Exelixis

Exelixis

Biopharmaceutical oncology company developing cancer therapies

Overview

Exelixis develops and commercializes medicines for cancer. Its products aim to treat advanced cancers, including renal cell carcinoma, by targeting multiple biological pathways and supporting combination regimens to achieve effective, tolerable, and durable responses. The company generates revenue from sales of approved therapies and strategic partnerships, backed by extensive research, clinical trials, and regulatory approvals to bring new drugs to market. Compared with peers, Exelixis focuses on a pipeline that combines multi-pathway targeting with combination therapies to improve patient outcomes. Its overall goal is to advance cancer treatment and offer patients better chances of remission through its ongoing drug development programs.

About Exelixis

Simplify's Rating
Why Exelixis is rated
B-
Rated B on Competitive Edge
Rated B on Growth Potential
Rated C on Differentiation

Industries

Biotechnology

Healthcare

Company Size

1,001-5,000

Company Stage

IPO

Headquarters

San Francisco, California

Founded

1994

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Simplify's Take

What believers are saying

  • FDA accepted zanzalintinib's mCRC NDA on February 2, 2026, with December 3 review.
  • STELLAR-303 data support zanzalintinib, and Exelixis plans STELLAR-316 initiation in mid-2026.
  • Q2 2026 revenue reached $628.7 million, while buybacks completed another $750 million program.

What critics are saying

  • Q2 2026 cabozantinib sales missed, and management cut 2026 revenue guidance on August 5.
  • Merck's LITESPARK-034 and belzutifan threaten zanzalintinib's RCC and colorectal positioning in 2026-2027.
  • Generic litigation with Handa and Intas targets cabozantinib and can erode Cabometyx cashflow.

What makes Exelixis unique

  • Cabometyx spans kidney, liver, thyroid, and neuroendocrine cancers, creating durable franchise breadth.
  • Zanzalintinib gives Exelixis a second growth engine after cabozantinib, with December 3, 2026 PDUFA.
  • Exelixis combines commercial scale, cash generation, and disciplined buybacks uncommon among oncology biotechs.

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Funding

Total Funding

$340.3M

Above

Industry Average

Funded Over

7 Rounds

Post IPO Equity funding comparison data is currently unavailable. We're working to provide this information soon!
Post IPO Equity Funding Comparison
Coming Soon

Benefits

Health Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

Health Savings Account/Flexible Spending Account

Unlimited Paid Time Off

Flexible Work Hours

Paid Vacation

Paid Sick Leave

Paid Holidays

401(k) Retirement Plan

401(k) Company Match

Performance Bonus

Employee Stock Purchase Plan

Stock Price

Growth & Insights and Company News

Headcount

6 month growth

2%

1 year growth

2%

2 year growth

2%
Investor's Business Daily
Aug 5th, 2026
Why this top-ranked IBD 50 stock just plummeted on its earnings.

Why this top-ranked IBD 50 stock just plummeted on its earnings. * ALLISON GATLIN * Updated 05:08 PM ET 08/05/2026 IBD 50 stock Exelixis (EXEL) toppled late Wednesday on a mixed second-quarter report, as sales of its bread-and-butter cancer drug, cabozantinib, lagged expectations. The biotech company sells cabozantinib under the brand names Cabometyx and Cometriq. The former - a treatment for kidney, liver and thyroid cancers as well as neuroendocrine tumors - brought in $570.6 million in quarterly sales. Cometriq, which treats a form of thyroid cancer, generated $2.4 million in sales. But analysts called for a healthier $578 million and $3 million in sales, respectively. Biotech's Next Boom? Inside The Multibillion Dollar Cancer Detection Market On this episode of Growth Stories, Investors take a look at the groundbreaking tests that could revolutionize cancer detection and what investors need to know about this evolving market. 0 seconds of 10 minutes, 57 secondsVolume 0% Biotech's Next Boom? Inside The Multibillion Dollar Cancer Detection Market See All Videos In response, Exelixis stock slumped more than 5% in after-hours trades on today's stock market, hitting 53.50. Exelixis' sales disappointment. The sales disappointment led Exelixis to cut its earnings outlook for the year. The company now sees $2.5 billion to $2.55 billion in sales. At the midpoint, that's a drop of $50 million from Exelixis' prior guidance from three months ago. More promisingly, Exelixis topped earnings forecasts, reporting an adjusted 91 cents per share, vs. the Street's forecast for 85 cents, according to FactSet. Earnings grew more than 21% as total sales climbed close to 11%, reaching $627.8 million. That includes sales of Cabometyx and Cometriq, as well as $53.2 million in royalties from partners Ipsen and Takeda Pharmaceutical. But sales lagged projections for $636 million. Investors are now watching closely the next steps for zanzalintinib. The Food and Drug Administration is reviewing the experimental prostate cancer treatment for potential approval in December. Exelixis stock is trading above its key moving averages with a nearly perfect IBD Digital Composite Rating of 98. The CR is a 1-99 measure of a stock's fundamental and technical performance. The stock also has a strong Relative Strength Rating of 90, putting its 12-month performance in the leading 10% of all stocks. Exelixis stock ranks No. 16 on the IBD 50 list of elite growth stocks. IBD newsletters. Get exclusive IBD analysis and actionable news daily. Follow Allison Gatlin on X/Twitter at @AGatlin_IBD. YOU MAY ALSO LIKE:

