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Clinical Trials/NCT00131742
NCT00131742
Completed
Phase 3

A Phase III Randomized, Double Blind Trial of LdT (Telbivudine) Versus Lamivudine in Chinese Adults With Compensated Chronic Hepatitis B

Novartis0 sitesJuly 2004

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Chronic Hepatitis B
Sponsor
Novartis
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

This study is being conducted to compare the effectiveness and safety of telbivudine (LdT) and lamivudine in Chinese adults.

Registry
clinicaltrials.gov
Start Date
July 2004
End Date
January 2007
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Novartis

Eligibility Criteria

Inclusion Criteria

  • Documented clinical history compatible with chronic hepatitis B infection
  • Other protocol-defined inclusion criteria may apply

Exclusion Criteria

  • Patient is pregnant or breastfeeding
  • Patient is co-infected with hepatitis C virus (HCV), hepatitis D virus (HDV) or HIV
  • Patient has previously received lamivudine or any investigational anti-HBV nucleoside or nucleotide analog
  • Other protocol-defined exclusion criteria may apply

Outcomes

Primary Outcomes

Not specified

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