Tenofovir for the treatment of breakthrough hepatitis caused by lamivudine and adefovir dipivoxil-resistant mutants of hepatitis B virus

Tenofovir for the treatment of breakthrough hepatitis caused by lamivudine and adefovir dipivoxil-resistant mutants of hepatitis B virus - GLSG,2006,tenofovir

Status

Active, not recruiting

Phases

Phase 4

Study type

Interventional

Source

JPRN

Registry ID

JPRN-C000000395

Enrollment

Registered

2012-10-01

Start date

2006-04-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic hepatitis B

Interventions

Viread (tenofovir) 300mg/day p.o.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: chronic hepatitis B Lamivudine and Adefovir dipivoxil-resistant mutants abnormal ALT positive test of HBV-DNA

Exclusion criteria

Exclusion criteria: Allergy to Lamivudine complication of chronic hepatitis coadministration of cytotoxic drugs leucopenia during pregnancy severe liver dysfunction

Design outcomes

Primary

Measure	Time frame
HBV-DNA	—

Secondary

Measure	Time frame
serum ALT side effects	—

Countries

Japan

Contacts

Public ContactKen Sato

Gunma University Graduate School of Medicine Department of Medicine and Molecular Science

satoken@showa.gunma-u.ac.jp027-220-8127

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026