Entecavir
DrugTablets, Oral, 0.5 mg, once daily (QD), 52 weeks
Other names: Baraclude, BMS-200475
NCT Number: NCT00718887
Switching to Entecavir will result in superior antiviral efficacy as compared to continuing with Adefovir in patients with a suboptimal response to Adefovir
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Notify Me16 year and older
All sexes
Interventional
Phase 4
Local Institution, Beijing, Beijing Municipality, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Tablets, Oral, 0.5 mg, once daily (QD), 52 weeks
Other names: Baraclude, BMS-200475
Tablets, Oral, 10-mg adefovir QD for 12 weeks followed by 0.5-mg entecavir QD for a maximum of 52 weeks
Other names: Baraclude, BMS-200475
Time frame: At Week 12 from Day 1
HBV DNA Level <50 IU/mL=approximately 300 copies/mL.
Time frame: At Week 48 from Day 1
HBV=hepatitis B virus. HBV DNA Level <50 IU/mL=approximately 300 copies/mL.
Time frame: At Weeks 12 and 48 from Day 1
HBV=hepatitis B virus
Time frame: At Weeks 12 and 48 from Day 1
ULN=upper limit of normal. ALT normalization= ≤1*ULN, among participants with baseline ALT >1*ULN
Time frame: At Weeks 12 and 48 from Day 1
Time frame: At Weeks 12 and 48 from Day 1
Time frame: At Week 48 from Day 1
Time frame: Continually from Day 1 through Week 48, and through 24-week follow-up period
AE=any new unfavorable symptom, sign, or disease or worsening of a preexisting condition that may not have a causal relationship with treatment. SAE=a medical event that at any dose results in death, persistent or significant disability/incapacity, or drug dependency/abuse; is life-threatening, an important medical event, or a congenital anomaly/birth defect; or requires or prolongs hospitalization. Treatment-related=possibly, probably, or certainly related to and of unknown relationship to study drug.
Time frame: Day 1 through Week 48
Hematology testing assessed levels of hemoglobin, white blood cells, platelets, neutrophils, international normalized ration, red blood cells, lymphocytes, and monocytes.
Bristol-Myers Squibb
Industry
A Comparative Study of the Week 12 Antiviral Efficacy and Safety of Switching to Entecavir vs. Continuing Adefovir Treatment in Adults With Chronic Hepatitis B and Suboptimal Response to Adefovir
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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