Safety and Efficacy Study of LB80380 in the Treatment-naive Patients of Chronic Hepatitis B

PHASE2CompletedINTERVENTIONAL
Enrollment

115

Participants

Timeline

Start Date

August 31, 2009

Primary Completion Date

November 30, 2010

Study Completion Date

May 31, 2011

Conditions
Chronic Hepatitis B
Interventions
DRUG

LB80380 90 mg

LB80380 90 mg + placebo tablets, once daily, for 48 weeks

DRUG

LB80380 150 mg

LB80380 60 mg + 90 mg tablets, once daily, for 48 weeks

DRUG

entecavir 0.5 mg

entecavir 0.5 mg tablet, once daily, for 48 weeks

Trial Locations (10)

Unknown

Queen Mary Hospital, Hong Kong

Hanyang University Guri Hospital, Guri-si

Inha University Hospital, Incheon

Kyungpook National University Hospital, Daegu

Pusan National University Yangsan Hospital, Pusan

Kangnam Severance Hospital, Yonsei University, Seoul

Korea University Medical Center, Seoul

Severance Hospital of Yonsei University, Seoul

The Catholic University of Korea, Seoul St. Mary's Hospital, Seoul

Ulsan University Hospital, Ulsan

Sponsors

Lead Sponsor

All Listed Sponsors
lead

LG Life Sciences

INDUSTRY

NCT01026610 - Safety and Efficacy Study of LB80380 in the Treatment-naive Patients of Chronic Hepatitis B | Biotech Hunter | Biotech Hunter