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    Wolfe Research initiated coverage on Exelixis

    11/18/25 8:22:21 AM ET
    $EXEL
    Biotechnology: Biological Products (No Diagnostic Substances)
    Health Care
    Get the next $EXEL alert in real time by email
    Wolfe Research initiated coverage of Exelixis with a rating of Peer Perform
    Get the next $EXEL alert in real time by email

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    Recent Analyst Ratings for
    $EXEL

    DatePrice TargetRatingAnalyst
    1/8/2026$48.00Overweight → Equal-Weight
    Morgan Stanley
    1/5/2026$41.00Neutral → Underperform
    BofA Securities
    11/18/2025Peer Perform
    Wolfe Research
    11/3/2025Buy → Neutral
    Guggenheim
    10/21/2025$48.00Market Perform → Outperform
    Leerink Partners
    9/19/2025$40.00Equal Weight
    Barclays
    9/17/2025$40.00Equal Weight
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    9/17/2025$47.00Buy
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    Exelixis Announces Results from Subgroup Analysis of Phase 3 CABINET Pivotal Trial Evaluating CABOMETYX® (cabozantinib) in Non-Functional and Functional Neuroendocrine Tumors at ASCO 2026

    – CABOMETYX significantly reduced the risk of disease progression or death by 74% and 60% in patients with non-functional and functional advanced NET, respectively, versus placebo – Exelixis, Inc. (NASDAQ:EXEL) today announced results from a subgroup analysis of the phase 3 CABINET pivotal trial, which showed that CABOMETYX® (cabozantinib) provided significant improvements in progression-free survival (PFS) versus placebo in patients with previously treated advanced neuroendocrine tumors (NET) regardless of functional status. These data will be presented at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting to be held from May 29 – June 2 in Chicago. "Understanding the

    5/30/26 10:00:00 AM ET
    $EXEL
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    Exelixis to Webcast Fireside Chats as Part of Upcoming Investor Conferences in June

    - Presentations to be webcast on www.exelixis.com - Exelixis, Inc. (NASDAQ:EXEL) today announced that company management will participate in fireside chats at the following investor conferences in June: 2026 Jefferies Global Healthcare Conference: Exelixis is scheduled to present at 11:05 a.m. ET / 8:05 a.m. PT on Wednesday, June 3 in New York City. Goldman Sachs 47th Annual Global Healthcare Conference: Exelixis is scheduled to present at 10:40 a.m. ET / 7:40 a.m. PT on Tuesday, June 9 in Miami. To access the webcast links, log onto www.exelixis.com and proceed to the Event Calendar page under the Investors & News heading. Replays will also be available at the same location for

    5/27/26 4:05:00 PM ET
    $EXEL
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    Exelixis Announces Presentations at ASCO 2026 Highlighting Ongoing Studies in Diverse Tumor Types

    – Findings in neuroendocrine tumors, kidney cancer, advanced colorectal cancer and other tumors to be presented – Exelixis, Inc. (NASDAQ:EXEL) today announced presentations for its flagship product, CABOMETYX® (cabozantinib), and its investigational oral kinase inhibitor, zanzalintinib, at the 2026 American Society of Clinical Oncology (ASCO) Annual Meeting to be held from May 29 – June 2 in Chicago. "The presentations at ASCO this year highlight the continued progress of our strategy to build upon the well-established therapeutic profile of CABOMETYX and accelerate the development of zanzalintinib, our next oncology franchise molecule," said Dana T. Aftab, Ph.D., Executive Vice Preside

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    Director Johnson David Edward bought $1,187,235 worth of shares (27,532 units at $43.12) (SEC Form 4)

    4 - EXELIXIS, INC. (0000939767) (Issuer)

    11/26/25 4:05:28 PM ET
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    Johnson David Edward bought $8,733,955 worth of shares (425,000 units at $20.55) (SEC Form 4)

    4 - EXELIXIS, INC. (0000939767) (Issuer)

    5/30/24 7:50:14 PM ET
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    Johnson David Edward bought $3,932,734 worth of shares (190,000 units at $20.70) (SEC Form 4)

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    FDA Approval for CABOMETYX issued to EXELIXIS INC

