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Clinical Trial Summary

To assess the safety and tolerability of SHR-A1912 in patients with B cell lymphoma, to determine the dose-limiting toxicity (DLT), maximum tolerated dose (MTD), and recommended phase II dose (RP2D) of SHR-A1912.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05113069
Study type Interventional
Source Shanghai Hengrui Pharmaceutical Co., Ltd.
Contact
Status Enrolling by invitation
Phase Phase 1
Start date December 22, 2021
Completion date March 30, 2025

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