Website that reads as follows but I can't make out who is who on the screenshot I have provided, can someone please tell me which one is which.
The United States Food and Drug Administration (FDA) has accepted for priority review Mesoblast’s Biologics License Application (BLA) to seek approval of RYONCIL for acute GVHD in children. The FDA has set a Prescription Drug User Fee Act (PDUFA) action date of September 30, 2020. If approved, Mesoblast will make RYONCIL immediately available in the United States.On the website it reads as follows...
A little clarification please
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