[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Jiangsu Healthy Life Innovation Medical Technology Co., Ltd\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":88},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,40,66],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100489464","phase-3-clinical-study-of-tumor-treating-fields-combined-with-gemcitabine-and-albumin-bound-paclitaxel-in-the-first-line-treatment-of-locally-advanced-pancreatic-cancer-100489464",false,"NCT05653453","Clinical Study of Tumor Treating Fields Combined with Gemcitabine and Albumin-bound Paclitaxel in the First-line Treatment of Locally Advanced Pancreatic Cancer","Inclusion Criteria:\n\n1. Subjects aged between 18 and 75 (including 18 and 75) of both genders;\n2. Expected survival time ≥3 months;\n3. Pancreatic adenocarcinoma confirmed by histology\u002Fcytology;\n4. Locally advanced lesions meeting any of the following criteria without distant metastasis: ① Pancreatic head and neck tumors: a. The tumor invaded the Superior Mesenteric Artery (SMA) more than 180°; b. The tumor invaded the celiac trunk more than 180°; c. Unresectable reconstruction of superior mesenteric vein or portal vein due to tumor invasion or embolism (tumor thrombus or thrombus); d. The tumor extensively invaded the distal jejunal drainage branch of the superior mesenteric vein. ② Pancreatic body\u002Ftail tumor: a. The tumor invaded the superior mesenteric artery or celiac trunk more than 180°; b. Celiac trunk and abdominal aorta involvement; c. The superior mesenteric vein or portal vein cannot be resected and reconstructed due to tumor invasion or embolism (tumor thrombus or thrombus).\n5. At least one measurable lesion according to revised RECIST version 1.1;\n6. ECOG score 0-1;\n7. Be able to receive gemcitabine for injection and paclitaxel for injection (albumin-bound) combined therapy according to medical advice;\n8. Able to operate tumor treating fields independently or with the help of nursing staff;\n9. AE should be restored to normal or CTCAE1 grade after previous treatment;\n10. The serum pregnancy test results of female subjects of reproductive age were negative. Female subjects of reproductive age agree to use effective contraception (e.g. hormonal or barrier methods or abstinence) during the study period and for 6 months after the last dose of chemotherapy drugs;\n11. Male subjects agree to use effective birth control (such as barrier method or abstinence) and not to donate sperm during the study and within 3 months after the last chemotherapy drug administration;\n12. Voluntarily sign the informed consent.\n\nExclusion Criteria:\n\n1. The subjects has previously received first-line treatment for pancreatic adenocarcinoma;\n2. Subjects with contraindications to treatment with gemcitabine for injection and\u002For paclitaxel for injection (albumin-bound) or known severe allergies to gemcitabine for injection and\u002For paclitaxel for injection (albumin-bound);\n3. Patients had cancer requiring other antitumor therapy within 2 years before enrollment, excluding treated stage I prostate cancer, cervical cancer in situ, breast cancer in situ, and non-melanoma skin cancer;\n4. Abnormal bone marrow, heart, liver and kidney function: a. Neutrophil count \\\u003C 1.5 × 10\\^9\u002FL, platelet count \\\u003C 100 × 10\\^9\u002FL, hemoglobin \\\u003C 90g\u002FL; The use of blood transfusion, platelet transfusion and erythropoietin was prohibited within 14 days before C1D1, and the use of Leukocytotropic drug such as G-CSF, fegrasstim, pefegrasstim, etc., was prohibited within 7 days before C1D1.b. Total bilirubin \\> 1.5× Upper Limit of Normal (ULN); Subjects with a total bilirubin \\> 2×ULN that is elevated due to pancreatic cancer compression of the bile duct but has been fitted with a bile duct stent for drainage can be enrolled. AST and\u002For ALT\\> 2.5×ULN; the use of drugs that improve liver function, such as reducing transaminase was prohibited within 7 days before C1D1. c. Serum creatinine \\> 1.5×ULN; d. A history of severe cardiovascular disease, including but not limited to second or third degree heart block; Severe ischemic