Camrelizumab Combined With Famitinib Malate for Treatment of Recurrent/Metastatic Cervical Cancer
- Sponsor
- Jiangsu HengRui Medicine Co., Ltd.
- Study ID
- NCT04906993
- Phase
- PHASE3
- Status
- Active Not Recruiting
Conditions
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- camrelizumab; famitinib malate — DRUGCamrelizumab intravenously ; Famitinib Orally
- platinum-based chemotherapy — DRUGPhysician's choice chemotherapy
Study Details
This study is a randomized, open-label, controlled, multi-center Phase III clinical study, aimed to evaluate the efficacy and safety of camrelizumab combined with famitinib malate versus platinum-based chemotherapy in the treatment of recurrent/metastatic cervical cancer. All enrolled patients will be randomly divided into 2 groups and continuously treated until any event that meets the criteria for end of the clinical trial.
Key Dates
- Start date
- Jul 23, 2021
- Status verified
- Sep 2025
- Primary completion
- Jun 10, 2025
- Completion
- May 31, 2027
Study Design
- Enrollment
- 443 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: camrelizumab combined with famitinib malate
- Active Comparator: platinum-based chemotherapy
Primary Outcome Measure
Progression-free survival (PFS) assessed by the BIRC based on RECIST V1.1 criteria [ Time Frame: up to 2 years ]
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