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Clinical Trial EndPoint
CRO
FDA draft recommends all cancer trials collect OS data
Even when OS is not used as the primary endpoint, the FDA still advises that trial sponsors collect and submit survival data to the regulator.
Darren Incorvaia
Aug 20, 2025 10:59am
Athersys stock plunges 60% after stroke stem cell therapy miss
May 20, 2022 10:26am
Icon to validate PROs as measurement of FDA clinical endpoints
Feb 22, 2017 10:45am