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ArriVent BioPharma, Inc.Bullish
ArriVent BioPharma announced the publication of Phase 1b (FURMO-002) results for firmonertinib in Cancer Cell, demonstrating significant clinical activity in EGFR PACC-mutant NSCLC patients. The study reported confirmed overall response rates of 43% at 160 mg and 68% at 240 mg, supporting the company's ongoing global Phase 3 ALPACCA trial. This data reinforces the potential of firmonertinib as a first-in-class targeted therapy for this underserved patient population.…more
ArriVent BioPharma, Inc.
Six entities, including Vivo Opportunity Fund Holdings, L.P., have filed a Schedule 13G to report their collective ownership stake in ArriVent BioPharma, Inc. The investors have agreed to jointly file any subsequent amendments regarding their holdings.…more
ArriVent BioPharma, Inc.
ArriVent BioPharma has successfully dosed the first patient in its U.S. Phase 1 clinical trial for ARR-002, a novel MUC16/NaPi2b dual-target tetravalent antibody-drug conjugate (ADC) targeting ovarian and endometrial cancer. This milestone marks the expansion of the company's clinical pipeline beyond its existing programs in lung and gastrointestinal cancers.…more
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ArriVent Reports Encouraging Phase 1 Data for CDH17-targeted ADC ARR-217…more
ArriVent announced positive initial Phase 1 results for its CDH17-targeting ADC, ARR-217, demonstrating significant anti-tumor activity in gastrointestinal cancer patients. The company plans to advance the candidate into a Phase 1b dose optimization study based on these findings.…more
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ArriVent will present initial safety and efficacy data from the Phase 1 study of its CDH17-targeted ADC, ARR-217, in patients with gastrointestinal cancers at the ESMO Congress 2026. The company plans to host a virtual webinar to discuss the clinical findings following the presentation.…more
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ArriVent BioPharma announced the publication of Phase 1b clinical results for its lung cancer candidate, firmonertinib, in the journal Cancer Cell. While the data highlights potential efficacy in EGFR PACC-mutant NSCLC, the company is currently advancing toward Phase 3 trials, making the impact of this publication neutral.…more
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