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Clinical Trial Summary

The purpose of this study is to evaluate the safety and tolerability of talectrectinib as treatment for Stage IV ILC with CDH1 mutation


Clinical Trial Description

Invasive lobular cancer (ILC) represents 10-15% of all breast cancers, up to 75% of ILCs carry a mutation in CDH1 gene which encodes for e-cadherin (ECAD), which is a cell adhesion glycoprotein. Preclinical data using patient derived xenografts have shown loss of ECAD due to CDH1 mutation is associated with an upregulation ROS1 activity, and ROS1 inhibitors have demonstrated synthetic lethality in CDH1-mutated cell lines. Taletrectinib is a novel ROS1/NTRK inhibitor with demonstrated activity in ROS1 mutated non-small cell lung cancer. The purpose of the trial is to estimate the activity of taletrectinib in previously treated CDH1-mutated metastatic breast ILC. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06214793
Study type Interventional
Source Case Comprehensive Cancer Center
Contact Megan Kruse, MD
Phone 216-956-5147
Email krusem@ccf.org
Status Not yet recruiting
Phase Phase 2
Start date October 1, 2024
Completion date January 1, 2030

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