Suboptimal Responders to Adefovir Switching to Entecavir

PHASE4CompletedINTERVENTIONAL
Enrollment

228

Participants

Timeline

Start Date

July 31, 2008

Primary Completion Date

December 31, 2009

Study Completion Date

January 31, 2011

Conditions
Hepatitis B, Chronic
Interventions
DRUG

Entecavir

Tablets, Oral, 0.5 mg, once daily (QD), 52 weeks

DRUG

Adefovir/Entecavir

Tablets, Oral, 10-mg adefovir QD for 12 weeks followed by 0.5-mg entecavir QD for a maximum of 52 weeks

Trial Locations (8)

100011

Local Institution, Beijing

110004

Local Institution, Shenyang

130021

Local Institution, Changchun

200235

Local Institution, Shanghai

210002

Local Institution, Nanjing

330006

Local Institution, Nanchang

550004

Local Institution, Guiyang

Unknown

Local Institution, Shanghai

Sponsors
All Listed Sponsors
lead

Bristol-Myers Squibb

INDUSTRY