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临床试验/JPRN-UMIN000038604
JPRN-UMIN000038604已完成未知

Efficacy and safety of Ledipasvir Plus Sofosbuvir in Patients With Hepatitis C Virus Genotype 2 Infection - Harvoni in Genotype 2 HCV patients

Ogaki Municipal Hospital0 个研究点目标入组 126 人开始时间: 2019年12月1日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
入组人数
126

研究概览

简要总结

The overall SVR rates of the ITT and mITT populations were 87.3% (95% confidence interval [CI] 80.2-92.6) (110/126) and 97.3% (95% CI 92.4-99.4) (110/113), respectively. In the mITT population, the percentages of patients with undetectable HCV RNA at 4, 8, and 12 weeks after the start of therapy were 92.9% (95% CI 86.5-96.9) (105/113), 99.1% (95% CI 95.2-100.0) (112/113), and 100.0% (95% CI 97.4-100.0) (113/113), respectively.

研究设计

研究类型
Observational

入排标准

年龄范围
20years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • Prior exposure to a direct-acting antiviral agent targeting HCV NS5A or NS5B Decompensated cirrhosis Creatinine clearance (Cockcroft-Gault) less than 30 mL/min

研究者

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