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A robust estimation of infliximab pharmacokinetic parameters in Crohn’s disease

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References

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Acknowledgments

Measurements of infliximab serum concentrations were carried out within the CePiBAc platform. CePiBAc was cofinanced by the European Union. Europe is committed to the region center with the European Regional Development Fund. This work was partly supported by the French Higher Education and Research ministry under the program ‘Investissements d’avenir’ Grand Agreement: LabEx MAbImprove ANR-10-LABX-53-01. The authors would like to thank Dr. Charlotte Magdelaine, Prof. Hervé Watier, and Dr. Danielle Degenne for the ATI assay management and Anne-Claire Duveau, Caroline Brochon, and Audrey Farnault for the technical assistance with infliximab and ATI assays.

Contribution of authors statement

D. Aubourg analyzed and interpreted the data and wrote the manuscript; Dr. Picon participated actively in execution of the study; Dr. Lecomte participated in the execution of the study; Dr. Paintaud participated in the interpretation of the data in manuscript writing; Dr. Paintaud participated in the interpretation of the data in manuscript writing; Dr Ternant participated in the data analysis, interpretation, and in manuscript writing.

Conflict of interest

Dr. Paintaud reports grants from Novartis, grants from Roche Pharma, grants from Genzyme, grants from MSD, grants from Servier, grants from Pfizer, outside the submitted work.

Dr. Aubourg, Dr Picon, Dr. Lecomte, Dr. Bejan-Angoulvant and Dr. Ternant declare that they have no conflict of interest.

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Correspondence to David Ternant.

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Aubourg, A., Picon, L., Lecomte, T. et al. A robust estimation of infliximab pharmacokinetic parameters in Crohn’s disease. Eur J Clin Pharmacol 71, 1541–1542 (2015). https://doi.org/10.1007/s00228-015-1942-8

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  • DOI: https://doi.org/10.1007/s00228-015-1942-8

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