$AVBP

ArriVent BioPharma, Inc.

8
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No SEC Form 4 filings for $AVBP in the last 30 days.

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ArriVent Announces Initial Phase 1 Data for CDH17-targeted ADC ARR-217 in Patients with Gastrointestinal Cancers at ESMO Congress 2026

ArriVent BioPharma, Inc. (AVBP) filed an SEC Form 8-K — Other Events. Exhibit 99.1 ArriVent Announces Initial Phase 1 Data for CDH17-targeted ADC ARR-217 in Patients with Gastrointestinal Cancers at ESMO Congress 2026 · 44.8% ORR at 6mg/kg dose in late-line CRC patients · ARR-217 was generally well-tolerated · ArriVent to host virtual webinar on Mo

AVBP sentiment & insider activity

Over the past 7 days, AlphAI's AI scored 8 news stories mentioning AVBP (ArriVent BioPharma, Inc.). Coverage has skewed bullish: 8 bullish, 0 neutral, and 0 bearish.

What's driving AVBP

  • Analysts raised ArriVent BioPharma's 12-month price target from $22.91 to $24, suggesting 14% upside. The consensus rating remains 'Buy' among 12 analysts. Forecasts range from $15 to $30 per share, according to estimates.

    tradingview.com · Oct 26, 2026

  • Positive Phase 1 results are likely to lift AVBP stock as investors price in potential efficacy and future trial milestones.

    SEC EDGAR 8-K · Oct 26, 2026

  • Positive Phase 1 results may lift AVBP as investors anticipate further development and potential market potential.

    stocktitan.net · Oct 25, 2026

  • Positive early-phase data could lift AVBP on expectations of further development and potential partnerships.

    stocktitan.net · Oct 23, 2026

  • Strong early‑stage data may boost investor confidence and drive short‑term price appreciation.

    SEC EDGAR 8-K · Oct 19, 2026

AlphAI scores every news story that mentions AVBP with an AI model for sentiment and relevance, and aggregates insider trades from ArriVent BioPharma, Inc.'s SEC EDGAR Form 4 filings. Figures refresh continuously.

News on $AVBP

Score
$AVBPMedAI 9/10

ArriVent Announces Initial Phase 1 Data for CDH17-targeted ADC ARR-217 in Patients with Gastrointestinal Cancers at ESMO Congress 2026

ArriVent BioPharma, Inc. (AVBP) filed an SEC Form 8-K — Other Events. Exhibit 99.1 ArriVent Announces Initial Phase 1 Data for CDH17-targeted ADC ARR-217 in Patients with Gastrointestinal Cancers at ESMO Congress 2026 · 44.8% ORR at 6mg/kg dose in late-line CRC patients · ARR-217 was generally well-tolerated · ArriVent to host virtual webinar on Mo

$AVBPMedAI 8/10

At one dose, an experimental cancer drug had a 44.8% response rate after earlier colorectal cancer treatments.

ArriVent BioPharma (AVBP) reported Phase 1 results for ARR-217, showing a 44.8% response rate in colorectal cancer patients at a 6mg/kg dose. The drug was generally well-tolerated. ArriVent plans a Phase 1b dose optimization study, with data expected in 2027. ARR-217 is a cadherin-17-targeting antibody-drug conjugate developed with Lepu Biopharma.

$AVBPMedAI 8/10

First human data on an experimental cancer drug will be presented in a late-breaking session.

ArriVent BioPharma (Nasdaq: AVBP) announced that initial safety and efficacy data from its Phase 1 study of ARR-217, a CDH17-targeted ADC for gastrointestinal cancers, will be presented at ESMO Congress 2026. The company will host a webinar on October 26, 2026, to discuss the data. ARR-217 is ArriVent's lead clinical candidate, obtained via a collaboration with Lepu Biopharma.

$AVBPHighAI 8/10

ArriVent Announces Cancer Cell Publication Highlighting Firmonertinib in EGFR PACC-Mutant Non-Small Cell Lung Cancer

ArriVent BioPharma, Inc. (AVBP) filed an SEC Form 8-K — Regulation FD Disclosure. Exhibit 99.1 ArriVent Announces Cancer Cell Publication Highlighting Firmonertinib in EGFR PACC-Mutant Non-Small Cell Lung Cancer NEWTOWN SQUARE, PA, October 19, 2026 (GLOBE NEWSWIRE) -- ArriVent BioPharma, Inc. (Company or ArriVent) (Nasdaq: AVBP), a clinical-stage company dedic

$AVBPHighAI 9/10

A lung cancer drug showed a 68% response rate at the higher dose. No targeted standard exists for this mutation.

ArriVent BioPharma (AVBP) reported Phase 1b trial results for firmonertinib, showing 43% and 68% response rates at different doses in EGFR PACC-mutant NSCLC. The drug demonstrated intracranial activity and manageable safety. ArriVent is advancing a Phase 3 trial (ALPACCA) for this underserved lung cancer population, with no current standard treatment.

$AVBPMedAI 8/10

ArriVent Announces First Patient Dosed with Novel Tetravalent MUC16/NaPi2b Dual Target ADC, ARR-002

ArriVent BioPharma, Inc. (AVBP) filed an SEC Form 8-K — Other Events. Exhibit 99.1 ArriVent Announces First Patient Dosed with Novel Tetravalent MUC16/NaPi2b Dual Target ADC, ARR-002 NEWTOWN SQUARE, PA, October 12, 2026 (GLOBE NEWSWIRE) -- ArriVent BioPharma, Inc. (Company or ArriVent) (Nasdaq: AVBP), a clinical-stage company dedicated to accelerat

$AVBPMedAI 8/10

A cancer drug targets two proteins in ovarian and endometrial tumors. Its first patient has been dosed.

ArriVent BioPharma (AVBP) dosed the first patient in a Phase 1 trial for ARR-002, a dual-target ADC for ovarian and endometrial cancer. The company licensed ARR-002 to Allist for Greater China. ARR-002 targets MUC16 and NaPi2b, aiming to overcome limitations of single-target ADCs. Preclinical data showed improved activity and stability. ArriVent's pipeline includes lung and gastrointestinal cancer programs.

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