Arrivent Presents the Final Analysis of Firmonertinib Monotherapy Data from Global Phase 1b Study in EGFR PACC Mutant Non-Small Cell Lung Cancer at the 2025 World Conference on Lung Cancer
ArriVent BioPharma, Inc. (AVBP)
Company Research
Source: GlobeNewswire
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) 14.6 months by BICR in first-line patientsConfirmed CNS (central nervous system) responses with firmonertinib including complete responses (CRs) by BICRFirmonertinib rapidly decreased or cleared PACC circulating tumor DNA (ctDNA) in frontline patients across PACC mutation types (frequent, less frequent and compound PACC) consistent with broad PACC activityEnrollment of the first patient in the global pivotal Phase 3 ALPACCA study in first-line EGFR PACC mutant non-small cell lung (NSCLC) cancer expected in the second half of 2025 NEWTOWN SQUARE, Pa., Sept. 09, 2025 (GLOBE NEWSWIRE) -- ArriVent BioPharma, Inc. (Company or ArriVent) (Nasdaq: AVBP), a clinical-stage company dedicated to accelerating the global development of innovative biopharmaceutical therapeutics,
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News
- ArriVent BioPharma (NASDAQ:AVBP) was upgraded by analysts at Truist Financial Corporation to a "strong-buy" rating.MarketBeat
- ArriVent BioPharma (NASDAQ:AVBP) was given a new $43.00 price target on by analysts at Truist Financial Corporation.MarketBeat
- ArriVent BioPharma (NASDAQ:AVBP) had its price target lowered by analysts at Citigroup Inc. from $33.00 to $31.00. They now have a "buy" rating on the stock.MarketBeat
- ArriVent BioPharma Reports Third Quarter 2025 Financial Results [Yahoo! Finance]Yahoo! Finance
- ArriVent BioPharma Reports Third Quarter 2025 Financial ResultsGlobeNewswire
AVBP
Earnings
- 11/10/25 - Miss
AVBP
Sec Filings
- 11/14/25 - Form SCHEDULE
- 11/10/25 - Form 10-Q
- 11/10/25 - Form 8-K
- AVBP's page on the SEC website