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Regulatory bodies, including the FDA and EMA, require comprehensive immunogenicity testing during clinical development, including method validation, sample handling, and data traceability

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On the basis of various factors, such as the concentration of active ingredients or the patient's condition, the combination according to the invention can be marketed as a food supplement, a nutritional supplement, or as a therapeutic product on sale with or without a compulsory doctor's prescription

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Increased FUS levels in astrocytes leads to astrocyte and microglia activation and neuronal death

First, the reassuring part