Trials / Withdrawn
WithdrawnNCT00986778
Entecavir Plus Adefovir in Lamivudine-Resistant Patients
A Comparative Study of Entecavir vs Adefovir Plus Lamivudine vs Combination Entecavir Plus Adefovir in Lamivudine-Resistant Chronic Hepatitis B Chinese Subjects
- Status
- Withdrawn
- Phase
- Phase 4
- Study type
- Interventional
- Enrollment
- 0 (actual)
- Sponsor
- Bristol-Myers Squibb · Industry
- Sex
- All
- Age
- 16 Years
- Healthy volunteers
- Not accepted
Summary
Combination therapy with entecavir 1.0 mg plus adefovir 10 mg has superior antiviral activity compared with either entecavir monotherapy 1.0 mg or adefovir 10 mg plus lamivudine 100 mg in Chinese adults with lamivudine-resistant chronic hepatitis B infection
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lamivudine | Tablets, Oral, 100mg, once daily, 48-96 weeks depending on response |
| DRUG | Entecavir | Tablets, Oral, 1mg, once daily, 48-96 weeks depending on response |
| DRUG | Adefovir | Tablets, Oral, 10mg, once daily, 48-96 weeks depending on response |
Timeline
- Start date
- 2009-12-01
- Primary completion
- 2012-12-01
- Completion
- 2014-06-01
- First posted
- 2009-09-30
- Last updated
- 2015-09-01
Source: ClinicalTrials.gov record NCT00986778. Inclusion in this directory is not an endorsement.