heart disease; New York Heart Association (NYHA) class II or higher congestive heart failure (mild physical activity limitation; Comfortable at rest, but normal activities can cause fatigue, palpitations, or difficulty breathing);\n5. Subjects who were required to receive systemic corticosteroids (doses equivalent to \\> 10 mg prednisone\u002Fday) or other immunosuppressive agents within 14 days before enrollment or during the study period. Subjects were eligible for enrollment if: a. The use of topical or inhaled glucocorticoids is permitted; b. Allow short-term (≤7 days) use of glucocorticoids for the prevention or treatment of non-autoimmune allergic diseases;\n6. Those who had severe infection before the first dose were judged ineligible for the study by the investigator;\n7. History of human immunodeficiency virus (HIV) infection (known HIV1\u002F2 antibody positive);\n8. The presence of active hepatitis B, active hepatitis C, or other active infections that may affect the patient's treatment as determined by the investigator;\n9. Subjects with a clear history of neurological or psychiatric disorders, such as epilepsy, dementia, or substance abuse (including alcohol) within the last year, and possibly affecting compliance;\n10. Infected, ulcerated or unhealed wounds exist on the skin where the tumor treating fields is applied;\n11. Having an implantable electronic medical device, such as a pacemaker;\n12. Metal medical instruments are implanted in the chest and abdomen such as bone nails;\n13. Known allergies to medical adhesives or hydrogels;\n14. Pregnant or breastfeeding;\n15. Subjects participated in clinical trials of other drugs within 3 months before enrollment, or participated in clinical trials of other devices within 1 month before enrollment;\n16. Subjects with poor compliance or other factors as judged by the investigator.","ALL","18 Years","75 Years",{"count":19,"type":20},512,"ESTIMATED","INTERVENTIONAL",[23],"PHASE3","The Objectives of this clinical trial is to evaluate the efficacy and safety of tumor treating fields combined with gemcitabine and albumin bound paclitaxel in the treatment of locally advanced pancreatic cancer.",[26],"Locally Advanced Pancreatic Cancer","RECRUITING","2025-03-20",{"date":30,"type":31},"2025-03-24","ACTUAL",{"date":33,"type":31},"2022-12-20",{"date":35,"type":20},"2027-09-28",{"name":37,"class":38},"Jiangsu Healthy Life Innovation Medical Technology Co., Ltd","INDUSTRY",5,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":47,"targetDuration":4,"studyType":21,"phases":49,"briefSummary":51,"conditions":52,"keywords":54,"overallStatus":57,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":4},"100571171","tumor-treating-fields-ttf-in-combination-with-stereotactic-radiosurgerysrs-for-brain-metastases-from-non-small-cell-lung-cancer-100571171","NCT06716775","Tumor Treating Fields (TTF) in Combination with Stereotactic Radiosurgery(SRS) for Brain Metastases from Non-small Cell Lung Cancer.","Tumor Treating Fields (TTF) in Combination with Stereotactic Radiosurgery(SRS) for Brain Metastases from Non-small Cell Lung Cancer: a Randomized, Controlled, Open-label Study.","Inclusion Criteria:\n\n1. The age of the subject was between 18 and 75 years old (inclusive), regardless of gender;\n2. The predicted survival time was ≥3 months;\n3. Newly diagnosed with NSCLC brain metastasis;\n4. MRI imaging showed 1-10 unresectable brain metastases;\n5. Karnofsky performance status (KPS) score ≥70;\n6. Able to operate the TTF independently or with the help of a caregiver;\n7. Subjects of childbearing potential had to agree to use effective contraception for the duration of the trial;\n8. Voluntarily signed the informed consent form.