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v3.26.3
Collaboration Agreements And Business Development Activities - Royalty Pharma and GSK - Narrative (Details) - USD ($)
$ in Millions
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Collaborative Arrangements with Glaxo Smith Kline        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Percent of royalty on net sale     3.00%  
Collaborative Arrangements with Royalty Pharma        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Royalty expense $ 24.5 $ 22.2 $ 71.6 $ 63.9
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v3.26.3
Collaboration Agreements And Business Development Activities - Takeda Collaboration - Narrative (Details) - Collaborative Arrangement with Takeda
$ in Millions
9 Months Ended
Oct. 02, 2026
USD ($)
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]  
Net revenue from sales milestone $ 7.8
Revenue from contract with customer, regulatory milestone 8.0
Cumulative net sales milestone 300.0
License revenues  
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]  
Revenue from contract with customer, commercial sales milestone 5.3
Collaboration services revenues  
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]  
Revenue from contract with customer, commercial sales milestone $ 2.5
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v3.26.3
Net Income Per Share - Potential Shares of Common Stock Not Included in the Computation of Diluted Net Income Per Share (Details) - shares
shares in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Share-based Payment Arrangement        
Antidilutive Securities Excluded from Computation of Earnings Per Share [Line Items]        
Anti-dilutive securities and contingently issuable shares excluded (in shares) 2,017 2,133 2,593 1,856
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v3.26.3
Commitments and Contingencies
9 Months Ended
Oct. 02, 2026
Commitments and Contingencies Disclosure [Abstract]  
COMMITMENTS AND CONTINGENCIES COMMITMENTS AND CONTINGENCIES
Legal Proceedings
MSN ANDA Litigation
Consolidated lawsuits in the United States District Court for the District of Delaware (the Delaware District Court), numbered Civil Action Nos. 19-02017 and 20-00633 (collectively referred to as MSN I), related to an Abbreviated New Drug Application (ANDA) submitted to the FDA and an amendment thereto by MSN Pharmaceuticals, Inc. (individually and collectively with certain of its affiliates, including MSN Laboratories Private Limited, referred to as MSN), requesting approval to market a generic version of CABOMETYX tablets. The litigation included U.S. Patents No. 7,579,473, composition of matter (the ’473 Patent), 8,497,284, methods of treatment (the ’284 Patent), 8,877,776, salt and polymorphic forms (the ’776 Patent), 9,724,342, formulations (the ’342 Patent), 10,034,873, methods of treatment (the ’873 Patent), and 10,039,757, methods of treatment (the ’757 Patent), which are listed in the Approved Drug Products with Therapeutic Equivalence Evaluations, also referred to as the Orange Book, for CABOMETYX. On January 19, 2023, the
Delaware District Court issued a ruling rejecting MSN’s invalidity challenge to the ’473 Patent. The Delaware District Court also ruled that MSN’s proposed ANDA product does not infringe the ’776 Patent. In accordance with these rulings, the Delaware District Court entered judgment that the effective date of any final FDA approval of MSN’s ANDA shall not be a date earlier than August 14, 2026, the expiration date of the ’473 Patent. Final judgment was entered on January 30, 2023. This ruling in MSN I did not impact our separate MSN II lawsuit (as defined below).
On January 11, 2022, we received notice from MSN that it had further amended its ANDA to assert additional Paragraph IV certifications. In particular, the January 11, 2022 amended ANDA requested approval to market a generic version of CABOMETYX tablets prior to expiration of three previously-unasserted CABOMETYX patents that are now listed in the Orange Book: U.S. Patents No. 11,091,439, crystalline salt forms (the ’439 Patent), 11,091,440, pharmaceutical composition (the ’440 Patent), and 11,098,015, methods of treatment (the ’015 Patent). On February 23, 2022, we filed a complaint in the Delaware District Court for patent infringement against MSN asserting infringement of the ’439, ’440, and ’015 Patents arising from MSN’s further amendment of its ANDA filing with the FDA. On February 25, 2022, MSN filed its response to the complaint, alleging that the asserted claims of the ’439, ’440, and ’015 Patents are invalid and not infringed. On June 7, 2022, we received notice from MSN that it had further amended its ANDA to assert an additional Paragraph IV certification. As currently amended, MSN’s ANDA now requests approval to market a generic version of CABOMETYX tablets prior to expiration of a previously-unasserted CABOMETYX patent that is now listed in the Orange Book: U.S. Patent No. 11,298,349, pharmaceutical composition (the ’349 Patent). On July 18, 2022, we filed a complaint in the Delaware District Court for patent infringement against MSN asserting infringement of the ’349 Patent arising from MSN’s further amendment of its ANDA filing with the FDA. On August 9, 2022, MSN filed its response to the complaint, alleging that the asserted claims of the ’349 Patent are invalid and not infringed and amended its challenges to the ’439, ’440, and ’015 Patents to allege that these patents are not enforceable based on equitable grounds. The two lawsuits comprising this litigation (collectively referred to as MSN II), numbered Civil Action Nos. 22-00228 and 22-00945, were consolidated in October 2022 and involve Exelixis patents that are different from those asserted in the MSN I litigation described above.
On June 21, 2022, pursuant to a stipulation between us and MSN, the Delaware District Court entered an order that (i) MSN’s submission of its ANDA constitutes infringement of certain claims relating to the ’439, ’440, and ’015 Patents, if those claims are not found to be invalid, and (ii) upon approval, MSN’s commercial manufacture, use, sale or offer for sale within the U.S., and importation into the U.S., of MSN’s proposed ANDA product prior to the expiration of these patents would also infringe certain claims of each patent, if those claims are not found to be invalid. In our MSN II complaints, we sought, among other relief, an order that the effective date of any FDA approval of MSN’s ANDA would be a date no earlier than the expiration of the ’439, ’440, ’015, and ’349 Patents, the latest of which expires on February 10, 2032, and equitable relief enjoining MSN from infringing these patents. On September 28, 2023, the Delaware District Court granted the parties’ stipulation of dismissal of MSN’s equitable defenses and counterclaims. A bench trial occurred in October 2023, and on October 15, 2024, the Delaware District Court issued a ruling rejecting MSN’s invalidity challenge to each of the ’439, ’440, and ’015 Patents. The Delaware District Court also ruled that the ’349 Patent is not invalid and that MSN’s proposed ANDA product does not infringe this patent. In accordance with these rulings, the Delaware District Court entered final judgment on October 23, 2024, that, should the FDA ultimately approve MSN’s ANDA, the effective date of any such approval of MSN’s ANDA shall not be a date earlier than January 15, 2030, the expiration date of each of the ’439, ’440, and ’015 Patents, subject to our potential additional regulatory exclusivity.
On November 22, 2024, MSN noticed an appeal to the Court of Appeals for the Federal Circuit (CAFC) and we noticed a cross-appeal on November 26, 2024. On April 1, 2025, MSN filed its Opening Brief arguing that the asserted claims of the ’439, ’440, ’015, and ’349 Patents are invalid. On June 10, 2025, the CAFC granted our request to dismiss our cross-appeal. On June 11, 2025, we filed our Response Brief. On August 1, 2025, MSN filed its Reply Brief. Oral argument in this matter was held on June 4, 2026. On August 31, 2026, the CAFC issued its opinion, where it affirmed that the asserted claims of the ’439, ’440, and ’015 patents are not invalid, dismissed MSN’s appeal as to the asserted claim of the ’349 patent, which expires on February 10, 2032, and vacated the district court’s judgment with respect to the validity of the asserted claim of the ’349 patent. Based on the CAFC’s opinion, the effective date of any final approval by the FDA of MSN’s ANDA shall not be a date earlier than January 15, 2030, the expiration date of each of the ’439, ’440, and ’015 patents, subject to any further appellate proceedings, applicable regulatory exclusivity, and the outcome of separate litigation involving the ’039 Patent (as defined below), which expires in February 2032 and for which trial is currently scheduled to begin in November 2026. MSN has until October 30, 2026 to seek rehearing at the CAFC.
In February 2025, we received another notice letter from MSN regarding its ANDA, requesting FDA approval to market a generic version of CABOMETYX tablets. MSN’s notice letter included a Paragraph IV certification with respect to Orange Book-listed patent U.S. Patent No. 12,128,039, low impurity (the ’039 Patent), which expires in 2032. On March 19, 2025, we filed a complaint in the Delaware District Court for patent infringement against MSN asserting infringement of this
patent arising from MSN’s further amendment of its ANDA filing with the FDA. On April 10, 2025, MSN filed its response to the complaint, alleging that the asserted claims of the ’039 Patent are invalid, unenforceable, and not infringed. On May 1, 2025, we filed our answer to MSN’s counterclaim. On August 18, 2025, pursuant to a stipulation between us and MSN, the Delaware District Court entered an order that (i) MSN’s submission of its ANDA constitutes infringement of certain claims relating to the ’039 Patent, if those claims are not found to be invalid or unenforceable, and (ii) upon approval, MSN’s commercial manufacture, use, sale or offer for sale within the U.S., and importation into the U.S., of MSN’s proposed ANDA product prior to the expiration of the ’039 Patent would also infringe certain claims of the patent, if those claims are not found to be invalid or unenforceable. This litigation has been consolidated with the Azurity Pharmaceuticals, Inc. (Azurity) litigation for the trial scheduled for November 2, 2026 (Consolidated Litigation). For additional information on the Consolidated Litigation, see “– Legal Proceedings – Consolidated Litigation.”
Azurity 505(b)(2) NDA Litigation
In March 2025, we received a notice letter regarding a 505(b)(2) New Drug Application (NDA) submitted to the FDA by Azurity, requesting approval to market cabozantinib tablets. Azurity’s notice letter included a Paragraph IV certification with respect to the ’776 Patent, the ’342 Patent, the ’873 Patent, the ’757 Patent, the ’439 Patent, the ’440 Patent, the ’015 Patent, the ’349 Patent, and the ’039 Patent, which are listed in the Orange Book, for CABOMETYX. On April 18, 2025, we filed a complaint in the Delaware District Court for patent infringement against Azurity asserting infringement of the ’776, ’439, ’440, ’015, ’349, and ’039 Patents. On April 24, 2025, we filed our First Amended Complaint alleging infringement of the same patents. On June 11, 2025, Azurity filed its response to the complaint, alleging that the asserted claims of the patents at issue are not infringed and/or invalid. On July 2, 2025, we filed our answer to Azurity’s counterclaims. On July 28, 2025, Azurity filed motions for judgment on the pleadings regarding the non-infringement of the ’776, ’439, ’440, ’015, ’349, and ’039 Patents. On August 25, 2025, we filed our answering briefs to Azurity’s motions for judgment on the pleadings. On September 15, 2025, Azurity filed its reply briefs. On October 5, 2026, the Delaware District Court denied Azurity’s motions for judgment on the pleadings. On October 22, 2026, pursuant to a stipulation between us and Azurity, the Delaware District Court entered an order that (i) Azurity’s submission of its 505(b)(2) NDA constitutes infringement of certain claims relating to the ’349 and ’039 Patents, if those claims are not found to be invalid, and (ii) upon approval, Azurity’s commercial manufacture, use, sale or offer for sale within the U.S., and importation into the U.S., of Azurity’s proposed 505(b)(2) NDA product prior to the expiration of the ’349 and ’039 Patents would also infringe certain claims of those patents, if those claims are not found to be invalid. This Azurity litigation was consolidated in the Consolidated Litigation. On October 28, 2026, we entered into a settlement and license agreement with Azurity (the Azurity Settlement Agreement) to resolve the Azurity litigation. Pursuant to the terms of the Azurity Settlement Agreement, we will grant Azurity a license to market its proposed 505(b)(2) NDA product in the U.S. beginning on December 1, 2030, if approved by the FDA and subject to conditions and exceptions customary for agreements of this type. The effective date for the proposed generic cabozantinib products where we have a settlement and license agreement remains January 1, 2031, subject to conditions and exceptions customary for agreements of this type.
Consolidated Litigation
On August 8, 2025, the Delaware District Court ordered that the then-pending abovementioned MSN and Azurity district court litigations be consolidated with the trial scheduled for November 2, 2026. In accordance with the Azurity Settlement Agreement, within three (3) business days after the effective date, we and Azurity will jointly file a stipulated dismissal (the Azurity Dismissal) terminating all ongoing litigation between us and Azurity in the Consolidated Litigation. The Azurity Dismissal will not affect our litigation with MSN, which remains pending in the Consolidated Litigation.
Handa 505(b)(2) NDA Litigation
In November 2025, we received a notice letter regarding a 505(b)(2) NDA submitted to the FDA by Handa Oncology, LLC (Handa), requesting approval to market cabozantinib capsules (in the form of cabozantinib lauryl sulfate). Handa’s notice letter included a Paragraph IV certification with respect to the ’776 Patent, the ’342 Patent, the ’873 Patent, the ’757 Patent, the ’439 Patent, the ’440 Patent, the ’015 Patent, the ’349 Patent, and the ’039 Patent, which are listed in the Orange Book, for CABOMETYX. Handa’s notice letter also included a Paragraph III certification with respect to the ’473 Patent. In April 2026, we filed a citizen petition with the FDA pursuant to section 505(q) of the Food, Drug, and Cosmetic Act notifying the FDA that Handa’s application raises new questions of safety and effectiveness requiring clinical data to support approval. On July 6, 2026, we filed a complaint in the Delaware District Court for patent infringement against Handa asserting infringement of U.S. Patent Nos. 9,174,947, method of use and process for preparing compounds, 9,365,516, process for preparing compounds, 9,969,692, process for preparing compounds, 10,123,999, process for preparing compounds, and 10,736,886, method of use and process for preparing compounds arising from Handa’s 505(b)(2) NDA
filing with the FDA. On August 31, 2026, the Delaware District Court granted our request to dismiss the July 6, 2026 complaint without prejudice. On September 3, 2026, the FDA responded to our citizen petition denying our requests and, on the same day, granted full approval to Handa’s 505(b)(2) NDA. In its response, the FDA stated that it had carefully considered the issues raised in the petition and concluded, based on its review of the data submitted in support of Handa’s NDA, that Handa was not required to submit additional data to support the safety and effectiveness of its product. We continue to evaluate all legal and strategic options with respect to Handa’s approved product.
