Special Drug Use Investigation for ZEFIX (Lamivudine) Tablet (HBV Cirrhosis)

NCT01376154 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 342

Last updated 2017-05-22

No results posted yet for this study

Summary

The purpose of this study is to confirm efficacy and safety when administering lamivudine tablet alone in subjects with hepatitis B virus-induced liver cirrhosis.

Conditions

  • Hepatitis B, Chronic

Interventions

DRUG

Lamivudine

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-06-30
Primary Completion
2009-12-31
Completion
2011-02-28

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01376154 on ClinicalTrials.gov