\n\nExclusion Criteria:\n\n1. Positive driver genes;\n2. Recurrent brain metastasis of NSCLC;\n3. Suffering from severe cerebral edema;\n4. Leptomeningeal metastases;\n5. Participants had to meet certain criteria for bone marrow, liver and kidney function before enrollment, and were not eligible if they had any of the following:\n\n   1. platelet count \\\u003C 100×103\u002FμL;\n   2. absolute neutrophil count \\\u003C 1.5×103\u002FμL;\n\n   d. AST or ALT exceeding 2.5 times the upper limit of normal; c.Total bilirubin more than 1.5 times the upper limit of the normal range; d.Severe renal impairment (serum creatinine \\>1.7 mg\u002FdL, or \\>150 μmol\u002FL);\n6. There were infection, ulcer and unhealed wound in the skin where the electrode was applied；\n7. Patients allergic to conductive hydrogels or medical adhesives;\n8. Those who are pregnant or preparing to become pregnant or who are breastfeeding;\n9. Patients with poor compliance, as judged by the investigator, or other factors considered by the investigator to be not suitable for the study.",{"count":48,"type":20},200,[50],"NA","This is a randomized, controlled, open-label, phase III trials. The main purpose of this study is to evaluate the effectiveness and safety of tumor treating felds (TTF) combined with stereotactic radiosurgery (SRS) in the treatment of brain metastases from non-small cell lung cancer (NSCLC) .",[53],"NSCLC Brain Metastasis",[55,56],"TTF","NSCLC brain metastasis","NOT_YET_RECRUITING","2024-12-02",{"date":60,"type":31},"2024-12-04",{"date":62,"type":20},"2024-12-20",{"date":64,"type":20},"2028-10-30",{"name":37,"class":38},{"id":67,"slug":68,"hasResults":11,"nctId":69,"briefTitle":70,"officialTitle":71,"acronym":4,"eligibilityCriteria":72,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":17,"enrollmentInfo":73,"targetDuration":4,"studyType":21,"phases":75,"briefSummary":76,"conditions":77,"keywords":4,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":79,"lastUpdatePostDateStruct":80,"startDateStruct":82,"completionDateStruct":84,"leadSponsor":86,"locationsCount":87},"100563067","a-study-of-tumor-treating-fields-in-combination-with-durvalumab-and-gemcitabinecisplatin-in-biliary-tract-cancers-100563067","NCT06611345","A Study of Tumor-Treating Fields in Combination With Durvalumab and Gemcitabine\u002FCisplatin in Biliary Tract Cancers","A Single-Arm, Phase 1b Study to Assess Tumor-Treating Fields (TTF) in Combination With Durvalumab and Gemcitabine\u002FCisplatin (GemCis) as the First-Line Treatment of Unresectable Biliary Tract Cancers (BTC)","Inclusion Criteria:\n\n1. Willing and able to provide written informed consent for the trial.\n2. Male or female patients between the ages of 18 and 75 years (including 18 and 75 years).\n3. Body weight \\> 30 kg.\n4. Histologically confirmed, unresectable adenocarcinoma of the biliary tract, including cholangiocarcinoma (intrahepatic or extrahepatic) and gallbladder carcinoma.\n5. Patients with the previously untreated disease if unresectable or metastatic at initial diagnosis will be eligible.\n6. Patients with recurrent disease \\>6 months after curative surgery or \\>6 months after the completion of adjuvant therapy (chemotherapy and\u002For radiation) will be eligible (but he\u002Fshe does not receive systemic treatment as the first-line therapy).\n7. At least 1 measurable lesion that qualifies as a RECIST 1.1 Target Lesion (TL) at baseline.\n8. ECOG PS of 0 or 1.\n9. Life expectancy ≥12 weeks at the time of screening.\n10. No prior exposure to immune-mediated therapy, including, but not limited to, other anti-CTLA-4, anti-PD-1, anti-PD-L1, and anti-PD-L2 antibodies, excluding therapeutic anticancer vaccines.\n11. Patients must have adequate organ function as indicated by the following laboratory values: Hemoglobin ≥9.0 g\u002FdL; Absolute neutrophil count ≥1.5 ×109\u002FL; Platelet count ≥100 ×109\u002FL. No blood transfusion, granulocyte colony-stimulating factor (G-CSF), filgrastim and other drugs are used within 2 weeks before the examination. Serum bilirubin ≤2.0 × the upper limit of normal (ULN); This will not apply to patients with confirmed Gilbert's syndrome. Any clinically significant biliary obstruction should be resolved before treatment. Alanine aminotransferase (ALT) and aspartate aminotransferase (AST) ≤2.5 × ULN; for patients with hepatic metastases, ALT and AST ≤5 × ULN. Creatinine clearance (CL) \\>50 mL\u002Fmin per 24-hour urine or as calculated by Cockroft and Gault formula (using actual body weight).