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Clinical Trial Summary

This is a single arm, open label, single center, and prospective, interventional study to explore clinical efficacy of afatinib in patients with chordoma of skull base. Subject meeting the inclusion criteria will take afatinib (40 mg daily) orally, 4 weeks for a cycle. The primary objective is to assess the efficacy of afatinib in chordoma of skull base by objective response rate (ORR). The Secondary objectives is to assess progression free survival (PFS), overall survival (OS), tumor response duration and tumor shrinkage degree in patients with chordoma of skull base after using afatinib; to evaluate the safety and tolerability of afatinib in patients with chordoma of skull base.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT05519917
Study type Interventional
Source Huashan Hospital
Contact Qilin Zhang, MD
Phone 86-21-52889999
Email zhangqlhuashan@163.com
Status Not yet recruiting
Phase Phase 2
Start date October 1, 2022
Completion date December 30, 2025