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Clinical Trial Summary

Patients with recurrent or metastatic uterine cervical squamous carcinoma have very poor prognosis. For eligible patients, radiotherapy remains the choice, which has the most effective impact on the survival periods. On the hand, anti-angiogenic therapy has been proved to be promising treatment for recurrent or advanced cervical carcinomas. This study aims to discover the objective response of combination therapy with nimotuzumab (an anti-epidermal growth factor receptor [EGFR] IgG1 humanized monoclonal antibody) and radiotherapy in recurrent or metastatic uterine cervical squamous carcinoma in a single-arm, open, phase 2 clinical trial. The primary endpoint is the objective response rate evaluated by imaging methods. The second endpoints are the progression-free survival and overall survival. The treatment toxicity is regarded as one the second endpoint.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04664244
Study type Interventional
Source Peking Union Medical College Hospital
Contact Lei Li, M.D
Phone 86-139-1198-8831
Email lileigh@163.com
Status Recruiting
Phase Phase 2
Start date December 19, 2020
Completion date December 31, 2023

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