Merus Announces FDA Approval of BIZENGRI® (zenocutuzumab-zbco) for NRG1+ Pancreatic Adenocarcinoma and NRG1+ Non–Small Cell Lung Cancer (NSCLC) Based on Safety and Efficacy Data From the eNRGy Study
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Merus N.V. announced FDA approval for BIZENGRI® (zenocutuzumab-zbco) for treating NRG1+ pancreatic adenocarcinoma and NSCLC. The approval is based on safety and efficacy data from the eNRGy study, with a focus on overall response rate and duration of response.
December 04, 2024 | 10:15 pm
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Merus N.V. received FDA approval for BIZENGRI®, a treatment for NRG1+ pancreatic adenocarcinoma and NSCLC. This approval could boost Merus' market position and stock value.
The FDA approval of BIZENGRI® is a significant milestone for Merus, as it is the first treatment for specific advanced cancers with NRG1 gene fusion. This approval is likely to enhance Merus' market position and could lead to an increase in stock value due to the potential market for this treatment.
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