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Serplulimab Plus Chemoradiotherapy for Stage III-IVA Cervical Cancer - Trial NCT06419673

Access comprehensive clinical trial information for NCT06419673 through Pure Global AI's free database. This Phase 2 trial is sponsored by Cancer Institute and Hospital, Chinese Academy of Medical Sciences and is currently Recruitment Completed. The study focuses on Cervical Cancer. Target enrollment is 240 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT06419673
Phase 2
Recruitment Completed
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06419673
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Serplulimab Plus Chemoradiotherapy for Stage III-IVA Cervical Cancer
Induced and Concurrent Serplulimab Plus Chemoradiotherapy Followed by Toripalimab Maintenance Therapy for Stage III-IVA Cervical Cancer: a Prospective, Multicenter, Randomized, Open Controlled Clinical Trial

Study Focus

Cervical Cancer

Serplulimab

Interventional

drug

Sponsor & Location

Cancer Institute and Hospital, Chinese Academy of Medical Sciences

Beijing, China

Timeline & Enrollment

Phase 2

May 01, 2024

May 31, 2028

240 participants

Primary Outcome

Progression-Free Survival(PFS) at Month 36

Summary

This study is a prospective, multicenter, randomized, open controlled clinical trial aimed at
 evaluating the effectiveness and safety of serplulimab plus chemoradiotherapy in FIGO 2018
 stage III or IVA cervical squamous cell carcinoma, adenocarcinoma, and adenosquamous cell
 carcinoma patients who have not received prior treatment.

ICD-10 Classifications

Severe cervical dysplasia, not elsewhere classified
Mild cervical dysplasia
Moderate cervical dysplasia
Carcinoma in situ: Cervix, unspecified
Cervical root disorders, not elsewhere classified

Data Source

ClinicalTrials.gov

NCT06419673

Non-Device Trial