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They cannot by themselves establish: A safe human amount A safe route of administration Long-term human safety Interaction risks Reproductive or developmental safety Clinical effectiveness Which individuals, if any, might be suitable for an authorised use The number of animal papers should not be presented as equivalent to a programme of large, well-controlled human clinical trials

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The subjects response time or motor function may become slightly impaired or decreased after administration of higher doses

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A pending CagriSema submission means cagrilintide is basically approved. It does not