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临床试验/JPRN-UMIN000008045
JPRN-UMIN000008045已完成未知

Prospective observational study on efficacy and safety of PEGASYS for the treatment of patients with HBeAg positive or HBeAg negative chronic active hepatitis B - Prospective observational study of PEGASYS for hepatitis B

Chugai Pharmaceutical Co., Ltd.0 个研究点目标入组 536 人开始时间: 2012年5月29日最近更新:

试验速览

阶段
未知
状态
已完成
入组人数
536

研究概览

简要总结

The incidence of ADRs in the 536 patients in the safety analysis set was 47.76% (256/536 patients), with 565 events reported. By system organ class (SOC), the most common ADRs (5% incidence) in the 536 patients in the safety analysis set were investigations (28.92%, 155/536 patients), general disorders and administration site condition (12.31%, 66/536 patients), and skin and subcutaneous tissue disorders (9.33%, 50/536 patients.

研究设计

研究类型
Observational

入排标准

年龄范围
ot applicable 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • chronic active hepatitis B patients without HBeAg data

研究者

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