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Systematic Review of Antiretroviral Treatments for Chronic Hepatitis B (CHB)

Bristol-Myers Squibb (BMS) logo

Bristol-Myers Squibb (BMS)

Status

Completed

Conditions

Hepatitis B, Chronic

Study type

Observational

Funder types

Industry

Identifiers

NCT01155427
AI463-186

Details and patient eligibility

About

The purpose of this study is to support the clinical value of entecavir by assessing the relationship between viral load and histological improvement.

Full description

Systematic review of prospective clinical trials

Enrollment

100 patients

Sex

All

Ages

16+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with CHB diagnosis and no co-infection with Hep A, Hep C, Hep D, or HIV
  • Age 16 years or older
  • No post-transplant patients
  • RCT, non-randomized trials, prospective cohort studies, prospectively analyses case series published since 2003
  • At least one arm of trial must include monotherapy with entecavir, lamivudine, tenofovir, adefovir, or telbivudine
  • Study arms must include at least 10 patients
  • Follow-up of at least 48 weeks
  • Published results available in English language

Exclusion criteria

  • N/A

Trial design

100 participants in 5 patient groups

entecavir
Description:
Patients initiating special antiviral treatments for CHB
tenofovir
Description:
Patients initiating special antiviral treatments for CHB
lamivudine
Description:
Patients initiating special antiviral treatments for CHB
telbivudine
Description:
Patients initiating special antiviral treatments for CHB
adefovir
Description:
Patients initiating special antiviral treatments for CHB

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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