NSCLC Clinical Trial - Efficacy & Safety of Furmonertinib in Patients With

Clinical Trial Summary

This study is a a single-arm, single-center, open-label, prospective phase II trial. The aim of this phase II study is to evaluate the efficacy and safety of Furmonertinib in patients with EGFR mutation (including 19del or 21L858R or T790M) in advanced NSCLC with brain metastases.

See also
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NCT number	NCT05465343
Study type	Interventional
Source	Peking Union Medical College
Contact	Junling Li, Professor
Phone	010-87788495
Email	lijunling@cicams.ac.cn
Status	Recruiting
Phase	Phase 2
Start date	July 11, 2022
Completion date	June 30, 2023

Efficacy and Safety of Furmonertinib in Patients With EGFR Mutations in Advanced NSCLC With Brain Metastases: A Single-center, Open-label, Phase II Trial（iFORCE）

Clinical Trial Summary

Clinical Trial Description

Study Design

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