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survival time
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
Long survival spurs Ultimovacs to mull ways to end cancer trial
Aug 22, 2023 10:00am
Celgene's phase 3 AML test chalks up a win
Sep 13, 2019 8:08am