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FIGURES/TABLES SUMMARY PAGE

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Treatment of Hepatitis B e Antigen–Positive Chronic Hepatitis with Telbivudine or Adefovir

A Randomized Trial


Figure 1
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Figure 1. Study flow diagram.

Primary exclusion criteria are listed; some patients met more than 1 exclusion criterion. One patient assigned to adefovir withdrew before initiation of treatment; thus, the intention-to-treat sample was 135 patients, of whom 45, 44, and 46 were assigned to receive telbivudine, adefovir, or adefovir for 24 weeks and then telbivudine for the remaining 28 weeks, respectively. One adefovir recipient withdrew before the week-24 analysis; 1 additional adefovir recipient and 2 telbivudine recipients withdrew before the week-52 analysis. ALT = alanine aminotransferase; HBeAg = hepatitis B e antigen; HBV = hepatitis B virus.

 

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Table 1. Baseline Characteristics

 

Figure 2
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Figure 2. Changes in serum hepatitis B virus (HBV) markers from baseline to week 52.

Top. Mean serum HBV DNA levels. Bottom. Proportion of patients with hepatitis B e antigen (HBeAg) seroconversion. ADV = adefovir; ADV/LdT = adefovir to telbivudine; LdT = telbivudine.

 

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Table 2. Efficacy Results at Week 24 of Treatment

 

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Table 3. Efficacy Results at Week 52 of Treatment

 

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Table 4. Effect of Viral Load at Week 24 on Efficacy Outcomes at Week 52

 

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Table 5. Clinical Adverse Events

 





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