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This applies if you take straight-up L-carnitine, L-carnitine L-tartrate, or propionyl-L-carnitine
PMC 4108183
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For example, a patient may have a documented clinical need that an FDA-approved product cant meet, such as an allergy to an inactive ingredient or a required dose or formulation that isnt commercially available
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Similar to an IND, a Clinical Trial Authorization (CTA) application must be submitted to the NCAs
![PDF] Role of Glutathione in the Regulation of Cisplatin Resistance in Cancer Chemotherapy](https://figures.semanticscholar.org/b26931d7caa6d8c9a5e19bd18eba3188c8291c7a/4-Figure2-1.png)
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