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This study is designed to support the optimal use of telbivudine by providing data to refine our understanding of telbivudine efficacy and resistance in real life clinical setting in patients with chronic hepatitis B with defined baseline characteristics and 24-week PCR negativity.
This study will be multicenter, open-label and observational data collection of patients on telbivudine who meet baseline characteristics defined as the majority of patients seen in the clinic setting. Data collection will take place after enrollment, at Week 12, 24, 52, 76 and 104 for efficacy assessments. In patients who discontinue observational drug earlier, clinical information would be kept following for assessment as well.
Study purpose:
This study is designed to evaluate the efficacy of telbivudine in real-life clinical settings with the use of the Roadmap Concept in chronic hepatitis B treatment.
Objectives:
Primary:
To observe telbivudine's 2-year efficacy in real-world clinical setting of achieving HBV-DNA < 60 IU/ml and HBeAg seroconversion rate in patients with defined baseline characteristics and 24-week treatment PCR negativity as previously reported in GLOBE study's sub-analysis.
Secondary:
Population:
The study population will consist of a representative group of 500 chronic hepatitis B patients with detectable HBsAg for more than 6 months who need telbivudine therapy based on investigators' judgment in 16 medical centers located in Taiwan.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| CHB patients without cirrhosis |
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| Measure | Description | Time Frame |
|---|---|---|
| PCR negativity | week 52 | |
| HBeAg seroconversion rate | week 52 | |
| PCR negativity | week 104 | |
| HBeAg seroconversion rate | week 104 |
| Measure | Description | Time Frame |
|---|---|---|
| Rate of ALT normalization | week 52 | |
| Genotypic resistance | week 52 | |
| Rate of ALT normalization |
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Inclusion Criteria:
Male or female 18 to 65 years of age
Documented chronic hepatitis B defined by ALL of following:
Exclusion Criteria:
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Chronic hepatitis B patients without cirrhosis
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| Name | Affiliation | Role |
|---|---|---|
| Jia-Horng Kao, Professor | National Taiwan University Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| National Taiwan University Hospital | Taipei | 100 | Taiwan |
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| ID | Term |
|---|---|
| D019694 | Hepatitis B, Chronic |
| ID | Term |
|---|---|
| D006509 | Hepatitis B |
| D000086982 | Blood-Borne Infections |
| D003141 | Communicable Diseases |
| D007239 | Infections |
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10 c.c whole blood
| week 104 |
| Genotypic resistance | week 104 |
| D018347 |
| Hepadnaviridae Infections |
| D004266 | DNA Virus Infections |
| D014777 | Virus Diseases |
| D006525 | Hepatitis, Viral, Human |
| D006521 | Hepatitis, Chronic |
| D006505 | Hepatitis |
| D008107 | Liver Diseases |
| D004066 | Digestive System Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |