Clinical Trial ResultsFirmonertinib demonstrated a best overall response rate of 81.8% at the 240 mg daily dose, including all unconfirmed responses, showcasing its promising efficacy in EGFR PACC NSCLC.
Financial PositionArriVent 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.
Market PotentialThere is no FDA approved agent for NSCLC patients with EGFR PACC mutations and no broadly utilized standard of care treatment, highlighting a significant opportunity for firmonertinib to address an unmet need.