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Discover all trending biotech companies
Discover all trending biotech companies
Company Research Platform
Annual Revenue
$ 161,900,000
Global Employees
181
This segment focuses on the research, development, and commercialization of targeted therapies for pediatric cancers, with a primary focus on low-grade gliomas. Research and development activities include clinical trials for DAY101, a brain-penetrant type II pan-RAF kinase inhibitor, and the development of Pimasertib, an inhibitor of mitogen-activated protein kinase kinases 1 and 2. Technologies employed include small molecule drug development and clinical trial management. The segment aims to improve outcomes for children with life-threatening cancers by providing innovative treatment options. Day One Biopharmaceuticals is positioning itself as a leader in pediatric oncology, addressing a significant unmet medical need. Future opportunities include expanding the pipeline with additional pediatric cancer therapies and securing regulatory approvals for DAY101. Partnerships with leading clinical oncologists and research institutions are crucial for advancing clinical trials and expanding market access.
This segment encompasses the development and commercialization of targeted therapies for genetically defined cancers in both pediatric and adult populations. The core focus is on precision medicine, utilizing advanced technologies to identify and develop drugs that specifically target cancer cells. Research and development efforts include preclinical studies, clinical trials, and the evaluation of biomarkers to identify patients most likely to benefit from treatment. The segment leverages small molecule drug discovery and development platforms. The goal is to improve patient outcomes by providing more effective and less toxic cancer treatments. Day One Biopharmaceuticals aims to establish a strong market position by focusing on innovative therapies with the potential to address unmet medical needs. Future growth will be driven by expanding the pipeline, securing regulatory approvals, and establishing strategic partnerships. Regulatory and clinical aspects are critical, with a focus on obtaining FDA approval for lead product candidates. Collaborations with pharmaceutical companies and research institutions are essential for advancing drug development and commercialization.