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临床试验/NCT03707080
NCT03707080已完成不适用

DAA-PASS: A Post-Authorisation Safety Study of Early Recurrence of Hepatocellular Carcinoma in HCV-Infected Patients After Direct-Acting Antiviral Therapy

Target PharmaSolutions, Inc.61 个研究点 分布在 3 个国家目标入组 42 人开始时间: 2018年3月9日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
42
试验地点
61
主要终点
Time to HCC recurrence - Prospective Cohort

研究概览

简要总结

This is an independent optional sub-study parallel to TARGET-HCC (NCT02954094). The purpose of Direct-Acting Antiviral-Post Authorization Safety Study (DAA-PASS) is to investigate the impact of exposure to direct-acting antivirals (DAAs) on early recurrence of hepatocellular carcinoma (HCC) in hepatitis C virus (HCV)-infected patients following successful HCC treatment interventions.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Current participant in TARGET-HCC
  • Adults, age ≥18 years
  • First diagnosis of HCC (mixed HCC/cholangiocarcinoma may be included). Diagnosis may be histological/cytological and/or radiological.
  • BCLC Stage A
  • Underwent, undergoing, or planned to undergo therapy for HCC, with exception that transplant as prior or planned treatment for HCC is excluded.
  • HCV RNA positive

排除标准

  • Inability to provide informed consent
  • HCC-free imaging (as defined in Section 9.1.1) after treatment of initial HCC prior to Screening (see Section 9.2.9 for imaging details)
  • Prior liver transplantation
  • Hepatitis B Virus (HBV) surface antigen positive (HBsAg)
  • Previously treated with direct-acting antiviral agents (not DAA-naïve); Note that prior (peg)IFN and/or ribavirin therapy is allowed
  • Enrollment Inclusion Criteria:
  • Continued participation in TARGET-HCC
  • No recurrence or progression of initial HCC beyond BCLC Stage A prior to Enrollment/Baseline
  • HCC-free imaging (as defined in Section 9.1.1) at Enrollment/Baseline (see Section 9.2.9 for imaging details; participants may remain in Screening until an HCC-free image is obtained)
  • Remains DAA-naïve (prior therapy with (peg)IFN and/or ribavirin is allowed)
  • Enrollment Exclusion Criteria:
  • Liver transplantation since Screening

结局指标

主要结局

Time to HCC recurrence - Prospective Cohort

时间窗: up to 24 months

Time to HCC recurrence associated with DAA therapy relative to no DAA therapy in the prospective cohort.

次要结局

  • Number of events of early HCC recurrence - Prospective Cohort(up to 24 months)
  • Number of events of early HCC recurrence - Prospective Cohort relative to Historical Cohort(up to 24 months)
  • Time to HCC recurrence - Prospective Cohort relative to Historical Cohort(up to 24 months)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (61)

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