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Clinical Trial Summary

To assess the safety and tolerability of SHR-1802 combined with camrelizumab and famitinib in subjects with advanced solid tumor and to determine the dose-limiting toxicity (DLT),recommended phase II dose (RP2D) and assess objective response rate (ORR) assessed by the investigator based on RECIST v1.1 criteria.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05208177
Study type Interventional
Source Jiangsu HengRui Medicine Co., Ltd.
Contact Quanren Wang, Ph.D.
Phone 86-021-23511999
Email [email protected]
Status Not yet recruiting
Phase Phase 2
Start date March 1, 2022
Completion date December 1, 2024

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