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Pregnancy Nursing Mothers: Pediatric Use: ADVERSE REACTIONS These statements have not been evaluated by the Food and Drug Administration (FDA)

Results from the phase 2 TROPION-Lung05 trial published in the Journal of Clinical Oncology revealed that among 137 patients given 6 mg/kg of dato-DXd every 21 days for pretreated NSCLC, the confirmed ORR was 35.8% (95% CI, 27.8%-44.4%), including 32.8% of patients experiencing a partial response and 2.9% having a complete response

Efficacy and safety of long-acting glucagon-like peptide-1 receptor agonists compared with exenatide twice daily and sitagliptin in type 2 diabetes mellitus: a systematic review and meta-analysis

Regular supplementation may preserve focus, memory, and clarity as part of a proactive brain health or longevity care plan

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93% reduction in shedding in clinical trial