Study to Evaluate Efficacy and Safety of Firmonertinib Compared With Investigator's Choice of EGFR Inhibitor as First-Line Treatment in Participants Who Have Locally Advanced or Metastatic NSCLC With EGFR P-Loop and Alpha C-Helix Compressing (PACC) Uncommon Mutations
Eligible age
18+ yrs
Accepts
All genders
Locations
10 states
Healthy volunteers
No
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About this study
Global, Phase 3, randomized, multicenter, open-label study evaluating the efficacy and safety of firmonertinib at a dose level of 240 mg QD compared to investigator's choice of osimertinib (80 mg QD) or afatinib (40 mg QD) in participants who have locally advanced or metastatic NSCLC with EGFR PACC mutations, and who have not received any prior therapy for advanced disease. Participants will be randomized in a 1:1 ratio to treatment with firmonertinib or osimertinib or afatinib and will take the assigned dose daily.
Sponsor: ArriVent BioPharma, Inc.
Where it's recruiting
Fullerton · Los Angeles · Orange · Sacramento …
Aurora
Arlington Heights · Chicago
Detroit
Lake Success · New York
Columbus
Philadelphia
Dallas · Houston
Charlottesville · Fairfax · Winchester
Edmonds
Source: ClinicalTrials.gov · NCT07185997 · last updated 2026-09-01