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临床试验/NCT05489289
NCT05489289招募中3 期

A Randomized, Double-blind, Phase III Clinical Study on the Efficacy and Safety of AK104 Versus Placebo as Adjuvant Therapy for Hepatocellular Carcinoma With High Risk of Recurrence After Curative Resection

Akeso1 个研究点 分布在 1 个国家目标入组 570 人开始时间: 2023年1月5日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
招募中
发起方
入组人数
570
试验地点
1
主要终点
Recurrence free survival (RFS) by BICR

研究概览

简要总结

The efficacy and safety of AK104 as adjuvant therapy in hepatocellular carcinoma of high recurrence risk after curative resection.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Pathological diagnosis of HCC without any metastasis;
  • Receiving radical resection as the only anti-tumor treatment;
  • No evidence of residual cancer found during or after the operation;
  • Presence of any high risk factor of postoperative recurrence;
  • Child-Pugh grade: A;
  • ECOG score: 0;
  • Controlled underlying causes of HCC.

排除标准

  • Fibrolamellar hepatocellular carcinoma, sarcoma-like hepatocellular carcinoma, cholangiocarcinoma, etc;
  • Any anti-tumor treatment other than radical surgery before randomization;
  • Precarious liver function indicated by severe complications;
  • Recent procedures or medications leading to high risk of bleeding;
  • Poorly controlled or symptomatic hypertension, congestive heart failure, arrhythmia, etc;
  • Failure of performing enhanced CT or MRI scans of the liver;
  • Recent severe infections or systemic antibiotics use;
  • Active autoimmune diseases;
  • History of other incurable malignant tumors;
  • History of transplantation;

研究组 & 干预措施

AK104

Active Comparator

AK104 IV every three weeks

干预措施: AK104 (Biological)

placebo

Placebo Comparator

Placebo IV every three weeks

干预措施: placebo (Biological)

结局指标

主要结局

Recurrence free survival (RFS) by BICR

时间窗: Up to 48 months

The time comfirmed by BICR from randomization to recurrence or death.

次要结局

  • 12-months recurrence free survival (RFS-12)(12 months)
  • Time to recurrence (TTR)(Up to 48 months)
  • 24-months recurrence free survival (RFS-24)(24 months)
  • Types and proportions of adverse events (AEs)(Up to 48 months)
  • Overall survival (OS)(Up to 48 months)

研究者

发起方
Akeso
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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