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Updated: 3-ArriVent’s cancer drug failed to “significantly” delay disease progression, stock price plummeted

Updated: 3-ArriVent’s cancer drug failed to “significantly” delay disease progression, stock price plummeted

路透社路透社2026/10/06 15:18
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Updated stock data and added analyst comments in paragraphs 8 and 10 Christy Santhosh - Reuters, October 6 - ArriVent BioPharma (AVBP.O) announced on Tuesday that its oral therapy for a rare form of lung cancer failed to significantly delay disease progression in a late-stage clinical trial, causing the company's share price to plunge by nearly 60% in early trading. The therapy, firmonertinib, was tested in treatment-naïve advanced non-small cell lung cancer (NSCLC) patients carrying a gene mutation known as EGFR exon 20 insertion, which may promote cancer growth. This mutation accounts for about 0.5% to 1% of all NSCLC cases. NSCLC makes up around 85% of all lung cancer cases. An assessment by independent reviewers showed that ArriVent’s 240 mg dose therapy extended median progression-free survival to 11 months in the trial, compared to just 9.5 months for the chemotherapy group. CEO Bing Yao stated that the improvement in progression-free survival (i.e., the period during which a patient's cancer does not worsen or spread) was not "significant". "These disappointing results are not what we had hoped for, especially for patients who... are in urgent need of more effective treatment options." The company said it is reviewing the complete dataset to determine the most appropriate development path for firmonertinib, and no new safety signals were observed in the trial. BTIG analyst Jeet Mukherjee noted that the main reason the trial appears to have failed was the control group's performance exceeding expectations—their progression-free survival reached 9.5 months, when only 7.5 to 8 months was anticipated; firmonertinib’s 11-month result matched the expected range of 9 to 11 months. Additionally, firmonertinib is currently undergoing an advanced clinical trial in NSCLC patients with rare EGFR PACC mutations in their tumors. "This result is a significant setback for the exon 20 mutation treatment space, but the PACC program still has clinical support," said Clear Street analyst Kaveri Pohlman. The therapy has been approved in China for NSCLC patients carrying specific mutations. (To aid non-English speakers, Reuters has automated the translation of its reports into several other languages. As automated translations may contain errors or lack necessary context, Reuters does not guarantee the accuracy of these translated texts and they are provided for reader convenience only. Reuters is not responsible for any damages or losses arising from the use of automated translation features.)

Stock price data updated, and analyst comments added in paragraphs 8 and 10

Christy Santhosh

- ArriVent BioPharma (AVBP.O) said on Tuesday that its oral therapy for a rare form of lung cancer failed to significantly delay disease progression in a late-stage clinical trial, sending the company’s shares plunging nearly 60% in early trading.

The therapy, firmonertinib, was tested in patients with previously untreated advanced non-small cell lung cancer (NSCLC) who carry a gene variant called EGFR exon 20 insertion mutation, which may promote cancer growth.

This mutation accounts for about 0.5% to 1% of all non-small cell lung cancer (NSCLC) cases. NSCLC accounts for about 85% of all lung cancer cases.

An independent review found that in the trial, ArriVent’s 240 mg dose therapy extended the median progression-free survival to 11 months, compared with just 9.5 months for the chemotherapy group.

Chief Executive Officer Bing Yao said the improvement in progression-free survival – the time patients lived without the disease worsening or spreading – was not “significant.”

“These disappointing results are not what we had hoped for, especially for patients who... are in urgent need of more effective treatment options.”

The company said it is evaluating the full data set to determine the most appropriate development path for firmonertinib, and no new safety signals were observed in the trial.

BTIG analyst Jeet Mukherjee noted that the main reason the trial appears to have failed is that the control group outperformed expectations—the progression-free survival reached 9.5 months versus the expected 7.5 to 8 months, while the 11 months seen with firmonertinib was in line with the expected range of 9 to 11 months.

In addition, firmonertinib is currently being tested in a late-stage clinical trial in NSCLC patients with rare EGFR PACC mutations in their tumors.

“This is a major setback for the exon 20 mutation treatment field, but the PACC program still has clinical support,” said Clear Street analyst Kaveri Pullman.

The therapy has been approved in China for NSCLC patients carrying certain mutations.


(To make its reporting more accessible to non-native English speakers, Reuters automatically translates its articles into several other languages. Automatic translation may contain errors or omit context, so Reuters does not guarantee the accuracy of such translations, which are provided for reader convenience only. Reuters accepts no responsibility for any damage or loss resulting from the use of automatic translation.)

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