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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

$EXELPress releaseMay 30, 2026, 10:00 AM ETRead the release

Exelixis presented positive subgroup data from the Phase 3 CABINET trial, showing cabozantinib significantly improved progression-free survival in both functional and non-functional neuroendocrine tumors. In non-functional NET, the hazard ratio was 0.26 (74% risk reduction) with a median PFS of 9.4 months versus 3.1 months for placebo. In functional NET, the hazard ratio was 0.40 (60% risk reduction) with a median PFS of 12.7 months versus 5.4 months for placebo.

Key figures

Drug Name
CABOMETYX (cabozantinib)
Phase Of Trial
Phase 3
Pfs functional hr
0.4
Pfs non functional hr
0.26
Total patients enrolled
298
Risk reduction functional
60%
Pfs functional median months
12.7
Pfs functional placebo months
5.4
Risk reduction non functional
74%
Pfs non functional median months
9.4
Pfs non functional placebo months
3.1

AI analysis

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    EXEL: 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 — AI Analysis | Signal8