Day One Biopharmaceuticals reported its first quarter 2024 financial results, including a net loss of $62.4 million and cash, cash equivalents, and short-term investments totaling $317.9 million.
OJEMDA is now approved and available in the U.S., with first prescriptions received.
Patients have begun enrolling in EveryDay Support From Day One program.
The Phase 3 FIREFLY-2/LOGGIC clinical trial continues to enroll at over 90 sites.
The Company received a rare pediatric disease priority review voucher from the FDA upon OJEMDA’s approval.
Results from the FIRELIGHT-1 Phase 1b and next steps are expected in the second half of 2024.
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