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Clinical Trial Summary

This is a Phase 1b, open-label, multi-center, dose-escalation and dose expansion study designed to evaluate the safety, pharmacokinetics (PK), and preliminary antitumor activity of furmonertinib in patients with advanced or metastatic non-small cell lung cancer (NSCLC) with activating, including uncommon, Epidermal Growth Factor Receptor (EGFR) or Human Epidermal Growth Factor Receptor 2 (HER2) mutations. Patients will be enrolled into one of 2 stages: Stage 1 (Dose Escalation and Backfill Cohorts) and Stage 2 (Dose Expansion).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05364073
Study type Interventional
Source ArriVent BioPharma, Inc.
Contact Nichole Baio
Phone 628-277-4836
Email FURMO002CT@arrivent.com
Status Recruiting
Phase Phase 1
Start date June 30, 2022
Completion date September 2025

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