Exelixis has received U.S. FDA approval of Cabometyx in patients 12 years and older with previously treated radioactive iodine-refractory differentiated thyroid cancer.
- Approval ahead of PDUFA target date of Dec. 4, 2021
- Approval based on results from COSMIC-311 trial
- Co. says it’s prepared to fully support expanded indication immediately
- Exelixis shares up over 2% in extended trading
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