Articles with "drug drug" as a keyword



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Safely Prescribing Nirmatrelvir and Ritonavir-Avoiding Drug-Drug Interactions.

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Published in 2023 at "JAMA internal medicine"

DOI: 10.1001/jamainternmed.2022.6834

Abstract: This Teachable Moment discusses drug-drug interactions with nirmatrelvir and ritonavir (Paxlovid) treatment for COVID-19 and considerations when prescribing. read more here.

Keywords: drug interactions; drug drug; nirmatrelvir ritonavir; safely prescribing ... See more keywords
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Association of polypharmacy and potential drug‐drug interactions with adverse treatment outcomes in older adults with advanced cancer

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Published in 2023 at "Cancer"

DOI: 10.1002/cncr.34642

Abstract: Polypharmacy is common in older adults who are starting cancer treatment and is associated with an increased risk of potentially inappropriate medications (PIMs) and potential drug‐drug interactions (PDIs). The authors evaluated the association of medication… read more here.

Keywords: potential drug; older adults; drug interactions; drug drug ... See more keywords
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Drug‐Drug Interaction of Letermovir and Atorvastatin in Healthy Participants

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Published in 2022 at "Clinical Pharmacology in Drug Development"

DOI: 10.1002/cpdd.1071

Abstract: Letermovir (MK‐8228/AIC246) is a cytomegalovirus (CMV) DNA terminase complex inhibitor for CMV prophylaxis in adult patients undergoing hematopoietic stem cell transplant. It is cytochrome P450 (CYP) 3A inhibitor and inhibits organic anion transporting polypeptide 1B1/3… read more here.

Keywords: atv cmax; coadministration; drug drug; letermovir ... See more keywords
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A Phase 1, Open-Label, Fixed-Sequence, Drug-Drug Interaction Study of Zanubrutinib with Rifabutin in Healthy Volunteers.

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Published in 2023 at "Clinical pharmacology in drug development"

DOI: 10.1002/cpdd.1250

Abstract: Zanubrutinib is a second-generation Bruton tyrosine kinase inhibitor that is primarily metabolized by CYP3A enzymes. Previous drug-drug interaction (DDI) studies have demonstrated that co-administration of zanubrutinib with rifampin, a strong CYP3A inducer, reduces zanubrutinib plasma… read more here.

Keywords: open label; zanubrutinib; drug drug; phase open ... See more keywords
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Evaluation of the Cytochrome P450 3A and P-glycoprotein Drug-Drug Interaction Potential of Futibatinib.

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Published in 2023 at "Clinical pharmacology in drug development"

DOI: 10.1002/cpdd.1259

Abstract: Futibatinib, a selective, irreversible fibroblast growth factor receptor 1-4 inhibitor, is being investigated for tumors harboring FGFR aberrations and was recently approved for the treatment of FGFR2 fusion/rearrangement-positive intrahepatic cholangiocarcinoma. In vitro studies identified cytochrome… read more here.

Keywords: cyp3a; plasma concentration; drug drug; cytochrome p450 ... See more keywords
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Evaluation of Pharmacokinetics, Safety, and Drug‐Drug Interactions of an Oral Suspension of Edaravone in Healthy Adults

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Published in 2021 at "Clinical Pharmacology in Drug Development"

DOI: 10.1002/cpdd.925

Abstract: Intravenous (IV) edaravone is approved as an amyotrophic lateral sclerosis (ALS) treatment. Because IV administration places a burden on patients, development of orally administered ALS treatments is needed. Therefore, 2 phase 1 studies of oral… read more here.

Keywords: formulation; edaravone healthy; drug; edaravone ... See more keywords
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Prediction of the Impact of Cytochrome P450 2C9 Genotypes on the Drug–Drug Interaction Potential of Siponimod With Physiologically‐Based Pharmacokinetic Modeling: A Comprehensive Approach for Drug Label Recommendations

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Published in 2019 at "Clinical Pharmacology and Therapeutics"

DOI: 10.1002/cpt.1547

Abstract: We predicted the drug–drug interaction (DDI) potential of siponimod in presence of cytochrome P450 (CYP)2C9/CYP3A4 inhibitors/inducers in subjects with different CYP2C9 genotypes by physiologically‐based pharmacokinetic (PK) modeling. The model was established using in vitro and… read more here.

Keywords: siponimod; drug interaction; potential siponimod; drug ... See more keywords
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Physiologically‐Based Pharmacokinetic Models for Evaluating Membrane Transporter Mediated Drug–Drug Interactions: Current Capabilities, Case Studies, Future Opportunities, and Recommendations

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Published in 2019 at "Clinical Pharmacology and Therapeutics"

DOI: 10.1002/cpt.1693

Abstract: Physiologically‐based pharmacokinetic (PBPK) modeling has been extensively used to quantitatively translate in vitro data and evaluate temporal effects from drug–drug interactions (DDIs), arising due to reversible enzyme and transporter inhibition, irreversible time‐dependent inhibition, enzyme induction,… read more here.

Keywords: based pharmacokinetic; pbpk modeling; physiologically based; drug ... See more keywords
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Drugs in COVID‐19 Clinical Trials: Predicting Transporter‐Mediated Drug‐Drug Interactions Using In Vitro Assays and Real‐World Data

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Published in 2021 at "Clinical Pharmacology and Therapeutics"

DOI: 10.1002/cpt.2236

Abstract: Numerous drugs are currently under accelerated clinical investigation for the treatment of coronavirus disease 2019 (COVID‐19); however, well‐established safety and efficacy data for these drugs are limited. The goal of this study was to predict… read more here.

Keywords: real world; drug interactions; drug; clinical trials ... See more keywords
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Oral Glucose Tolerance Test: An Informative Endpoint or an Added Burden in Metformin Drug–Drug Interaction Studies?

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Published in 2022 at "Clinical Pharmacology and Therapeutics"

DOI: 10.1002/cpt.2650

Abstract: For drugs that inhibit organic cation transporters and/or multidrug and toxin extrusion proteins, a metformin clinical drug– drug interaction (DDI) study is recommended to assess the impact on metformin’s systemic exposure. An oral glucose tolerance… read more here.

Keywords: tolerance test; glucose tolerance; drug drug; oral glucose ... See more keywords
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The key role of organic anion transporter 3 in the drug-drug interaction between tranilast and methotrexate.

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Published in 2022 at "Journal of biochemical and molecular toxicology"

DOI: 10.1002/jbt.22983

Abstract: Tranilast, N-(3',4'-dimethoxycinnamoyl)-anthranilic acid, is an anti-allergic drug and is considered for use in the treatment of rheumatoid arthritis. Methotrexate, an antimetabolite and folate antagonist to treat some cancers, is also a first-line drug for RA.… read more here.

Keywords: mtx; drug drug; drug; methotrexate ... See more keywords