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News articleYahoo Finance· May 21, 2026

Exelixis Announces Presentations at ASCO 2026 Highlighting Ongoing Studies in Diverse Tumor Types

View original at finance.yahoo.com
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 – ALAMEDA, Calif., May 21, 2026--(BUSINESS WIRE)--Exelixis, Inc…
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  • The collective ASCO 2026 data sets demonstrate Exelixis's dedication to improving standards of care for patients with cancer

    60% confidence
  • Findings from the phase 3 STELLAR-303 pivotal trial evaluating zanzalintinib in metastatic colorectal cancer will be presented at ASCO 2026

    60% confidence
  • New analyses from the phase 3 CABINET pivotal trial further reinforce the foundational role of CABOMETYX in patient care

    60% confidence
  • In 2016, Exelixis granted Ipsen Pharma SAS exclusive rights for the commercialization and further clinical development of cabozantinib outside of the U.S. and Japan

    60% confidence
  • In 2017, Exelixis granted Takeda Pharmaceutical Company Limited exclusive rights for cabozantinib commercialization and development for all future indications in Japan

    60% confidence
  • CABOMETYX tablets have received regulatory approvals in over 65 countries outside the U.S. and Japan, including the EU

    60% confidence
  • The ASCO 2026 presentations highlight continued progress of Exelixis's strategy to build upon the well-established therapeutic profile of CABOMETYX and accelerate the development of zanzalintinib as the next oncology franchise molecule

    60% confidence
  • Exelixis holds the exclusive rights to develop and commercialize cabozantinib in the U.S.

    60% confidence

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Q4 2026 Clinical Catalyst Season: Big-Pharma Data Flow, Regulatory Milestones, and a Thin AI-Drug Fringe
October 2026 conferences (EASD, IGCS, NACFC, HFSA) are producing a dense run of late-stage readouts from Novo Nordisk, Lilly, Roche, Bayer, Vertex and Galderma. Regulatory milestones are scheduled behind them: the ivonescimab BLA PDUFA date on 2026-11-14, FDA acceptance of Roche's vamikibart BLA, and Scholar Rock's EMA resubmission. The AI-and-finance angle is peripheral. It consists of the AI-designed drug Rentosertib and QAIAx, a speculative microcap whose trial claims (the QIII pilot, anticipated 2027-01-01, and a patent update) are forecasts and filings rather than data, so they warrant skepticism.
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EPKINLY Regulatory-Clinical Success Cascade
High probability of expanded label indications, additional combination approvals, and competitive positioning strength in follicular lymphoma market. Predicts positive commercial uptake and potential accelerated review for related indications.
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ING Group
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