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Clinical Trial Summary

To Observe the Efficacy and Safety of Pyrotinib Maleate in Patients With HER2-positive Advanced Colorectal Cancer


Clinical Trial Description

This study is an investigator-initiated, open-label, two-cohort phase II trial, assessing the objective response rate (ORR) of pyrotinib monotherapy (Cohort 1) or in combination with trastuzumab (Cohort 2), in HER2-positive advanced colorectal cancer. HER2 positivity is centrally established by immunohistochemistry (IHC) and silver in situ hybridization (SISH). To be HER2 eligible the original tumor, or the biopsied metastasis (whichever is last available), must be IHC 3+ or 2+ in more than 50% of cells, confirmed by SISH or fluorescence in situ hybridization (FISH) with a HER2:CEP17 ratio ≥ 2.0. For IHC a positive staining (3+) is defined as an intense membrane staining which can be circumferential, basolateral, or lateral of the tumor cells. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04380012
Study type Interventional
Source Second Affiliated Hospital, School of Medicine, Zhejiang University
Contact Ying Yuan, Doctor
Phone +86 13858193601
Email yuany@z2hospital.com
Status Recruiting
Phase Phase 2
Start date December 17, 2019
Completion date June 17, 2022

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