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FDA delays review of Exelixis' zanzalintinib by 3 months, no new safety issues found

Analyst Insights
14 Sep 2026
Seeking Alpha
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Bullish
FDA delays review of Exelixis' zanzalintinib by 3 months, no new safety issues found

The FDA extended its review of Exelixis' cancer drug zanzalintinib by three months without revealing any new clinical failures or safety concerns. This delay reduces the drug's present value by about 2.35%, which is less than the initial market loss. Exelixis' other drug, CABOMETYX, continues to grow, and the company's 2026 revenue guidance does not include zanzalintinib sales. The stock trades at a reasonable valuation, and the analyst maintains a Buy rating with a $68 price target.

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