[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"childhood-solid-tumor\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:childhood-solid-tumor":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,56,84],{"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":25,"conditions":26,"keywords":32,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":44,"lastUpdatePostDateStruct":45,"startDateStruct":48,"completionDateStruct":50,"leadSponsor":52,"locationsCount":55},"100532119","phase-1-optimal-precision-therapies-to-customise-care-in-childhood-and-adolescent-cancer-100532119",false,"NCT06208657","Optimal Precision TherapIes to CustoMISE Care in Childhood and Adolescent Cancer","Inclusion Criteria:\n\n1. Patients must be diagnosed with a solid tumor, CNS tumor or lymphoma that has progressed despite standard therapy, or for which no effective standard therapy exists.\n2. Age \\\u003C21 years at inclusion; patients 21 years and older may be included after approval by the Study Chair if they have a pediatric type recurrent\u002Frefractory malignancy.\n3. Patients must be enrolled on a precision medicine study (i.e. PROFYLE, ZERO or equivalent as agreed with Study Chair).\n4. Patients enrolled in a Phase I cohort must have either evaluable or measurable disease.\n5. Patients enrolled in a Phase II cohort must have measurable disease. Evaluable and measurable disease are defined by standard imaging criteria for the patient's tumor type.\n6. Disease evaluations, laboratory tests, and other clinical assessments that are considered standard of care may be undertaken at the patient's local oncology treatment centre with results transferred to study site for evaluation.\n7. Performance status: Karnofsky performance status (for patients \\> 16 years of age) or Lansky play score (for patients ≤ 16 years of age) ≥ 50%.\n8. Life expectancy ≥ 6 weeks.\n9. Patients must have fully recovered from the acute toxic effects of all prior anticancer therapy and must meet the following minimum duration from prior anticancer-directed therapy prior to enrolment.\n10. Adequate organ function.\n11. Able to comply with scheduled follow-up and with management of toxicity.\n12. Females of childbearing potential must have a negative serum or urine pregnancy test.\n13. Fertile males must agree to use adequate contraception during the study and following completion of treatment.\n14. Provide a signed and dated informed consent form.\n\nExclusion Criteria:\n\n1. Patients with symptomatic central nervous system (CNS) primary or metastatic tumours who are neurologically unstable or require increasing doses of corticosteroids or local CNS-directed therapy to control their CNS disease. Patients on stable doses of corticosteroids for at least 7 days prior to receiving study drug may be included.\n2. Impairment of gastrointestinal (GI) function or GI disease that may significantly alter drug absorption of oral drugs (e.g., ulcerative diseases, uncontrolled nausea, vomiting, diarrhoea, or malabsorption syndrome) - only for arms that include orally administered therapeutic agents.\n3. Clinically significant, uncontrolled heart disease (including history of any cardiac arrhythmias, e.g., ventricular, supraventricular, nodal arrhythmias, or conduction abnormality), unstable ischemia, congestive heart failure within 12 months of screening.\n4. Known active viral hepatitis or human immunodeficiency virus (HIV) infection or any other uncontrolled infection.\n5. Major surgery within 21 days of the first dose of investigational drug. Gastrostomy, ventriculo-peritoneal shunt, endoscopic ventriculostomy, tumour biopsy and insertion of central venous access devices are not considered major surgery, but for these procedures, a 48-hour interval must be maintained before the first dose of the investigational drug is administered.\n6. Known hypersensitivity to any study drug or component of the formulation.\n7. Pregnant or nursing (lactating) females.