TTrialPathMatch Me to Trials
← Back to trials
RecruitingNon-Small-Cell Lung CancerMetastatic Non-Small-Cell Lung CancerAdvanced Non-Small-Cell Lung Cancer

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

See if you qualify for this study

Answer a few quick questions about your location and health. Takes about a minute.

Check my eligibility →

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

California

Fullerton · Los Angeles · Orange · Sacramento …

Colorado

Aurora

Illinois

Arlington Heights · Chicago

Michigan

Detroit

New York

Lake Success · New York

Ohio

Columbus

Pennsylvania

Philadelphia

Texas

Dallas · Houston

Virginia

Charlottesville · Fairfax · Winchester

Washington

Edmonds

Source: ClinicalTrials.gov · NCT07185997 · last updated 2026-09-01

Study to Evaluate Efficacy and Safety of Firmonertinib Compared With I · TrialPath