Clinical TrialsFirmonertinib demonstrated a 78.6% and 46.2% ORR in treatment-naïve and pretreated patients, respectively, which compares favorably to those achieved by the majority of competitor agents.
Financial PerformanceArriVent ended 3Q24 with $282.9M in cash, cash equivalents, and marketable securities, which should provide an operational runway into 2026 and through multiple clinical data readouts.
Regulatory OutlookThe probability of approval for firmonertinib in EGFR PACC+ NSCLC was raised to 50% from the prior 40%.