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Clinical Trial EndPoint

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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
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Athersys stock plunges 60% after stroke stem cell therapy miss

May 20, 2022 10:26am
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Icon to validate PROs as measurement of FDA clinical endpoints

Feb 22, 2017 10:45am

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