ArriVent Says Cancer Drug Candidate Firmonertinib Misses Primary Endpoint in Phase 3 Trial; Shares Fall Pre-Bell
MT newswire2026/10/06 12:5008:50 AM EDT, 10/06/2026 (MT Newswires) -- ArriVent BioPharma's (AVBP) phase 3 Furvent trial of firmonertinib did not achieve its primary progression-free survival goal in previously untreated patients with EGFR exon 20 insertion-mutated non-small cell lung cancer, the company said Tuesday. According to the study, media progression-free survival was 11 months for the 240mg firmonertinib dose; 8.4 months for 160mg, and 9.5 months for the control arm, while confirmed response rates were 60%, 35% and 33%, respectively. The safety profile was consistent with prior studies, with no new safety signals. Grade 3 or higher adverse events occurred in 52% of patients on the 240mg dose, 53% on the 160mg dose, and 55% in the control arm, the company said. Shares of ArriVent fell more than 56% in recent premarket activity Tuesday. Price: 12.50, Change: -15.96, Percent Change: -56.08
Disclaimer: The content of this article solely reflects the author's opinion and does not represent the platform in any capacity. This article is not intended to serve as a reference for making investment decisions.
You may also like
Former BioNTech executive leads Bambusa Therapeutics (BBTX.US) in sprint to Nasdaq, "boosting" eczema drug trials
Bambusa Therapeutics Inc. has filed for an initial public offering, planning to raise funds for clinical trials of treatments for eczema and other inflammatory diseases.
JPMorgan raises AbbVie target price to $300