[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"GT Medical Technologies, Inc.\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":83},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,55],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":43,"lastUpdatePostDateStruct":44,"startDateStruct":47,"completionDateStruct":49,"leadSponsor":51,"locationsCount":54},"100607979","phase-3-beginning-radiation-immediately-with-gammatile-at-gbm-excision-versus-standard-of-care-100607979",false,"NCT07195591","Beginning Radiation Immediately With GammaTile at GBM Excision Versus Standard of Care","Randomized Study of Resection and GammaTile® Followed by Concurrent External Beam Radiation Therapy (EBRT) and Temozolomide (TMZ) and Adjuvant TMZ Versus Standard of Care in Newly Diagnosed Glioblastoma (GBM)","BRIDGES","Major Criteria Includes the Following:\n\nInclusion Criteria\n\n* Patients must be ≥18 years of age.\n* Have radiographic suspicion of newly diagnosed glioblastoma (GBM).\n\n  o If final pathology reports IDH mutant glioma, then the patients found to have an IDH mutation will be followed for safety and QoL measures but will not be included in the primary and secondary comparative survival and efficacy analyses.\n* Are medically and surgically appropriate for resection.\n* Have an estimated Karnofsky Performance Scale (KPS) score of ≥70.\n* Are able to receive standard of care treatment.\n\nExclusion Criteria\n\n* A previous biopsy diagnosis other than IDH wild-type GBM.\n* Have contraindications to TMZ, magnetic resonance imaging, gadolinium, or non-contrast computed tomography.\n* Have multi-focal enhancing tumors that cannot be encompassed in one operative field.","ALL","18 Years",{"count":20,"type":21},766,"ESTIMATED","INTERVENTIONAL",[24],"PHASE3","This is a Phase 3 prospective, randomized, superiority, open-label, multi-site study. The overview of this study is as follows:\n\n* A Screening\u002FBaseline Period of 21 days. During this time, patients will be randomized into a 1:2 allocation of Arm A:Arm B.\n* A Perioperative\u002FOperative Phase where patients will undergo tumor resection (Arm A) or tumor resection plus GammaTile implantation (Arm B).\n* An EBRT Prior to Start Period. This occurs within 10 business days prior to EBRT and Concurrent TMZ Phase.\n* An EBRT and Concurrent TMZ Phase, which will begin 30 ±10 days post-surgery. EBRT (30 fractions) and TMZ will be administered up to 5 days a week for 6 weeks in Arm A, and EBRT (20 fractions) and TMZ will be administered for up to 5 days a week for 4 weeks in Arm B. TMZ will be administered at a dose of 75 mg\u002Fm2\u002Fday orally for each Arm.\n* An Adjuvant TMZ Phase, which begins 28 ±7 days following the EBRT and Concurrent TMZ Phase, and is comprised of six 28-day cycles. TMZ (150-200 mg\u002Fm2\u002Fday orally) will be administered for the first 5 days of each 28-day cycle for each Arm. Tumor treating fields are allowed but are not mandated during this phase. Up to 6 additional cycles (for a total of 12) can be completed at the discretion of the Investigator.\n* An Early Discontinuation\u002FFollow-Up Phase will occur 28 ±7 days after completion of Cycle 6 of the Adjuvant TMZ Phase, regardless of the total number of cycles completed or any delays in cycle start. If fewer than six cycles are completed, the first follow-up assessment will occur 28 ±7 days after the last administered dose of adjuvant TMZ. If patient has a qualifying event requiring entrance to Early Discontinuation Phase, the first follow-up assessment will occur as soon as feasible, but within 28 days.\n\nFor any unscheduled visits, data collected should be documented in the case report form (CRF) and must include, but are not limited to, safety evaluations, survival status, and disease status.",[27],"Glioblastoma",[27,29,30,31,32,33,34,35,36,37,38,39,15,40,41],"Newly Diagnosed","GammaTile","External Beam Radiation Therapy","Temozolomide","Brain","Tumor","Brachytherapy","Radiation Therapy","Surgery","Resection","GBM","EBRT","TMZ","RECRUITING","2026-05-28",{"date":45,"type":46},"2026-05-29","ACTUAL",{"date":48,"type":46},"2025-12-10",{"date":50,"type":21},"2031-12",{"name":52,"class":53},"GT Medical Technologies, Inc.","INDUSTRY",5,{"id":56,"slug":57,"hasResults":11,"nctId":58,"briefTitle":59,"officialTitle":60,"acronym":4,"eligibilityCriteria":61,"healthyVolunteers":11,"sex":17,"minAge":4,"maxAge":4,"enrollmentInfo":62,"targetDuration":64,"studyType":65,"phases":4,"briefSummary":66,"conditions":67,"keywords":4,"overallStatus":42,"whyStopped":4,"lastUpdateSubmitDate":74,"lastUpdatePostDateStruct":75,"startDateStruct":77,"completionDateStruct":79,"leadSponsor":81,"locationsCount":82},"100395308","registry-of-patients-with-brain-tumors-treated-with-start-gammatiles-100395308","NCT04427384","Registry of Patients With Brain Tumors Treated With STaRT (GammaTiles)","A Multicenter Observational Study of GammaTile™ Surgically Targeted Radiation Therapy (STaRT) in Intracranial Brain Neoplasms","Inclusion Criteria:\n\n1. Patients who undergo maximum safe resection of intracranial neoplasm(s) AND implantation of GammaTiles.\n2. Willing and able to provide informed consent and to participate in all evaluations.\n\nExclusion Criteria:\n\n1. Inability to undergo pre-operative and post-operative imaging for disease and implant assessment.\n2. Major medical or psychiatric illness, which, in the investigator's opinion would prevent completion of treatment, ability to complete assessments at the time of enrollment, and\u002For interfere with follow ups.\n3. Subjects who, in the investigator's opinion, are unable to understand the protocol or to give informed consent, have a history of poor cooperation, noncompliance with medical treatment, or difficulty in returning for follow up care. A legally authorized representative may provide consent if the potential subject lacks the capacity to provide consent themselves.",{"count":63,"type":21},600,"5 Years","OBSERVATIONAL","The objectives of this registry study are to evaluate real-world clinical outcomes and patient reported outcomes that measure the effectiveness and safety of STaRT.",[68,69,70,71,72,73],"Brain Tumor, Recurrent","Brain Tumor","Brain Tumor, Primary","Brain Tumor - Metastatic","Brain Tumor, Adult: Glioblastoma","Brain Tumor, Adult Meningioma","2026-02-11",{"date":76,"type":46},"2026-02-13",{"date":78,"type":46},"2020-09-11",{"date":80,"type":21},"2028-12-31",{"name":52,"class":53},54,""]