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This substantial participant database provides meaningful safety evidence across varied dosing regimens, administration routes (oral and injectable), and treatment durations, making it one of the more extensively studied peptide fragments in human clinical trials

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These characteristics provide answers to problems like drug resistance and inefficiencies in standard antibiotic treatment (Lim et al., 2016)

Autophagy in cisplatin ototoxicity In the study of cisplatin resistance, it was found that cancer cells can reduce cisplatin therapy efficacy by triggering autophagy and autophagy-modulating agents as chemosensitizers for cisplatin therapy in cancer