{"id":9040,"date":"2026-04-16T10:56:01","date_gmt":"2026-04-16T08:56:01","guid":{"rendered":"https:\/\/inoc.it\/clinical-trials\/"},"modified":"2026-07-30T10:34:56","modified_gmt":"2026-07-30T08:34:56","slug":"clinical-trials","status":"publish","type":"page","link":"https:\/\/inoc.it\/en\/clinical-trials\/","title":{"rendered":"Clinical Trials"},"content":{"rendered":"\n<p class=\"wp-block-paragraph\">INOC is currently conducting <strong>over 200 clinical trials<\/strong> <strong>registered on international platforms<\/strong>, ranging from interventional studies\u2014across various stages of drug development\u2014to nursing and surgical studies. Among the areas of greatest innovation are: cell therapies and CAR-T therapies, cancer vaccines, oncolytic viruses, bispecific antibodies, antibody-drug conjugates, and molecularly targeted therapies. <\/p>\n\n<p class=\"wp-block-paragraph\">To support this research, INOC\u2019s advanced <strong>molecular diagnostics service<\/strong> is capable, for certain clinical cases, of <strong>analyzing over 500 genetic variants<\/strong> associated with more than 28 types of cancer, enabling precise guidance in treatment selection and facilitating access to targeted clinical trials.<\/p>\n\n<p class=\"wp-block-paragraph\"><strong>Use the search engine to find active clinical trials<\/strong> and see if there are any opportunities to participate that are suitable for your medical condition.<\/p>\n\t<div id=\"block_69fc900fe1f8d\" class=\"spacer-block acf-block\">\n\t\t\t\n\n<div class=\"w-full h-px my-6 lg:my-12\"><\/div>\n\n\t<\/div>\n\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-8f761849 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-constrained wp-block-column-is-layout-constrained\" style=\"flex-basis:33.33%\">\n<div class=\"facetwp-facet facetwp-facet-sc_search facetwp-type-search\" data-name=\"sc_search\" data-type=\"search\"><\/div>\n\n\n\n<div class=\"facetwp-facet facetwp-facet-sc_patologia facetwp-type-dropdown\" data-name=\"sc_patologia\" data-type=\"dropdown\"><\/div>\n\n\n\n<div class=\"facetwp-facet facetwp-facet-sc_fase facetwp-type-dropdown\" data-name=\"sc_fase\" data-type=\"dropdown\"><\/div>\n\n\n\n<div class=\"facetwp-facet facetwp-facet-sc_sperimentatore facetwp-type-dropdown\" data-name=\"sc_sperimentatore\" data-type=\"dropdown\"><\/div>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:66.66%\">\n<div class=\"wp-block-columns risultati is-layout-flex wp-container-core-columns-is-layout-8f761849 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<div class=\"facetwp-facet facetwp-facet-sc_risultati facetwp-type-pager\" data-name=\"sc_risultati\" data-type=\"pager\"><\/div>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<div class=\"facetwp-facet facetwp-facet-sc_clear facetwp-type-reset\" data-name=\"sc_clear\" data-type=\"reset\"><\/div>\n<\/div>\n<\/div>\n\n\n\n<hr class=\"azzurro\"\/><br\/>\n\n\n\t<div id=\"block_69fc900fe1fb6\" class=\"spacer-block acf-block\">\n\t\t\n\n<div class=\"w-full h-px my-2 lg:my-4\"><\/div>\n\n\t<\/div>\n\n\n\n<div class=\"facetwp-template\" data-name=\"studi_clinici\"><div class=\"fwpl-layout el-ozb9ph\"><div class=\"fwpl-result r1\"><div class=\"fwpl-row el-kr0ko\"><div class=\"fwpl-col fwpl-col el-z6g91n\"><div class=\"fwpl-item el-ekcivf sc_result_title\"><a href=\"https:\/\/inoc.it\/en\/clinical-study\/1456-0001\/\">1456-0001<\/a><\/div><div class=\"fwpl-item el-rloj4n sc_result_title_full\">A study to evaluate different doses of BI 18 31169, either alone or in combination with an anti-PD-1 antibody, in people with various types of advanced cancer (solid tumors).<\/div><div class=\"fwpl-item el-ozb9ph sc_result_patologia\">Diseases: <span class=\"fwpl-term fwpl-term-gastroenteric fwpl-tax-patologia\">Gastrointestinal tumor (GI tumor)<\/span>, <span class=\"fwpl-term fwpl-term-head-neck fwpl-tax-patologia\">Head and neck cancers<\/span>, <span class=\"fwpl-term fwpl-term-melanoma fwpl-tax-patologia\">Melanoma<\/span>, <span class=\"fwpl-term fwpl-term-pancreas fwpl-tax-patologia\">Pancreatic cancer<\/span><\/div><div class=\"fwpl-item el-82qagl sc_result_farmaco\">Medication: BI 1831169 (VSV-GP)\r\nBI 754091 (Ezabenlimab; anti-PD-1 mAb)<\/div><div class=\"fwpl-item el-akg5f sc_result_fase\"><span class=\"fwpl-term fwpl-term-fase-i fwpl-tax-fase\">FASE I<\/span><\/div><\/div><\/div><\/div><div class=\"fwpl-result r2\"><div class=\"fwpl-row el-kr0ko\"><div class=\"fwpl-col fwpl-col el-z6g91n\"><div class=\"fwpl-item el-ekcivf sc_result_title\"><a href=\"https:\/\/inoc.it\/en\/clinical-study\/8951-0305\/\">8951-0305<\/a><\/div><div class=\"fwpl-item el-rloj4n sc_result_title_full\">A Phase 3, Double-Blind, Randomized Study of Zolbetuximab in Combination with Pembrolizumab and Chemotherapy (CAPOX or mFOLFOX6) for the first-line treatment of locally advanced, unresectable, or metastatic gastric or gastroesophageal adenocarcinoma in participants whose tumors are HER2-negative, Claudin (CLDN) 18.2-positive, and whose combined positive scores (CPS) are greater than or equal to 1.<\/div><div class=\"fwpl-item el-ozb9ph sc_result_patologia\">Diseases: <span class=\"fwpl-term fwpl-term-gastroenteric fwpl-tax-patologia\">Gastrointestinal tumor (GI tumor)<\/span><\/div><div class=\"fwpl-item el-82qagl sc_result_farmaco\">Medication: Zolbetuximab in combination with pembrolizumab + (CAPOX or mFOLFOX6)  <\/div><div class=\"fwpl-item el-akg5f sc_result_fase\"><span class=\"fwpl-term fwpl-term-fase-iii fwpl-tax-fase\">FASE III<\/span><\/div><\/div><\/div><\/div><div class=\"fwpl-result r3\"><div class=\"fwpl-row el-kr0ko\"><div class=\"fwpl-col fwpl-col el-z6g91n\"><div class=\"fwpl-item el-ekcivf sc_result_title\"><a href=\"https:\/\/inoc.it\/en\/clinical-study\/andrometa-lung-713-m25-713\/\">AndroMETa-Lung-713 M25-713<\/a><\/div><div class=\"fwpl-item el-rloj4n sc_result_title_full\">A Phase 2\/3, open-label, randomized study of telisotuzumab adizutecan compared with standard of care in patients with locally advanced or metastatic non-squamous non-small cell lung cancer with an EGFR mutation, following progression on a third-generation TKI.<\/div><div class=\"fwpl-item el-ozb9ph sc_result_patologia\">Diseases: <span class=\"fwpl-term fwpl-term-polmone fwpl-tax-patologia\">Lung Cancer<\/span><\/div><div class=\"fwpl-item el-82qagl sc_result_farmaco\">Medication: Osimertinib \n, Telisotuzumab Adizutecan  <\/div><div class=\"fwpl-item el-akg5f sc_result_fase\"><span class=\"fwpl-term fwpl-term-fase-ii fwpl-tax-fase\">FASE II<\/span><\/div><\/div><\/div><\/div><div class=\"fwpl-result r4\"><div class=\"fwpl-row el-kr0ko\"><div class=\"fwpl-col fwpl-col el-z6g91n\"><div class=\"fwpl-item el-ekcivf sc_result_title\"><a href=\"https:\/\/inoc.it\/en\/clinical-study\/artemide-lung-04-d702gc00001\/\">Artemide Lung 04 - D702GC00001<\/a><\/div><div class=\"fwpl-item el-rloj4n sc_result_title_full\">A global, randomized, double-blind, multicenter Phase III study of Rilvegostomig or Pembrolizumab in combination with platinum-based chemotherapy for the first-line treatment of patients with metastatic non-small cell lung cancer whose tumors express PD-L1 (D702BC00001).