Pharmacokinetic/pharmacodynamic drug-drug interactions of avatrombopag when coadministered with dual or selective CYP2C9 and CYP3A interacting drugs

Author:

Nomoto Maiko1ORCID,Zamora Cynthia A.2,Schuck Edgar3,Boyd Peter4,Chang Min-Kun3,Aluri Jagadeesh3,Siu Y. Amy5,Lai W. George5,Yasuda Sanae1,Ferry Jim3,Rege Bhaskar3

Affiliation:

1. Eisai Co., Ltd.; Tokyo Japan

2. Worldwide Clinical Trials; San Antonio TX USA

3. Eisai, Inc.; Woodcliff Lake NJ USA

4. Eisai Ltd; Hatfield UK

5. Eisai, Inc.; Andover MA USA

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference22 articles.

1. AKR-501 (YM477) in combination with thrombopoietin enhances human megakaryocytopoiesis;Fukushima-Shintani;Exp Haematol,2008

2. AKR-501 (YM477) a novel orally-active thrombopoietin receptor agonist;Fukushima-Shintani;Eur J Haematol,2009

3. Relative contributions of the five major human cytochromes P450, 1A2, 2C9, 2C19, 2D6, and 3A4, to the hepatic metabolism of the proteasome inhibitor vortezomib;Uttamsingh;Drug Metab Dispos,2005

4. Pharmacokinetics, pharmacodynamics, pharmacogenomics, safety and tolerability of avatrombopag in healthy Japanese and Caucasian subjects;Nomoto;Clin Pharm Drug Dev,2018

5. European Medicines Agency Guideline on the investigation of drug interactions http://www.ema.europa.eu/docs/en_GB/document_library/Scientific_guideline/2012/07/WC500129606.pdf

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