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In cases where FDA-approved medications are not suitable for treating a particular patient, such as when a patient is allergic to an ingredient in the medication or when the medicine is in tablet form, which children or elderly individuals cannot swallow, compounding is performed to make the medication suitable for the patient

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Sunlenca was also granted approval by the European Commission supported by data from the Phase 2/3 CAPELLA study

[25] The results were reproduced when NAD+ was replaced by giving several NAD+ precursor molecules, demonstrating that the positive effects are caused by NAD+ replacement