[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"cholangiocarcinoma-recurrent\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:cholangiocarcinoma-recurrent":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100482949","phase-1-synkir-110-for-mesothelin-expressing-ovarian-cancer-cholangiocarcinoma-or-mesothelioma-100482949",false,"NCT05568680","SynKIR-110 for Mesothelin Expressing Ovarian Cancer, Cholangiocarcinoma or Mesothelioma","A Phase 1 Study of SynKIR-110, Autologous T Cells Transduced With Mesothelin KIR-CAR, in Subjects With Mesothelin-Expressing Advanced Ovarian Cancer, Cholangiocarcinoma, or Mesothelioma","Inclusion Criteria:\n\n* Pathologically confirmed recurrent or relapsed advanced ovarian cancer, primary peritoneal cancer, fallopian tube cancer, cholangiocarcinoma, or epithelial mesothelioma (pleural or peritoneal) after at least 1 prior line of systemic therapy for advanced disease\n* Adult 18 years of age or older.\n* Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1.\n* Has at least 1 measurable lesion by iRECIST for ovarian cancer or cholangiocarcinoma or lesions measurable for mRECIST for mesothelioma.\n* Satisfactory Blood coagulation parameters\n* Satisfactory organ and bone marrow function\n\nExclusion Criteria:\n\n* Active invasive cancers other than mesothelioma, cholangiocarcinoma, and ovarian unless surgically and medically cured without evidence of recurrent disease for 5 years.\n* History of T or B cell malignancies or previous gene-engineered T cell therapies.\n* Sarcomatoid\u002Fbiphasic mesothelioma.\n* Pulmonary exclusions\n* Have acquired hereditary, congenital immunodeficiency or have recognized immunodeficiency disease\n* Active hepatitis B, active hepatitis C, or any HIV infection at the time of screening\n* Active autoimmune disease","ALL","18 Years",{"count":19,"type":20},42,"ESTIMATED","INTERVENTIONAL",[23],"PHASE1","This first-in-human (FIH) trial is designed to assess the safety, feasibility, and potential activity of a single intravenous (IV) dose of SynKIR-110 administered to subjects with mesothelin-expressing advanced ovarian cancer, mesothelioma, and cholangiocarcinoma.",[26,27,28],"Ovarian Cancer","Cholangiocarcinoma Recurrent","Mesothelioma, Malignant","RECRUITING","2026-06-23",{"date":32,"type":33},"2026-06-24","ACTUAL",{"date":35,"type":33},"2023-03-30",{"date":37,"type":20},"2027-12",{"name":39,"class":40},"Verismo Therapeutics","INDUSTRY",5,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":21,"phases":53,"briefSummary":55,"conditions":56,"keywords":59,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":72},"100581472","en-bloc-resection-of-the-liver-and-pancreas-with-a-non-touch-technique-followed-by-liver-transplantation-to-improve-the-overall-survival-in-patients-with-non-resectable-hilar-cholangiocarcinoma-beyond-the-mayo-clinic-transplant-criteria-100581472","NCT06850753","En Bloc Resection of the Liver and Pancreas With a \"Non-touch\" Technique Followed by Liver Transplantation to Improve the Overall Survival in Patients With Non-resectable Hilar Cholangiocarcinoma Beyond the Mayo Clinic Transplant Criteria","Superior Right Abdominal Excentration and Liver Transplantation (SURE-LT) for Perihilar Cholangiocarcinoma","SURE-LT","Inclusion Criteria:\n\n* Histologically verified or strong suspicion of cholangiocarcinoma based on radiology and endoscopy and elevated Ca 19-9 \\> 100U\u002FL\n* Perihilar cholangiocarcinoma that is deemed unresectable based on tumor location or severity of the underlying liver disease. Perihilar recurrence in PSC patients more than 24 months following the previous resection (N0, R0, no macrovascular involvement) is accepted.\n* Patients should not be eligible for liver transplantation according to the Mayo protocol criteria.\n* Tumor involvement of the hepatic artery distal to the gastroduodenal artery or the portal vein without tumor thrombus is accepted.\n* No evidence of distant metastasis or metastatic lymph node (M1) involvement (para-aortic, coeliac or para-colic)\n* Good performance status Eastern Cooperative Oncology Group (ECOG) performance status score 0 or 1\n* At least 6 months of observation time during which the patient should be treated by chemotherapy and radiation (hyperfractioned 30-50 Gy) with response or stable disease before listing for LT. Patients with PSC and significant liver dysfunction that restricts the tolerability of chemoradiotherapy may be considered on an individual basis\n\nExclusion Criteria:\n\n* Radiological signs of tumor invasion along intended resection borders\n* Direct tumor invasion of the pancreatic head\n* Signs of spread to the para-aortic, superior mesenteric, or coeliac lymph nodes\n* Perforation of the visceral peritoneum\n* Weight loss \\>10% in the last six months\n* Patient BMI \\> 30 kg\u002Fm2\n* Other malignancies, except curatively treated basal cell carcinoma or other tumors with disease-free interval \\> five years without relapse. The final decision on acceptable previous cancer diagnoses is at the principal investigator's discretion.