RE:RE:RE:RE:RE:RE:RE:New Press Release - Oncolytics Biotech® Announces Productive FDA Type C Meeting on its Metastatic Breast Cancer ProgramThat said ... PFS is considered by the FDA to be a "validated" surrogate endpoint that can also lead times an Accelerated Approval.
CelTil is a novel biomarker/surrogate endpoint that applies breast, pancreatic, CRC and anal caner which can lead to Accelerated Approval particularly involving pelareorep in combination with ICIs, such as Tecentriq.