[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100637803":3},{"organization":4,"armGroups":7,"interventions":16,"overallOfficials":11,"centralContacts":30,"locations":11,"responsibleParty":36,"collaborators":11,"id":38,"slug":39,"hasResults":40,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":11,"eligibilityCriteria":44,"healthyVolunteers":40,"sex":45,"minAge":46,"maxAge":47,"enrollmentInfo":48,"targetDuration":11,"studyType":51,"phases":52,"briefSummary":54,"conditions":55,"keywords":57,"overallStatus":59,"whyStopped":11,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":64,"completionDateStruct":66,"leadSponsor":68,"locationsCount":11},{"fullName":5,"class":6},"Hunan Cancer Hospital","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Camrelizumab combined with famitinib malate and chemotherapy","EXPERIMENTAL",null,[13,14,15],"Drug: Camrelizumab","Drug: Famitinib Malate","Drug: Chemotherapy",[17,22,26],{"type":18,"name":19,"description":20,"armGroupLabels":21,"otherNames":11},"DRUG","Camrelizumab","Intravenous (IV) on Day 1 of each cycle",[9],{"type":18,"name":23,"description":24,"armGroupLabels":25,"otherNames":11},"Famitinib Malate","Famitinib po qd",[9],{"type":18,"name":27,"description":28,"armGroupLabels":29,"otherNames":11},"Chemotherapy","Paclitaxel + cisplatin or carboplatin",[9],[31],{"name":32,"role":33,"phone":34,"phoneExt":11,"email":35},"Jie Tang","CONTACT","0731-89762071","tangjie@hnca.org.cn",{"type":37,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100637803","phase-2-camrelizumab-combined-with-famitinib-malate-and-chemotherapy-for-treatment-of-recurrent-metastatic-cervical-cancer-100637803",false,"NCT07627620","Camrelizumab Combined With Famitinib Malate and Chemotherapy for Treatment of Recurrent\u002F Metastatic Cervical Cancer","A Multi-Center Phase II Clinical Study of Camrelizumab Combined With Famitinib Malate and Platinum-based Chemotherapy in the Treatment of Recurrent\u002FMetastatic Cervical Cancer","Inclusion Criteria:\n\n1. Female aged 18-75 years.\n2. Histopathologically confirmed recurrent\u002Fmetastatic cervical squamous cell carcinoma, adenocarcinoma or adenosquamous cell carcinoma that cannot be radically treated by surgery, radiotherapy or chemoradiotherapy.\n3. No prior systemic anti-cancer therapy for recurrent\u002Fmetastatic disease.\n4. According to RECIST v1.1 criteria, the patient must have at least one measurable lesion.\n5. Able to normally swallow drug tablets\n6. Has adequate organ function.\n7. Willing to participate and able to comply with research programme requirements.\n8. Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.\n9. Estimated life expectancy of more than 3 months.\n\nExclusion Criteria:\n\n1. Has any malignancy \\\u003C5 years prior to study entry.\n2. Known to have brain or meningeal metastasis.\n3. Known to have autoimmune disease.\n4. Received live vaccinations 4 weeks before randomization or during the study period.\n5. Known allergies and contraindications to the investigational drug or any of its components.","FEMALE","18 Years","75 Years",{"count":49,"type":50},54,"ESTIMATED","INTERVENTIONAL",[53],"PHASE2","This study is an open-label, multi-center Phase II clinical study, aimed to evaluate the efficacy and safety of camrelizumab combined with famitinib malate and platinum-based chemotherapy in the treatment of recurrent\u002Fmetastatic cervical cancer.",[56],"Cervical Cancer",[56,27,19,58],"Famitinib malate","NOT_YET_RECRUITING","2026-05-31",{"date":62,"type":63},"2026-06-04","ACTUAL",{"date":65,"type":50},"2026-06-30",{"date":67,"type":50},"2029-03-30",{"name":5,"class":6}]