To Explore the Efficacy and Safety of Camrelizumab Combined With SHR1020 in the Treatment of Advanced Melanoma
- Sponsor
- Peking University Cancer Hospital & Institute
- Study ID
- NCT05051865
- Phase
- PHASE2
- Status
- Unknown
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- camrelizumab — DRUGcamrelizumab combined with SHR1020 for advanced melanoma
- SHR1020 — DRUGcamrelizumab combined with SHR1020 for advanced melanoma
Study Details
This study is being conducted to explore the efficacy and safety of camrelizumab combined with SHR1020 in the treatment of advanced melanoma.
Key Dates
- Start date
- Oct 9, 2021
- Status verified
- Nov 2022
- Primary completion
- Aug 30, 2024
- Completion
- Aug 30, 2024
Study Design
- Enrollment
- 60 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Camrelizumab Combined With SHR1020Camrelizumab combined with SHR1020 for advanced melanoma.
Primary Outcome Measure
ORR (Objective Response Rate) [ Time Frame: From date of first dose until the date of first documented progression or date of death from any cause, whichever came first, assessed up to 12 months ]
Central Contacts
- Lili Mao, MD13261859885
- Jun Guo, MD
Related Studies
- Evaluation for NCI Surgery Branch Clinical Research ProtocolsRecruiting · National Cancer Institute (NCI) · Bethesda, Maryland
- Clinical, Laboratory, and Epidemiologic Characterization of Individuals and Families at High Risk of MelanomaRecruiting · National Cancer Institute (NCI) · Bethesda, Maryland
- Harvesting Cells for Experimental Cancer TreatmentsEnrolling By Invitation · National Cancer Institute (NCI) · Bethesda, Maryland
- Follow Up Protocol for Subjects Previously Enrolled on NCI Surgery Branch StudiesEnrolling By Invitation · National Cancer Institute (NCI) · Bethesda, Maryland