Clinical Assessment of Breast Cancer Resistance Protein (BCRP)-Mediated Drug–Drug Interactions of Sepiapterin with Curcumin and Rosuvastatin in Healthy Volunteers

Oral coadministration of the BCRP inhibitor curcumin slightly increased the plasma exposure of sepiapterin and its metabolite BH<sub>4</sub> in healthy volunteers. This modest increase was deemed not clinically meaningful. Sepiapterin did not alter the pharmacokinetics of the BCRP substrate rosuvastatin.

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Publication Details

Journal
Drugs in R&D
Published
2024-09-01
DOI
https://doi.org/10.1007/s40268-024-00488-0
Citations
5
Primary Topic
Drug Transport and Resistance Mechanisms
Type
article
Field-Weighted Citation Impact
1.41

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article

Clinical Assessment of Breast Cancer Resistance Protein (BCRP)-Mediated Drug–Drug Interactions of Sepiapterin with Curcumin and Rosuvastatin in Healthy Volunteers

Kimberly Ingalls, Sarah Milner, Diksha Kaushik, Ronald Kong et al.
5 citations
Drugs in R&D
Drug Transport and Resistance Mechanisms
1.41
article

Clinical Assessment of Breast Cancer Resistance Protein (BCRP)-Mediated Drug–Drug Interactions of Sepiapterin with Curcumin and Rosuvastatin in Healthy Volunteers

Kimberly Ingalls, Sarah Milner, Diksha Kaushik, Ronald Kong, Lan Gao, Neil Smith
article en
5 citations

Abstract

Oral coadministration of the BCRP inhibitor curcumin slightly increased the plasma exposure of sepiapterin and its metabolite BH<sub>4</sub> in healthy volunteers. This modest increase was deemed not clinically meaningful. Sepiapterin did not alter the pharmacokinetics of the BCRP substrate rosuvastatin.

Drugs in R&DVol. 24(3)
Pfeiffer Medical Center (US), PTC Therapeutics (United States) (US)
PTC Therapeutics
Good health and well-being
Openalex Percentile: Top 15%
Drug Transport and Resistance Mechanisms
1.41
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