\n8. Any other concomitant serious medical condition or organ dysfunction that in the opinion of the investigator would either compromise patient safety or interfere with the evaluation of the safety of the investigational drug(s).","ALL","0 Years","21 Years",{"count":19,"type":20},90,"ESTIMATED","INTERVENTIONAL",[23,24],"PHASE1","PHASE2","A companion platform trial to test novel targeted agents based on the patient's tumor profile.",[27,28,29,30,31],"Childhood Cancer","Childhood Solid Tumor","Childhood Brain Tumor","Recurrent Cancer","Refractory Cancer",[33,34,35,36,37,38,39,40,41,42],"children","basket trial","platform study","pediatric","solid tumor","paediatric","solid tumour","CNS tumor","CNS tumour","lymphoma","RECRUITING","2026-01-26",{"date":46,"type":47},"2026-01-28","ACTUAL",{"date":49,"type":47},"2024-07-10",{"date":51,"type":20},"2035-12",{"name":53,"class":54},"Australian & New Zealand Children's Haematology\u002FOncology Group","OTHER",14,{"id":57,"slug":58,"hasResults":11,"nctId":59,"briefTitle":60,"officialTitle":60,"acronym":61,"eligibilityCriteria":62,"healthyVolunteers":11,"sex":15,"minAge":16,"maxAge":63,"enrollmentInfo":64,"targetDuration":4,"studyType":66,"phases":4,"briefSummary":67,"conditions":68,"keywords":71,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":75,"lastUpdatePostDateStruct":76,"startDateStruct":78,"completionDateStruct":80,"leadSponsor":82,"locationsCount":83},"100478038","precision-medicine-for-every-child-with-cancer-100478038","NCT05504772","Precision Medicine for Every Child With Cancer","ZERO2","Inclusion Criteria:\n\n1. Age \\\u003C 18 years Note: Individual patients aged 19 - 25 years old with a pediatric cancer, e.g., neuroblastoma, may be enrolled after discussion with, and at the discretion of, the Study Chair or their delegate.\n2. Life expectancy \\>6 weeks at time of enrolment\n3. Consent i. Signed and dated informed consent for study enrolment from participant aged ≥ 18 years or from parent\u002Fguardian of participant aged \\\u003C18 years. ii. Separate signed and dated informed consent for understanding the role of germline testing and choice for the return of germline results.","25 Years",{"count":65,"type":20},3500,"OBSERVATIONAL","To improve outcomes for childhood cancer patients through the implementation of precision medicine.",[27,28,29,69,31,70],"Childhood Leukemia","Relapsed Cancer",[33,72,73,74,36,38],"precision medicine","personalised medicine","molecular profiling","2024-07-16",{"date":77,"type":47},"2024-07-17",{"date":79,"type":47},"2022-12-16",{"date":81,"type":20},"2030-07",{"name":53,"class":54},11,{"id":85,"slug":86,"hasResults":11,"nctId":87,"briefTitle":88,"officialTitle":89,"acronym":90,"eligibilityCriteria":91,"healthyVolunteers":11,"sex":15,"minAge":4,"maxAge":92,"enrollmentInfo":93,"targetDuration":4,"studyType":66,"phases":4,"briefSummary":95,"conditions":96,"keywords":4,"overallStatus":43,"whyStopped":4,"lastUpdateSubmitDate":97,"lastUpdatePostDateStruct":98,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":107},"100180217","french-childhood-cancer-survivor-study-100180217","NCT01620372","French Childhood Cancer Survivor Study","Constitution d'Une Cohorte Nationale rétrospective de Survivants d'un Cancer Solide de l'Enfant diagnostiqué Avant 2000","FCCSS","Inclusion Criteria:\n\n* All types of solid childhood cancer in France\n* Age at diagnosis: Below age 19\n* Period of diagnosis: between 1st January 1942 and 31st December 1999\n* Complete identification (first name, last name, date of birth and place of birth)\n\nExclusion Criteria:\n\n* Leukaemia cases","18 Years",{"count":94,"type":20},18000,"The FCCSS is a multicentric national large-scale collaborative population-based study of children treated for a solid tumor before 2000 in France and before the age of 19 years.\n\nThe study is concerned by improving knowledge about the long-term effects caused by cancer and its treatments including adverse health and social outcomes.\n\nThe main reason of the FCCSS is to estimate the risk of adverse health and social outcomes that may occur after a cancer treatment and to prevent them by providing adapted follow-up care.\n\nThe cohort will be followed for up to 20 years from 2011.",[28],"2012-10-08",{"date":99,"type":20},"2012-10-10",{"date":101,"type":4},"2011-11",{"date":103,"type":20},"2031-11",{"name":105,"class":106},"Institut National de la Santé Et de la Recherche Médicale, France","OTHER_GOV",36]