A Study of CM350 in Patients With Advanced Solid Tumors

Status Recruiting

Clinical Trial Summary

This is an open label, dose escalation and expansion Phase I/II study to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, immunogenicity, and preliminary efficacy of CM350 in patients with advanced solid tumors. The phase I study consists of a dose escalation part (Part A) and a dose extension part (Part B). The safety and tolerability of CM350 and the maximum tolerated dose (MTD) will be evaluated in Part A. The safety, tolerability and efficacy of CM350 at MTD and/or the dose of one level less than MTD (MTD-1), and the recommended dose level for the phase II study will be determined in Part B.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05263960
Study type	Interventional
Source	Keymed Biosciences Co.Ltd
Contact	Qian Jia
Phone	+862888610620
Email	qianjia@keymedbio.com
Status	Recruiting
Phase	Phase 1/Phase 2
Start date	April 21, 2022
Completion date	March 2025

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