Recent advancements in diabetes management have highlighted the efficacy of semaglutide, particularly in patients with type 2 diabetes and chronic kidney disease (CKD). In a study involving 3,533 participants, semaglutide demonstrated a significant reduction in the risk of clinically important kidney outcomes and cardiovascular mortality, with a mean annual eGFR slope that was less steep by 1.16 ml/min/1.73 m² compared to placebo (ref: Perkovic doi.org/10.1056/NEJMoa2403347/). Additionally, zodasiran, an RNAi therapeutic targeting ANGPTL3, showed promising results in reducing triglyceride levels significantly across various dosages, indicating its potential in managing mixed hyperlipidemia (ref: Rosenson doi.org/10.1056/NEJMoa2404147/). Furthermore, the SELECT trial revealed that semaglutide not only aids in weight loss but also maintains its effects over an extended period, with participants experiencing sustained weight loss for up to four years (ref: Ryan doi.org/10.1038/s41591-024-02996-7/). These findings underscore the importance of innovative pharmacological approaches in diabetes care, particularly in populations at high risk for cardiovascular events and kidney failure. Moreover, the role of melatonin supplements in diabetes risk has been explored, suggesting a potential protective effect against type 2 diabetes and cardiovascular diseases, especially among individuals with irregular work schedules (ref: Li doi.org/10.1016/S2213-8587(24)00096-2/). This highlights the multifaceted nature of diabetes management, where lifestyle interventions and pharmacotherapy can be integrated to optimize patient outcomes. The systematic review on the demographic representation in obesity medication trials also emphasizes the need for inclusivity in clinical research to ensure that findings are applicable to diverse populations (ref: Alsaqaaby doi.org/10.1016/S2213-8587(24)00098-6/).