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WithdrawnNCT00986778

Entecavir Plus Adefovir in Lamivudine-Resistant Patients

A Comparative Study of Entecavir vs Adefovir Plus Lamivudine vs Combination Entecavir Plus Adefovir in Lamivudine-Resistant Chronic Hepatitis B Chinese Subjects

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Bristol-Myers Squibb · Industry
Sex
All
Age
16 Years
Healthy volunteers
Not accepted

Summary

Combination therapy with entecavir 1.0 mg plus adefovir 10 mg has superior antiviral activity compared with either entecavir monotherapy 1.0 mg or adefovir 10 mg plus lamivudine 100 mg in Chinese adults with lamivudine-resistant chronic hepatitis B infection

Conditions

Interventions

TypeNameDescription
DRUGLamivudineTablets, Oral, 100mg, once daily, 48-96 weeks depending on response
DRUGEntecavirTablets, Oral, 1mg, once daily, 48-96 weeks depending on response
DRUGAdefovirTablets, Oral, 10mg, once daily, 48-96 weeks depending on response

Timeline

Start date
2009-12-01
Primary completion
2012-12-01
Completion
2014-06-01
First posted
2009-09-30
Last updated
2015-09-01

Source: ClinicalTrials.gov record NCT00986778. Inclusion in this directory is not an endorsement.

Entecavir Plus Adefovir in Lamivudine-Resistant Patients (NCT00986778) · Clinical Trials Directory