Press Releases Day One Biopharmaceuticals, Inc.

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US23954D1090

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07/05	HC Wainwright Adjusts Price Target on Day One Biopharmaceuticals to $40 From $50, Maintains Buy Rating	MT
06/05	Day One Biopharmaceuticals, Inc. Reports Earnings Results for the First Quarter Ended March 31, 2024	CI

Press Releases

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Day One Reports First Quarter 2024 Financial Results and Corporate Progress	07/05	GL
Day One Biopharmaceuticals : Corporate Presentation - April 2024	24/04	PU
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	24/04	GL
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	24/04	AQ
Day One Reports Fourth Quarter and Full Year 2023 Financial Results and Corporate Progress	27/02	GL
Day One Announces Two New Appointments to Board of Directors	17/01	GL
Day One to Present at the 42nd Annual J.P. Morgan Healthcare Conference	19/12	GL
Day One Announces Tovorafenib FIREFLY-1 Data Published in Nature Medicine	17/11	GL
Day One Announces Tovorafenib FIREFLY-1 Data Published in Nature Medicine	17/11	AQ
Day One Biopharmaceuticals : Change in Certifying Accountants - Form 8-K	16/11	PU
Day One to Participate in the Piper Sandler 35th Annual Healthcare Conference	14/11	GL
Day One Reports Third Quarter 2023 Financial Results and Corporate Progress	07/11	GL
Day One Reports Third Quarter 2023 Financial Results and Corporate Progress	07/11	AQ
Day One Biopharmaceuticals : Corporate Presentation - October 2023	30/23/30	PU
Day One Announces FDA Acceptance of NDA and Priority Review for Tovorafenib in Relapsed or Progressive Pediatric Low-Grade Glioma (pLGG)	30/23/30	GL
Day One Announces FDA Acceptance of NDA and Priority Review for Tovorafenib in Relapsed or Progressive Pediatric Low-Grade Glioma (pLGG)	30/23/30	AQ
Day One Announces Updated FIREFLY-1 Data for Tovorafenib and Completion of Rolling NDA Submission to FDA for Relapsed or Progressive Pediatric Low-Grade Glioma (pLGG)	11/23/11	GL
Day One Announces VRK1 License Agreement and Research Collaboration with Sprint Bioscience	16/23/16	GL
Sprint Bioscience licenses the VADA (VRK1) program to Day One Biopharmaceuticals	16/23/16	AQ
Day One Announces VRK1 License Agreement and Research Collaboration with Sprint Bioscience	16/23/16	AQ

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Press Releases Day One Biopharmaceuticals, Inc.

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