Geneva, Feb. 13 -- International Clinical Trials Registry received information related to the study (ChiCTR2600118532) titled 'A prospective, single-arm, open-label Phase II clinical study on the efficacy and safety of Serplulimab combined with TPC(Nab-paclitaxel, cisplatin, and capecitabine) regimen as neoadjuvant therapy followed by concurrent chemoradiotherapy in locally advanced cervical cancer' on Feb. 6.
Study Type: Interventional study
Study Design:
Single arm
Primary Sponsor: Huizhou Central People's Hospital
Condition:
Cervical Cancer
Intervention:
Intervention group:Serplulimab + Nab-paclitaxel + Cisplatin + Capecitabine for 2 cycles
Recruitment Status: Not Recruiting
Phase: 2
Date of First Enrollment: 2026-02-24
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