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EXEL

EXELIXIS, INC.

EXELIXIS, INC. Q3 FY2025 earnings call

November 4, 2025 · fiscal period ended 2024-10

EPS · actual vs est

$0.78 / $0.69Beat +13.9%

Revenue · actual vs est

$597.8M / $590.2MBeat +1.3%
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Summary

Generated 2025-11-04

Management highlights

  • R&D Momentum: Zanzalintinib is the focus of seven pivotal trials, with positive results from STELLAR-303 in CRC. Early-stage pipeline has four molecules in Phase I clinical development.
  • Commercial Execution: Cabozantinib U.S. business strong with growth in demand and revenue; NET launch in neuroendocrine tumors off to a great start with over 40% new patient share. Plan to expedite build-out of GI sales team.
  • Pipeline Update: Early-stage pipeline includes molecules like XL309, XB010, XB628, and XB371, with Phase I studies progressing well.
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Segment performance

Cabozantinib: U.S. net product revenues grew approximately 14% year-over-year to $543 million in the third quarter of 2025 compared to $478 million in the third quarter of 2024. Global Cabo franchise and their product revenues generated by Exelixis and partners were approximately $739 million in Q3 2025 vs. $653 million in Q3 2024. Cabo demand in neuroendocrine tumors grew about 50% and contributed approximately 6% of Q3 business, with revenue for 2025 expected to exceed $100 million. Zanzalintinib: Rapidly advancing with seven ongoing and soon-to-start pivotal trials, with positive results from STELLAR-303 in CRC, showing a 20% reduction in death risk in the ITT population.

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Guidance

  • Revised total revenue guidance: $2.3 billion to $2.35 billion; net product revenue: $2.1 billion to $2.15 billion.
  • Cost of goods guidance: ~4% of net product revenues.
  • R&D expense guidance: $850 million to $900 million (lowered by $75 million).
  • SG&A expense guidance: $500 million to $525 million.
  • Effective tax rate guidance: 17% to 18%.
View in transcript ↓

Risks

  • Regulatory Risks: Uncertainties in regulatory review and approval processes for trials and product launches.
  • Competitive Risks: Intense market competition in the oncology space.
  • Clinical Trial Risks: Uncertainties in clinical trial outcomes and the ability to meet trial endpoints.
View in transcript ↓

Q&A highlights

Q: Capital allocation strategy between R&D, BD, and share repurchases A: Chris Senner said they plan to fund R&D, business development, and share repurchases with revenue growth and prudent expense management.

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Key numbers

Reported versus consensus

Earnings calendar feed

MetricReportedConsensusDeltaPrior year
EPS$0.78$0.69+13.9%
Revenue$597.8M$590.2M+1.3%

Transcript

November 4, 2025

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