Y-mAbs Submits Omburtamab Marketing Authorization Application to the European Medicines Agency
"We believe omburtamab is on track to potentially become the first EMA approved targeted therapy for pediatric patients with CNS/leptomeningeal metastasis from neuroblastoma," said
In addition, Y-mAbs recently concluded a Type B meeting with the
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About Y-mAbs
Y-mAbs is a commercial-stage biopharmaceutical company focused on the development and commercialization of novel, antibody-based therapeutic products for the treatment of cancer. The Company has a broad and advanced product pipeline, including one FDA approved product, DANYELZA® (naxitamab-gqgk), which targets tumors that express GD2, and one pivotal-stage product candidate, omburtamab, which targets tumors that express B7-H3.
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“Y-mAbs®” and “DANYELZA®” are registered trademarks of
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Source: Y-mAbs Therapeutics, Inc