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临床试验/NCT03941795
NCT03941795Unknown2 期

A Randomized, Controlled, Multicenter Phase II Clinical Study to Evaluate the Efficacy and Safety of Toripalimab Injection Combined With Axitinib in the First-Line Treatment of Patients With Advanced Mucosal Melanoma

Peking University Cancer Hospital & Institute2 个研究点 分布在 1 个国家目标入组 99 人开始时间: 2019年11月11日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
发起方
入组人数
99
试验地点
2
主要终点
the progression-free survival (PFS)

研究概览

简要总结

This is a randomized, controlled, multicenter Phase II clinical study to evaluate the efficacy and safety of toripalimab injection combined with axitinib in the first-line treatment of patients with advanced mucosal melanoma. The target population is the patients with previously untreated, histopathologically confirmed, unresectable or metastatic mucosal melanoma. At the randomization, patients are randomized 1:1:1 into three groups with approximately 33 subjects in each group to receive toripalimab injection plus axitinib, toripalimab injection monotherapy (subjects who meet the criteria after disease progression may cross over to receive toripalimab plus axitinib), or axitinib monotherapy (subjects who meet the criteria after disease progression may cross over to receive toripalimab plus axitinib); when the patient has disease progression or intolerable toxicity, the treatment is terminated, and the survival follow-up will be initiated.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

JS001(Toripalimab Injection) Combined With Axitinib

Experimental

干预措施: JS001 and Axitinib (Other)

JS001 alone

Experimental

干预措施: JS001(Toripalimab Injection) (Biological)

Axitinib alone

Active Comparator

干预措施: Axitinib 1 MG [Inlyta] (Drug)

结局指标

主要结局

the progression-free survival (PFS)

时间窗: 36 months

Progression-free survival (PFS) per RECIST 1.1 criteria: Time from the date of randomization to the first documented disease progression (per RECIST 1.1 criteria), or death from any cause, whichever occurs first.

次要结局

  • INV-ORR(36 months)
  • ORR(36 months)
  • PFS(36 months)
  • DOR(36 months)
  • TTR(36 months)
  • DCR(36 months)
  • OS(36 months)
  • safety: Number of Participants With Abnormal Laboratory Values and/or Adverse Events That Are Related to Treatment(36 months)

研究者

发起方
Peking University Cancer Hospital & Institute
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jun Guo

Director of department of renal cancer and melanoma

Peking University Cancer Hospital & Institute

研究点 (2)

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