<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(12)</volume><submitter>Goosen TC</submitter><pubmed_abstract>Isavuconazole is a broad-spectrum triazole approved for the treatment of invasive aspergillosis or mucormycosis in adults and children aged ≥ 1 year. Current prescribing information lacks guidance regarding the co-administration of isavuconazole with anticancer drugs-limited by the availability of clinical drug-drug interaction (DDI) data in the patient population. This study utilized physiologically-based pharmacokinetic (PBPK) modeling to evaluate the DDI risk of isavuconazole compared with other azoles and provide dosing recommendations when co-administered with anticancer drugs (ibrutinib, venetoclax, and midostaurin). PBPK models were developed in the Simcyp simulator using physiochemical properties, in vitro, and clinical pharmacokinetic data. The model well-predicted isavuconazole p</pubmed_abstract><journal>CPT: pharmacometrics &amp; systems pharmacology</journal><pagination>2198-2209</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12706401</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Comparative Analysis of Isavuconazole DDIs With Other Azole Antifungal Drugs and PBPK Model-Informed Dosing Recommendations for Anticancer Drugs.</pubmed_title><pmcid>PMC12706401</pmcid><pubmed_authors>Raber SR</pubmed_authors><pubmed_authors>Cheruvu N</pubmed_authors><pubmed_authors>Varma MVS</pubmed_authors><pubmed_authors>Goosen TC</pubmed_authors><pubmed_authors>Lin J</pubmed_authors><pubmed_authors>de Figueiredo MLN</pubmed_authors><pubmed_authors>Wu X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Comparative Analysis of Isavuconazole DDIs With Other Azole Antifungal Drugs and PBPK Model-Informed Dosing Recommendations for Anticancer Drugs.</name><description>Isavuconazole is a broad-spectrum triazole approved for the treatment of invasive aspergillosis or mucormycosis in adults and children aged ≥ 1 year. Current prescribing information lacks guidance regarding the co-administration of isavuconazole with anticancer drugs-limited by the availability of clinical drug-drug interaction (DDI) data in the patient population. This study utilized physiologically-based pharmacokinetic (PBPK) modeling to evaluate the DDI risk of isavuconazole compared with other azoles and provide dosing recommendations when co-administered with anticancer drugs (ibrutinib, venetoclax, and midostaurin). PBPK models were developed in the Simcyp simulator using physiochemical properties, in vitro, and clinical pharmacokinetic data. The model well-predicted isavuconazole p</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-07T05:04:54.254Z</modification><creation>2026-06-07T03:06:55.281Z</creation></dates><accession>S-EPMC12706401</accession><cross_references><pubmed>41104611</pubmed><doi>10.1002/psp4.70123</doi></cross_references></HashMap>