<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Kim C</submitter><pubmed_abstract>18F-GP1 is a derivative of elarofiban with a high affinity to activated platelet glycoprotein IIb/IIIa (GPIIb/IIIa) and favorable in vivo characteristics for thrombus imaging in preclinical models. We aimed to explore the detection rate of thromboembolic foci with 18F-GP1 positron emission tomography/computed tomography (PET/CT) in patients with acute venous thromboembolism (VTE), and to evaluate the safety, biodistribution, pharmacokinetics, and metabolism of 18F-GP1. Methods: We studied patients who had signs or symptoms of acute deep vein thrombosis (DVT) of the leg or acute pulmonary embolism (PE) within 14 days prior to 18F-GP1 PET/CT, and had thromboembolic foci confirmed by conventional imaging (n = 10 for DVT and n = 10 for PE). Dynamic whole-body PET/CT images were acquired for up</pubmed_abstract><journal>Journal of nuclear medicine : official publication, Society of Nuclear Medicine</journal><pagination>jnumed.118.212084</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8833852</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Glycoprotein IIb/IIIa receptor imaging with 18F-GP1 positron emission tomography for acute venous thromboembolism: an open-label, non-randomized, first-in-human phase 1 study.</pubmed_title><pmcid>PMC8833852</pmcid><pubmed_authors>Kim C</pubmed_authors><pubmed_authors>Son HJ</pubmed_authors><pubmed_authors>Chae SY</pubmed_authors><pubmed_authors>Kim B</pubmed_authors><pubmed_authors>Lee SJ</pubmed_authors><pubmed_authors>Jin S</pubmed_authors><pubmed_authors>Han Y</pubmed_authors><pubmed_authors>Kwon TW</pubmed_authors><pubmed_authors>Cho YP</pubmed_authors><pubmed_authors>Koglin N</pubmed_authors><pubmed_authors>Lee JS</pubmed_authors><pubmed_authors>Jang S</pubmed_authors><pubmed_authors>Berndt M</pubmed_authors><pubmed_authors>Lee DH</pubmed_authors><pubmed_authors>Oh SJ</pubmed_authors><pubmed_authors>Sung C</pubmed_authors><pubmed_authors>Oh JS</pubmed_authors><pubmed_authors>Moon DH</pubmed_authors><pubmed_authors>Stephens AW</pubmed_authors></additional><is_claimable>false</is_claimable><name>Glycoprotein IIb/IIIa receptor imaging with 18F-GP1 positron emission tomography for acute venous thromboembolism: an open-label, non-randomized, first-in-human phase 1 study.</name><description>18F-GP1 is a derivative of elarofiban with a high affinity to activated platelet glycoprotein IIb/IIIa (GPIIb/IIIa) and favorable in vivo characteristics for thrombus imaging in preclinical models. We aimed to explore the detection rate of thromboembolic foci with 18F-GP1 positron emission tomography/computed tomography (PET/CT) in patients with acute venous thromboembolism (VTE), and to evaluate the safety, biodistribution, pharmacokinetics, and metabolism of 18F-GP1. Methods: We studied patients who had signs or symptoms of acute deep vein thrombosis (DVT) of the leg or acute pulmonary embolism (PE) within 14 days prior to 18F-GP1 PET/CT, and had thromboembolic foci confirmed by conventional imaging (n = 10 for DVT and n = 10 for PE). Dynamic whole-body PET/CT images were acquired for up</description><dates><release>2018-01-01T00:00:00Z</release><publication>2018 Jun</publication><modification>2025-06-01T00:52:08.948Z</modification><creation>2024-11-13T10:45:03.903Z</creation></dates><accession>S-EPMC8833852</accession><cross_references><pubmed>29959214</pubmed><doi>10.2967/jnumed.118.212084</doi></cross_references></HashMap>