Drug Use Investigation for HEPSERA (Adefovir) Tablet

NCT01863589 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 436

Last updated 2013-05-29

No results posted yet for this study

Summary

This post-marketing surveillance (PMS) is conducted to collect safety and efficacy data among subjects with chronic hepatitis B and hepatic cirrhosis B who is treated with adefovir tablets.

Conditions

Interventions

DRUG

Adefovir tablets

Administered according to the prescribing information in the locally approved label by the authorities.

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-02-28
Primary Completion
2007-06-30
Completion
2012-07-31

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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 NCT01863589 on ClinicalTrials.gov