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Clinical Trial Summary

This study will evaluate the safety and tolerability of APL-102 Capsule and characterize the pharmacokinetic (PK) profile in advanced solid tumor patients.


Clinical Trial Description

This study is an open, multicenter dose-escalation study to evaluate the safety and tolerance of APL-102 and obtain the relevant data of APL-102 in patients with advanced solid tumors. In the dose escalation stage, based on the incidence of dose limited toxicity (DLT) and adverse event (AE), explore and determine the maximum tolerated dose (MTD) and phase II recommended dose (RP2D). After RP2D and administration protocol are determined, an extended study will be conducted on 6-10 subjects to further evaluate the safety and antitumor activity of APL-102. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05055518
Study type Interventional
Source Apollomics Inc.
Contact Zhejiang CrownMab Ltd.
Phone 0571-83521933
Email ClinicalTrialsChina@apollomicsinc.com
Status Recruiting
Phase Phase 1
Start date August 2, 2021
Completion date December 31, 2023

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