CYP3A4-mediated effects of rifampicin on the pharmacokinetics of vilaprisan and its UGT1A1-mediated effects on bilirubin glucuronidation in humans

Author:

Chattopadhyay Niladri1,Kanacher Tobias1,Casjens Manuela2,Frechen Sebastian1,Ligges Sandra1,Zimmermann Torsten1,Rottmann Antje1,Ploeger Bart1,Höchel Joachim1,Schultze-Mosgau Marcus-Hillert1ORCID

Affiliation:

1. Bayer AG; Berlin Germany

2. CRS Clinical Research Services Berlin GmbH; Berlin Germany

Publisher

Wiley

Subject

Pharmacology (medical),Pharmacology

Reference41 articles.

1. Interaction of sodium warfarin and rifampin;O'Reilly;Ann Intern Med,1974

2. US Department of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research (CDER) Clinical drug interaction studies - study design, data analysis, and clinical implications. Guidance for industry. Draft guidance [online] https://www.fda.gov/downloads/Drugs/GuidanceComplianceRegulatoryInformation/Guidances/UCM292362.pdf

3. Physiologically based pharmacokinetic modeling of CYP3A4 induction by rifampicin in human: influence of time between substrate and inducer administration;Baneyx;Eur J Pharm Sci,2014

4. BAY 1002670: a novel, highly potent and selective progesterone receptor modulator for gynaecological therapies;Wagenfeld;Hum Reprod,2013

5. Pharmacodynamics and safety of the novel selective progesterone receptor modulator vilaprisan: a double-blind, randomized, placebo-controlled phase 1 trial in healthy women;Schütt;Hum Reprod,2016

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