[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT05799248":3,"trial-entities:NCT05799248":97,"trial-summary:NCT05799248":102},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":6,"overall_status":7,"completion_date":8,"status_verified_date":9,"last_update_date":10,"start_date":11,"sponsor_name":12,"lead_sponsor_class":13,"has_dmc":14,"brief_summary":15,"detailed_description":16,"conditions":17,"keywords":19,"study_type":20,"primary_purpose":21,"phases":22,"enrollment_info":24,"interventions":27,"primary_outcomes":36,"secondary_outcomes":41,"sex":57,"minimum_age":58,"maximum_age":59,"healthy_volunteers":14,"eligibility_criteria":60,"std_ages":64,"locations":67,"central_contacts":89,"overall_officials":92,"references":95,"see_also_links":96},"NCT05799248","BED-IIT-437","Role of rhPSMA-7.3 PET\u002FCT Imaging in Men With High-Risk Prostate Cancer Following Conventional Imaging and Associated Changes in Medical Management","UNKNOWN","2024-05-28","2024-05","2024-05-24","2023-04-27","MidLantic Urology","OTHER",false,"Study Title: Role of rhPSMA-7.3 PET\u002FCT imaging in men with High-Risk prostate cancer following conventional imaging and associated changes in medical management Protocol number: BED-IIT-437 Phase: 3b Sponsor: MidLantic Urology Funding Organization: Blue Earth Diagnostics Ltd Study Design: This is a Phase 3b, multi-center, single-arm, diagnostic imaging study designed to detect metastatic lesions in men diagnosed with high-risk prostate cancer.","Consented patients will be screened to determine eligibility for the study prior to investigational product (IP) administration. In addition to their routine clinical work-up, which will include 99mtechnetium-biphosphonate bone scan and abdominal\u002Fpelvic computed tomography (CT) or magnetic resonance imaging (MRI) and chest CT per local practice, and before the scheduled radical prostatectomy (RP) and pelvic lymph node dissection (PLND), or radical pelvic radiation therapy, patients will receive 8 mCi (296 MBq) ± 20% rhPSMA-7.3, delivered as an intravenous (IV) bolus injection, followed by PET imaging. For each patient, the PET imaging results will be reported to the responsible physician prior to the planned treatment. Imaging results and further procedures\u002Ftreatment plan should be discussed with the patient within 7 days after rhPSMA-7.3 imaging (this may be conducted by telephone at the clinician's discretion). Within 45 days post-IP administration, the patient will receive treatment as follows:\n\n* Standard of care surgical treatment of PCa, including PLND; or\n* If the rhPSMA-7.3 PET scan detects M1 lesion(s):\n\n  * A biopsy\u002Fsurgery and\u002For additional imaging to confirm M1 lesion(s) will be required prior to initiation of treatment.\n\nThe purpose of this study is to assess the accuracy of rhPSMA-7.3 PET\u002FCT with conventional imaging for detecting metastatic disease in men with high-risk prostate cancer and the impact on medical management of these men. Accurate staging of newly diagnosed PCa assists in directing appropriate treatment strategies. In patients with high-risk PCa, the primary goal of imaging is to detect extra-prostatic disease. The identification of metastatic disease may significantly change the planned treatment regimen from locoregional to systemic therapy",[18],"Prostate Cancer",[],"INTERVENTIONAL","DIAGNOSTIC",[23],"PHASE3",{"count":25,"type":26},113,"ESTIMATED",[28],{"type":29,"name":30,"description":31,"armGroupLabels":32,"otherNames":34},"DRUG","rhPSMA-7.3 (18F)","Patients will receive a dose with an administered activity of 8 mCi (296 MBq) ± 20% of rhPSMA-7.3, delivered as an IV bolus injection with a 10 mL fast 0.9% sodium chloride flush, followed by PET imaging.",[33],"rhPSMA-7.3",[35],"radiohybrid PSMA-targeted PET imaging agent, Radioligand for PET CT scanning",[37],{"measure":38,"description":39,"timeFrame":40},"Prostate cancer upstaging","Compare the accuracy of rhPSMA-7.3 PET\u002FCT with conventional imaging for detecting metastatic disease and up-staging of disease in men with high-risk prostate cancer","15 months",[42,45,48,51,54],{"measure":43,"description":44,"timeFrame":40},"Verified Detection Rate of rhPSMA-7.3","To assess the Verified Detection Rate (VDR) for M1 disease of rhPSMA-7.3 PET\u002FCT findings (as determined by central BIE) on a patient level in with high-risk prostate cancer",{"measure":46,"description":47,"timeFrame":40},"Positive predictive value of rhPSMA-7.3","To assess the VDR and determine PPV for M1 disease of rhPSMA-7.3 PET\u002FCT findings (as determined by central BIE) on a patient