drugset / Trial / NCT01938820
Optimized Treatment and Regression of HBV-induced Early Cirrhosis
Phase 4
Completed
82 enrolled
Beijing Friendship Hospital
Beijing 302 Hospital · collabBeijing Ditan Hospital · collabBeijing Tiantan Hospital · collabBeijing YouAn Hospital · collabFifth Hospital of Shijiazhuang City · collabFudan University · 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 early cirrhosis S4 (similar to metavir F4, Ishak 5/6) are randomly assigned in a 1:1 ratio. One arm is entecavir alone for 2 years; the other is entecavir for the first 0.5 year, entecavir plus thymosin 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, 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 | Thymalfasin | Peptide | 1.6 ug | — |
| Background | Entecavir | Small molecule | 0.5 mg | Oral |