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Clinical Trials/NCT03941795
NCT03941795
Unknown
Phase 2

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 sites in 1 country99 target enrollmentNovember 11, 2019

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.

Registry
clinicaltrials.gov
Start Date
November 11, 2019
End Date
December 2022
Last Updated
6 years ago
Study Type
Interventional
Study Design
Crossover
Sex
All

Investigators

Sponsor
Peking University Cancer Hospital & Institute
Responsible Party
Principal Investigator
Principal Investigator

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)

Study Sites (2)

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