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临床试验/JPRN-jRCT1031210167
JPRN-jRCT1031210167招募中3 期

Randomized phase III trial of Sorafenib versus Lenvatinib as a second-line treatment after immune check point inhibitor for advanced hepatocellular carcinoma - JON2102-H (SUCCEED)

eno Makoto0 个研究点目标入组 164 人开始时间: 2021年6月28日最近更新:
适应症

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
164

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • 1. Advanced hepatocellular carcinoma (HCC) confirmed by Radiological or histological assessment
  • 2. Not amenable to a liver directed therapy
  • 3. Intolerant or refractory to first-line systemic treatment containing immune check point inhibitor
  • 4. No prior therapy of EGFR-TKI or Ramucirumab
  • 5. ECOG performance status (PS) of 0-1
  • 6. Age >= 20 years old
  • 7. Adequate hematologic and renal function
  • 8. Child-Pugh class A
  • 9. More than two weeks from the last treatment
  • 10. Expected prognosis of more than 12 weeks
  • 11. Provided written informed consent

排除标准

  • 1. Moderate or severe pleural effusion
  • 2. Uncontrollable hypertension
  • 3. Urinary protein excretion of 2g/day or over
  • 4. With hepatic encephalopathy
  • 5. Synchronous or metachronous malignancies
  • 6. Active infection requiring systemic treatment
  • 7. Inability of oral food intake
  • 8. Brain or meningeal metastasis
  • 9. Pregnant and lactating females, and males and females unwilling to use contraception
  • 10. Severe psychosis
  • 11. Continuous use of systemic steroid or immune suppressant
  • 12. Interstitial pneumonia, fibroid lung, or severe emphysema
  • 13. Severe concomitant disease, such as cardiovascular, renal and gastrointestinal disorders, and uncontrolled diabetes mellitus)
  • 14. Unstable angina pectoris, or history of myocardial infarction within 6 months
  • 15. Hemorrhagic or thrombotic disease
  • 16. Blood transfusion or use of G-CSF within 2 weeks
  • 17. Other conditions not suitable for this study

研究者

发起方
eno Makoto

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