Outcomes

  • Percentage of Participants Who Achieved Sustained HBeAg Seroconversion During Off-treatment Follow up Among Participants Who Achieved HBeAg Seroconversion at End of Dosing (EOD).(Week 48, EOD (2 years))
  • Percentage of Participants With Serum Alanine Aminotransferase ≤1*Upper Limit of Normal at Week 48(At Week 48)
  • Percentage of Participants With Hepatitis B e Antigen (HBeAg) Seroconversion at Week 48 (Undetectable HBeAg and Presence of Anti-HBeAb)(At Week 48)
  • Percentage of Participants With Hepatitis B Virus DNA <Limit of Quantitation (LOQ) at Week 48(At Week 48)
  • Histological Analysis (Percentage) Among Participants With Available Liver Biopsy Data(Between weeks 48 and 96)
  • Percentage of Participants With Hepatitis B Virus (HBV) DNA <50 IU/mL at Week 48(At Week 48)
  • Number of Participants With Laboratory Test Results Meeting the Criteria for Abnormality (Grades 1-4)(Day 1 through Week 48 on blinded therapy)
  • Number of Participants With Adverse Events (Including Palatability Issues), SAEs, Discontinuous Due to Adverse Events, and HBV Disease Progression Through Week 48(Day 1 through Week 48 on blinded therapy)
  • Percentage of Participants With Death as Outcome, Serious Adverse Events (SAEs), Discontinuations Due to Adverse Events (AEs), Related AEs, Grade 2-4 Related AEs, Grade 3-4 AEs, Malignancies, ALT Flares, and Hepatic Disease Progression Through Week 96(Day 1 through Week 96)
  • Number of Participants With Laboratory Test Results Meeting the Criteria for Abnormality (Grades 1-4) (Continued)(Day 1 through Week 48 on blinded therapy)
  • Percentage of Participants Who Maintained HBeAg Seroconversion at Week 96 (End of Blinded Therapy) Among Participants With HBeAg Seroconversion at Week 48(At Week 96)
  • Percentage of Participants With HBeAg Seroconversion on ETV Over-time at Week 96 (All ETV Cohort)(At Week 96)
  • Percentage of Participants With HBeAg Seroconversion (Undetectable HBeAg and Presence of Anti-HBeAb) up to Week 96(up to week 96)
  • Percentage of Participants With HbeAg Loss at Weeks 48 and 96(At 48 and 96 weeks)

Study Sites (16)

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