Agilent has received FDA approval for PD-L1 IHC 22C3 pharmDx, Code SK006, as a companion diagnostic to identify patients with esophageal or gastroesophageal junction carcinoma eligible for ...
A Nature study identifies a previously unknown protein modification, O-2-hydroxyglutarylation, driven by the oncometabolite ...
BioNTech SE will present the latest clinical updates from its late-stage lung cancer portfolio at ELCC 2026, highlighting ...
Mayo Clinic has launched the first U.S. clinical research program using magnetic nanoparticle-mediated hyperthermia for ...
The FDA has approved nivolumab (Opdivo) plus AVD as first-line treatment for advanced classical Hodgkin lymphoma in patients ...
Phase 3 WU-KONG28 trial met its primary endpoint, showing that once-daily oral sunvozertinib significantly improved ...
TG Therapeutics secured $500 million in non-dilutive capital through a new credit facility, supporting the expansion of ...
Phase 3 TALAPRO-3 results show that talazoparib plus enzalutamide significantly improves radiographic progression-free ...
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