Exelixis Provides 2026 Financial Guidance: Anticipates $2.525B to $2.625B in Revenue
Written by Emily J. Thompson, Senior Investment Analyst
Updated: Jan 11 2026
0mins
Source: Businesswire
- Financial Outlook: Exelixis anticipates total revenues for 2026 to range from $2.525 billion to $2.625 billion, representing a significant growth from $2.320 billion in 2025, indicating strong potential in the oncology treatment sector.
- Product Revenue Growth: The company expects net product revenues to reach $2.325 billion to $2.425 billion in 2026, reflecting CABOMETYX's sustained leadership in the renal cell carcinoma and neuroendocrine tumor markets, further solidifying its market share.
- Increased R&D Investment: Research and development expenses are projected to rise to $875 million to $925 million in 2026, up from $825 million in 2025, demonstrating the company's commitment to advancing new drug development and clinical trials.
- Stock Repurchase Program: Since March 2023, Exelixis has repurchased $2.16 billion in stock and plans to buy back an additional $750 million by the end of 2026, aimed at enhancing shareholder value and boosting market confidence.
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Analyst Views on EXEL
Wall Street analysts forecast EXEL stock price to fall
16 Analyst Rating
7 Buy
8 Hold
1 Sell
Moderate Buy
Current: 51.450
Low
30.00
Averages
44.09
High
52.00
Current: 51.450
Low
30.00
Averages
44.09
High
52.00
About EXEL
Exelixis, Inc. is an oncology company. The Company has produced four marketed pharmaceutical products, two of which are formulations of its flagship molecule, cabozantinib. It is also advancing and evolving its product pipeline portfolio, including its lead investigational asset, zanzalintinib. Cabozantinib is an inhibitor of multiple tyrosine kinases, including MET, AXL, VEGF receptors and RET and has been also approved as CABOMETYX tablets for advanced renal cell carcinoma, for previously treated hepatocellular carcinoma and for previously treated, radioactive iodine-refractory differentiated thyroid cancer, and as COMETRIQ capsules for progressive, metastatic medullary thyroid cancer. The Company's other two products are COTELLIC, an inhibitor of MEK approved as part of multiple combination regimens to treat specific forms of advanced melanoma and MINNEBRO an oral, non-steroidal, selective blocker of the mineralocorticoid receptor approved the treatment of hypertension in Japan.
About the author

Emily J. Thompson
Emily J. Thompson, a Chartered Financial Analyst (CFA) with 12 years in investment research, graduated with honors from the Wharton School. Specializing in industrial and technology stocks, she provides in-depth analysis for Intellectia’s earnings and market brief reports.
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- New Drug Presentation: Exelixis will showcase its flagship product CABOMETYX® and investigational oral kinase inhibitor zanzalintinib at the 2026 ASCO Annual Meeting, highlighting ongoing progress in tumor treatment, which is expected to attract investor interest and boost market confidence.
- Clinical Trial Results: CABOMETYX has demonstrated significant efficacy in multiple clinical trials, including studies targeting renal cell carcinoma and neuroendocrine tumors, further solidifying its foundational role in patient care and potentially driving sales growth.
- Strategic Development: Dana T. Aftab, Exelixis' EVP of Research and Development, stated that the presented datasets affirm the company's commitment to improving cancer care standards, which may lay the groundwork for future product line expansions.
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- Strong Stock Performance: Exelixis has seen its stock price rise by 101% over the past five years, outperforming the S&P 500, indicating robust performance in the biotech sector, with potential for another doubling in the next five years attracting investor interest.
- Cabometyx Growth: The company's flagship product, Cabometyx, generated $610.8 million in revenue in Q1 2023, a 10% year-over-year increase, with projected revenue of $2.58 billion for fiscal year 2026, underscoring its strong market position in liver and kidney cancers.
- Next-Gen Drug Potential: Exelixis is developing zanzalintinib, which has completed phase 3 trials and is awaiting regulatory approval for metastatic colorectal cancer, addressing a significant unmet need with projected peak sales of $5 billion, enhancing the company's growth prospects.
- Diverse Pipeline Strategy: Beyond Cabometyx, Exelixis is testing zanzalintinib for various cancers, including renal cell carcinoma, and successful indications could provide substantial financial support, ensuring continued growth in the competitive oncology market.
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- Strong Stock Performance: Exelixis shares have risen 101% over the past five years, slightly outperforming the S&P 500, indicating robust performance and investment appeal in the biotech sector.
- Cabometyx Drives Growth: As Exelixis' flagship product, Cabometyx saw a 10% year-over-year revenue increase to $610.8 million in Q1, with projected midpoint revenue of $2.58 billion for FY 2026, reflecting sustained demand and strong sales capabilities in the cancer treatment market.
- New Drug Development Progress: The investigational drug zanzalintinib has completed phase 3 trials and is awaiting regulatory approval for metastatic colorectal cancer, with potential peak sales of $5 billion, showcasing the company's strategic focus on addressing unmet medical needs.
- Optimistic Future Outlook: Despite the impending patent cliff for Cabometyx, Exelixis has several early-stage pipeline candidates expected to drive financial growth in the coming years, suggesting a bright medium-term outlook with potential for stock doubling by 2031.
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- CABOMETYX Growth Momentum: Exelixis reported the highest number of new patient starts for CABOMETYX in Q1, with TRx market share increasing from 44% to 47%, indicating strong demand in the renal cell carcinoma and neuroendocrine tumor markets, further solidifying its leadership position.
- Capital Repurchase Plan: The company repurchased approximately $430.8 million of stock in Q1 and received board approval for a new $750 million stock repurchase plan, aimed at enhancing shareholder confidence while providing funding for future R&D investments.
- ZANZA R&D Progress: Management emphasized that the CRC NDA application for ZANZA and atezolizumab is the company's top priority, with a PDUFA expected in early December 2026, highlighting the strategic focus on colorectal cancer treatment.
- Strong Financial Performance: Q1 total revenues were approximately $611 million, with GAAP net income around $210.5 million, demonstrating effective control over operating expenses despite pressures from the 340B program and Medicare discounts.
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