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This dual-agent compound includes both a long-acting amylin analog (Cagrilintide) and a GLP-1 (Sema) receptor agonist, facilitating synergistic modulation of satiety and glycemic pathways in preclinical settings

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By integrating insights from redox biology and nanotechnology, this review offers a timely and original perspective on the opportunities and challenges of exploiting tumor redox imbalance for precision drug delivery and cancer therapy