Accord ANDA Litigation
In May 2026, we received a notice letter regarding an ANDA submitted to the FDA by Intas Pharmaceuticals Ltd. and Accord Healthcare, Inc. (collectively, Accord), requesting approval to market cabozantinib tablets. Accord’s notice letter included a Paragraph IV certification with respect to the ’776 Patent, the ’342 Patent, the ’873 Patent, the ’757 Patent, the ’439 Patent, the ’440 Patent, the ’015 Patent, the ’349 Patent, and the ’039 Patent, which are listed in the Orange Book, for CABOMETYX. On July 6, 2026, we filed a complaint in the Delaware District Court for patent infringement against Accord asserting infringement of the ’776, ’439, ’440, ’015, and ’039 Patents arising from Accord’s ANDA filing with the FDA. On September 22, 2026, Accord filed its response to the complaint, alleging that the asserted claims of the patents at issue are not infringed, invalid, and/or unenforceable. On October 20, 2026, we filed our answer to Accord’s counterclaims.
Other
In May 2026, we received a notice letter regarding a 505(b)(2) NDA submitted to the FDA by Almatica Pharma, LLC (Almatica), requesting approval to market cabozantinib tablets (in the form of cabozantinib fumarate). Almatica’s notice letter included a Paragraph IV certification with respect to the ’776 Patent, the ’342 Patent, the ’873 Patent, the ’757 Patent, the ’439 Patent, the ’440 Patent, the ’015 Patent, the ’349 Patent, and the ’039 Patent, which are listed in the Orange Book, for CABOMETYX. We continue to evaluate all legal and strategic options with respect to Almatica’s product.
In September 2026, we received a notice letter regarding a 505(b)(2) NDA submitted to the FDA by MSN Pharmaceuticals, Inc. and MSN Private Laboratories Limited (the September 2026 Notice Letter), requesting approval to market cabozantinib tablets (in the form of cabozantinib fumarate). The September 2026 Notice Letter included a Paragraph IV certification with respect to the ’776 Patent, the ’342 Patent, the ’873 Patent, the ’757 Patent, the ’439 Patent, the ’440 Patent, the ’015 Patent, the ’349 Patent, and the ’039 Patent, which are listed in the Orange Book, for CABOMETYX. We continue to evaluate all legal and strategic options with respect to the fumarate product of MSN Pharmaceuticals, Inc. and MSN Private Laboratories Limited.
The sale of any cabozantinib products, including tablets and/or capsules, besides CABOMETYX significantly earlier than CABOMETYX’s patent expiration could decrease our revenues derived from the U.S. sales of CABOMETYX and thereby materially harm our business, financial condition and results of operations. It is not possible at this time to determine the likelihood of an unfavorable outcome or estimate of the amount or range of any potential loss.
We may also from time-to-time become a party or subject to various other legal proceedings and claims, either asserted or unasserted, which arise in the ordinary course of business. Some of these proceedings have involved, and may involve in the future, claims that are subject to substantial uncertainties and unascertainable damages.
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v3.26.3
Revenues - Revenues Disaggregated by Concentration Risks (Details) - Customer Concentration Risk
3 Months Ended 9 Months Ended 12 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Jan. 02, 2026
Affiliates of Cencora, Inc. | Revenue          
Concentration Risk [Line Items]          
Percent of total revenues 20.00% 20.00% 21.00% 22.00%  
Affiliates of Cencora, Inc. | Accounts Receivable          
Concentration Risk [Line Items]          
Percent of total revenues     24.00%   23.00%
Affiliates of McKesson Corporation | Revenue          
Concentration Risk [Line Items]          
Percent of total revenues 20.00% 20.00% 20.00% 19.00%  
Affiliates of McKesson Corporation | Accounts Receivable          
Concentration Risk [Line Items]          
Percent of total revenues     25.00%   25.00%
Affiliates of CVS Health Corporation | Revenue          
Concentration Risk [Line Items]          
Percent of total revenues 16.00% 15.00% 15.00% 15.00%  
Affiliates of CVS Health Corporation | Accounts Receivable          
Concentration Risk [Line Items]          
Percent of total revenues     13.00%   13.00%
Affiliates of Optum Specialty Pharmacy | Revenue          
Concentration Risk [Line Items]          
Percent of total revenues 11.00%   10.00%    
Accredo Health Group, Inc. | Revenue          
Concentration Risk [Line Items]          
Percent of total revenues   11.00% 10.00% 12.00%  
Ipsen Pharma SAS | Accounts Receivable          
Concentration Risk [Line Items]          
Percent of total revenues     15.00%   19.00%
Cardinal Health, Inc. | Revenue          
Concentration Risk [Line Items]          
Percent of total revenues 10.00%        
Cardinal Health, Inc. | Accounts Receivable          
Concentration Risk [Line Items]          
Percent of total revenues     12.00%   12.00%
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Cash And Marketable Securities - Narrative (Details)
Oct. 02, 2026
USD ($)
investment
Jan. 02, 2026
USD ($)
investment
Investments, Debt and Equity Securities [Abstract]    
Interest receivable $ 9,800,000 $ 12,400,000
Number of investments in an unrealized loss position | investment 356 35
Allowance for credit losses $ 0  
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v3.26.3
Segment Reporting
9 Months Ended
Oct. 02, 2026
Segment Reporting [Abstract]  
SEGMENT REPORTING SEGMENT REPORTING
We operate in one business segment that focuses on the discovery, development and commercialization of new medicines for difficult-to-treat cancers. Our President and Chief Executive Officer, as the chief operating decision-maker, manages and allocates resources to our operations on a total consolidated basis. Consistent with this decision-making process, our President and Chief Executive Officer uses net income to monitor budget versus actual results for purposes of evaluating performance and to make decisions about the allocation of resources.
Our significant segment expenses that are regularly provided to our President and Chief Executive Officer and included in the measure of segment net income consist of consolidated expenses for our operational departments: drug discovery, development, and selling, general and administrative and other segment items.
The segment and consolidated net income, including significant segment expenses were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Revenues$658,696 $597,755 $1,898,198 $1,721,463 
Less:
Cost of goods sold26,233 18,574 66,843 57,216 
Drug discovery17,144 23,838 54,872 63,448 
Development147,739 133,645 433,976 421,021 
Selling, general, and administrative136,910 103,129 387,193 336,835 
Other segment items(1)
62,200 82,078 186,816 206,212 
Interest income(14,315)(15,922)(44,652)(51,787)
Provision for income taxes64,690 58,835 172,538 150,476 
Segment and consolidated net income$218,095 $193,578 $640,612 $538,042 
_________________
(1) Other segment items include stock-based compensation, restructuring expenses, other research and development expenses, including the allocation of general corporate costs to research and development services and development cost reimbursements in connection with certain of our collaboration arrangements, and other income (expenses), net.
All of our long-lived assets are located in the U.S. See “Note 3. Revenues” for enterprise-wide disclosures about product sales, revenues from major customers and revenues by geographic region.
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Segment Reporting - Narrative (Details)
9 Months Ended
Oct. 02, 2026
segment
Segment Reporting [Abstract]  
Number of business segments 1
Number of reportable segments 1
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Stockholders’ Equity (Tables)
9 Months Ended
Oct. 02, 2026
Share-Based Payment Arrangement [Abstract]  
Schedule of Allocated Stock-Based Compensation
We allocated stock-based compensation for the 2017 Plan and the 2000 Employee Stock Purchase Plan (as amended and restated, the Amended ESPP) as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Research and development$11,069 $10,353 $35,731 $34,018 
Selling, general and administrative17,649 20,532 54,600 58,868 
Total stock-based compensation$28,718 $30,885 $90,331 $92,886 
Stock-based compensation for each type of award under the 2017 Plan and the Amended ESPP were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Stock options$206 $493 $673 $2,224 
Restricted stock units27,830 29,660 86,533 87,388 
Performance-based restricted stock units— — — 241 
Employee stock purchase plan
682 732 3,125 3,033 
Total stock-based compensation$28,718 $30,885 $90,331 $92,886 
Schedule Of Share-Based Payment Award, Equity Instruments Other Than Options, Valuation Assumptions
We used a Monte Carlo simulation model and the following assumptions to determine the grant date fair value of $55.31 per share for the 2026 TSR-based RSUs:
2026 TSR-based RSUs
Fair value of Exelixis common stock on grant date
$44.28 
Expected volatility
35.5%
Risk-free interest rate
3.4%
Dividend yield
—%
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Restructuring
9 Months Ended
Oct. 02, 2026
Restructuring and Related Activities [Abstract]  
RESTRUCTURING RESTRUCTURING
In the third quarter of fiscal year 2025, our Board of Directors authorized, and we implemented, a corporate reorganization plan (the 2025 Plan) to reorganize our workforce and close our office located in King of Prussia, Pennsylvania. Restructuring expenses incurred under the 2025 Plan were primarily severance and employee-related costs. During the three and nine months ended September 30, 2025, we recognized $19.8 million in expenses associated with the 2025 Plan, which are presented in restructuring in the accompanying Condensed Consolidated Statements of Income. We incurred the majority of the charges related to the 2025 Plan during the third quarter of 2025 and substantially completed the 2025 Plan by the end of the fiscal year 2025. For more information about our restructuring expenses, see “Note 13. Restructuring” of the “Notes to Consolidated Financial Statements” included in Part II, Item 8 of our Fiscal 2025 Form 10-K.
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Stockholders’ Equity - Employee Service Share - Based Compensation (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]        
Total stock-based compensation $ 28,718 $ 30,885 $ 90,331 $ 92,886
Stock options        
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]        
Total stock-based compensation 206 493 673 2,224
Restricted stock units        
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]        
Total stock-based compensation 27,830 29,660 86,533 87,388
Performance-based restricted stock units        
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]        
Total stock-based compensation 0 0 0 241
Employee stock purchase plan        
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]        
Total stock-based compensation $ 682 $ 732 $ 3,125 $ 3,033
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v3.26.3
Collaboration Agreements And Business Development Activities
9 Months Ended
Oct. 02, 2026
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
COLLABORATION AGREEMENTS AND BUSINESS DEVELOPMENT ACTIVITIES COLLABORATION AGREEMENTS AND BUSINESS DEVELOPMENT ACTIVITIES
We have established multiple collaborations with leading biopharmaceutical companies for the commercialization and further development of our cabozantinib franchise. Additionally, we have made considerable progress under our existing research collaboration and in-licensing arrangements to further enhance our pipeline and expand our ability to discover, develop and commercialize novel therapies with the goal of providing new treatment options for cancer patients. Historically, we also entered into other collaborations with leading biopharmaceutical companies pursuant to which we out-licensed other compounds and programs in our portfolio.
See “Note 4. Collaboration Agreements and Business Development Activities” of the “Notes to Consolidated Financial Statements” included in Part II, Item 8 of our Fiscal 2025 Form 10-K for additional information on certain of our collaboration agreements and in-licensing arrangements.
Cabozantinib Commercial Collaborations
Ipsen Collaboration
In February 2016, we entered into a collaboration and license agreement with Ipsen for the commercialization and further development of cabozantinib, which was subsequently amended and restated to, among other things, modify the amount of reimbursements we receive for costs associated with pharmacovigilance activities. The parties’ efforts are governed through a joint steering committee and appropriate subcommittees established to guide and oversee the collaboration’s operation and strategic direction; provided, however, that we retain final decision-making authority with respect to cabozantinib’s ongoing development.
Revenues under the collaboration agreement with Ipsen were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
License revenues$49,071 $47,313 $143,142 $120,832 
Collaboration services revenues(4,773)(2,347)(13,269)(6,127)
Total collaboration revenues$44,298 $44,966 $129,873 $114,705 
During the three and nine months ended September 30, 2025, we recognized $4.3 million in license revenues and $0.4 million in collaboration services revenues in connection with a $5.0 million regulatory milestone payment, upon approval by the European Commission for the treatment of patients with either advanced pancreatic neuroendocrine tumors or advanced extra-pancreatic neuroendocrine tumors.
Takeda Collaboration
In January 2017, we entered into a collaboration and license agreement with Takeda, which was subsequently amended, to, among other things, modify the amount of reimbursements we receive for costs associated with our required pharmacovigilance activities and milestones we are eligible to receive, as well as modify certain cost-sharing obligations related to the Japan-specific development costs associated with certain studies for the commercialization and further
development of cabozantinib and also grant Exelixis the right to develop and commercialize a competing product in Japan and modify certain costs sharing and milestone payments that may become payable if Takeda opts into certain studies. The operation and strategic direction of the parties’ collaboration is governed through a joint executive committee and appropriate subcommittees.
Revenues under the collaboration agreement with Takeda were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
License revenues$2,691 $3,299 $13,003 $9,891 
Collaboration services revenues136 936 3,375 3,346 
Total collaboration revenues$2,827 $4,235 $16,378 $13,237 
During the nine months ended September 30, 2026, we recognized $7.8 million in revenues in connection with an $8.0 million commercial milestone payment from Takeda, which was earned upon their achievement of $300.0 million of cumulative net sales of cabozantinib in Japan. Of the revenues recognized from this milestone, $5.3 million was allocated to license revenues and $2.5 million was allocated to collaboration services revenues. Upon the achievement of this commercial milestone, the tiered royalty rate on annual net sales reset to 20% and will reset each calendar year, thereafter.
Royalty Pharma and GSK
In October 2002, we established a product development and commercialization collaboration agreement with GlaxoSmithKline (now GSK plc, or GSK), that required us to pay a 3% royalty to GSK on the worldwide net sales of any product containing cabozantinib sold by us and our collaboration partners. Effective January 1, 2021, Royalty Pharma plc (Royalty Pharma) acquired from GSK all rights, title and interest in royalties on net product sales containing cabozantinib for non-U.S. markets for the full term of the royalty and for the U.S. market through September 2026, after which time U.S. royalties reverted back to GSK. Royalty fees earned in connection with cabozantinib sales are recognized in cost of goods sold for our sales and as a reduction of collaboration services revenues for sales made by our collaboration partners. Such royalty fees earned were $24.5 million and $71.6 million during the three and nine months ended September 30, 2026, respectively, as compared to $22.2 million and $63.9 million, respectively, for the corresponding prior year periods.
Research Collaborations, In-Licensing Arrangements and Other Business Development Activities
We enter into collaborative arrangements with other pharmaceutical or biotechnology companies to develop and commercialize oncology assets or other intellectual property. Our research collaborations and in-licensing arrangements are intended to enhance our pipeline and expand our ability to discover, develop and commercialize novel therapies with the goal of providing new treatment options for cancer patients. Our research collaborations, in-licensing arrangements and other strategic transactions generally include upfront payments for the purchase or in-licensing of intellectual property, development, regulatory and commercial milestone payments and royalty payments, in each case contingent upon the occurrence of certain future events linked to the success of the asset in development. Certain of our research collaborations provide us exclusive options that give us the right to license programs or acquire the intellectual property developed under the research collaborations for further discovery and development. When we decide to exercise the options, we are required to pay an exercise fee and then assume the responsibilities for all subsequent development, manufacturing and commercialization.
During the three and nine months ended September 30, 2026, we recognized $3.2 million and $20.3 million, respectively, as compared to $8.4 million and $19.3 million, respectively, for the corresponding prior year periods, within research and development expenses on the Condensed Consolidated Statements of Income, primarily related to development milestone payments for the cost of intellectual property that have not yet achieved technological feasibility, research and development funding and other fees.
As of September 30, 2026, in conjunction with the active collaborative in-licensing arrangements and asset purchase agreements, we are subject to potential future development milestone payments of up to $441.5 million, regulatory milestone payments of up to $278.0 million and commercial milestone payments of up to $2.5 billion, each in the aggregate per product or target, as well as royalties on future net sales of products.
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Inventory (Tables)
9 Months Ended
Oct. 02, 2026
Inventory Disclosure [Abstract]  
Schedule of Inventory
Inventory consisted of the following (in thousands):
 
September 30, 2026December 31, 2025
Raw materials$798 $894 
Work in process45,803 53,531 
Finished goods17,917 5,942 
Total$64,518 $60,367 
Balance Sheet classification:
Current portion included in inventory$29,871 $21,686 
Non-current portion included in other non-current assets34,647 38,681 
Total
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CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME (Parenthetical) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Statement of Comprehensive Income [Abstract]        
Net unrealized gains (losses) on available-for-sale debt securities, tax impact $ 1,357 $ (659) $ 2,979 $ (1,445)
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v3.26.3
Collaboration Agreements And Business Development Activities - Collaboration Revenues under the Collaboration Agreement with Takeda (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Total revenues $ 658,696 $ 597,755 $ 1,898,198 $ 1,721,463
Collaborative Arrangement with Takeda        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Total revenues 2,827 4,235 16,378 13,237
License revenues        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Total revenues 58,408 56,236 175,166 148,017
License revenues | Collaborative Arrangement with Takeda        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Total revenues 2,691 3,299 13,003 9,891
Collaboration services revenues        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Total revenues (4,636) (1,411) (9,894) (2,781)
Collaboration services revenues | Collaborative Arrangement with Takeda        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Total revenues $ 136 $ 936 $ 3,375 $ 3,346
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Net Income Per Share - Computation of Basic and Diluted Net Income Per Share (Details) - USD ($)
$ / shares in Units, shares in Thousands, $ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
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v3.26.3
Revenues - Contract Assets and Liabilities (Details) - USD ($)
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Jan. 02, 2026
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v3.26.3
Stockholders’ Equity - Estimate Grant-Date Fair Value (Details) - 2026 TSR-based RSUs
9 Months Ended
Oct. 02, 2026
$ / shares
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]  
Weighted average grant date fair value, awarded (in dollars per share) $ 44.28
Expected volatility 35.50%
Risk-free interest rate 3.40%
Dividend yield 0.00%
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v3.26.3
Net Income Per Share
9 Months Ended
Oct. 02, 2026
Earnings Per Share [Abstract]  
NET INCOME PER SHARE NET INCOME PER SHARE
Net income per share — basic and diluted, were computed as follows (in thousands, except per share amounts):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Numerator:
Net income$218,095 $193,578 $640,612 $538,042 
Denominator:
Weighted-average common shares outstanding — basic246,756 268,421 251,964 273,269 
Dilutive securities8,998 10,114 8,953 10,432 
Weighted-average common shares outstanding — diluted255,754 278,535 260,917 283,701 
Net income per share — basic$0.88 $0.72 $2.54 $1.97 
Net income per share — diluted$0.85 $0.69 $2.46 $1.90 
The basic net income per share is computed using the weighted-average number of common shares outstanding during the periods. The diluted net income per share is computed using the weighted-average number of common shares outstanding and dilutive potential common shares outstanding during the periods. Dilutive common shares outstanding include the dilutive effect of in-the-money options, unvested RSUs (including market condition-based RSUs), unvested PSUs when the performance condition is met and ESPP contributions. The dilutive effect of such equity awards is calculated based on the average share price for each fiscal period using the treasury stock method.
Certain potential common shares were excluded from our calculation of weighted-average common shares outstanding — diluted because either they would have had an anti-dilutive effect on net income per share or they were related to shares from PSUs or from market condition-based RSUs that were contingently issuable, and the contingency had not been satisfied at the end of the reporting period.
The weighted-average potential common shares excluded from our calculation were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Anti-dilutive securities and contingently issuable shares excluded2,017 2,133 2,593 1,856 
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v3.26.3
Fair Value Measurements - Fair Value of Financial Assets Measured on a Recurring Basis (Details) - USD ($)
$ in Thousands
Oct. 02, 2026
Jan. 02, 2026
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale $ 1,213,635 $ 1,291,842
Total financial assets carried at fair value 1,399,777 1,662,582
Money market funds    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Cash and cash equivalents 139,503 304,352
Certificates of deposit    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Cash and cash equivalents 46,639 66,388
Commercial paper    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 257,762 241,439
Corporate bonds    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 785,501 886,500
U.S. Treasury and government-sponsored enterprises    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 163,579 155,139
Municipal bonds    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 6,793 8,764
Level 1    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 0 0
Total financial assets carried at fair value 139,503 304,352
Level 1 | Money market funds    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Cash and cash equivalents 139,503 304,352
Level 1 | Certificates of deposit    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Cash and cash equivalents 0
Level 1 | Commercial paper    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 0 0
Level 1 | Corporate bonds    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 0 0
Level 1 | U.S. Treasury and government-sponsored enterprises    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 0 0
Level 1 | Municipal bonds    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 0 0
Level 2    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 1,213,635 1,291,842
Total financial assets carried at fair value 1,260,274 1,358,230
Level 2 | Money market funds    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Cash and cash equivalents 0 0
Level 2 | Certificates of deposit    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Cash and cash equivalents 46,639 66,388
Level 2 | Commercial paper    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 257,762 241,439
Level 2 | Corporate bonds    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 785,501 886,500
Level 2 | U.S. Treasury and government-sponsored enterprises    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale 163,579 155,139
Level 2 | Municipal bonds    
Fair Value, Assets and Liabilities Measured on Recurring and Nonrecurring Basis [Line Items]    
Total debt securities available-for-sale $ 6,793 $ 8,764
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v3.26.3
CONDENSED CONSOLIDATED STATEMENTS OF INCOME - USD ($)
shares in Thousands, $ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Revenues:        
Total revenues $ 658,696 $ 597,755 $ 1,898,198 $ 1,721,463
Operating expenses:        
Cost of goods sold 26,233 18,574 66,843 57,216
Research and development 209,481 199,164 621,384 611,753
Selling, general and administrative 154,559 123,661 441,793 395,703
Restructuring 0 19,816 0 19,816
Total operating expenses 390,273 361,215 1,130,020 1,084,488
Income from operations 268,423 236,540 768,178 636,975
Interest income 14,315 15,922 44,652 51,787
Other income (expenses), net 47 (49) 320 (244)
Income before income taxes 282,785 252,413 813,150 688,518
Provision for income taxes 64,690 58,835 172,538 150,476
Segment and consolidated net income $ 218,095 $ 193,578 $ 640,612 $ 538,042
Net income per share:        
Basic (in dollars per share) $ 0.88 $ 0.72 $ 2.54 $ 1.97
Diluted (in dollars per share) $ 0.85 $ 0.69 $ 2.46 $ 1.90
Weighted-average common shares outstanding:        
Basic (in shares) 246,756 268,421 251,964 273,269
Diluted (in shares) 255,754 278,535 260,917 283,701
Net product revenues        
Revenues:        
Total revenues $ 604,924 $ 542,930 $ 1,732,926 $ 1,576,227
Collaboration revenues        
Revenues:        
Total revenues $ 53,772 $ 54,825 $ 165,272 $ 145,236
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v3.26.3
CONDENSED CONSOLIDATED STATEMENTS OF COMPREHENSIVE INCOME - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Statement of Comprehensive Income [Abstract]        
Net income $ 218,095 $ 193,578 $ 640,612 $ 538,042
Other comprehensive income (loss):        
Net unrealized gains (losses) on available-for-sale debt securities, net of tax impact of $1,357, $(659), $2,979 and $(1,445), respectively (4,576) 2,216 (10,065) 4,912
Comprehensive income $ 213,519 $ 195,794 $ 630,547 $ 542,954
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Amount after tax of increase (decrease) in equity from transactions and other events and circumstances from net income and other comprehensive income, attributable to parent entity. Excludes changes in equity resulting from investments by owners and distributions to owners.

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v3.26.3
Cash And Marketable Securities - Investments by Security Type (Details) - USD ($)
$ in Thousands
Oct. 02, 2026
Jan. 02, 2026
Debt securities available-for-sale:    
Amortized Cost $ 1,221,830 $ 1,286,993
Gross Unrealized Gains 87 4,887
Gross Unrealized Losses (8,282) (38)
Fair Value 1,213,635 1,291,842
Cash, Cash Equivalents, Restricted Cash and Restricted Cash Equivalents    
Amortized Cost 1,407,972 1,657,845
Gross Unrealized Gains 87 4,887
Gross Unrealized Losses (8,282) (38)
Fair Value 1,399,777 1,662,694
Commercial paper    
Debt securities available-for-sale:    
Amortized Cost 257,765 241,439
Gross Unrealized Gains 0 0
Gross Unrealized Losses (3) 0
Fair Value 257,762 241,439
Corporate bonds    
Debt securities available-for-sale:    
Amortized Cost 792,197 882,390
Gross Unrealized Gains 84 4,138
Gross Unrealized Losses (6,780) (28)
Fair Value 785,501 886,500
U.S. Treasury and government-sponsored enterprises    
Debt securities available-for-sale:    
Amortized Cost 165,033 154,449
Gross Unrealized Gains 3 700
Gross Unrealized Losses (1,457) (10)
Fair Value 163,579 155,139
Municipal bonds    
Debt securities available-for-sale:    
Amortized Cost 6,835 8,715
Gross Unrealized Gains 0 49
Gross Unrealized Losses (42) 0
Fair Value 6,793 8,764
Cash    
Cash, Cash Equivalents, Restricted Cash and Restricted Cash Equivalents    
Amortized Cost   112
Gross Unrealized Gains   0
Gross Unrealized Losses   0
Fair Value   112
Money market funds    
Cash, Cash Equivalents, Restricted Cash and Restricted Cash Equivalents    
Amortized Cost 139,503 304,352
Gross Unrealized Gains 0 0
Gross Unrealized Losses 0 0
Fair Value 139,503 304,352
Certificates of deposit    
Cash, Cash Equivalents, Restricted Cash and Restricted Cash Equivalents    
Amortized Cost 46,639 66,388
Gross Unrealized Gains 0 0
Gross Unrealized Losses 0 0
Fair Value $ 46,639 $ 66,388
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v3.26.3
Cash And Marketable Securities
9 Months Ended
Oct. 02, 2026
Investments, Debt and Equity Securities [Abstract]  
CASH AND MARKETABLE SECURITIES CASH AND MARKETABLE SECURITIES
Cash, Cash Equivalents and Marketable Securities
Cash, cash equivalents and marketable securities consisted of the following (in thousands):
September 30, 2026
Amortized Cost
Gross Unrealized Gains
Gross Unrealized Losses
Fair Value
Debt securities available-for-sale:
Commercial paper$257,765 $— $(3)$257,762 
Corporate bonds792,197 84 (6,780)785,501 
U.S. Treasury and government-sponsored enterprises165,033 3 (1,457)163,579 
Municipal bonds6,835 — (42)6,793 
Total debt securities available-for-sale1,221,830 87 (8,282)1,213,635 
Money market funds139,503 — — 139,503 
Certificates of deposit46,639 — — 46,639 
Total cash, cash equivalents and marketable securities$1,407,972 $87 $(8,282)$1,399,777 

December 31, 2025
Amortized Cost
Gross Unrealized Gains
Gross Unrealized Losses
Fair Value
Debt securities available-for-sale:
Commercial paper$241,439 $— $— $241,439 
Corporate bonds882,390 4,138 (28)886,500 
U.S. Treasury and government-sponsored enterprises154,449 700 (10)155,139 
Municipal bonds8,715 49 — 8,764 
Total debt securities available-for-sale1,286,993 4,887 (38)1,291,842 
Cash112 — — 112 
Money market funds304,352 — — 304,352 
Certificates of deposit66,388 — — 66,388 
Total cash, cash equivalents and marketable securities$1,657,845 $4,887 $(38)$1,662,694 
Interest receivable was $9.8 million and $12.4 million as of September 30, 2026 and December 31, 2025, respectively, and is included in prepaid expenses and other current assets in the accompanying Condensed Consolidated Balance Sheets.
Realized gains and losses on the sales of marketable securities were immaterial during the three and nine months ended September 30, 2026 and 2025.
We manage credit risk associated with our marketable securities portfolio through our investment policy, which limits purchases to high-quality issuers and the amount of our portfolio that can be invested in a single issuer. The fair value and gross unrealized losses on debt securities available-for-sale in an unrealized loss position were as follows (in thousands):
September 30, 2026
In an Unrealized Loss Position Less than 12 MonthsIn an Unrealized Loss Position 12 Months or GreaterTotal
Fair ValueGross Unrealized LossesFair ValueGross Unrealized LossesFair ValueGross Unrealized Losses
Commercial Paper$26,354 $(3)$— $— $26,354 $(3)
Corporate bonds680,392 (6,780)— — 680,392 (6,780)
U.S. Treasury and government-sponsored enterprises147,881 (1,407)4,948 (50)152,829 (1,457)
Municipal Bonds6,793 (42)— — 6,793 (42)
Total
$861,420 $(8,232)$4,948 $(50)$866,368 $(8,282)
December 31, 2025
In an Unrealized Loss Position Less than 12 MonthsIn an Unrealized Loss Position 12 Months or GreaterTotal
Fair Value
Gross Unrealized Losses
Fair ValueGross Unrealized LossesFair ValueGross Unrealized Losses
Corporate bonds$46,851 $(25)$5,104 $(3)$51,955 $(28)
U.S. Treasury and government-sponsored enterprises11,350 (5)4,991 (5)16,341 (10)
Total$58,201 $(30)$10,095 $(8)$68,296 $(38)
There were 356 and 35 debt securities available-for-sale in an unrealized loss position as of September 30, 2026 and December 31, 2025, respectively. During the three and nine months ended September 30, 2026, we did not record an allowance for credit losses or other impairment charges on our marketable securities. Based upon our quarterly impairment review, we determined that the unrealized losses were not attributed to credit risk but were primarily associated with changes in interest rates and market liquidity. Based on the scheduled maturities of our marketable securities, we determined that it was more likely than not that we will hold these marketable securities for a period of time sufficient for a recovery of our cost basis.
The fair values of debt securities available-for-sale by contractual maturity were as follows (in thousands):
 
September 30, 2026December 31, 2025
Maturing in one year or less$705,875 $691,409 
Maturing after one year through five years507,760 600,433 
Total debt securities available-for-sale$1,213,635 $1,291,842 
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v3.26.3
CONDENSED CONSOLIDATED STATEMENTS OF STOCKHOLDERS’ EQUITY - USD ($)
shares in Thousands, $ in Thousands
Total
Common Stock
Additional Paid-in Capital
Accumulated Other Comprehensive Income (loss)
Accumulated Deficit
Beginning balance (in shares) at Jan. 03, 2025   281,732      
Beginning balance at Jan. 03, 2025 $ 2,244,203 $ 282 $ 2,343,915 $ (1,347) $ (98,647)
Increase (Decrease) in Stockholders' Equity [Roll Forward]          
Net income 538,042       538,042
Other comprehensive income (loss) 4,912     4,912  
Issuance of common stock under the equity incentive plans and stock purchase plan (in shares)   4,328      
Issuance of common stock under the equity incentive plan and stock purchase plan 41,350 $ 4 41,346    
Stock transactions associated with taxes withheld on equity awards (66,422)   (66,422)    
Repurchases of common stock (in shares)   (17,962)      
Repurchases of common stock (695,038) $ (18) (149,564)   (545,456)
Stock-based compensation 93,653   93,653    
Ending balance (in shares) at Oct. 03, 2025   268,098      
Ending balance at Oct. 03, 2025 2,160,700 $ 268 2,262,928 3,565 (106,061)
Beginning balance (in shares) at Jul. 04, 2025   270,132      
Beginning balance at Jul. 04, 2025 2,033,536 $ 270 2,251,456 1,349 (219,539)
Increase (Decrease) in Stockholders' Equity [Roll Forward]          
Net income 193,578       193,578
Other comprehensive income (loss) 2,216     2,216  
Issuance of common stock under the equity incentive plans and stock purchase plan (in shares)   340      
Issuance of common stock under the equity incentive plan and stock purchase plan 3,500 $ 0 3,500    
Stock transactions associated with taxes withheld on equity awards (3,363)   (3,363)    
Repurchases of common stock (in shares)   (2,374)      
Repurchases of common stock (99,891) $ (2) (19,789)   (80,100)
Stock-based compensation 31,124   31,124    
Ending balance (in shares) at Oct. 03, 2025   268,098      
Ending balance at Oct. 03, 2025 $ 2,160,700 $ 268 2,262,928 3,565 (106,061)
Beginning balance (in shares) at Jan. 02, 2026 262,483 262,483      
Beginning balance at Jan. 02, 2026 $ 2,161,319 $ 262 2,234,411 3,476 (76,830)
Increase (Decrease) in Stockholders' Equity [Roll Forward]          
Net income 640,612       640,612
Other comprehensive income (loss) (10,065)     (10,065)  
Issuance of common stock under the equity incentive plans and stock purchase plan (in shares)   3,210      
Issuance of common stock under the equity incentive plan and stock purchase plan 26,225 $ 4 26,221    
Stock transactions associated with taxes withheld on equity awards (73,909)   (73,909)    
Repurchases of common stock (in shares)   (21,015)      
Repurchases of common stock (1,001,079) $ (21) (178,474)   (822,584)
Stock-based compensation $ 90,729   90,729    
Ending balance (in shares) at Oct. 02, 2026 244,678 244,678      
Ending balance at Oct. 02, 2026 $ 1,833,832 $ 245 2,098,978 (6,589) (258,802)
Beginning balance (in shares) at Jul. 03, 2026   248,885      
Beginning balance at Jul. 03, 2026 1,843,762 $ 249 2,108,059 (2,013) (262,533)
Increase (Decrease) in Stockholders' Equity [Roll Forward]          
Net income 218,095       218,095
Other comprehensive income (loss) (4,576)     (4,576)  
Issuance of common stock under the equity incentive plans and stock purchase plan (in shares)   274      
Issuance of common stock under the equity incentive plan and stock purchase plan 3,395 $ 0 3,395    
Stock transactions associated with taxes withheld on equity awards (3,357)   (3,357)    
Repurchases of common stock (in shares)   (4,481)      
Repurchases of common stock (252,313) $ (4) (37,945)   (214,364)
Stock-based compensation $ 28,826   28,826    
Ending balance (in shares) at Oct. 02, 2026 244,678 244,678      
Ending balance at Oct. 02, 2026 $ 1,833,832 $ 245 $ 2,098,978 $ (6,589) $ (258,802)
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Revenues - Net Product Revenues Disaggregated by Product (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
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Net product revenues        
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CABOMETYX        
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v3.26.3
Stockholders’ Equity
9 Months Ended
Oct. 02, 2026
Share-Based Payment Arrangement [Abstract]  
STOCKHOLDERS’ EQUITY STOCKHOLDERS’ EQUITY
Stock-based Compensation
We have an equity incentive plan under which we grant stock options and restricted stock units (RSUs), including market condition-based RSUs and performance-based RSUs (PSUs) to employees and directors. On May 26, 2026, at the 2026 Annual Meeting of Stockholders, our stockholders approved the amendment and restatement of the Exelixis, Inc. 2017 Equity Incentive Plan (as amended and restated, the 2017 Plan). The amendment and restatement increased the share reserve, under the 2017 Plan, by 2,000,000 shares. As of September 30, 2026, 17.0 million shares were available for grant under the 2017 Plan. The share reserve is reduced by 1 share for each share issued pursuant to any award granted on or after May 26, 2026, including stock options, RSUs and PSUs. In addition, for each share that becomes available again for issuance under the terms of the 2017 Plan on or after May 26, 2026, the share reserve will be increased by the same number of shares by which the share reserve was reduced at the time the applicable award was granted.
We allocated stock-based compensation for the 2017 Plan and the 2000 Employee Stock Purchase Plan (as amended and restated, the Amended ESPP) as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Research and development$11,069 $10,353 $35,731 $34,018 
Selling, general and administrative17,649 20,532 54,600 58,868 
Total stock-based compensation$28,718 $30,885 $90,331 $92,886 
Stock-based compensation for each type of award under the 2017 Plan and the Amended ESPP were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Stock options$206 $493 $673 $2,224 
Restricted stock units27,830 29,660 86,533 87,388 
Performance-based restricted stock units— — — 241 
Employee stock purchase plan
682 732 3,125 3,033 
Total stock-based compensation$28,718 $30,885 $90,331 $92,886 
As of September 30, 2026, there were 1.1 million stock options outstanding and $0.6 million of related unrecognized stock-based compensation.
In February 2026, we awarded to certain employees an aggregate of 0.7 million RSUs (the target number) that are subject to a total shareholder return (TSR) market condition and a time-based service condition (the 2026 TSR-based RSUs). The TSR market condition is based on our relative TSR percentile rank compared to companies in the Nasdaq Biotechnology Index during the performance period, which is January 3, 2026 through December 29, 2028. Depending on the results relative to the TSR market condition, the holders of the 2026 TSR-based RSUs may earn up to 200% of the target number of shares. Following achievement of the market condition at the end of the performance period and upon employee’s continuous service through the vesting dates, 50% of the shares earned pursuant to the 2026 TSR-based RSUs will vest shortly after the end of the performance period, and the remainder will vest approximately one year later. The 2026 TSR-based RSUs will be forfeited if the market condition at or above a threshold level is not achieved, and/or the time-based service condition is not fulfilled, by the end of the performance period and through the vesting dates.
We used a Monte Carlo simulation model and the following assumptions to determine the grant date fair value of $55.31 per share for the 2026 TSR-based RSUs:
2026 TSR-based RSUs
Fair value of Exelixis common stock on grant date
$44.28 
Expected volatility
35.5%
Risk-free interest rate
3.4%
Dividend yield
—%
The Monte Carlo simulation model for our 2026 TSR-based RSUs assumed correlations of returns of the stock prices of Exelixis common stock and the common stock of a peer group of companies and historical stock price volatility of the peer group of companies. The valuation model also used terms based on the remaining length of the performance period and compound annual growth rate goals for TSR based on the provisions of the awards. Stock-based compensation related to RSUs with a market condition is recognized regardless of the outcome of the market condition.
During the nine months ended September 30, 2026, we granted 2.0 million service-based RSUs with a weighted- average grant date fair value of $45.38 per share. As of September 30, 2026, there were 15.8 million RSUs outstanding, including RSUs that are subject to market conditions, and $307.3 million of related unrecognized stock-based compensation. Service-based RSUs granted to employees during the nine months ended September 30, 2026, have vesting conditions and contractual lives of a similar nature to those described in “Note 9. Stockholders’ Equity” of the “Notes to Consolidated Financial Statements” included in Part II, Item 8 of our Fiscal 2025 Form 10-K.
Common Stock Repurchases
In October 2025, our Board of Directors authorized a stock repurchase program (SRP) to acquire up to $750.0 million of our outstanding common stock before December 31, 2026 (the October 2025 SRP). As of June 30, 2026, we completed the repurchase of 17.2 million shares of outstanding common stock for an aggregate purchase price of $750.0 million pursuant to the October 2025 SRP. In May 2026, our Board of Directors authorized the repurchase of up to an additional $750.0 million of our outstanding common stock before December 31, 2027 (the May 2026 SRP). Under the May 2026 SRP, as of September 30, 2026, we repurchased 7.4 million shares of common stock for an aggregate purchase price of $402.1 million. As of September 30, 2026, approximately $347.9 million remained available for future stock repurchases before December 31, 2027. Stock repurchases under the May 2026 SRP may be made from time to time through a variety of methods, which may include open market purchases, in block trades, Rule 10b5-1 trading plans, accelerated share repurchase transactions, exchange transactions, or any combination of such methods. The timing and amount of any stock repurchases under the SRP will be based on a variety of factors, including ongoing assessments of the capital needs of the business, alternative investment opportunities, the market price of our common stock and general market conditions. The SRP does not obligate us to acquire any amount of our common stock, and the SRP may be modified, suspended or discontinued at any time without prior notice.
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v3.26.3
Cash And Marketable Securities - Fair Value and Gross Unrealized Losses of Investments Available-for-Sale in an Unrealized Loss Position (Details) - USD ($)
$ in Thousands
Oct. 02, 2026
Jan. 02, 2026
Fair Value    
In an Unrealized Loss Position Less than 12 Months $ 861,420 $ 58,201
In an Unrealized Loss Position 12 Months or Greater 4,948 10,095
Total 866,368 68,296
Gross Unrealized Losses    
In an Unrealized Loss Position Less than 12 Months (8,232) (30)
In an Unrealized Loss Position 12 Months or Greater (50) (8)
Total (8,282) (38)
Commercial paper    
Fair Value    
In an Unrealized Loss Position Less than 12 Months 26,354  
In an Unrealized Loss Position 12 Months or Greater 0  
Total 26,354  
Gross Unrealized Losses    
In an Unrealized Loss Position Less than 12 Months (3)  
In an Unrealized Loss Position 12 Months or Greater 0  
Total (3)  
Corporate bonds    
Fair Value    
In an Unrealized Loss Position Less than 12 Months 680,392 46,851
In an Unrealized Loss Position 12 Months or Greater 0 5,104
Total 680,392 51,955
Gross Unrealized Losses    
In an Unrealized Loss Position Less than 12 Months (6,780) (25)
In an Unrealized Loss Position 12 Months or Greater 0 (3)
Total (6,780) (28)
U.S. Treasury and government-sponsored enterprises    
Fair Value    
In an Unrealized Loss Position Less than 12 Months 147,881 11,350
In an Unrealized Loss Position 12 Months or Greater 4,948 4,991
Total 152,829 16,341
Gross Unrealized Losses    
In an Unrealized Loss Position Less than 12 Months (1,407) (5)
In an Unrealized Loss Position 12 Months or Greater (50) (5)
Total (1,457) $ (10)
Municipal bonds    
Fair Value    
In an Unrealized Loss Position Less than 12 Months 6,793  
In an Unrealized Loss Position 12 Months or Greater 0  
Total 6,793  
Gross Unrealized Losses    
In an Unrealized Loss Position Less than 12 Months (42)  
In an Unrealized Loss Position 12 Months or Greater 0  
Total $ (42)  
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v3.26.3
CONDENSED CONSOLIDATED BALANCE SHEETS - USD ($)
$ in Thousands
Oct. 02, 2026
Jan. 02, 2026
Current assets:    
Cash and cash equivalents $ 304,774 $ 482,488
Marketable securities 587,244 576,603
Trade receivables, net 328,466 286,916
Inventory 29,871 21,686
Prepaid expenses and other current assets 71,267 75,596
Total current assets 1,321,622 1,443,289
Non-current marketable securities 507,759 603,603
Property and equipment, net 87,276 98,960
Deferred tax assets, net 295,561 292,582
Goodwill 63,684 63,684
Right-of-use assets and other non-current assets 237,587 342,305
Total assets 2,513,489 2,844,423
Current liabilities:    
Accounts payable 30,833 29,623
Accrued compensation and benefits 100,493 102,218
Accrued clinical trial liabilities 70,316 65,742
Rebates and fees due to customers 70,767 59,896
Accrued collaboration liabilities 24,627 22,783
Other current liabilities 114,841 125,382
Total current liabilities 411,877 405,644
Non-current operating lease liabilities 162,201 173,038
Other non-current liabilities 105,579 104,422
Total liabilities 679,657 683,104
Commitments and contingencies (Note 11)
Stockholders’ equity:    
Preferred stock, $0.001 par value, 10,000 shares authorized and no shares issued 0 0
Common stock, $0.001 par value; 400,000 shares authorized; issued and outstanding: 244,678 and 262,483 at September 30, 2026, and December 31, 2025, respectively 245 262
Additional paid-in-capital 2,098,978 2,234,411
Accumulated other comprehensive income (loss) (6,589) 3,476
Accumulated deficit (258,802) (76,830)
Total stockholders’ equity 1,833,832 2,161,319
Total liabilities and stockholders’ equity $ 2,513,489 $ 2,844,423
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v3.26.3
Revenues - Narrative (Details) - USD ($)
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Jan. 02, 2026
Disaggregation of Revenue [Line Items]          
Contract assets $ 0   $ 0   $ 0
Contract revenue recognized, including revenue from deferred revenue beginning balance 1,000,000.0 $ 1,000,000.0 3,100,000 $ 3,100,000  
Ipsen And Takeda Collaborations          
Disaggregation of Revenue [Line Items]          
Revenues recognized for performance obligations satisfied in previous periods 58,000,000.0 $ 57,600,000 177,900,000 $ 151,300,000  
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v3.26.3
Organization and Summary of Significant Accounting Policies
9 Months Ended
Oct. 02, 2026
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES ORGANIZATION AND SUMMARY OF SIGNIFICANT ACCOUNTING POLICIES
Organization
Exelixis, Inc. (Exelixis, we, our or us) is an oncology company innovating next-generation medicines and regimens at the forefront of cancer care. We have produced four marketed pharmaceutical products, two of which are formulations of our flagship molecule, cabozantinib, and we are steadily advancing and evolving our product pipeline portfolio, including our lead clinical asset, zanzalintinib, currently under review by the U.S. Food and Drug Administration (FDA) for the treatment of certain forms of colorectal cancer, as well as the focus of an extensive late-stage clinical development program in other indications. With a rational and disciplined approach to investment, we are leveraging our internal experience and expertise, and the strength of strategic partnerships, to identify and pursue opportunities across the landscape of scientific modalities, including small molecules and biotherapeutics, such as antibody-drug conjugates.
Sales related to cabozantinib account for the majority of our revenues. Cabozantinib is an inhibitor of multiple tyrosine kinases, including MET, AXL, VEGF receptors and RET and has been approved by the FDA, and in other countries for all or a combination of, the following: as CABOMETYX® (cabozantinib) tablets for advanced renal cell carcinoma (RCC) (both alone and in combination with Bristol-Myers Squibb Company’s nivolumab (OPDIVO®)), previously treated hepatocellular carcinoma, previously treated, radioactive iodine-refractory differentiated thyroid cancer, and previously treated, unresectable, locally advanced or metastatic, well-differentiated pancreatic neuroendocrine tumors and extra-pancreatic neuroendocrine tumors; and as COMETRIQ® (cabozantinib) capsules for progressive, metastatic medullary thyroid cancer. For physicians treating these types of cancer, cabozantinib has become or is becoming an important medicine in their selection of effective therapies.
The other two products resulting from our discovery efforts are: COTELLIC® (cobimetinib), an inhibitor of MEK, approved as part of multiple combination regimens to treat specific forms of advanced melanoma and marketed under a collaboration with Genentech, Inc. (a member of the Roche Group) (Genentech); and MINNEBRO® (esaxerenone), an oral, non-steroidal, selective blocker of the mineralocorticoid receptor, approved for the treatment of hypertension in Japan and licensed to Daiichi Sankyo Company, Limited.
Basis of Presentation
The accompanying unaudited Condensed Consolidated Financial Statements include the accounts of Exelixis and those of our wholly owned subsidiaries. These entities’ functional currency is the U.S. dollar. All intercompany balances and transactions have been eliminated.
We use a 52- or 53-week fiscal year policy that generally ends on the Friday closest to December 31. Fiscal year 2026, which is a 52-week fiscal year, will end on January 1, 2027 and fiscal year 2025, which was a 52-week fiscal year, ended on January 2, 2026. For convenience, references in this report as of and for the fiscal periods ended October 2, 2026, October 3, 2025, July 3, 2026 and July 4, 2025, and as of and for the fiscal year ending January 1, 2027 and the fiscal years ended January 2, 2026 and January 3, 2025, are indicated as being as of and for the periods ended September 30, 2026, September 30, 2025, June 30, 2026 and June 30, 2025, and the year ending December 31, 2026, and the years ended December 31, 2025, and December 31, 2024, respectively.
The accompanying Condensed Consolidated Financial Statements have been prepared in accordance with accounting principles generally accepted in the U.S. for interim financial information and pursuant to Form 10-Q and Article 10 of Regulation S-X of the Securities and Exchange Commission (SEC). Accordingly, they do not include all of the information and footnotes required by U.S. generally accepted accounting principles for complete financial statements. In our opinion, all adjustments (consisting only of normal recurring adjustments) considered necessary for a fair presentation of our financial statements for the periods presented have been included. Operating results for the nine months ended September 30, 2026 are not necessarily indicative of the results that may be expected for the year ending December 31, 2026 or for any future period. The accompanying Condensed Consolidated Financial Statements and Notes thereto should be read in conjunction with our Consolidated Financial Statements and Notes thereto for the fiscal year ended December 31, 2025, included in Part II, Item 8 of our Annual Report on Form 10-K, filed with the SEC on February 10, 2026 (Fiscal 2025 Form 10-K).
Use of Estimates
The preparation of the accompanying Condensed Consolidated Financial Statements conforms to accounting principles generally accepted in the U.S., which requires management to make judgments, estimates and assumptions that affect the reported amounts of assets, liabilities, equity, revenues and expenses and related disclosures. On an ongoing basis, we evaluate our significant estimates. We base our estimates on historical experience and on various other market-specific and other relevant assumptions that we believe to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results could differ materially from those estimates.
Significant Accounting Policies
There have been no material changes to our significant accounting policies during the nine months ended September 30, 2026, as compared to the significant accounting policies disclosed in “Note 1. Organization and Summary of Significant Accounting Policies” of the “Notes to Consolidated Financial Statements” included in Part II, Item 8 of our Fiscal 2025 Form 10-K.
Recently Adopted Accounting Pronouncements
There were no new accounting pronouncements adopted by us since our filing of the Fiscal 2025 Form 10-K, which could have a significant effect on our Condensed Consolidated Financial Statements.
Recent Accounting Pronouncements Not Yet Adopted
In November 2024, the Financial Accounting Standards Board (FASB) issued Accounting Standards Update (ASU) 2024-03, Income Statement – Reporting Comprehensive Income – Expense Disaggregation Disclosures (Subtopic 220-40): Disaggregation of Income Statement Expenses (ASU 2024-03), which enhances the disclosures required for expense disaggregation in our annual and interim consolidated financial statements. In January 2025, the FASB issued ASU 2025-01, Income Statement – Reporting Comprehensive Income – Expense Disaggregation Disclosures (Subtopic 220-40) – Clarifying the effective Date (ASU 2025-01), which clarifies the effective date of ASU 2024-03 for companies with a non-calendar year end. ASU 2024-03 is effective for us in our annual reporting for fiscal year 2027, and in our interim periods beginning in fiscal year 2028. Early adoption and retrospective application are permitted. We are currently evaluating the impact of ASU 2024-03 on our Consolidated Financial Statements.
In September 2025, the FASB issued ASU 2025-06, Intangibles – Goodwill and Other – Internal-Use Software (Subtopic 350-40): Targeted Improvements to the Accounting for Internal-Use Software (ASU 2025-06) to clarify and modernize the accounting for costs related to internal-use software by removing all references to software development project stages and clarifying the threshold entities apply to begin capitalizing costs. ASU 2025-06 is effective for us in our annual reporting for fiscal year 2028. Early adoption and retrospective reporting are permitted. We do not expect the adoption of ASU 2025-06 to have a material impact on our Consolidated Financial Statements.
In December 2025, the FASB issued ASU 2025-11, Interim Reporting (Topic 270): Narrow-Scope Improvements (ASU 2025-11), which clarifies the guidance in Topic 270 to improve the consistency of interim financial reporting. ASU 2025-11 provides a comprehensive list of required interim disclosures and introduces a disclosure principle requiring entities to disclose events since the end of the last annual reporting period that have a material impact on the entity. ASU 2025-11 is effective for us in our annual reporting for fiscal year 2028, and in our interim periods beginning in fiscal year 2028. Early adoption and retrospective application are permitted. We do not expect the adoption of ASU 2025-11 to have a material impact on our Consolidated Financial Statements.
In December 2025, the FASB issued ASU 2025-12, Codification Improvements (ASU 2025-12), which addresses 33 issues, representing amendments to Accounting Standards Codification (ASC) topics that clarify, correct errors or make minor improvements. ASU 2025-12 makes the ASC topics easier to understand and apply. ASU 2025-12 is effective for us in our annual reporting for fiscal year 2027, and in our interim periods beginning in fiscal year 2027. Early adoption and retrospective application are permitted on an issue-by-issue basis. We are currently evaluating the impact of ASU 2025-12 on our Consolidated Financial Statements.
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Cash And Marketable Securities (Tables)
9 Months Ended
Oct. 02, 2026
Investments, Debt and Equity Securities [Abstract]  
Schedule of Investments by Security Type
Cash, cash equivalents and marketable securities consisted of the following (in thousands):
September 30, 2026
Amortized Cost
Gross Unrealized Gains
Gross Unrealized Losses
Fair Value
Debt securities available-for-sale:
Commercial paper$257,765 $— $(3)$257,762 
Corporate bonds792,197 84 (6,780)785,501 
U.S. Treasury and government-sponsored enterprises165,033 3 (1,457)163,579 
Municipal bonds6,835 — (42)6,793 
Total debt securities available-for-sale1,221,830 87 (8,282)1,213,635 
Money market funds139,503 — — 139,503 
Certificates of deposit46,639 — — 46,639 
Total cash, cash equivalents and marketable securities$1,407,972 $87 $(8,282)$1,399,777 

December 31, 2025
Amortized Cost
Gross Unrealized Gains
Gross Unrealized Losses
Fair Value
Debt securities available-for-sale:
Commercial paper$241,439 $— $— $241,439 
Corporate bonds882,390 4,138 (28)886,500 
U.S. Treasury and government-sponsored enterprises154,449 700 (10)155,139 
Municipal bonds8,715 49 — 8,764 
Total debt securities available-for-sale1,286,993 4,887 (38)1,291,842 
Cash112 — — 112 
Money market funds304,352 — — 304,352 
Certificates of deposit66,388 — — 66,388 
Total cash, cash equivalents and marketable securities$1,657,845 $4,887 $(38)$1,662,694 
Schedule of Fair Value and Gross Unrealized Losses of Investments Available-for-Sale in an Unrealized Loss Position The fair value and gross unrealized losses on debt securities available-for-sale in an unrealized loss position were as follows (in thousands):
September 30, 2026
In an Unrealized Loss Position Less than 12 MonthsIn an Unrealized Loss Position 12 Months or GreaterTotal
Fair ValueGross Unrealized LossesFair ValueGross Unrealized LossesFair ValueGross Unrealized Losses
Commercial Paper$26,354 $(3)$— $— $26,354 $(3)
Corporate bonds680,392 (6,780)— — 680,392 (6,780)
U.S. Treasury and government-sponsored enterprises147,881 (1,407)4,948 (50)152,829 (1,457)
Municipal Bonds6,793 (42)— — 6,793 (42)
Total
$861,420 $(8,232)$4,948 $(50)$866,368 $(8,282)
December 31, 2025
In an Unrealized Loss Position Less than 12 MonthsIn an Unrealized Loss Position 12 Months or GreaterTotal
Fair Value
Gross Unrealized Losses
Fair ValueGross Unrealized LossesFair ValueGross Unrealized Losses
Corporate bonds$46,851 $(25)$5,104 $(3)$51,955 $(28)
U.S. Treasury and government-sponsored enterprises11,350 (5)4,991 (5)16,341 (10)
Total$58,201 $(30)$10,095 $(8)$68,296 $(38)
Schedule of Fair Value of Cash Equivalents and Investments by Contractual Maturity
The fair values of debt securities available-for-sale by contractual maturity were as follows (in thousands):
 
September 30, 2026December 31, 2025
Maturing in one year or less$705,875 $691,409 
Maturing after one year through five years507,760 600,433 
Total debt securities available-for-sale$1,213,635 $1,291,842 
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Collaboration Agreements And Business Development Activities - Research Collaborations and In-Licensing Arrangements Narrative (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Asset Acquisition [Line Items]        
Research and development $ 209,481 $ 199,164 $ 621,384 $ 611,753
Research Collaborations, In-Licensing Arrangements and Other Business Development Activities        
Asset Acquisition [Line Items]        
Research and development 3,200 $ 8,400 20,300 $ 19,300
Collaborative arrangement, maximum aggregate development milestone payments 441,500   441,500  
Collaborative arrangement, maximum aggregate regulatory milestone payments 278,000   278,000  
Collaborative arrangement, rights and obligations, maximum aggregate commercial milestone payments $ 2,500,000   $ 2,500,000  
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Segment Reporting - Segment and Consolidated Net Income (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Segment Reporting [Line Items]        
Revenues $ 658,696 $ 597,755 $ 1,898,198 $ 1,721,463
Less:        
Cost of goods sold 26,233 18,574 66,843 57,216
Interest income (14,315) (15,922) (44,652) (51,787)
Provision for income taxes 64,690 58,835 172,538 150,476
Segment and consolidated net income 218,095 193,578 640,612 538,042
Reportable Segment        
Segment Reporting [Line Items]        
Revenues 658,696 597,755 1,898,198 1,721,463
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Cost of goods sold 26,233 18,574 66,843 57,216
Drug discovery 17,144 23,838 54,872 63,448
Development 147,739 133,645 433,976 421,021
Selling, general, and administrative 136,910 103,129 387,193 336,835
Other segment items 62,200 82,078 186,816 206,212
Interest income (14,315) (15,922) (44,652) (51,787)
Provision for income taxes 64,690 58,835 172,538 150,476
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v3.26.3
Provision For Income Taxes
9 Months Ended
Oct. 02, 2026
Income Tax Disclosure [Abstract]  
PROVISION FOR INCOME TAXES PROVISION FOR INCOME TAXES
The effective tax rates for the three and nine months ended September 30, 2026 were 22.9% and 21.2%, respectively, as compared to 23.3% and 21.9% for the corresponding prior year periods. The effective tax rates for the three months ended September 30, 2026, differed from the U.S. federal statutory tax rate of 21%, primarily due to state taxes, partially offset by the Foreign-Derived Intangible Income (FDII) deduction. The effective tax rate for the nine months ended September 30, 2026, differed from the U.S. federal statutory rate of 21% primarily due to state taxes, offset by excess tax
benefits related to certain stock grants and the FDII deduction. The effective tax rates for the three and nine months ended September 30, 2025, differed from the U.S. federal statutory tax rate of 21%, primarily due to state taxes, offset by excess tax benefits related to certain stock grants.
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v3.26.3
Organization and Summary of Significant Accounting Policies (Policies)
9 Months Ended
Oct. 02, 2026
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
Basis of Consolidation
The accompanying unaudited Condensed Consolidated Financial Statements include the accounts of Exelixis and those of our wholly owned subsidiaries. These entities’ functional currency is the U.S. dollar. All intercompany balances and transactions have been eliminated.
Fiscal Period
We use a 52- or 53-week fiscal year policy that generally ends on the Friday closest to December 31. Fiscal year 2026, which is a 52-week fiscal year, will end on January 1, 2027 and fiscal year 2025, which was a 52-week fiscal year, ended on January 2, 2026. For convenience, references in this report as of and for the fiscal periods ended October 2, 2026, October 3, 2025, July 3, 2026 and July 4, 2025, and as of and for the fiscal year ending January 1, 2027 and the fiscal years ended January 2, 2026 and January 3, 2025, are indicated as being as of and for the periods ended September 30, 2026, September 30, 2025, June 30, 2026 and June 30, 2025, and the year ending December 31, 2026, and the years ended December 31, 2025, and December 31, 2024, respectively.
Basis of Presentation
The accompanying Condensed Consolidated Financial Statements have been prepared in accordance with accounting principles generally accepted in the U.S. for interim financial information and pursuant to Form 10-Q and Article 10 of Regulation S-X of the Securities and Exchange Commission (SEC). Accordingly, they do not include all of the information and footnotes required by U.S. generally accepted accounting principles for complete financial statements. In our opinion, all adjustments (consisting only of normal recurring adjustments) considered necessary for a fair presentation of our financial statements for the periods presented have been included. Operating results for the nine months ended September 30, 2026 are not necessarily indicative of the results that may be expected for the year ending December 31, 2026 or for any future period. The accompanying Condensed Consolidated Financial Statements and Notes thereto should be read in conjunction with our Consolidated Financial Statements and Notes thereto for the fiscal year ended December 31, 2025, included in Part II, Item 8 of our Annual Report on Form 10-K, filed with the SEC on February 10, 2026 (Fiscal 2025 Form 10-K).
Use of Estimates
The preparation of the accompanying Condensed Consolidated Financial Statements conforms to accounting principles generally accepted in the U.S., which requires management to make judgments, estimates and assumptions that affect the reported amounts of assets, liabilities, equity, revenues and expenses and related disclosures. On an ongoing basis, we evaluate our significant estimates. We base our estimates on historical experience and on various other market-specific and other relevant assumptions that we believe to be reasonable under the circumstances, the results of which form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources. Actual results could differ materially from those estimates.
Recently Adopted Accounting Pronouncements
Recently Adopted Accounting Pronouncements
There were no new accounting pronouncements adopted by us since our filing of the Fiscal 2025 Form 10-K, which could have a significant effect on our Condensed Consolidated Financial Statements.
Recent Accounting Pronouncements Not Yet Adopted
In November 2024, the Financial Accounting Standards Board (FASB) issued Accounting Standards Update (ASU) 2024-03, Income Statement – Reporting Comprehensive Income – Expense Disaggregation Disclosures (Subtopic 220-40): Disaggregation of Income Statement Expenses (ASU 2024-03), which enhances the disclosures required for expense disaggregation in our annual and interim consolidated financial statements. In January 2025, the FASB issued ASU 2025-01, Income Statement – Reporting Comprehensive Income – Expense Disaggregation Disclosures (Subtopic 220-40) – Clarifying the effective Date (ASU 2025-01), which clarifies the effective date of ASU 2024-03 for companies with a non-calendar year end. ASU 2024-03 is effective for us in our annual reporting for fiscal year 2027, and in our interim periods beginning in fiscal year 2028. Early adoption and retrospective application are permitted. We are currently evaluating the impact of ASU 2024-03 on our Consolidated Financial Statements.
In September 2025, the FASB issued ASU 2025-06, Intangibles – Goodwill and Other – Internal-Use Software (Subtopic 350-40): Targeted Improvements to the Accounting for Internal-Use Software (ASU 2025-06) to clarify and modernize the accounting for costs related to internal-use software by removing all references to software development project stages and clarifying the threshold entities apply to begin capitalizing costs. ASU 2025-06 is effective for us in our annual reporting for fiscal year 2028. Early adoption and retrospective reporting are permitted. We do not expect the adoption of ASU 2025-06 to have a material impact on our Consolidated Financial Statements.
In December 2025, the FASB issued ASU 2025-11, Interim Reporting (Topic 270): Narrow-Scope Improvements (ASU 2025-11), which clarifies the guidance in Topic 270 to improve the consistency of interim financial reporting. ASU 2025-11 provides a comprehensive list of required interim disclosures and introduces a disclosure principle requiring entities to disclose events since the end of the last annual reporting period that have a material impact on the entity. ASU 2025-11 is effective for us in our annual reporting for fiscal year 2028, and in our interim periods beginning in fiscal year 2028. Early adoption and retrospective application are permitted. We do not expect the adoption of ASU 2025-11 to have a material impact on our Consolidated Financial Statements.
In December 2025, the FASB issued ASU 2025-12, Codification Improvements (ASU 2025-12), which addresses 33 issues, representing amendments to Accounting Standards Codification (ASC) topics that clarify, correct errors or make minor improvements. ASU 2025-12 makes the ASC topics easier to understand and apply. ASU 2025-12 is effective for us in our annual reporting for fiscal year 2027, and in our interim periods beginning in fiscal year 2027. Early adoption and retrospective application are permitted on an issue-by-issue basis. We are currently evaluating the impact of ASU 2025-12 on our Consolidated Financial Statements.
Segment Reporting
We operate in one business segment that focuses on the discovery, development and commercialization of new medicines for difficult-to-treat cancers. Our President and Chief Executive Officer, as the chief operating decision-maker, manages and allocates resources to our operations on a total consolidated basis. Consistent with this decision-making process, our President and Chief Executive Officer uses net income to monitor budget versus actual results for purposes of evaluating performance and to make decisions about the allocation of resources.
Our significant segment expenses that are regularly provided to our President and Chief Executive Officer and included in the measure of segment net income consist of consolidated expenses for our operational departments: drug discovery, development, and selling, general and administrative and other segment items.
Revenues
Total revenues include net product revenues attributed to geographic regions based on the ship-to location and license and collaboration services revenues attributed to geographic regions based on the location of our collaboration partners’ headquarters.
Net product revenues and license revenues are recorded in accordance with ASC Topic 606, Revenue from Contracts with Customers (Topic 606). License revenues include the recognition of the portion of milestone payments allocated to the transfer of intellectual property licenses for which it had become probable in the current period that the milestone would be achieved and a significant reversal of revenues would not occur, as well as royalty revenues and our share of profits under our collaboration agreement with Genentech. Collaboration services revenues are recorded in accordance with ASC Topic 808, Collaborative Arrangements. Collaboration services revenues include the recognition of deferred revenues for the portion of upfront and milestone payments allocated to our research and development services performance obligations, development cost reimbursements earned under our collaboration agreements, product supply revenues, net of product supply costs and the royalties we paid on sales of products containing cabozantinib by our collaboration partners. License revenues and collaboration services revenues are presented in collaboration revenues in the accompanying Condensed Consolidated Statements of Income.
The allowance for chargebacks, discounts for prompt payment and other are recorded as a reduction of trade receivables, net, and the remaining reserves are recorded as rebates and fees due to customers in the accompanying Condensed Consolidated Balance Sheets.
Contract Assets and Liabilities
We receive payments from our collaboration partners based on billing schedules established in each contract. Amounts are recorded as accounts receivable when our right to consideration is unconditional. We may also recognize revenue in advance of the contractual billing schedule and such amounts are recorded as a contract asset when recognized. We may be required to defer recognition of revenue for upfront and milestone payments until we perform our obligations under these arrangements, and such amounts are recorded as deferred revenue upon receipt or when due. For those contracts that have multiple performance obligations, contract assets and liabilities are reported on a net basis at the contract level. There were no contract assets as of September 30, 2026 and December 31, 2025. Contract liabilities are primarily related to deferred revenues from Ipsen Pharma SAS (Ipsen) and Takeda Pharmaceutical Company Limited (Takeda).