\n12. Patients (women of childbearing potential and males with fertile female partners) must be willing to use the currently accepted reliable contraception method from the time of screening throughout the total duration of the study treatment and the drug washout period (180 days after the last dose of GemCis or 90 days after the last dose of durvalumab monotherapy). These measures include, but are not limited to, oral or implantable injections of hormonal contraceptives; intrauterine birth control ring or placement of IUS intrauterine device); or use of barrier methods such as condoms or septum and spermicide products. Postmenopausal women over 50 years of age must have been amenorrheic for at least 12 months to be considered non-childbearing potential.\n13. Patients with HBV infection (as characterized by positive hepatitis B surface antigen \\[HBsAg\\] and\u002For anti-hepatitis B core antibodies (anti-HBc) with detectable HBV deoxyribonucleic acid (DNA) \\[above the limit of detection per local laboratory\\]) must receive antiviral therapy prior to treatment per institutional practice to ensure adequate viral suppression. Patients must remain on antiviral therapy for the study duration and for 6 months after the last dose of study treatment. Patients who test positive for anti-HBc with undetectable HBV DNA (under the limit of detection per local laboratory) do not require antiviral therapy unless HBV DNA reaches detectable limits per local laboratory during the course of treatment. Patients with active co-infection of HBV and HCV as evidenced by positive anti-HCV antibody and actively co-infected with HBV and hepatitis D virus are not eligible.\n14. Able to operate TTF device independently or with the help of a caregiver.\n\nExclusion Criteria:\n\n1. Patients previously received systemic treatment as the first-line therapy.\n2. Ampullary carcinoma.\n3. History of allogeneic organ transplantation.\n4. Active or prior documented autoimmune or inflammatory disorders (including inflammatory bowel disease \\[e.g., colitis or Crohn's disease\\], diverticulitis \\[with the exception of diverticulosis\\], systemic lupus erythematosus, Sarcoidosis syndrome, or Wegener syndrome \\[granulomatosis with polyangiitis, Graves' disease, rheumatoid arthritis, hypophysitis, uveitis, etc.\\]). The following are exceptions to this criterion: Patients with vitiligo or alopecia; Patients with hypothyroidism (e.g., following Hashimoto syndrome) are stable on hormone replacement; Any chronic skin condition that does not require systemic therapy; Patients without active disease in the last 5 years may be included but only after consultation with the investigator\u002F Study Physician; Patients with celiac disease controlled by diet alone.\n5. Uncontrolled intercurrent illness, including, but not limited to, symptomatic congestive heart failure, uncontrolled hypertension, unstable angina pectoris, uncontrolled cardiac arrhythmia, active interstitial lung disease (ILD), serious chronic gastrointestinal conditions associated with diarrhea, or psychiatric illness\u002Fsocial situations that would limit compliance with study requirement, substantially increase the risk of incurring AEs, or compromise the ability of the patient to give written informed consent.\n6. History of another primary malignancy, except for: Malignancy was treated with curative intent and with no known active disease ≥5 years before the first dose of the investigational product (IP) and of low potential risk for recurrence; Adequately treated non-melanoma skin cancer or lentigo maligna without evidence of disease; Adequately treated carcinoma in situ without evidence of disease.\n7. History of leptomeningeal carcinomatosis.\n8. History of active primary immunodeficiency.\n9. Active infection, including tuberculosis (clinical evaluation that includes clinical history, physical examination and radiographic findings, and tuberculosis testing in line with local practice), or human immunodeficiency virus (positive HIV 1\u002F2 antibodies).