Business Wire
Aug 5th, 2026
Exelixis reports Q2 2026 revenues of $628.7M, up 11% on cabozantinib growth

Exelixis reported second quarter 2026 total revenues of $628.7 million, up from $568.3 million in the same period last year. Net product revenues reached $573.0 million, compared to $520.0 million in 2025, driven primarily by increased sales volume. The company reported GAAP net income of $212.1 million, or $0.82 per diluted share, versus $184.8 million, or $0.65 per diluted share, in the prior year period. Research and development expenses increased to $212.0 million from $200.4 million. Exelixis is preparing for a potential launch of zanzalintinib in metastatic colorectal cancer, pending regulatory approval. The FDA assigned a target action date of 3 December 2026 for the new drug application. The company expects topline results from its phase 3 STELLAR-304 trial in the second half of 2026.

San Francisco Biotechnology Network
May 30th, 2026
Exelixis announces results from subgroup analysis of phase 3 CABINET pivotal trial evaluating CABOMETYX(R)(cabozantinib) in non-functional and functional neuroendocrine tumors at ASCO 2026.

Exelixis announces results from subgroup analysis of phase 3 CABINET pivotal trial evaluating CABOMETYX(R)(cabozantinib) in non-functional and functional neuroendocrine tumors at ASCO 2026. May 30, 2026 san francisco biotechnology network news news, syndication comments off on exelixis announces results from subgroup analysis of phase 3 CABINET pivotal trial evaluating CABOMETYX(R)(cabozantinib) in non-functional and functional neuroendocrine tumors at ASCO 2026. ALAMEDA, Calif.-(BUSINESS WIRE)-Exelixis, Inc. (Nasdaq: EXEL) today announced results from a subgroup analysis of the phase 3 CABINET pivotal trial, which showed that CABOMETYX(R)(cabozantinib) provided significant improvements in progression-free survival (PFS) versus placebo in patients with previously treated advanced neuroendocrine tumors (NET) regardless of functional status. These data will be presented at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting to be held fr Click here to view original post

Yahoo Finance
May 22nd, 2026
Exelixis posts $611M Q1 revenue, FDA accepts colorectal cancer drug application

Exelixis, an oncology-focused biopharmaceutical company, reported total revenues of $610.8 million for Q1 2026, up from $555.4 million in Q1 2025. US net product revenues from its cabozantinib franchise reached $555 million, whilst collaboration revenues rose to $55.8 million. The company achieved GAAP net income of $210.5 million and non-GAAP net income of $232.8 million. The US FDA accepted Exelixis's first NDA for zanzalintinib combined with atezolizumab for previously treated metastatic colorectal cancer, with a target action date of 3 December. The company is progressing multiple zanzalintinib clinical trials, including upcoming data readouts for STELLAR-303 and STELLAR-304 studies. Exelixis expects to complete its $750 million share repurchase programme this month. The Board authorised a new $750 million buyback programme through end-2027.

Yahoo Finance
May 5th, 2026
Exelixis reports Q1 earnings of $210.5M, beating analyst expectations at 87 cents per share

Exelixis reported first-quarter earnings of $210.5 million, with net income of 79 cents per share. Adjusted earnings reached 87 cents per share, exceeding Wall Street's average estimate of 75 cents per share from seven analysts surveyed by Zacks Investment Research. The Alameda, California-based drug developer posted revenue of $610.8 million for the period, slightly below analyst forecasts of $612.6 million. The company has issued full-year revenue guidance of $2.53 billion to $2.63 billion.

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