FDA Approval and Launch of OJEMDA
OJEMDA was approved by the FDA for relapsed/refractory pediatric low-grade glioma, marking a significant achievement for Day One Biopharmaceuticals and offering a new treatment option for patients.
Strong Revenue Growth
OJEMDA generated over $57 million in net product revenues in 2024, with fourth-quarter revenues reaching $29 million, representing a 44% growth compared to Q3.
Ex-U.S. Partnership with Ipsen
Day One established an exclusive licensing arrangement with Ipsen for ex-U.S. rights to OJEMDA, potentially expanding access to international markets.
Advancement of Clinical Trials
The FIREFLY-2 trial for tovorafenib is now open at over 110 sites globally, with full enrollment expected by the first half of 2026. The DAY301 program has also cleared the first dose cohort in its trial.
Strong Financial Position
Day One ended 2024 with over $500 million in cash, enabling continued investment in pipeline advancement without requiring external financing.