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
Overview
- Phase
- Phase 2
- Intervention
- JS001 and Axitinib
- Conditions
- Advanced Mucosal Melanoma
- Sponsor
- Peking University Cancer Hospital & Institute
- Enrollment
- 99
- Locations
- 2
- Primary Endpoint
- the progression-free survival (PFS)
- Last Updated
- 6 years ago
Overview
Brief Summary
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.
Investigators
Jun Guo
Director of department of renal cancer and melanoma
Peking University Cancer Hospital & Institute
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- Not provided
Arms & Interventions
JS001(Toripalimab Injection) Combined With Axitinib
Intervention: JS001 and Axitinib
JS001 alone
Intervention: JS001(Toripalimab Injection)
Axitinib alone
Intervention: Axitinib 1 MG [Inlyta]
Outcomes
Primary Outcomes
the progression-free survival (PFS)
Time Frame: 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.
Secondary Outcomes
- 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)