30
Participants
Start Date
March 31, 2008
Primary Completion Date
December 31, 2009
Study Completion Date
December 31, 2009
Telbivudine
Arm 1: 600 mg/day, oral telbivudina for 24 weeks
oral adefovir
Arm 2: 600 mg/day, oral telbivudina plus 10 mg/day oral adefovir for 24 weeks
Novartis Investigative Site, Barcelona
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY