<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-04-18T06:10:13Z</responseDate><request verb="GetRecord" identifier="oai:www.recercat.cat:11351/12812" metadataPrefix="oai_dc">https://recercat.cat/oai/request</request><GetRecord><record><header><identifier>oai:recercat.cat:11351/12812</identifier><datestamp>2025-10-24T10:28:44Z</datestamp><setSpec>com_2072_378070</setSpec><setSpec>com_2072_378040</setSpec><setSpec>col_2072_378092</setSpec></header><metadata><oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:doc="http://www.lyncode.com/xoai" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
   <dc:title>Open-label, phase Ia study of STING agonist BI 1703880 plus ezabenlimab for patients with advanced solid tumors</dc:title>
   <dc:creator>Harrington, Kevin</dc:creator>
   <dc:creator>Kitano, Shigehisa</dc:creator>
   <dc:creator>Parkes, Eileen</dc:creator>
   <dc:creator>Moreno, Irene</dc:creator>
   <dc:creator>Alonso-Casal, Guzman</dc:creator>
   <dc:creator>Gambardella, Valentina</dc:creator>
   <dc:contributor>Institut Català de la Salut</dc:contributor>
   <dc:contributor>[Harrington K] The Institute of Cancer Research/The Royal Marsden NHS Foundation Trust, London, UK. [Kitano S] Japanese Foundation for Cancer Research, Tokyo, Japan. [Gambardella V] INCLIVA Biomedical Research Institute, Hospital Clínico de Valencia, Valencia, Spain. [Parkes EE] Department of Oncology, University of Oxford, Churchill Hospital, Oxford, UK. [Moreno I] START Madrid, CIOCC, Centro Integral Oncológico Clara Campal, Madrid, Spain. [Alonso G] Vall d’Hebron Hospital Universitari, Barcelona, Spain</dc:contributor>
   <dc:contributor>Vall d'Hebron Barcelona Hospital Campus</dc:contributor>
   <dc:subject>Quimioteràpia combinada</dc:subject>
   <dc:subject>Càncer - Immunoteràpia</dc:subject>
   <dc:subject>Posologia</dc:subject>
   <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Therapeutics::Therapeutics::Drug Therapy::Antineoplastic Protocols::Therapeutics::Drug Therapy::Antineoplastic Combined Chemotherapy Protocols</dc:subject>
   <dc:subject>DISEASES::Neoplasms</dc:subject>
   <dc:subject>Other subheadings::Other subheadings::Other subheadings::/drug therapy</dc:subject>
   <dc:subject>ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Investigative Techniques::Toxicity Tests::Maximum Tolerated Dose</dc:subject>
   <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::terapéutica::farmacoterapia::protocolos antineoplásicos::terapéutica::farmacoterapia::protocolos de quimioterapia antineoplásica combinada</dc:subject>
   <dc:subject>ENFERMEDADES::neoplasias</dc:subject>
   <dc:subject>Otros calificadores::Otros calificadores::Otros calificadores::/farmacoterapia</dc:subject>
   <dc:subject>TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::técnicas de investigación::pruebas de toxicidad::dosis máxima tolerada</dc:subject>
   <dc:description>PD-1 antibody; Cancer; Immunotherapy</dc:description>
   <dc:description>Anticuerpo PD-1; Cáncer; Inmunoterapia</dc:description>
   <dc:description>Anticòs PD-1; Càncer; Immunoteràpia</dc:description>
   <dc:description>BI 1703880, a novel STimulator of INterferon Genes (STING) agonist, has demonstrated preclinical antitumor activity. As STING activation can upregulate programmed death ligand 1 and human leukocyte antigen in tumor cells, a combination of BI 1703880 and an anti-programmed cell death protein 1-antibody, such as ezabenlimab, may improve efficacy. This first-in-human phase Ia study (NCT05471856) is evaluating BI 1703880 plus ezabenlimab in patients with advanced solid tumors. The study utilizes an innovative lead-in design; all patients receive BI 1703880 monotherapy in Cycle 1 and combination therapy from Cycle 2. The primary endpoint is dose-limiting toxicities during the maximum tolerated dose evaluation period. Results will inform the future development of BI 1703880 for treatment of metastatic or recurrent malignancies.&#xd;
Clinical Trial number: NCT05471856</dc:description>
   <dc:description>This article was funded by Boehringer Ingelheim International GmbH.</dc:description>
   <dc:date>2025-03-21T09:31:00Z</dc:date>
   <dc:date>2025-03-21T09:31:00Z</dc:date>
   <dc:date>2025-01-16</dc:date>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:identifier>Harrington K, Kitano S, Gambardella V, Parkes EE, Moreno I, Alonso G, et al. Open-label, phase Ia study of STING agonist BI 1703880 plus ezabenlimab for patients with advanced solid tumors. Futur Oncol. 2025 Jan 16;21(2):195-200.</dc:identifier>
   <dc:identifier>1744-8301</dc:identifier>
   <dc:identifier>http://hdl.handle.net/11351/12812</dc:identifier>
   <dc:identifier>10.1080/14796694.2024.2441107</dc:identifier>
   <dc:identifier>39817655</dc:identifier>
   <dc:identifier>001398428300001</dc:identifier>
   <dc:identifier>http://hdl.handle.net/11351/12812</dc:identifier>
   <dc:language>eng</dc:language>
   <dc:relation>Future Oncology;21(2)</dc:relation>
   <dc:relation>https://doi.org/10.1080/14796694.2024.2441107</dc:relation>
   <dc:rights>Attribution-NonCommercial-NoDerivatives 4.0 International</dc:rights>
   <dc:rights>http://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:format>application/pdf</dc:format>
   <dc:publisher>Taylor &amp; Francis</dc:publisher>
   <dc:source>Scientia</dc:source>
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