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Clinical Trial Summary

This is an open label, phase 1 clinical study to evaluate the safety and tolerability of different doses of QLH11906 monotherapy in patients with relapsed/refractory, unresectable locally advanced or metastatic advanced solid tumors with abnormal MAPK pathway, and determine the Maximum Tolerated Dose (MTD) or Maximum Administered Dose (MAD, if MTD cannot be determined) and Recommended Dose in Phase II Clinical Studies (Recommended Phase II Dose, RP2D).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05488821
Study type Interventional
Source Qilu Pharmaceutical Co., Ltd.
Contact Lianghua Fang
Phone 86-13645192882
Email lianghua.fang@qilu-pharma.com
Status Recruiting
Phase Phase 1
Start date June 14, 2022
Completion date July 1, 2025