\n10. Any unresolved toxicity NCI CTCAE Grade ≥2 from a previous anticancer therapy, with the exception of alopecia, vitiligo, and the laboratory values defined in the inclusion criteria. Patients with Grade ≥2 neuropathy will be evaluated on a case-by-case basis after consultation with the Study Physician. Patients with irreversible toxicity not reasonably expected to be exacerbated by treatment with durvalumab may be included only after consultation with the Study Physician.\n11. Brain metastases or spinal cord compression (including asymptomatic and adequately treated disease). Patients with suspected brain metastases at screening should have an MRI (preferred) or CT scan, each preferably with IV contrast of the brain prior to study entry.\n12. Known allergy or hypersensitivity to any of the study drugs or any of the study drug excipients.\n13. Any concurrent chemotherapy, IP, biologic, or hormonal therapy for cancer treatment. Concurrent use of hormonal therapy for non-cancer-related conditions (e.g., hormone replacement therapy) is acceptable.\n14. Radiation therapy, including palliative radiation, is not allowed before the study, with an exception of radiation given in an adjuvant setting.\n15. Receipt of live attenuated vaccine within 30 days prior to the first dose of IP. Note that patients, if enrolled, should not receive a live vaccine while receiving IP and up to 30 days after the last dose of IP.\n16. Major surgical procedure (as defined by the investigator) within 28 days prior to the first dose of IP. Note that minor surgery of isolated lesions for palliative intent is acceptable if performed more than 14 days prior to the first dose of IP.\n17. Patients who have received prior immune-mediated therapy, including, but not limited to, other anti-PD-1, anti-PD-L1, or anti-CTLA-4.\n18. Prior locoregional therapy such as radioembolization.\n19. Current or prior use of immunosuppressive medication within 14 days before the first dose of durvalumab. The following are exceptions to this criterion: Intranasal, inhaled, or topical steroids, or local steroid injections (e.g., intra-articular injection); Systemic corticosteroids at physiologic doses not to exceed 10 mg\u002Fday of prednisone or its equivalent; Steroids as premedication for hypersensitivity reactions (e.g., CT scan premedication).\n20. Participation in another clinical study with an IP administered in the last 3 months.\n21. Previous IP assignment in the present study.\n22. Concurrent enrollment in another clinical study, unless it is an observational (non-interventional) clinical study or during the follow-up period of an interventional study.\n23. Prior randomization or treatment in a previous durvalumab clinical study, regardless of treatment arm assignment.\n24. Female patients who are pregnant or breastfeeding or male or female patients of reproductive potential who are not willing to use effective birth control from screening to 180 days after the last dose of GemCis or 90 days after the last dose of durvalumab monotherapy.\n25. Judgment by the investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions, and requirements.\n26. Active infection of hepatitis C as evidenced by detectable HCV RNA per local laboratory. Patients who test positive for hepatitis C (HCV) antibody may be enrolled if HCV RNA is undetectable.\n27. Known allergy or hypersensitivity to medical adhesives or hydrogel.\n28. Implantable electronic medical devices such as cardiac pacemakers.\n29. Metallic medical devices, such as bone nails, were implanted in the chest and abdomen.\n30. Patients with infection, ulcer or unhealed wound at the electrode application site.\n31. Patients with symptomatic ascites, pleural effusion, pericardial effusion, etc., unless the condition is well controlled after clinical treatment (including therapeutic puncture).",{"count":74,"type":20},60,[50],"Unresectable BTC represents an area of unmet medical need due to its very aggressive nature, limited treatment options, and poor prognosis. This study is to evaluate the efficacy and safety of adding TTF to the established regimen of durvalumab plus GemCis for the treatment of patients with previously untreated, unresectable BTC.",[78],"Biliary Tract Cancers (BTC)","2024-10-24",{"date":81,"type":31},"2024-10-26",{"date":83,"type":31},"2024-10-21",{"date":85,"type":20},"2027-03-30",{"name":37,"class":38},1,""]