EXEL stock fell 12.17% following STELLAR-303 Phase 3 trial results. The trial showed a 20% reduction in death risk with zanzalintinib. Median overall survival was 10.9 months versus 9.4 months for regorafenib. Superiority in progression-free survival (PFS) remains inconclusive currently. Investors may be reacting negatively to the lack of definitive results.
Exelixis announced positive STELLAR-303 trial results for zanzalintinib. Zanzalintinib increased overall survival compared to regorafenib in metastatic CRC. Analysts project U.S. peak sales of $875 million for zanzalintinib. Cabometyx regulatory approval in Europe anticipated in 2025. EXEL stock rose 11.1% to $44.85 following the announcement.
EXEL reported Q1 2025 earnings of 62 cents, surpassing expectations. Quarterly sales reached $555.45 million, beating the consensus of $498.18 million. Cabometyx's demand has surged following FDA approval in neuroendocrine tumors. 2025 revenue guidance raised by $100 million to between $2.25B-$2.35B. EXEL advances into phase 1 study for XB628 in solid tumors.
- EXEL reported lower-than-expected Q1 results, with earnings and revenues missing estimates. - Net product revenues increased, but Cabometyx sales fell short of expectations. - Company undertook a corporate restructuring program by reducing headcount by 13%. - Management focuses on label expansion for Cabometyx and accelerating the development of other drugs. Price Impact Rating: Bearish Impact Horizon Rating: Short-term Type: Earnings