<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>11(9)</volume><submitter>Kassir N</submitter><pubmed_abstract>Etrolizumab is an IgG1-humanized monoclonal anti-β7 integrin antibody. Phase III trials with induction and/or maintenance phases were conducted in patients with moderately-to-severely active ulcerative colitis (UC) who were either previously treated with tumor necrosis factor (TNF) inhibitors (HICKORY) or were TNF inhibitor naïve (HIBISCUS I/II, LAUREL, and GARDENIA). A total of eight exposure-response analyses were conducted for two clinical outcomes (remission and endoscopic improvement) at the end of induction for studies HIBISCUS I/II (combined) and HICKORY and at the end of maintenance for studies HICKORY and LAUREL. Trough concentration at week 4 (C&lt;sub>trough,wk4&lt;/sub> ) of induction was selected as the exposure metric. Exposure-response (ER) modeling was conducted using logistic re</pubmed_abstract><journal>CPT: pharmacometrics &amp; systems pharmacology</journal><pagination>1234-1243</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9469693</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Exposure-response relationships of etrolizumab in patients with moderately-to-severely active ulcerative colitis.</pubmed_title><pmcid>PMC9469693</pmcid><pubmed_authors>Zhang W</pubmed_authors><pubmed_authors>Moein A</pubmed_authors><pubmed_authors>Oh YS</pubmed_authors><pubmed_authors>Langenhorst J</pubmed_authors><pubmed_authors>Kassir N</pubmed_authors><pubmed_authors>Ribbing J</pubmed_authors><pubmed_authors>Zhu R</pubmed_authors><pubmed_authors>Zhang R</pubmed_authors><pubmed_authors>Tang MT</pubmed_authors></additional><is_claimable>false</is_claimable><name>Exposure-response relationships of etrolizumab in patients with moderately-to-severely active ulcerative colitis.</name><description>Etrolizumab is an IgG1-humanized monoclonal anti-β7 integrin antibody. Phase III trials with induction and/or maintenance phases were conducted in patients with moderately-to-severely active ulcerative colitis (UC) who were either previously treated with tumor necrosis factor (TNF) inhibitors (HICKORY) or were TNF inhibitor naïve (HIBISCUS I/II, LAUREL, and GARDENIA). A total of eight exposure-response analyses were conducted for two clinical outcomes (remission and endoscopic improvement) at the end of induction for studies HIBISCUS I/II (combined) and HICKORY and at the end of maintenance for studies HICKORY and LAUREL. Trough concentration at week 4 (C&lt;sub>trough,wk4&lt;/sub> ) of induction was selected as the exposure metric. Exposure-response (ER) modeling was conducted using logistic re</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-05T10:46:03.563Z</modification><creation>2025-04-05T10:46:03.563Z</creation></dates><accession>S-EPMC9469693</accession><cross_references><pubmed>35789549</pubmed><doi>10.1002/psp4.12840</doi></cross_references></HashMap>