NCT06251388

A Study of Concurrent Chemoradiotherapy Followed by Cadonilimab(AK104) for Newly Diagnosed Local Advanced Cervical Cancer

A Prospective, Single Arm, Multicenter, Phase II Study to Evaluate the Efficacy and Safety of Concurrent Chemoradiotherapy Followed by Cadonilimab(AK104) for Newly Diagnosed Local Advanced Cervical Cancer
West China Second University Hospital·Phase 2·ClinicalTrials.gov·drugRecruiting
View on ClinicalTrials.gov
Study focus
Disease/Condition
Cervical Cancer
Drug/Device/Intervention
AK104
Study type
Interventional
Intervention type
drug
Sponsor & location
Primary sponsor
West China Second University Hospital
Location
Chengdu, China
Timeline & enrollment
Phase
Phase 2
Start date
Feb 20, 2024
End date
Oct 01, 2026
Enrollment
50 participants
Primary outcome

Progression-free survival

Summary

This study will evaluate the efficacy and safety of concurrent
 chemoradiotherapy(CCRT)followed by cadonilimab(AK104) in high risk local advanced cervical
 cancer.
 
 Participants received CCRT,efficacy evaluation of CCRT was no disease progression who
 maintained with AK104(10.0 mg/kg,Q3W)until drug exposure over 1 years or disease progression
 or intolerable toxicity.

ICD-10 classifications
Severe cervical dysplasia, not elsewhere classifiedMild cervical dysplasiaModerate cervical dysplasiaCarcinoma in situ: Cervix, unspecifiedCervical root disorders, not elsewhere classified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT06251388
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT06251388 through Pure Global AI's free database. This Phase 2 trial is sponsored by West China Second University Hospital and is currently Recruiting. The study focuses on Cervical Cancer. Target enrollment is 50 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.