level in patients with negative conventional imaging",{"measure":49,"description":50,"timeFrame":40},"Metastasis detection rate","Percentage of patients in which rhPSMA-7.3 PET\u002FCT imaging detects at least one verified M1 metastasis, as determined by central BIE",{"measure":52,"description":53,"timeFrame":40},"Metastasis detection rate with negative imaging","Percentage of patients with negative conventional imaging for M1 disease in whom rhPSMA-7.3 PET\u002FCT detects at least one verified M1 metastasis, as determined by central BIE",{"measure":55,"description":56,"timeFrame":40},"Positive predictive value of rhPSMA compared to biopsy","The PPV of rhPSMA-7.3 PET\u002FCT to detect distant disease compared to biopsy in those patients who undergo a distant disease biopsy on the basis of a rhPSMA-7.3 PET\u002FCT finding or in case of bony disease a correlation with MRI or biopsy","MALE","18 Years",null,{"inclusion":61,"exclusion":62,"raw_text":63},[],[],"Inclusion Criteria:\n\n1. Patient willing to provide signed informed consent and willing to comply with all required study schedule events, where safe and feasible.\n2. Patient is male and aged \\>18 years old.\n3. Histologically confirmed adenocarcinoma of the prostate.\n4. High risk prostate cancer. High-risk patients will be defined as having any of the following criteria: primary Gleason grade 4, or any Gleason grade 5, PSA ≥20, or clinical stage T3a (per NCCN Guidelines Version 2.2019; PROS-2).\n\nExclusion Criteria:\n\n1. Patients with any medical condition or circumstance (including receiving an IP) that the investigator believes may compromise the data collected or lead to a failure to fulfil the study requirements.\n2. Patients who are planned to have an x-ray contrast agent or other PET radiotracer \\\u003C24 hours prior to the PET scan.\n3. Patients currently receiving, or with a prior history of, androgen deprivation therapy (ADT; defined as surgical orchidectomy; luteinizing hormone-releasing hormone \\[LHRH\\] agonist alone \\[continuous or intermittent\\]; LHRH antagonist alone \\[continuous or intermittent\\]; administration or use of a first generation or second generation anti-androgen alone or in combination with an LHRH agonist\u002Fantagonist).\n4. Patients participating in an interventional clinical trial within 30 days and having received an IP within five biological half-lives prior to administration of rhPSMA-7.3.",[65,66],"ADULT","OLDER_ADULT",[68],{"facility":12,"status":69,"city":70,"state":71,"zip":72,"country":73,"contacts":74,"geoPoint":86},"RECRUITING","Bala-Cynwyd","Pennsylvania","19004","United States",[75,80,83],{"name":76,"role":77,"phone":78,"email":79},"Cheryl Zinar, RN, BSN","CONTACT","610-667-0458","czinar@midlanticurology.com",{"name":81,"role":82},"Laurence Belkoff, DO","PRINCIPAL_INVESTIGATOR",{"name":84,"role":85},"Zachariah Taylor, DO","SUB_INVESTIGATOR",{"lat":87,"lon":88},40.00761,-75.23407,[90],{"name":91,"role":77,"phone":78,"email":79},"Cheryl Zinar, RN,BSN",[93],{"name":94,"affiliation":12,"role":82},"Laurence Belkoff, DO, FACOS",[],[],{"nct_id":4,"conditions":98,"biomarkers":100},[99],"Prostate Carcinoma",[101],"KLK3 Gene",{"nct_id":4,"found":103,"summary":104,"prompt_version":114},true,{"design":105,"status":106,"heading":107,"summary":108,"follow_up":109,"word_count":110,"commitments":111,"compensation":112,"drugs_mentioned":113},"This is a Phase 3b study involving one group of participants. It is designed to test a diagnostic imaging method in men with high-risk prostate cancer.","completed","rhPSMA-7.3 PET\u002FCT Imaging for High-Risk Prostate Cancer","This study is looking at how a special imaging scan, called rhPSMA-7.3 PET\u002FCT, can help doctors treat men with high-risk prostate cancer. You would receive a dose of rhPSMA-7.3 (18F) through an IV, followed by a PET scan. This scan helps doctors find out if the cancer has spread. The main goal is to see if this scan changes how doctors plan your treatment, specifically if it leads to \"upstaging\" (meaning the cancer is found to be more advanced than initially thought). This study is for men aged 18 or older who have been diagnosed with high-risk prostate cancer. The study is currently unclear on its recruitment status and plans to enroll 113 participants.","The study will measure prostate cancer upstaging at 15 months after the imaging.",114,"You would have a rhPSMA-7.3 PET scan after your regular imaging tests. Your doctor will discuss the scan results with you within 7 days, and your treatment plan will be decided within 45 days.","Not stated in the trial record.",[30],"v2"]