Company intelligence / Profile preview
Day One Biopharmaceuticals
- Ownership
- Public · DAWN
- Development stage
- Commercial
Overview
Day One Biopharmaceuticals received FDA approval for OJEMDA™ (tovorafenib) in April 2024 for the treatment of patients 6 months of age and older with relapsed or refractory pediatric low-grade glioma (pLGG) harboring a BRAF fusion or rearrangement, or BRAF V600 mutation. The company reported preliminary 2024 OJEMDA™ net product revenue in January 2025 and is advancing multiple clinical programs.
- Therapeutic areas
- Oncology
- Modalities
- Small moleculesAntibody-drug conjugates (ADCs)
- Industry
- Biotech
Drug pipeline
6 assets5 more assets in the full pipeline.
Partnerships
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