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v3.26.3
CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS - USD ($)
$ in Thousands
9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Statement of Cash Flows [Abstract]    
Net income $ 640,612 $ 538,042
Adjustments to reconcile net income to net cash provided by operating activities:    
Depreciation and amortization 20,867 22,109
Stock-based compensation 90,331 92,886
Non-cash lease expense 17,808 18,210
Acquired in-process research and development technology 11,600 6,999
Other, net (4,556) (9,261)
Changes in operating assets and liabilities:    
Trade receivables, net (41,550) (44,207)
Inventory (3,753) (1,581)
Prepaid expenses and other assets 94,349 (36,737)
Accrued collaboration liabilities 844 1,544
Accounts payable and other liabilities 12,990 (37,252)
Net cash provided by operating activities 839,542 550,752
Cash flows from investing activities:    
Purchases of marketable securities (527,580) (477,556)
Proceeds from maturities and sales of marketable securities 582,646 833,527
Purchases of property, equipment and other, net (10,814) (7,272)
Acquired in-process research and development technology (10,600) (25,499)
Net cash provided by investing activities 33,652 323,200
Cash flows from financing activities:    
Payments for repurchases of common stock (1,003,289) (689,893)
Proceeds from issuance of common stock under the equity incentive plan and stock purchase plan 26,313 41,262
Taxes paid related to net share settlement of equity awards (73,932) (66,395)
Net cash used in financing activities (1,050,908) (715,026)
Net increase (decrease) in cash and cash equivalents (177,714) 158,926
Cash and cash equivalents at beginning of period 482,488 217,374
Cash and cash equivalents at end of period $ 304,774 $ 376,300
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v3.26.3
Inventory (Details) - USD ($)
$ in Thousands
Oct. 02, 2026
Jan. 02, 2026
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Work in process 45,803 53,531
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Trading Arrangements, by Individual  
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Revenues - Revenues Disaggregated by Geographic Region (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Disaggregation of Revenue [Line Items]        
Total revenues $ 658,696 $ 597,755 $ 1,898,198 $ 1,721,463
U.S.        
Disaggregation of Revenue [Line Items]        
Total revenues 609,099 546,461 1,746,006 1,588,413
Europe        
Disaggregation of Revenue [Line Items]        
Total revenues 44,298 44,966 129,873 114,705
Japan        
Disaggregation of Revenue [Line Items]        
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v3.26.3
Fair Value Measurements
9 Months Ended
Oct. 02, 2026
Fair Value Disclosures [Abstract]  
FAIR VALUE MEASUREMENTS FAIR VALUE MEASUREMENTS
Fair value reflects the amounts that would be received upon sale of an asset or paid to transfer a liability in an orderly transaction between market participants at the measurement date. The fair value hierarchy has the following three levels:
•Level 1 - quoted prices (unadjusted) in active markets for identical assets and liabilities;
•Level 2 - inputs other than Level 1 that are observable either directly or indirectly, such as quoted prices in active markets for similar instruments or on industry models using data inputs, such as interest rates and prices that can be directly observed or corroborated in active markets; and
•Level 3 - unobservable inputs that are supported by little or no market activity that are significant to the fair value measurement.
The classifications within the fair value hierarchy of our financial assets that were measured and recorded at fair value on a recurring basis were as follows (in thousands):
September 30, 2026
Level 1Level 2Total
Commercial paper$— $257,762 $257,762 
Corporate bonds— 785,501 785,501 
U.S. Treasury and government-sponsored enterprises— 163,579 163,579 
Municipal bonds— 6,793 6,793 
Total debt securities available-for-sale— 1,213,635 1,213,635 
Money market funds139,503 — 139,503 
Certificates of deposit46,639 46,639 
Total financial assets carried at fair value$139,503 $1,260,274 $1,399,777 
December 31, 2025
Level 1Level 2Total
Commercial paper$— $241,439 $241,439 
Corporate bonds— 886,500 886,500 
U.S. Treasury and government-sponsored enterprises— 155,139 155,139 
Municipal bonds— 8,764 8,764 
Total debt securities available-for-sale— 1,291,842 1,291,842 
Money market funds304,352 — 304,352 
Certificates of deposit— 66,388 66,388 
Total financial assets carried at fair value$304,352 $1,358,230 $1,662,582 
When available, we value marketable securities based on quoted prices for those financial instruments, which is a Level 1 input. Our remaining marketable securities are valued using third-party pricing sources, which use observable market prices, interest rates and yield curves observable at commonly quoted intervals for similar assets as observable inputs for pricing, which is a Level 2 input.
The carrying amount of our remaining financial assets and liabilities, which include cash, receivables and payables, approximate their fair values due to their short-term nature.
Forward Foreign Currency Contracts
We may enter into forward foreign currency exchange contracts that are not designated as hedges for accounting purposes to hedge certain operational exposures for the changes in foreign currency exchange rates associated with assets or liabilities denominated in foreign currencies, primarily the Euro.
As of September 30, 2026, we had one forward contract outstanding to sell €2.2 million. The forward contract with a maturity of three months is recorded at fair value and is included in other current liabilities in the accompanying Condensed Consolidated Balance Sheets. The unrealized gain on the forward contract was immaterial as of September 30, 2026. The forward contract is considered a Level 2 in the fair value hierarchy of our fair value measurements. The net realized gains and losses recognized upon maturity of forward contracts were immaterial for each of the three and nine months ended September 30, 2026 and 2025, and are included in other income (expenses), net in the accompanying Condensed Consolidated Statements of Income.
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Oct. 31, 2022
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€ in Millions
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EUR (€)
derivative_instrument
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Segment Reporting [Abstract]  
Schedule of Segment and Consolidated Net Income, Including Significant Segment Expenses
The segment and consolidated net income, including significant segment expenses were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Revenues$658,696 $597,755 $1,898,198 $1,721,463 
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Cost of goods sold26,233 18,574 66,843 57,216 
Drug discovery17,144 23,838 54,872 63,448 
Development147,739 133,645 433,976 421,021 
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62,200 82,078 186,816 206,212 
Interest income(14,315)(15,922)(44,652)(51,787)
Provision for income taxes64,690 58,835 172,538 150,476 
Segment and consolidated net income$218,095 $193,578 $640,612 $538,042 
_________________
(1) Other segment items include stock-based compensation, restructuring expenses, other research and development expenses, including the allocation of general corporate costs to research and development services and development cost reimbursements in connection with certain of our collaboration arrangements, and other income (expenses), net.
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Provision For Income Taxes (Details)
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Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Income Tax Disclosure [Abstract]        
Effective income tax rate (as percent) 22.90% 23.30% 21.20% 21.90%
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Stockholders' Equity - Narrative (Details) - USD ($)
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Jun. 30, 2026
May 26, 2026
Feb. 28, 2026
Oct. 02, 2026
May 31, 2026
Oct. 31, 2025
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]              
Reduction in share reserve after stock option or stock appreciation award (in shares)         1    
Options outstanding (in shares) 1,100,000       1,100,000    
Options, unrecognized stock-based compensation $ 600,000       $ 600,000    
May 2026 Repurchase Program              
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]              
Stock repurchase program, authorized amount           $ 750,000,000.0  
Repurchases of common stock (in shares) 7,400,000            
Repurchases of common stock $ 402,100,000            
Stock repurchase program, remaining authorized repurchase amount $ 347,900,000       $ 347,900,000    
October 2025 Repurchase Program              
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]              
Stock repurchase program, authorized amount             $ 750,000,000.0
Repurchases of common stock (in shares)   17,200,000          
Repurchases of common stock   $ 750,000,000.0          
2026 TSR-based RSUs              
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]              
Number of awards granted (in shares)       700,000      
Maximum potential to vest       200.00%      
Weighted average grant date fair value, awarded (in dollars per share)         $ 55.31    
2026 TSR-based RSUs | Share-based Payment Arrangement, Tranche One              
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]              
Vesting award percentage       50.00%      
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Share-based Compensation Arrangement by Share-based Payment Award [Line Items]              
Award vesting period (in years)       1 year      
Restricted stock units              
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]              
Number of awards granted (in shares)         2,000,000.0    
Weighted average grant date fair value, awarded (in dollars per share)         $ 45.38    
Number of awards outstanding (in shares) 15,800,000       15,800,000    
Share-based payment arrangement, nonvested award, excluding option, cost not yet recognized, amount $ 307,300,000       $ 307,300,000    
Amended And Restated 2017 Equity Incentive Plan              
Share-based Compensation Arrangement by Share-based Payment Award [Line Items]              
Amendment and restatement increase (in shares)     2,000,000        
Number of shares available for grant (in shares) 17,000,000.0       17,000,000.0    
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Inventory
9 Months Ended
Oct. 02, 2026
Inventory Disclosure [Abstract]  
INVENTORY INVENTORY
Inventory consisted of the following (in thousands):
 
September 30, 2026December 31, 2025
Raw materials$798 $894 
Work in process45,803 53,531 
Finished goods17,917 5,942 
Total$64,518 $60,367 
Balance Sheet classification:
Current portion included in inventory$29,871 $21,686 
Non-current portion included in other non-current assets34,647 38,681 
Total
$64,518 $60,367 
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v3.26.3
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9 Months Ended
Oct. 02, 2026
product
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Products Derived From Other Compounds  
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v3.26.3
Revenues (Tables)
9 Months Ended
Oct. 02, 2026
Revenue from Contract with Customer [Abstract]  
Schedule of Disaggregation of Revenue
Revenues consisted of the following (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Product revenues:
Gross product revenues$853,716 $780,272 $2,461,852 $2,247,263 
Discounts and allowances(248,792)(237,342)(728,926)(671,036)
Net product revenues604,924 542,930 1,732,926 1,576,227 
Collaboration revenues:
License revenues58,408 56,236 175,166 148,017 
Collaboration services revenues(4,636)(1,411)(9,894)(2,781)
Collaboration revenues
53,772 54,825 165,272 145,236 
Total revenues$658,696 $597,755 $1,898,198 $1,721,463 
Net product revenues by product were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
CABOMETYX$603,154 $539,878 $1,726,575 $1,568,640 
COMETRIQ 1,770 3,052 6,351 7,587 
Net product revenues$604,924 $542,930 $1,732,926 $1,576,227 
Schedule of Concentration Risks
The percentage of total revenues by customer who individually accounted for 10% or more of our total revenues were as follows:
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Affiliates of Cencora, Inc.20%20%21%22%
Affiliates of McKesson Corporation20%20%20%19%
Affiliates of CVS Health Corporation16%15%15%15%
Affiliates of Optum Specialty Pharmacy11%*10%*
Accredo Health Group, Inc.*11%10%12%
Cardinal Health, Inc.10%***
___________________
(*) Represents less than 10% of our total revenues in the applicable period.
The percentage of trade receivables by customer who individually accounted for 10% or more of our trade receivables were as follows:
September 30, 2026December 31, 2025
Affiliates of McKesson Corporation25%25%
Affiliates of Cencora, Inc.24%23%
Ipsen Pharma SAS15%19%
Affiliates of CVS Health Corporation13%13%
Cardinal Health, Inc.12%12%
Schedule of Revenues Disaggregated by Geographic Region
Total revenues by geographic region were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
U.S.$609,099 $546,461 $1,746,006 $1,588,413 
Europe44,298 44,966 129,873 114,705 
Japan5,299 6,328 22,319 18,345 
Total revenues$658,696 $597,755 $1,898,198 $1,721,463 
Schedule of Activities and Ending Reserve Balances for Significant Categories of Discounts and Allowances
The activities and ending reserve balances for each significant category of discounts and allowances (which constitute variable consideration) were as follows (in thousands):
Chargebacks, Discounts for Prompt Payment and Other
Other Customer Credits/Fees and Co-pay Assistance
Rebates
Total
Balance at December 31, 2025
$34,223 $23,612 $36,284 $94,119 
Provision related to sales made in:
Current period492,111 55,155 192,295 739,561 
Prior periods(10,015)(402)(218)(10,635)
Payments and customer credits issued(485,149)(56,113)(179,846)(721,108)
Balance at September 30, 2026
$31,170 $22,252 $48,515 $101,937 
Schedule of Other Assets and Other Liabilities
Contract liabilities were as follows (in thousands):
September 30, 2026December 31, 2025
Contract liabilities:
Current portion(1)
$1,081 $1,115 
Non-current portion(2)
4,041 6,112 
Total contract liabilities$5,122 $7,227 
____________________
(1) Presented in other current liabilities in the accompanying Condensed Consolidated Balance Sheets.
(2) Presented in other non-current liabilities in the accompanying Condensed Consolidated Balance Sheets.
