<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>17(1)</volume><submitter>Ding Z</submitter><funding>Eddingpharm Co., Ltd., China</funding><funding>Shionogi</funding><pubmed_abstract>&lt;h4>Purpose&lt;/h4>Probing efficacy and safety of lusutrombopag in Chinese chronic liver disease (CLD) and severe thrombocytopenia (PLT &lt; 50 × 10&lt;sup>9&lt;/sup>/L) patients undergoing elective invasive procedures.&lt;h4>Methods&lt;/h4>In this double-blind, parallel-group phase 3 study, 66 patients with CLD and severe thrombocytopenia were randomized 2:1 to lusutrombopag or placebo arm treatment regimens for seven days at 9 centers in China. Responders (PLT ≥ 50 × 10&lt;sup>9&lt;/sup>/L that increased to ≥ 20 × 10&lt;sup>9&lt;/sup>/L from the baseline and not received rescue therapy for bleeding) on Day 8 (the day after seven-day treatment) were assessed. PLT ≥ 50 × 10&lt;sup>9&lt;/sup>/L on or after Day 8 and within 2 days before invasive procedure (alternative criteria for not requiring platelet transfusion) were also</pubmed_abstract><journal>Hepatology international</journal><pagination>180-189</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9895009</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Lusutrombopag for thrombocytopenia in Chinese patients with chronic liver disease undergoing invasive procedures.</pubmed_title><pmcid>PMC9895009</pmcid><pubmed_authors>Fu X</pubmed_authors><pubmed_authors>Zeng Y</pubmed_authors><pubmed_authors>Meng Z</pubmed_authors><pubmed_authors>Kano T</pubmed_authors><pubmed_authors>Wu H</pubmed_authors><pubmed_authors>Pan H</pubmed_authors><pubmed_authors>Yang W</pubmed_authors><pubmed_authors>Fan J</pubmed_authors><pubmed_authors>Kuang M</pubmed_authors><pubmed_authors>Shi G</pubmed_authors><pubmed_authors>Chen Y</pubmed_authors><pubmed_authors>Zou S</pubmed_authors><pubmed_authors>Liu C</pubmed_authors><pubmed_authors>Wang X</pubmed_authors><pubmed_authors>Ding Z</pubmed_authors><pubmed_authors>Sun H</pubmed_authors><pubmed_authors>Lin K</pubmed_authors><pubmed_authors>Hao C</pubmed_authors><pubmed_authors>Chen R</pubmed_authors><pubmed_authors>Yang S</pubmed_authors><pubmed_authors>Liang R</pubmed_authors><pubmed_authors>Zhou J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lusutrombopag for thrombocytopenia in Chinese patients with chronic liver disease undergoing invasive procedures.</name><description>&lt;h4>Purpose&lt;/h4>Probing efficacy and safety of lusutrombopag in Chinese chronic liver disease (CLD) and severe thrombocytopenia (PLT &lt; 50 × 10&lt;sup>9&lt;/sup>/L) patients undergoing elective invasive procedures.&lt;h4>Methods&lt;/h4>In this double-blind, parallel-group phase 3 study, 66 patients with CLD and severe thrombocytopenia were randomized 2:1 to lusutrombopag or placebo arm treatment regimens for seven days at 9 centers in China. Responders (PLT ≥ 50 × 10&lt;sup>9&lt;/sup>/L that increased to ≥ 20 × 10&lt;sup>9&lt;/sup>/L from the baseline and not received rescue therapy for bleeding) on Day 8 (the day after seven-day treatment) were assessed. PLT ≥ 50 × 10&lt;sup>9&lt;/sup>/L on or after Day 8 and within 2 days before invasive procedure (alternative criteria for not requiring platelet transfusion) were also</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Feb</publication><modification>2025-04-26T18:09:22.206Z</modification><creation>2025-02-19T03:30:30.863Z</creation></dates><accession>S-EPMC9895009</accession><cross_references><pubmed>36258065</pubmed><doi>10.1007/s12072-022-10421-9</doi></cross_references></HashMap>