<\/div><div class=\"fwpl-item el-ozb9ph sc_result_patologia\">Diseases: <span class=\"fwpl-term fwpl-term-polmone fwpl-tax-patologia\">Lung Cancer<\/span><\/div><div class=\"fwpl-item el-82qagl sc_result_farmaco\">Medication: Rilvegostomig \n, Pembrolizumab<\/div><div class=\"fwpl-item el-akg5f sc_result_fase\"><span class=\"fwpl-term fwpl-term-fase-iii fwpl-tax-fase\">FASE III<\/span><\/div><\/div><\/div><\/div><div class=\"fwpl-result r5\"><div class=\"fwpl-row el-kr0ko\"><div class=\"fwpl-col fwpl-col el-z6g91n\"><div class=\"fwpl-item el-ekcivf sc_result_title\"><a href=\"https:\/\/inoc.it\/en\/clinical-study\/axin\/\">AxIn<\/a><\/div><div class=\"fwpl-item el-rloj4n sc_result_title_full\">A Phase II study comparing the intensification of axitinib in combination with nivolumab versus nivolumab alone following induction therapy with nivolumab plus ipilimumab in patients with metastatic renal cell carcinoma (mRCC) who have not previously achieved a complete response.<\/div><div class=\"fwpl-item el-ozb9ph sc_result_patologia\">Diseases: <span class=\"fwpl-term fwpl-term-rene fwpl-tax-patologia\">Kidney cancer (renal cancer)<\/span><\/div><div class=\"fwpl-item el-82qagl sc_result_farmaco\">Medication: Axitinib in combination with nivolumab or nivolumab alone  <\/div><div class=\"fwpl-item el-akg5f sc_result_fase\"><span class=\"fwpl-term fwpl-term-fase-ii fwpl-tax-fase\">FASE II<\/span><\/div><\/div><\/div><\/div><div class=\"fwpl-result r6\"><div class=\"fwpl-row el-kr0ko\"><div class=\"fwpl-col fwpl-col el-z6g91n\"><div class=\"fwpl-item el-ekcivf sc_result_title\"><a href=\"https:\/\/inoc.it\/en\/clinical-study\/beamion-bcgc-1\/\">Beamion BCGC-1<\/a><\/div><div class=\"fwpl-item el-rloj4n sc_result_title_full\">A multicenter, randomized, open-label, Phase Ib dose-escalation and Phase II dose-optimization study of oral zongertinib (BI 1810631) alone or in combination with other agents for the treatment of patients with advanced HER2-positive metastatic breast cancer (mBC) and metastatic gastric, gastroesophageal junction, or esophageal adenocarcinoma (mGEAC).<\/div><div class=\"fwpl-item el-ozb9ph sc_result_patologia\">Diseases: <span class=\"fwpl-term fwpl-term-mammella fwpl-tax-patologia\">Breast Cancer<\/span>, <span class=\"fwpl-term fwpl-term-gastroenteric fwpl-tax-patologia\">Gastrointestinal tumor (GI tumor)<\/span><\/div><div class=\"fwpl-item el-82qagl sc_result_farmaco\">Medication: Oral zongertinib (BI 1810631) alone or in combination with other standard therapeutic agents.<\/div><div class=\"fwpl-item el-akg5f sc_result_fase\"><span class=\"fwpl-term fwpl-term-fase-ii fwpl-tax-fase\">FASE II<\/span><\/div><\/div><\/div><\/div><div class=\"fwpl-result r7\"><div class=\"fwpl-row el-kr0ko\"><div class=\"fwpl-col fwpl-col el-z6g91n\"><div class=\"fwpl-item el-ekcivf sc_result_title\"><a href=\"https:\/\/inoc.it\/en\/clinical-study\/bl-b01d1-lung-101\/\">BL-B01D1-LUNG-101<\/a><\/div><div class=\"fwpl-item el-rloj4n sc_result_title_full\">A Phase 1 Study Evaluating the Safety, Tolerability, and Efficacy of BL-B01D1 in Patients with Metastatic or Unresectable Non-Small Cell Lung Cancer.<\/div><div class=\"fwpl-item el-ozb9ph sc_result_patologia\">Diseases: <span class=\"fwpl-term fwpl-term-mammella fwpl-tax-patologia\">Breast Cancer<\/span>, <span class=\"fwpl-term fwpl-term-male-urologic-cancers fwpl-tax-patologia\">Male urologic cancers (urological tumors)<\/span><\/div><div class=\"fwpl-item el-82qagl sc_result_farmaco\">Medication: BL-B01D1 (anti-EGFR and anti-HER3 antibody)<\/div><div class=\"fwpl-item el-akg5f sc_result_fase\"><span class=\"fwpl-term fwpl-term-fase-i fwpl-tax-fase\">FASE I<\/span><\/div><\/div><\/div><\/div><div class=\"fwpl-result r8\"><div class=\"fwpl-row el-kr0ko\"><div class=\"fwpl-col fwpl-col el-z6g91n\"><div class=\"fwpl-item el-ekcivf sc_result_title\"><a href=\"https:\/\/inoc.it\/en\/clinical-study\/bnt324-010\/\">BNT324-010<\/a><\/div><div class=\"fwpl-item el-rloj4n sc_result_title_full\">A Phase Ib\/II, multicenter, open-label, two-part study to evaluate the efficacy, safety, pharmacokinetics, and recommended dose of the combination of BNT324 and BNT327 in participants with advanced lung cancer.<\/div><div class=\"fwpl-item el-ozb9ph sc_result_patologia\">Diseases: <span class=\"fwpl-term fwpl-term-polmone fwpl-tax-patologia\">Lung Cancer<\/span><\/div><div class=\"fwpl-item el-82qagl sc_result_farmaco\">Medication: BNT324 (antibody conjugate targeting B7-H3)\nBNT327 - Pumitamig (bispecific antibody for PD-L1 and VEGF-A)<\/div><div class=\"fwpl-item el-akg5f sc_result_fase\"><span class=\"fwpl-term fwpl-term-fase-ii fwpl-tax-fase\">FASE II<\/span><\/div><\/div><\/div><\/div><div class=\"fwpl-result r9\"><div class=\"fwpl-row el-kr0ko\"><div class=\"fwpl-col fwpl-col el-z6g91n\"><div class=\"fwpl-item el-ekcivf sc_result_title\"><a href=\"https:\/\/inoc.it\/en\/clinical-study\/bnt324-03\/\">BNT324-03<\/a><\/div><div class=\"fwpl-item el-rloj4n sc_result_title_full\">A Phase III, randomized, open-label study comparing BNT324 with docetaxel plus prednisone\/prednisolone in patients with castration-resistant metastatic prostate cancer.<\/div><div class=\"fwpl-item el-ozb9ph sc_result_patologia\">Diseases: <span class=\"fwpl-term fwpl-term-male-urologic-cancers fwpl-tax-patologia\">Male urologic cancers (urological tumors)<\/span><\/div><div class=\"fwpl-item el-82qagl sc_result_farmaco\">Medication: BNT324 vs. Docetaxel <\/div><div class=\"fwpl-item el-akg5f sc_result_fase\"><span class=\"fwpl-term fwpl-term-fase-iii fwpl-tax-fase\">FASE III<\/span><\/div><\/div><\/div><\/div><div class=\"fwpl-result r10\"><div class=\"fwpl-row el-kr0ko\"><div class=\"fwpl-col fwpl-col el-z6g91n\"><div class=\"fwpl-item el-ekcivf sc_result_title\"><a href=\"https:\/\/inoc.it\/en\/clinical-study\/c6461013\/\">C6461013<\/a><\/div><div class=\"fwpl-item el-rloj4n sc_result_title_full\">A Phase 1\/2a, open-label, dose-finding study to evaluate the safety, tolerability, pharmacokinetics, and preliminary efficacy of combinations of BMS-986507 (BL-B01D1) in adult participants with advanced solid tumors.<\/div><div class=\"fwpl-item el-ozb9ph sc_result_patologia\">Diseases: <\/div><div class=\"fwpl-item el-82qagl sc_result_farmaco\">Medication: PF-08634404 as monotherapy versus standard combination therapy.<\/div><div class=\"fwpl-item el-akg5f sc_result_fase is-empty\"><\/div><\/div><\/div><\/div><\/div>\n<style>\n.fwpl-layout, .fwpl-row {\n    display: grid;\n}\n.fwpl-layout.el-ozb9ph {\n    grid-template-columns: repeat(1, 1fr);\n    grid-gap: 10px;\n}\n.fwpl-btn {\n    text-decoration: none;\n}\n.fwpl-row.el-kr0ko {\n    grid-template-columns: 1fr;\n}\n@media (max-width: 480px) { \n    body .facetwp-template .fwpl-layout,  \n    body .facetwp-template-static .fwpl-layout { grid-template-columns: 1fr; } \n} \n\n<\/style>\n<\/div>\n\n\n\n<div class=\"facetwp-facet facetwp-facet-sc_pager facetwp-type-pager\" data-name=\"sc_pager\" 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