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N/A N=12,378

Study of Entecavir in Patients With Chronic Hepatitis B Virus (HBV) Infection

Chronic Hepatitis B

Enrolled (actual)
12,378
Serious AEs
0.9%
Results posted
Jul 2018
Primary outcome: Primary: Number of Participants With Adjudicated Overall Malignant Neoplasms — 331; 337 Participants — p=0.3553

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
entecavir (Drug); Other anti-HBV medication (Drug)
Age
Pediatric, Adult, Older Adult · 16+ yrs
Sex
All
Sponsor
Bristol-Myers Squibb
Primary completion
Oct 2016

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Participants With Adjudicated Overall Malignant Neoplasms
331; 337 0.3553
PRIMARY
Number of Deaths
238; 264 0.0676
PRIMARY
Number of Participants With Liver-related HBV Disease Progression
350; 375 0.1182
SECONDARY
Number of Participants With Non-HCC Malignant Neoplasm
95; 81
SECONDARY
Number of Participants With HCC Malignant Neoplasm
240; 263
SECONDARY
Number of Participants With Liver-related Death
46; 48

Summary

The purpose of this study is to prospectively assess the long-term outcomes (benefits and risks) associated with entecavir (ETV) therapy as compared to other antivirals approved for the treatment of chronic HBV infection. For the China substudy, patients randomized to entecavir will have safety and efficacy assessments performed during the first year of the study.

Eligibility Criteria

Inclusion Criteria

  • Chronic HBV infection
  • HBV nucleoside/tide-naive or -experienced
  • Patients who, in opinion of investigator, are appropriate for initiating or modifying their HBV therapy and who are appropriate for a treatment regimen comprised of nucleoside/tide monotherapy with either ETV or another standard of care HBV nucleoside/tide analogue
  • Age 16 and older or minimum age required in a given country

Exclusion Criteria

  • Women who are pregnant or breastfeeding
  • Patients who, in the opinion of the investigator, are expected to have a liver transplant-free survival of less than one year
  • Patients who, in the opinion of the investigator, are virologically controlled on their current treatment regimen and clinically responding to treatment, unless the regimen needs to be modified for medication intolerance
  • Coinfection with HIV
  • History of malignant neoplasm(s), including hepatocellular carcinoma (HCC) and carcinoma in situ (CIS), but excluding non-melanoma skin cancers
  • Patients with chronic renal insufficiency, defined as a creatinine clearance < 50 ml/min who do not have either of the following means of dose reducing ETV:

i. an approved country-specific ETV label which includes the extended interval ETV dose modification method and/or ii. an approved country specific label for the ETV oral solution AND access to the oral solution

  • History of dysplastic liver nodules
  • Known history of allergy to nucleoside/tide analogues
  • Prior or current treatment with entecavir
  • An investigator proposed study regimen which will include only interferon-alfa
  • An investigator proposed study regimen of combination (two or more) HBV nucleoside/tide analogues
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00388674). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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