Abstract
Clinical development of new drugs may require dedicated drug–drug interaction (DDI) studies, such as to evaluate the effect of cytochrome P450 3A induction on the pharmacokinetics of investigational drugs. However, as a result of N-nitrosamine impurity findings in marketed rifampin formulations, the application of rifampin in DDI studies has been halted. This mini-review considers the root cause and impact of the nitrosamine impurity as well as alternative options for the continued conduct of DDIs.
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CITATION STYLE
van Haarst, A., Smith, S., Garvin, C., Benrimoh, N., & Paglialunga, S. (2023, April 1). Rifampin Drug–Drug–Interaction Studies: Reflections on the Nitrosamine Impurities Issue. Clinical Pharmacology and Therapeutics. John Wiley and Sons Inc. https://doi.org/10.1002/cpt.2652
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