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Clinical Trial Summary

The primary objective of this study is to evaluate the safety and tolerability of TYK-00540, with dose-escalation stage and dose-expansion stage.


Clinical Trial Description

To evaluate dose limiting toxicities (DLT) and determine the maximum tolerated dose (MTD) in subjects with locally advanced or metastatic solid tumors. To investigate the pharmacokinetic profile of TYK-00540 and its metabolites after single then multiple doses of TYK-00540 administered orally once daily. To assess preliminary effectiveness. ;


Study Design


Related Conditions & MeSH terms

  • Locally Advanced or Metastatic Solid Tumors
  • Neoplasms

NCT number NCT06246071
Study type Interventional
Source TYK Medicines, Inc
Contact Jian Zhang, MD
Phone 18017312991
Email syner2000@163.com
Status Recruiting
Phase Phase 1
Start date January 2, 2024
Completion date December 5, 2026

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