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survival rates
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
AstraZeneca, Daiichi unpack Dato-DXd's overall survival fail
Sep 10, 2024 6:00am
Differences in survival spark FDA hold on Oncopeptides' drug
Jul 8, 2021 8:05am
Takeda takes on multiple myeloma outcomes study, as Ninlaro flounders
Aug 31, 2016 8:00am
