
Gabriela Hobbs, MD, explains the importance of risk assessment and using disease factors to drive management approaches in myelofibrosis.
Experts across tumor types share their insights on the notable FDA regulatory decisions of 2025.
In 2025, more than 60 agents and combinations, including biosimilars, earned accelerated, regular, or expanded approvals from the FDA, reshaping the treatment paradigms of multiple disease states and offering additional options for patients.






