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Study identifier: NCT06288360 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Neoadjuvant Immunochemotherapy in PD-L1-negative LACC

Condition: Cervical Cancer · Locally Advanced Cervical Cancer · PD-L1 Negative  ·  Sponsor: Tongji Hospital

PhasePhase 2
Planned participants40
Who can joinFemale, 18 Years to 70 Years
Healthy volunteersNo

About this study

This is a multicenter, prospective, single-arm, phase 2 clinical trial designed to evaluate the therapeutic efficacy of the NACI (neoadjuvant chemotherapy plus Camrelizumab) for PD-L1-negative locally advanced cervical cancer.

This description comes directly from the study's public registry record.

Talk to the study team

Kezhen Li  ·  086-027-8362  ·  tjkeke@126.com

Jie Yang  ·  086-027-8362  ·  yangjie@tjh.tjmu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (12)

Anhui Provincial Cancer HospitalHefei, Anhui, ChinaRecruiting
Beiing Friendship Hospital, Capital Medical UniversityBeijing, Beijing Municipality, ChinaRecruiting
The First Affiliated Hospital (Southwest Hospital), Army Medical University (Third Military Medical University)Chongqing, Chongqing Municipality, ChinaRecruiting
Gansu Provincial Maternity and Child-care HospitalLanzhou, Gansu, ChinaRecruiting
The Affiliated Tumor Hospital of Guangxi Medical UniversityNanning, Guangxi, ChinaRecruiting
Tongji Hospital, Tongji Medical College, Huazhong University of Science and TechnologyWuhan, Hubei, ChinaRecruiting
Xiangya Hospital, Central South UniversityChangsha, Hunan, ChinaRecruiting
Shengjing Hospital of China Medical UniversityShenyang, Liaoning, ChinaRecruiting
Second People's Hospital of Sichuan (Sichuan Cancer Hospital)Chengdu, Sichuan, ChinaRecruiting
Tianjin Medical University General HospitalTianjin, Tianjin Municipality, ChinaRecruiting
Women's Hospital, Zhejiang University School of MedicineHangzhou, Zhejiang, ChinaRecruiting
Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of SciencesHangzhou, Zhejiang, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06288360