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
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
- 否
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
干预措施: JS001 and Axitinib (Other)
JS001 alone
干预措施: JS001(Toripalimab Injection) (Biological)
Axitinib alone
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
Jun Guo
Director of department of renal cancer and melanoma
Peking University Cancer Hospital & Institute
