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clinical trial design
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
Bayer boosts precision oncology efforts with multiyear AI deal
Apr 23, 2025 12:55pm
Clario acquires WCG's neuro-focused eCOA business
Mar 12, 2025 3:40pm
Fewer than 1% of trials include pregnant patients, study finds
Jan 29, 2025 2:06pm
FDA issues draft guidance on clinical trial tissue biopsies
Jan 6, 2025 2:55pm
Sanofi will deploy new AI tool in late-stage MS trials
Nov 13, 2024 7:40am
