drugset / Trial / NCT01143662
Efficacy and Safety of Ypeginterferon Alfa-2b in HBeAg Positive Chronic Hepatitis B
Phase 2
Completed
205 enrolled
Xiamen Amoytop Biotech Co., Ltd.
Peking University First Hospital · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
This study is a multi-center, randomized, open-label and positive controlled Phase II Clinical trial to assess efficacy and safety of Ypeginterferon alfa-2b, once a week, in 3 dose-groups: 90mcg, 135mcg and 180mcg, respectively, for treatment of chronic hepatitis B characterized by HBeAg positivity, with Pegasys 180mcg/week as positive control. It is aimed to establish a dose response and safety relationship sufficient to allow the subsequent design and conduct of Phase III trials, and generate pharmacokinetic data of Ypeginterferon alfa-2b in hepatitis B patients to satisfy regulatory requirements.
Timeline
- Start
- 2010-07
- Primary completion
- 2011-04
- Completion
- 2012-04
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Peginterferon alfa-2a | Protein / enzyme biologic | 180 ug | — |
| Subject | Peginterferon alfa-2b | Protein / enzyme biologic | 90 ug | — |
| Subject | Peginterferon alfa-2b | Protein / enzyme biologic | 135 ug | — |
| Subject | Peginterferon alfa-2b | Protein / enzyme biologic | 180 ug | — |