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Clinical Trial Summary

This is a phase I, multicenter, open-label study. The study will investigate the safety, tolerability, PK, and preliminary efficacy of TY-2699a on locally advanced or metastatic solid tumors.


Clinical Trial Description

To assess the safety and tolerability of TY-2699a when administered as a single agent in subjects with locally advanced or metastatic solid tumors. To determine the maximum tolerated dose (MTD), and the recommended phase 2 dose (RP2D) as a single agent in subjects with locally advanced or metastatic solid tumors. To evaluate the pharmacokinetics (PK) of TY-2699a administered at single and multiple oral doses. To assess the preliminary antitumor activity of TY-2699a as a single agent in subjects with locally advanced or metastatic solid tumors. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05866692
Study type Interventional
Source TYK Medicines, Inc
Contact
Status Recruiting
Phase Phase 1
Start date August 17, 2023
Completion date October 2026

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