    Submission status for EXELIXIS INC's drug CABOMETYX (SUPPL-16) with active ingredient CABOZANTINIB S-MALATE has changed to 'Approval' on 09/20/2023. Application Category: NDA, Application Number: 208692, Application Classification: Labeling

    9/21/23 4:37:02 AM ET
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    FDA Approval for CABOMETYX issued to EXELIXIS INC

    Submission status for EXELIXIS INC's drug CABOMETYX (SUPPL-14) with active ingredient CABOZANTINIB S-MALATE has changed to 'Approval' on 07/14/2022. Application Category: NDA, Application Number: 208692, Application Classification: Efficacy

    7/15/22 4:38:40 AM ET
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    FDA Approval for CABOMETYX issued to EXELIXIS INC

    Submission status for EXELIXIS INC's drug CABOMETYX (SUPPL-12) with active ingredient CABOZANTINIB S-MALATE has changed to 'Approval' on 09/17/2021. Application Category: NDA, Application Number: 208692, Application Classification: Efficacy

    9/20/21 3:53:29 PM ET
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    Director Wyszomierski Jack L sold $198,409 worth of shares (3,925 units at $50.55) as part of a pre-agreed trading plan, decreasing direct ownership by 1% to 284,384 units (SEC Form 4)

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    6/3/26 6:52:04 PM ET
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    Director Eckhardt Sue Gail sold $491,974 worth of shares (9,812 units at $50.14) as part of a pre-agreed trading plan, decreasing direct ownership by 38% to 16,079 units (SEC Form 4)

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    6/3/26 6:51:58 PM ET
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    Director Papadopoulos Stelios was granted 8,367 shares, increasing direct ownership by 0.70% to 1,197,595 units (SEC Form 4)

    4 - EXELIXIS, INC. (0000939767) (Issuer)

    5/29/26 5:43:52 PM ET
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    Exelixis downgraded by Morgan Stanley with a new price target

    Morgan Stanley downgraded Exelixis from Overweight to Equal-Weight and set a new price target of $48.00

    1/8/26 8:39:35 AM ET
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    Exelixis downgraded by BofA Securities with a new price target

    BofA Securities downgraded Exelixis from Neutral to Underperform and set a new price target of $41.00

    1/5/26 8:47:51 AM ET
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    Wolfe Research initiated coverage on Exelixis

    Wolfe Research initiated coverage of Exelixis with a rating of Peer Perform

    11/18/25 8:22:21 AM ET
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    Exelixis Inc. filed SEC Form 8-K: Leadership Update, Submission of Matters to a Vote of Security Holders, Financial Statements and Exhibits

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    SEC Form 10-Q filed by Exelixis Inc.

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    Exelixis Inc. filed SEC Form 8-K: Results of Operations and Financial Condition, Other Events, Financial Statements and Exhibits

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    10/21/25 8:05:00 AM ET
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    Exelixis Announces Appointment of Dana T. Aftab, Ph.D. as Executive Vice President, Research and Development

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    8/29/25 5:47:00 PM ET
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    SEC Form SC 13D/A filed by Exelixis Inc. (Amendment)

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    SEC Form SC 13G filed by Exelixis Inc.

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    2/13/24 9:19:48 AM ET
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    SEC Form SC 13D/A filed by Exelixis Inc. (Amendment)

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    Exelixis Announces First Quarter 2026 Financial Results and Provides Corporate Update

    - Total Revenues of $610.8 million, Cabozantinib Franchise U.S. Net Product Revenues of $555.0 million - - GAAP Diluted EPS of $0.79, Non-GAAP Diluted EPS of $0.87 - - Announced Additional Stock Repurchase Program for up to $750 million by the End of 2027 - - Conference Call and Webcast Today at 5:00 PM ET - Exelixis, Inc. (NASDAQ:EXEL) today reported financial results for the first quarter of 2026, provided an update on progress toward achieving key corporate objectives, and outlined its commercial, clinical and pipeline development milestones. "Exelixis made significant progress in the first quarter of 2026 as we remain focused on our goal of building next-generation oncology fr

    5/5/26 4:05:00 PM ET
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    Exelixis to Release First Quarter 2026 Financial Results on Tuesday, May 5, 2026

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    Exelixis Announces Fourth Quarter and Fiscal Year 2025 Financial Results and Provides Corporate Update

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    2/10/26 4:05:00 PM ET
    $EXEL
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