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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
slow economic growth

Long survival spurs Ultimovacs to mull ways to end cancer trial

Aug 22, 2023 10:00am
celgene

Celgene's phase 3 AML test chalks up a win

Sep 13, 2019 8:08am

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