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Clinical Trial Summary

Evaluate the efficacy and safety of Disitamb Vedotin in patients with HER2-positive or HER2-low expressing, locally advanced or metastatic breast cancer


Clinical Trial Description

The main goal of this clinical trial is to examinie the utilization of RC48 in different HER2 statuses, elucidating its clinical outcomes and safety, and investigating the factors that influence its clinical efficacy. The primary endpoint was the objective response rate (ORR) assessed by the primary researcher. Secondary endpoints included progression-free survival (PFS), overall survival (OS), disease control rate (DCR), time to progression, and safety. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06168227
Study type Observational
Source The First Affiliated Hospital with Nanjing Medical University
Contact
Status Completed
Phase
Start date October 1, 2021
Completion date September 30, 2023

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