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Day One Reports Fourth Quarter and Full Year 2024 Financial Results and Corporate Progress
DAWNDay One Biopharmaceuticals pany(DAWN) GlobeNewswire·2025-02-25 21:05

Core Insights - Day One Biopharmaceuticals reported Q4 2024 net product revenues of 29.0millionandfullyearrevenuesof29.0 million and full year revenues of 57.2 million for OJEMDA (tovorafenib) [1][5] - The company ended 2024 with a strong cash position of 531.7million[1][7]TheCEOhighlightedtheapprovalofOJEMDAasasignificantgrowthcatalystandexpressedconfidenceinthecompanyslongtermgrowthtrajectory[2]FinancialHighlightsOJEMDAnetproductrevenuesincreasedby44531.7 million [1][7] - The CEO highlighted the approval of OJEMDA as a significant growth catalyst and expressed confidence in the company's long-term growth trajectory [2] Financial Highlights - OJEMDA net product revenues increased by 44% from Q3 to Q4 2024 [5] - The company wrote over 1,600 OJEMDA prescriptions within eight months of its launch in April 2024 [5] - License revenue from the sale of ex-U.S. commercial rights for tovorafenib was 0.2 million for Q4 and 73.9millionforthefullyear[6]Researchanddevelopmentexpensesroseto73.9 million for the full year [6] - Research and development expenses rose to 61.8 million for Q4 and 227.7millionforthefullyear,comparedto227.7 million for the full year, compared to 37.3 million and 130.5millionin2023[6]Selling,generalandadministrativeexpenseswere130.5 million in 2023 [6] - Selling, general and administrative expenses were 29.8 million for Q4 and 115.5millionforthefullyear,upfrom115.5 million for the full year, up from 22.2 million and 75.6millionin2023[6]ThenetlossforQ4was75.6 million in 2023 [6] - The net loss for Q4 was 65.7 million and 95.5millionforthefullyear,withnoncashstockbasedcompensationexpensesof95.5 million for the full year, with non-cash stock-based compensation expenses of 11.0 million and $48.3 million respectively [6][7] Corporate Developments - OJEMDA received the Exclusively Pediatric designation, reducing its Medicaid and 340B minimum rebate percentage from 23.1% to 17.1% [5] - The DAY301 program, a PTK7-targeted ADC, successfully cleared the first dose cohort in its Phase 1a clinical trial [5] - Enrollment in the pivotal Phase 3 FIREFLY-2 clinical trial is advancing, with full enrollment expected in the first half of 2026 [5]