\n* Known history of human immunodeficiency virus (HIV) infection\n* Substance abuse, medical, psychological, or social conditions that may interfere with the patient's participation in the study or evaluation of the study results\n* Known hypersensitivity to rapamycin\n* Prior metastatic disease\n* Women who are pregnant or breastfeeding\n* Any reason why, in the opinion of the investigator, the patient should not participate","70 Years",{"count":52,"type":20},15,[54],"NA","Surgery for hilar cholangiocarcinoma (phCCA) remains a significant challenge. The minority of patients who are eligible for resection are exposed to high procedure-related morbidity and mortality, and despite apparent R0 resection, cancer recurrence is common. The benefit of R1 resection compared to the best palliative chemotherapy has been questioned. The concept of extended surgery to achieve better radicality is controversial and in many instances, associated with higher procedure-related risk and unclarified oncological benefit. For unresectable patients, liver transplantation, per the Mayo protocol, remains the only alternative for a few patients.\n\nOptimal staging pre- and intraoperatively is problematic since only the local biliary ductal involvement and, to a certain extent, lymph node dissemination can be reasonably correctly assessed. The reliability and validity of the intraoperative frozen section have been questioned. Furthermore, microscopic tumor cell affection leading to recurrent disease has been found in 16% of presumed N0 lymph nodes when analyzed by immunohistochemistry, and patients with nodal micrometastasis showed the same dismal survival as those with positive nodes on regular pathology (pN1).\n\nTaken together, there is a lack of good surgical options for patients with marginally or unresectable phCCA that do not satisfy current criteria for liver transplantation.\n\nThe practical problem in the current surgical techniques for hilar cholangiocarcinoma, particularly in locally advanced disease, is that the hepatoduodenal ligament, in most instances, represents an incompletely staged operative field, making the probability of obtaining true free margins uncertain.\n\nAn alternative procedure must, therefore, consider the anatomical and multidimensional pattern of dissemination and the limitations in the accurate staging of phCCA, and this suggests that a wider surgical margin is needed to obtain radical resection in locally advanced phCCA.\n\nThe aim of the current study is tho these the following hypothesis:\n\nLocally advanced hilar cholangiocarcinoma without M1 lymph node metastatic disease can be radically resected by extending the surgical margin to include the complete hepatobiliary axis and the main anatomical trajectories of local and regional dissemination through an \"en-bloc\" surgical approach.\n\nM1 metastatic disease is defined as positive nodes in the following locations at staging:\n\n* Station 9: lymph nodes around the celiac axis.\n* Station 14: lymph nodes along the superior mesenteric artery or vein.\n* Station 15: lymph nodes along the middle colic vein.\n* Station 16: para-aortic lymph nodes.\n\nPatients will be treated by chemotherapy and radiation therapy with an observation period of at least 6 months showing response or stable disease before final inclusion.\n\nThe operative procedure consists of a superior right abdominal exenteration, including the liver, pancreas, spleen, and vena cava + liver transplantation. If islets are available from the same donor, this will be administered postoperatively according to the institutional protocol.\n\nMain enpoint is overall survival at 1, 3 and 5 years",[57,27,58],"Cholangiocarcinoma Non-resectable","Liver Transplantation",[60,61],"hilar cholangiocarcinoma","Liver transplantation","2025-08-15",{"date":64,"type":33},"2025-08-21",{"date":66,"type":33},"2025-01-01",{"date":68,"type":20},"2030-12-31",{"name":70,"class":71},"Oslo University Hospital","OTHER",1]