This study is to evaluate the safety of telbivudine for up to 21 months of open-label treatment in patients with chronic hepatitis B who have completed the CLDT600A2407 trial. Patients treated with telbivudine during core phase will continue telbivudine and patients treated with entecavir during core phase will be switched to telbivudine if the patient is willing to enroll this study.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
44
Novartis Investigative Site (705-035)
Daegu, South Korea
Novartis Investigative Site , (420-717)
Gyeonggi-do, South Korea
Novartis Investigative Site , (405-760)
Incheon, South Korea
Novartis Investigative Site , (136-705)
Seoul, South Korea
Safety of telbivudine (LDT600) up to 21 additional months of open-label treatment in patients with chronic hepatitis B who have completed study CLDT600A2407 assessed by Adverse Events, data of vital signs and other tests
Safety of patients switched from entecavir to telbivudine compared with patients continuing telbivudine assessed by Adverse Events, data of vital signs and other tests
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Novartis Investigative Site , (150-590)
Seoul, South Korea
Novartis Investigative Site
Seoul, South Korea