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minimal residual disease
Biotech
FDA outlines draft policy on MRD for accelerated approval
The guidance provides recommendations for designing clinical trials that use MRD or CR as endpoints for accelerated approval in multiple myeloma.
Angus Liu
Jan 21, 2026 2:55pm
Natera buys Foresight Diagnostics in $450M cancer testing deal
Dec 5, 2025 11:57am
Roche sues Stanford, Foresight Diagnostics over trade secrets
Jul 3, 2024 10:44am
JPM24: Veracyte inks $95M deal to buy C2i Genomics
Jan 9, 2024 10:22am
ASCO: Inside C2i Genomics' precision oncology 'one-stop shop'
Jun 3, 2023 10:34pm
Quest pens $450M deal for cancer test maker Haystack Oncology
Apr 27, 2023 9:25am