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v3.26.3
CONDENSED CONSOLIDATED BALANCE SHEETS (Parenthetical) - $ / shares
Oct. 02, 2026
Jan. 02, 2026
Preferred stock    
Par value (in dollars per share) $ 0.001 $ 0.001
Shares authorized (in shares) 10,000,000 10,000,000
Shares issued (in shares) 0 0
Common stock    
Par value (in dollars per share) $ 0.001 $ 0.001
Shares authorized (in shares) 400,000,000 400,000,000
Shares issued (in shares) 244,678,000 262,483,000
Shares outstanding (in shares) 244,678,000 262,483,000
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v3.26.3
Collaboration Agreements And Business Development Activities - Collaboration Revenues under the Collaboration Agreement with Ipsen (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
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Collaborative Arrangement with Ipsen        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
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License revenues        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
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License revenues | Collaborative Arrangement with Ipsen        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
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Collaboration services revenues        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Total revenues (4,636) (1,411) (9,894) (2,781)
Collaboration services revenues | Collaborative Arrangement with Ipsen        
Collaborative Arrangement and Arrangement Other than Collaborative [Line Items]        
Total revenues $ (4,773) (2,347) $ (13,269) (6,127)
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Oct. 02, 2026
Jan. 02, 2026
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9 Months Ended
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v3.26.3
Restructuring (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Restructuring and Related Activities [Abstract]        
Restructuring $ 0 $ 19,816 $ 0 $ 19,816
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v3.26.3
Fair Value Measurements (Tables)
9 Months Ended
Oct. 02, 2026
Fair Value Disclosures [Abstract]  
Schedule of Fair Value of Financial Assets Measured on a Recurring Basis
The classifications within the fair value hierarchy of our financial assets that were measured and recorded at fair value on a recurring basis were as follows (in thousands):
September 30, 2026
Level 1Level 2Total
Commercial paper$— $257,762 $257,762 
Corporate bonds— 785,501 785,501 
U.S. Treasury and government-sponsored enterprises— 163,579 163,579 
Municipal bonds— 6,793 6,793 
Total debt securities available-for-sale— 1,213,635 1,213,635 
Money market funds139,503 — 139,503 
Certificates of deposit46,639 46,639 
Total financial assets carried at fair value$139,503 $1,260,274 $1,399,777 
December 31, 2025
Level 1Level 2Total
Commercial paper$— $241,439 $241,439 
Corporate bonds— 886,500 886,500 
U.S. Treasury and government-sponsored enterprises— 155,139 155,139 
Municipal bonds— 8,764 8,764 
Total debt securities available-for-sale— 1,291,842 1,291,842 
Money market funds304,352 — 304,352 
Certificates of deposit— 66,388 66,388 
Total financial assets carried at fair value$304,352 $1,358,230 $1,662,582 
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v3.26.3
Collaboration Agreements And Business Development Activities (Tables)
9 Months Ended
Oct. 02, 2026
Organization, Consolidation and Presentation of Financial Statements [Abstract]  
Schedule of Collaborative Revenues Under Collaboration and License Agreement
Revenues under the collaboration agreement with Ipsen were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
License revenues$49,071 $47,313 $143,142 $120,832 
Collaboration services revenues(4,773)(2,347)(13,269)(6,127)
Total collaboration revenues$44,298 $44,966 $129,873 $114,705 
Revenues under the collaboration agreement with Takeda were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
License revenues$2,691 $3,299 $13,003 $9,891 
Collaboration services revenues136 936 3,375 3,346 
Total collaboration revenues$2,827 $4,235 $16,378 $13,237 
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Net Income Per Share (Tables)
9 Months Ended
Oct. 02, 2026
Earnings Per Share [Abstract]  
Schedule of Computation of Basic and Diluted Net Income Per Share
Net income per share — basic and diluted, were computed as follows (in thousands, except per share amounts):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Numerator:
Net income$218,095 $193,578 $640,612 $538,042 
Denominator:
Weighted-average common shares outstanding — basic246,756 268,421 251,964 273,269 
Dilutive securities8,998 10,114 8,953 10,432 
Weighted-average common shares outstanding — diluted255,754 278,535 260,917 283,701 
Net income per share — basic$0.88 $0.72 $2.54 $1.97 
Net income per share — diluted$0.85 $0.69 $2.46 $1.90 
Schedule of Potential Shares of Common Stock Not Included in the Computation of Diluted Net Income Per Share
The weighted-average potential common shares excluded from our calculation were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Anti-dilutive securities and contingently issuable shares excluded2,017 2,133 2,593 1,856 
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Stockholders’ Equity - Allocated Stock-Based Compensation (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Employee Service Share-based Compensation, Allocation of Recognized Period Costs [Line Items]        
Total stock-based compensation $ 28,718 $ 30,885 $ 90,331 $ 92,886
Income Statement Location [Axis]: us-gaap:ResearchAndDevelopmentExpense        
Employee Service Share-based Compensation, Allocation of Recognized Period Costs [Line Items]        
Total stock-based compensation 11,069 10,353 35,731 34,018
Income Statement Location [Axis]: us-gaap:SellingGeneralAndAdministrativeExpense        
Employee Service Share-based Compensation, Allocation of Recognized Period Costs [Line Items]        
Total stock-based compensation $ 17,649 $ 20,532 $ 54,600 $ 58,868
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v3.26.3
Revenues - Activities and Ending Reserve Balances for Significant Categories of Discounts and Allowances (Details)
$ in Thousands
9 Months Ended
Oct. 02, 2026
USD ($)
SEC Schedule, 12-09, Movement in Valuation Allowances and Reserves [Roll Forward]  
Balance at December 31, 2025 $ 94,119
Provision related to sales made in:  
Current period 739,561
Prior periods (10,635)
Payments and customer credits issued (721,108)
Balance at September 30, 2026 101,937
Chargebacks, Discounts for Prompt Payment and Other  
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Balance at December 31, 2025 34,223
Provision related to sales made in:  
Current period 492,111
Prior periods (10,015)
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Balance at September 30, 2026 31,170
Other Customer Credits/Fees and Co-pay Assistance  
SEC Schedule, 12-09, Movement in Valuation Allowances and Reserves [Roll Forward]  
Balance at December 31, 2025 23,612
Provision related to sales made in:  
Current period 55,155
Prior periods (402)
Payments and customer credits issued (56,113)
Balance at September 30, 2026 22,252
Rebates  
SEC Schedule, 12-09, Movement in Valuation Allowances and Reserves [Roll Forward]  
Balance at December 31, 2025 36,284
Provision related to sales made in:  
Current period 192,295
Prior periods (218)
Payments and customer credits issued (179,846)
Balance at September 30, 2026 $ 48,515
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v3.26.3
Revenues - Revenues by Disaggregated Category (Details) - USD ($)
$ in Thousands
3 Months Ended 9 Months Ended
Oct. 02, 2026
Oct. 03, 2025
Oct. 02, 2026
Oct. 03, 2025
Disaggregation of Revenue [Line Items]        
Total revenues $ 658,696 $ 597,755 $ 1,898,198 $ 1,721,463
Gross product revenues        
Disaggregation of Revenue [Line Items]        
Total revenues 853,716 780,272 2,461,852 2,247,263
Discounts and allowances        
Disaggregation of Revenue [Line Items]        
Total revenues (248,792) (237,342) (728,926) (671,036)
Net product revenues        
Disaggregation of Revenue [Line Items]        
Total revenues 604,924 542,930 1,732,926 1,576,227
License revenues        
Disaggregation of Revenue [Line Items]        
Total revenues 58,408 56,236 175,166 148,017
Collaboration services revenues        
Disaggregation of Revenue [Line Items]        
Total revenues (4,636) (1,411) (9,894) (2,781)
Collaboration revenues        
Disaggregation of Revenue [Line Items]        
Total revenues $ 53,772 $ 54,825 $ 165,272 $ 145,236
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v3.26.3
Revenues
9 Months Ended
Oct. 02, 2026
Revenue from Contract with Customer [Abstract]  
REVENUES REVENUES
Revenues consisted of the following (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Product revenues:
Gross product revenues$853,716 $780,272 $2,461,852 $2,247,263 
Discounts and allowances(248,792)(237,342)(728,926)(671,036)
Net product revenues604,924 542,930 1,732,926 1,576,227 
Collaboration revenues:
License revenues58,408 56,236 175,166 148,017 
Collaboration services revenues(4,636)(1,411)(9,894)(2,781)
Collaboration revenues
53,772 54,825 165,272 145,236 
Total revenues$658,696 $597,755 $1,898,198 $1,721,463 
The percentage of total revenues by customer who individually accounted for 10% or more of our total revenues were as follows:
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
Affiliates of Cencora, Inc.20%20%21%22%
Affiliates of McKesson Corporation20%20%20%19%
Affiliates of CVS Health Corporation16%15%15%15%
Affiliates of Optum Specialty Pharmacy11%*10%*
Accredo Health Group, Inc.*11%10%12%
Cardinal Health, Inc.10%***
___________________
(*) Represents less than 10% of our total revenues in the applicable period.
The percentage of trade receivables by customer who individually accounted for 10% or more of our trade receivables were as follows:
September 30, 2026December 31, 2025
Affiliates of McKesson Corporation25%25%
Affiliates of Cencora, Inc.24%23%
Ipsen Pharma SAS15%19%
Affiliates of CVS Health Corporation13%13%
Cardinal Health, Inc.12%12%
Total revenues by geographic region were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
U.S.$609,099 $546,461 $1,746,006 $1,588,413 
Europe44,298 44,966 129,873 114,705 
Japan5,299 6,328 22,319 18,345 
Total revenues$658,696 $597,755 $1,898,198 $1,721,463 
Total revenues include net product revenues attributed to geographic regions based on the ship-to location and license and collaboration services revenues attributed to geographic regions based on the location of our collaboration partners’ headquarters.
Net product revenues and license revenues are recorded in accordance with ASC Topic 606, Revenue from Contracts with Customers (Topic 606). License revenues include the recognition of the portion of milestone payments allocated to the transfer of intellectual property licenses for which it had become probable in the current period that the milestone would be achieved and a significant reversal of revenues would not occur, as well as royalty revenues and our share of profits under our collaboration agreement with Genentech. Collaboration services revenues are recorded in accordance with ASC Topic 808, Collaborative Arrangements. Collaboration services revenues include the recognition of deferred revenues for the portion of upfront and milestone payments allocated to our research and development services performance obligations, development cost reimbursements earned under our collaboration agreements, product supply revenues, net of product supply costs and the royalties we paid on sales of products containing cabozantinib by our collaboration partners. License revenues and collaboration services revenues are presented in collaboration revenues in the accompanying Condensed Consolidated Statements of Income.
Net product revenues by product were as follows (in thousands):
Three Months Ended September 30,Nine Months Ended September 30,
2026202520262025
CABOMETYX$603,154 $539,878 $1,726,575 $1,568,640 
COMETRIQ 1,770 3,052 6,351 7,587 
Net product revenues$604,924 $542,930 $1,732,926 $1,576,227 
Product Sales Discounts and Allowances
The activities and ending reserve balances for each significant category of discounts and allowances (which constitute variable consideration) were as follows (in thousands):
Chargebacks, Discounts for Prompt Payment and Other
Other Customer Credits/Fees and Co-pay Assistance
Rebates
Total
Balance at December 31, 2025
$34,223 $23,612 $36,284 $94,119 
Provision related to sales made in:
Current period492,111 55,155 192,295 739,561 
Prior periods(10,015)(402)(218)(10,635)
Payments and customer credits issued(485,149)(56,113)(179,846)(721,108)
Balance at September 30, 2026
$31,170 $22,252 $48,515 $101,937 
The allowance for chargebacks, discounts for prompt payment and other are recorded as a reduction of trade receivables, net, and the remaining reserves are recorded as rebates and fees due to customers in the accompanying Condensed Consolidated Balance Sheets.
Contract Assets and Liabilities
We receive payments from our collaboration partners based on billing schedules established in each contract. Amounts are recorded as accounts receivable when our right to consideration is unconditional. We may also recognize revenue in advance of the contractual billing schedule and such amounts are recorded as a contract asset when recognized. We may be required to defer recognition of revenue for upfront and milestone payments until we perform our obligations under these arrangements, and such amounts are recorded as deferred revenue upon receipt or when due. For those contracts that have multiple performance obligations, contract assets and liabilities are reported on a net basis at the contract level. There were no contract assets as of September 30, 2026 and December 31, 2025. Contract liabilities are primarily related to deferred revenues from Ipsen Pharma SAS (Ipsen) and Takeda Pharmaceutical Company Limited (Takeda).
Contract liabilities were as follows (in thousands):
September 30, 2026December 31, 2025
Contract liabilities:
Current portion(1)
$1,081 $1,115 
Non-current portion(2)
4,041 6,112 
Total contract liabilities$5,122 $7,227 
____________________
(1) Presented in other current liabilities in the accompanying Condensed Consolidated Balance Sheets.
(2) Presented in other non-current liabilities in the accompanying Condensed Consolidated Balance Sheets.
During each of the three and nine months ended September 30, 2026, and 2025, we recognized $1.0 million and $3.1 million, respectively, of revenues that were included in the deferred revenues balance at the beginning of the respective periods.
During the three and nine months ended September 30, 2026, we recognized $58.0 million and $177.9 million, respectively, in revenues for performance obligations satisfied in previous periods, as compared to $57.6 million and $151.3 million, respectively, for the corresponding prior year periods. During the three and nine months ended September 30, 2026, such revenues were primarily related to royalty payments allocated to our license performance obligations for our collaborations with Ipsen and Takeda and the recognition of revenues for the achievement of milestones, including a commercial milestone achieved during the first quarter of 2026. During the three and nine months ended September 30, 2025, such revenues were primarily related to royalty payments allocated to our license performance obligations for our collaborations with Ipsen and Takeda and the recognition of revenues for the achievement of milestones, including a regulatory milestone achieved during the third quarter of 2025.
As of September 30, 2026, $16.0 million of the combined transaction prices for our Ipsen and Takeda collaborations were allocated to research and development services performance obligations that had not yet been satisfied. See “Note 4. Collaboration Agreements and Business Development Activities” of the “Notes to Consolidated Financial Statements” included in Part II, Item 8 of our Fiscal 2025 Form 10-K for additional information about the expected timing to satisfy these performance obligations.
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