RE:RE:RE:RE:How does Accelerated Approval work The FDA request for an Accelerated Approval is usually made with the filing of the Phase 3 design (which is then considered as the confirmatory study design) and the enrollment of the first number of trial patients. I would think that ONCY's partner or acquirer would want to be responsible for administering these final registration steps to ensure pelareorep's approval, and to ensure that pelareorep's cancer therapeutic applications can be efficiently expanded through its proposed combination with multiple other I/O agents, CAR-T, ADCs, and small molecule drugs, such as CDK4/6 and PARP inhibitors.