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An Open Label, Response Adaptive Study of Telbivudine in Adults With HBeAg Positive Compensated CHB
This study is to evaluate the antiviral efficacy of add-on adefovir to telbivudine in non-responders to telbivudine monotherapy after 24 and 36 initial weeks. Antiviral efficacy is assessed by hepatitis B virus (HBV) DNA non-detectability (PCR \<300 copies/ml) by week 104 with CHB.
Age
18 - No limit years
Sex
ALL
Healthy Volunteers
No
Novartis Investigative Site
Hyderabad, India
Novartis Investigative Site
Mumbai, India
Novartis Investigative Site
Vellore, India
Start Date
August 1, 2007
Primary Completion Date
June 1, 2011
Last Updated
June 23, 2017
100
ACTUAL participants
Telbivudine
DRUG
Lead Sponsor
Novartis Pharmaceuticals
NCT04166266
NCT06550622
Data Source & Attribution
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Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT05922306