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Clinical Trial Summary

This study will evaluate the efficacy and safety of SHR-1701 combined with radiotherapy and chemotherapy as perioperative treatment for locally advanced rectal cancer. Eligible patients will receive standard chemoradiation with SHR-1701 followed by XELOX combined with SHR-1701. In all subjects, restaging pelvic MRI with chest and abdominal CT will be performed after completion of neoadjuvant treatment to determine resectability and to rule out any evidence of metastases. Subjects who have resectable disease will undergo surgery. Adjuvant XELOX combined with SHR-1701 will be given after surgery.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05300269
Study type Interventional
Source Suzhou Suncadia Biopharmaceuticals Co., Ltd.
Contact Qing Yang, M.D
Phone +86 021-61053363
Email qing.yang@hengrui.com
Status Recruiting
Phase Phase 2
Start date July 5, 2022
Completion date October 31, 2026

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