FDA
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Day One Announces New OJEMDA™ (tovorafenib) Data to be Presented in Oral Session at the 2025 Society for Neuro-Oncology (SNO) Annual Meeting
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Day One Reports Fourth Quarter and Full Year 2024 Financial Results and Corporate Progress
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Day One (DAWN) Sells Priority Review Voucher for $108M
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Day One’s OJEMDA™ (tovorafenib) Receives US FDA Accelerated Approval for Relapsed or Refractory BRAF-altered Pediatric Low-Grade Glioma (pLGG), the Most Common Form of Childhood Brain Tumor
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Day One Biopharmaceuticals (DAWN) Announces Updated FIREFLY-1 Data for Tovorafenib
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Day One Announces Tovorafenib (DAY101) Data and Additional Abstracts to be Presented at the 2023 American Society of Clinical Oncology (ASCO) Annual Meeting
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Day One Reports Fourth Quarter and Full Year 2022 Financial Results and Corporate Progress
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