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Low Bioavailability of Oral Tacrolimus Suspension in Pediatric Kidney Transplant Patients

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Acknowledgements

The authors thank Chris Vermaat for the critical review of the manuscript and the information on the production process of the tacrolimus suspension.

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Corresponding author

Correspondence to Anne M. Schijvens.

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Funding

This study was funded by the Dutch Kidney Foundation (grant number 15OKG16, M.F. Schreuder).

Conflict of interest

The authors declare that they have no conflict of interest.

Ethics approval

The Ethics Committee of the Radboud University Medical Center waived the need for ethical approval according to the Dutch Law on Human Research, as only patient chart data were anonymously collected.

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Not applicable.

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Author contributions

Conception and study design: RtH, MS, AS; data acquisition: AS, FH; data analysis/interpretation: all authors. Each author contributed important intellectual content during manuscript drafting or revision, approved the submitted version of the manuscript, accepts personal accountability for the author’s own contributions, and agrees to ensure that questions pertaining to the accuracy or integrity of any portion of the work are appropriately investigated and resolved.

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Schijvens, A.M., de Wildt, S.N., Cornelissen, E.A.M. et al. Low Bioavailability of Oral Tacrolimus Suspension in Pediatric Kidney Transplant Patients. Clin Pharmacokinet 59, 1483–1485 (2020). https://doi.org/10.1007/s40262-020-00908-9

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  • DOI: https://doi.org/10.1007/s40262-020-00908-9

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