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Published in 2020 at "Drug metabolism and pharmacokinetics"
DOI: 10.1016/j.dmpk.2020.11.003
Abstract: Cytochrome P450 (CYP) 3A-related drug-drug interaction (DDI) studies are needed during drug development to determine clinical interaction effects. We aimed to evaluate DDI between sildenafil and two CYP3A inhibitors, clarithromycin and itraconazole, regarding the changes…
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Keywords:
endogenous markers;
cyp3a activity;
drug;
sildenafil ... See more keywords
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Published in 2021 at "Clinical and translational science"
DOI: 10.1111/cts.13142
Abstract: It remains uncertain whether pharmacokinetic changes following Roux-en-Y gastric bypass (RYGB) can be attributed to surgery-induced gastrointestinal alterations per se and/or the subsequent weight loss. The aim was to compare short- and long-term effects of…
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Keywords:
weight loss;
term;
cyp3a activity;
loss ... See more keywords
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Published in 2022 at "Clinical and Translational Science"
DOI: 10.1111/cts.13448
Abstract: Ibrutinib is an orally administered Bruton's tyrosine kinase inhibitor approved for the treatment of B‐cell malignancies, including chronic lymphocytic leukemia. Ibrutinib is metabolized primarily via oxidation by cytochrome P450 (CYP) 3A4/5 to M37 (the primary…
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Keywords:
formation;
cyp3a;
cholesterol ratio;
cyp3a activity ... See more keywords
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Published in 2020 at "Frontiers in Genetics"
DOI: 10.3389/fgene.2020.00944
Abstract: Human CYP3A enzymes (including CYP3A4 and CYP4A5) metabolize about 40% of all drugs and numerous other environmental and endogenous substances. CYP3A activity is highly variable within and between humans. As a consequence, therapy with standard…
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Keywords:
environmental factors;
variation;
cyp3a activity;
cyp3a ... See more keywords