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Clinical Trial Summary

The Primary purpose of this study is to evaluate the safety of SHR-1316 plus concurrent chemoradiotherapy in participants with locally advanced cervical cancer. The second purpose of this study is to evaluate the efficacy and PK traits; The exploratory study is to explore the biomarker 、immunogenicity and so on .


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06237257
Study type Interventional
Source Shanghai Shengdi Pharmaceutical Co., Ltd
Contact Yong Cao
Phone +0518-81220121
Email caoyong@hrs.com.cn
Status Recruiting
Phase Phase 2
Start date March 20, 2024
Completion date January 31, 2025

See also
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