{"id":1291,"date":"2021-05-21T11:48:00","date_gmt":"2021-05-21T09:48:00","guid":{"rendered":"https:\/\/lensounds.com\/science\/pertinence-a-pilot-study-to-assess-safety-tolerability-radiation-dosimetry-and-imaging-properties-of-89zr-labeled-girentuximab-in-non-muscle-invasive-bladder-cancer\/"},"modified":"2021-05-21T11:48:00","modified_gmt":"2021-05-21T09:48:00","slug":"pertinence-a-pilot-study-to-assess-safety-tolerability-radiation-dosimetry-and-imaging-properties-of-89zr-labeled-girentuximab-in-non-muscle-invasive-bladder-cancer","status":"publish","type":"science","link":"https:\/\/atonco-pharma.com\/en\/science\/pertinence-a-pilot-study-to-assess-safety-tolerability-radiation-dosimetry-and-imaging-properties-of-89zr-labeled-girentuximab-in-non-muscle-invasive-bladder-cancer\/","title":{"rendered":"PERTINENCE: A Pilot Study to Assess Safety, Tolerability, Radiation Dosimetry, and Imaging Properties of 89Zr-labeled Girentuximab in Non-Muscle Invasive Bladder Cancer"},"content":{"rendered":"<h2>Abstract<\/h2>\n<p>This early Phase I pilot open-label feasibility study evaluates the safety, tolerability, radiation dosimetry, and imaging properties of <sup>89<\/sup>Zr-labeled girentuximab, a radiopharmaceutical targeting the carbonic anhydrase IX (CAIX) antigen, for PET\/CT imaging in patients with non-muscle invasive bladder cancer (NMIBC). The study enrolled 6 patients with NMIBC to assess the diagnostic potential of this novel imaging agent. <sup>89<\/sup>Zr-girentuximab enables precise visualization of CAIX-expressing tumor cells, offering valuable insights for patient selection and treatment planning in targeted alpha therapy approaches. This monocentric, prospective study was conducted at Institut de Canc\u00e9rologie de l&#8217;Ouest (ICO) in collaboration with Atonco, contributing to the development of theranostic strategies combining diagnostic imaging with therapeutic applications using the anti-CAIX antibody girentuximab.<\/p>\n<h2>Publication Information<\/h2>\n<p><strong>Source:<\/strong> ClinicalTrials.gov<\/p>\n<p><strong>Trial Registration Date:<\/strong> May 21, 2021<\/p>\n<p><strong>Study Completion Date:<\/strong> September 26, 2022<\/p>\n<p><strong>Trial ID:<\/strong> NCT04897763<\/p>\n<p><strong>Study Status:<\/strong> COMPLETED<\/p>\n<p><strong>ClinicalTrials.gov Link:<\/strong> <a href=\"https:\/\/clinicaltrials.gov\/study\/NCT04897763\" target=\"_blank\" rel=\"noopener\">https:\/\/clinicaltrials.gov\/study\/NCT04897763<\/a><\/p>\n<h2>Authors<\/h2>\n<p><strong>Sponsor:<\/strong> Institut de Canc\u00e9rologie de l&#8217;Ouest (ICO)<\/p>\n<p><strong>Collaborator:<\/strong> Atonco<\/p>\n<p><strong>Principal Investigator:<\/strong> Caroline Rousseau, MD, PhD<\/p>\n<p><strong>Institutional Affiliation:<\/strong> Institut de Canc\u00e9rologie de l&#8217;Ouest, Saint-Herblain (44805), France<\/p>\n<p><strong>Phase:<\/strong> Early Phase I (Diagnostic)<\/p>\n<p><strong>Actual Enrollment:<\/strong> 6 patients<\/p>\n<p><strong>Study Timeline:<\/strong> October 1, 2021 \u2013 September 26, 2022<\/p>\n<p><strong>Study Design:<\/strong> Monocentric, open-label, prospective, single-arm<\/p>\n","protected":false},"excerpt":{"rendered":"<p> ClinicalTrials.gov ID: NCT04897763<br \/>\n  Sponsor: Institut de Canc\u00e9rologie de l&#8217;Ouest (ICO)<br \/>\n  Collaborator: Atonco<br \/>\n  ClinicalTrials.gov Link: https:\/\/clinicaltrials.gov\/study\/NCT04897763<\/p>\n","protected":false},"featured_media":0,"template":"","meta":[],"science_category":[50],"class_list":["post-1291","science","type-science","status-publish","hentry","science_category-ato-101-publications"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.3 - 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