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Clinical Trial Summary

The study is being conducted to evaluate the safety and tolerability of HRS2300 and combined with SHR-1316 or SHR-1701 or trametinib or Almonertinib.To Determine the maximum tolerated dose (MTD) and recommended Dose (RP2D) for HRS2300 monotherapy and combination therapy.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05048134
Study type Interventional
Source Jiangsu HengRui Medicine Co., Ltd.
Contact Yanjuan Liang, P.M
Phone +0518-82342973
Email yanjuan.liang@hengrui.com
Status Recruiting
Phase Phase 1
Start date October 25, 2021
Completion date March 30, 2025

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