已收盘 10-31 16:00:00 美东时间
+0.260
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ArriVent BioPharma announced the appointment of Brent S. Rice as Chief Commercial Officer. With over 25 years of experience in biotech and pharma, Rice will lead commercial efforts for firmonertinib, a potential treatment for EGFR mutant NSCLC, and advance the company's ADC portfolio. Previously, Rice served as CCO at Autolus Therapeutics and held leadership roles at Amgen and Juno Therapeutics, demonstrating success in launching therapies and bu...
09-22 20:05
16.0 months median progression free survival (mPFS) with firmonertinib 240 mg by blinded independent central review (BICR) in first-line patientsConfirmed overall response rate (cORR) 68.2% and duration of response (DOR)
09-09 20:07
ArriVent BioPharma presented positive data from the Phase 1b FURTHER trial of firmonertinib in first-line NSCLC patients with EGFR PACC mutations. Key findings include a 16.0-month median progression-free survival (mPFS) and a 68.2% confirmed overall response rate (cORR). Firmonertinib also demonstrated CNS responses, including complete responses, and rapidly cleared PACC ctDNA across mutation types. Enrollment in the Phase 3 ALPACCA trial is exp...
09-09 12:00
Citigroup analyst Yigal Nochomovitz maintains ArriVent BioPharma (NASDAQ:AVBP) with a Buy and lowers the price target from $40 to $33.
08-12 19:41
ArriVent BioPharma, Inc. ( ($AVBP) ) has released its Q2 earnings. Here is a br...
08-12 12:18
ArriVent BioPharma (NASDAQ:AVBP) reported quarterly losses of $(0.90) per share which missed the analyst consensus estimate of $(0.72) by 25.52 percent. This is a 38.46 percent decrease over losses of $(0.65) per share
08-11 20:12
ArriVent BioPharma reported positive interim Phase 1b data for firmonertinib in EGFR PACC mutant NSCLC, with plans to initiate the global pivotal Phase 3 ALPACCA study in 2H 2025. The first patient was dosed in the Phase 1 study of ARR-217, a CDH17-targeted ADC for gastrointestinal tumors. Top-line data from the FURVENT Phase 3 study for EGFR exon 20 insertion mutant NSCLC is expected in early 2026. The company had $254.5 million in cash and inve...
08-11 12:00
Enrollment in FURVENT was completed in Q1 2025Firmonertinib received FDA Breakthrough Therapy Designation in this patient population
07-21 20:13
今日重点评级关注:摩根大通:维持Cogent Biosciences"超配"评级,目标价从25美元升至29美元;摩根士丹利:维持Legend Biotech"超配"评级,目标价从80美元升至81美元
07-11 09:04
Goldman Sachs analyst Corinne Johnson reinstates ArriVent BioPharma (NASDAQ:AVBP) with a Buy and announces $33 price target.
07-11 02:13