drugset / Trial / NCT01938781
Optimized Treatment and Regression of HBV-induced Liver Fibrosis
Phase 4
Completed
400 enrolled
Beijing Friendship Hospital
Beijing 302 Hospital · collabBeijing Ditan Hospital · collabBeijing Tiantan Hospital · collabBeijing YouAn Hospital · collabFifth Hospital of Shijiazhuang City · collabHuashan Hospital · collabLogistics University of Chinese People's Armed Police Forces · collabNanfang Hospital, Southern Medical University · collabPeking Union Medical College Hospital · collabPeking University · collabPeking University First Hospital · collabPeking University People's Hospital · collabRenJi Hospital · collabShanghai General Hospital, Shanghai Jiao Tong University School of Medicine · collabShanghai Public Health Clinical Center · collabShanghai Zhongshan Hospital · collabSir Run Run Shaw Hospital · collabTang-Du Hospital · collabThe Affiliated Hospital of Yanbian University · collabThe First Affiliated Hospital of Shanxi Medical University · collabTongji Hospital · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
Patients with chronic hepatitis B histologically confirmed of liver fibrosis S2/S3 (similar to metavir F2/F3, Ishak 2/3/4) are randomly assigned in a 1:1 ratio. One arm is entecavir alone for 2 years; the other is entecavir alone for the first 0.5 year, entecavir plus pegylated interferon (peg-IFN) for 1 year, entecavir for another additional 0.5 year. Patients will be assessed at baseline, at every six months for blood count, liver function test, HBVDNA, AFP, prothrombin time, thyroid function, liver ultrasonography, and Fibroscan. The second liver biopsy will be performed to evaluate regression rate of liver fibrosis 1.5 years after initial therapy.
Timeline
- Start
- 2013-06
- Primary completion
- 2016-12
- Completion
- 2016-12
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Peginterferon alfa-2a | Protein / enzyme biologic | — | — |
| Background | Entecavir | Small molecule | 0.5 mg | Oral |