University of California San Francisco
UC San Francisco study data was instrumental in today’s approval by the Food and Drug Administration (FDA) of a PET imaging agent that helps physicians evaluate gliomas, a form of brain cancer.
The approval of floretyrosine F 18 (18F-FET) was supported by prospective clinical trial data generated at UCSF through a multi-year study. The agent addresses a persistent challenge in caring for people with gliomas: determining whether changes seen on conventional imaging represent tumor growth or changes caused by treatment.
A UCSF-developed program that integrates behavioral health support for children and caregivers into routine pediatric care is poised to extend across California with a $17 million investment from the California Department of Health Care Services (DHCS).