The FDA on September 17, 2021, approved CABOMETYX® (Cabozantinib) for adult and pediatric patients 12 years of age and older with locally advanced or metastatic Differentiated Thyroid Cancer (DTC) that has progressed following prior VEGFR-targeted therapy and who are ineligible or refractory to Radioactive Iodine. CABOMETYX® is a product of Exelixis, Inc.
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