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RIBBON-1: Randomized, double-blind, placebo-controlled, phase III trial of chemotherapy with or without bevacizumab for first-line treatment of human epidermal growth factor receptor 2-negative, locally recurrent or metastatic breast cancer

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Although some peptides like tesamorelin have received formal FDA approval, many others fall under compounding provisions of the Federal Food, Drug, and Cosmetic Act503A (patient-specific prescriptions by state-licensed pharmacies) and 503B (FDA-regulated outsourcing facilities operating under cGMP)

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Furthermore, the Philippines Food and Drug Administration (FDA) has sanctioned its application as an adjunctive treatment to mitigate the neurotoxic effects of cisplatin chemotherapy[3]