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Exelixis' Partner Ipsen Receives European Commission Approval for CABOMETYX® (cabozantinib) for Patients with Previously Treated Advanced Neuroendocrine Tumors

1. Ipsen received EC approval for CABOMETYX® in pancreatic neuroendocrine tumors. 2. This could expand market opportunities for Exelixis and influence EXEL's stock performance.

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Why Bullish?

EC approval for CABOMETYX® enhances its therapeutic value, likely increasing sales. Historical approvals often led to stock price increases for similar biotech firms.

How important is it?

The article directly highlights a significant regulatory approval that can drive future revenue for EXEL, thus substantially affecting investor sentiment and stock price.

Why Long Term?

The approval opens new markets for CABOMETYX®, potentially increasing revenues over time, similar to prior drug launches that created sustained growth for companies.

Related Companies

ALAMEDA, Calif.--(BUSINESS WIRE)--Exelixis, Inc. (Nasdaq: EXEL) today announced that its partner Ipsen received approval from the European Commission (EC) for CABOMETYX® (cabozantinib) for the treatment of adult patients with unresectable or metastatic, well-differentiated pancreatic (pNET) and extra-pancreatic (epNET) neuroendocrine tumors who have progressed following at least one prior systemic therapy other than somatostatin analogues. This approval follows the positive opinion received fro.

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