[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"autoimmune-lymphoproliferative-syndrome\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:autoimmune-lymphoproliferative-syndrome":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,48],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":28,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":36,"lastUpdatePostDateStruct":37,"startDateStruct":40,"completionDateStruct":42,"leadSponsor":44,"locationsCount":47},"100572196","phase-2-study-of-the-itk-inhibitor-soquelitinib-to-reduce-lymphoproliferation-and-improve-cytopenias-in-autoimmune-lymphoproliferative-syndrome-alps-fas-patients-100572196",false,"NCT06730126","Study of the ITK Inhibitor Soquelitinib to Reduce Lymphoproliferation and Improve Cytopenias in Autoimmune Lymphoproliferative Syndrome (ALPS)-FAS Patients","A Phase 2a Study of the ITK Inhibitor Soquelitinib to Reduce Lymphoproliferation and Improve Cytopenias in Autoimmune Lymphoproliferative Syndrome (ALPS)-FAS Patients","* INCLUSION CRITERIA:\n\nTo be eligible to participate in this study and to re-enroll, an individual must meet all the following criteria:\n\n1. Aged \\>= 16 years.\n2. Able to provide informed consent (for ages \\>= 18 years) or has a parent(s) or guardian(s) who can provide permission to participate on their behalf (for ages \\\u003C18 years).\n3. Has a documented diagnosis of ALPS-FAS.\n4. Has clinical evidence of active disease, defined as at least one enlarged lymph node and\u002For enlarged spleen.\n5. If currently on corticosteroid therapy, then dose is less than 20 mg\u002Fday (prednisone equivalent) and has been stable for at least 4 weeks.\n6. For participants to be seen at the NIH CC, co-enrolled on NIH protocol 93-I-0063.\n7. Participants who can become pregnant or who can impregnate their partner must agree to either remain sexually abstinent or use two highly effective methods of contraception when engaging in sexual activities that can result in pregnancy, beginning 28 days before baseline until 3 months after the last dose. One method must be a barrier (eg, internal or external condom, cervical cap, or diaphragm). The second method may be any of the following:\n\n7a. Oral contraceptive pill or hormonal patch or ring.\n\n7b. Parenteral hormonal contraceptive implant.\n\n7c. Intrauterine device.\n\nEXCLUSION CRITERIA:\n\nAn individual who meets any of the following criteria will be excluded from participation or re-enrollment in this study:\n\n1. Profound grade 3 or 4 cytopenias that cannot be improved with immunomodulatory treatments prior to enrolling in the clinical trial and starting the study drug. Per investigator discretion, individuals on a single agent may be included if the dose is stable for 12 weeks at screening and is not expected to confer additive toxicity.\n2. Renal impairment, defined as serum creatinine \\>1.5 mg\u002FdL (or 133 micromol\u002FL) or estimated glomerular filtration rate \\\u003C60 mL\u002Fmin\u002F1.73 m\\^2.\n3. Liver impairment, defined as bilirubin, alanine aminotransferase, or aspartate aminotransferase greater than 2.5 times the upper limit of normal.\n4. History of EBV-associated lymphoma.\n5. Active EBV infection with EBV load \\>300 copies\u002FmL.\n6. Tuberculosis infection (active or latent) or undergoing tuberculosis treatment.\n7. Infection with HIV or hepatitis B or C.\n8. Current other invasive or systemic fungal, bacterial, or viral infection requiring therapy.\n9. History of opportunistic infection within the previous 180 days.\n10. History of invasive malignancy that required systemic therapy within the last 3 years.\n11. Current use of moderate or strong cytochrome P450 isozyme (CYP)3A inhibitors or inducers that cannot be stopped before day 0.\n12. Current use of P-glycoprotein (P-gp) inhibitors that cannot be stopped before day 0.\n13. Known hypersensitivity or contraindication to CT contrast agent.\n14. Pregnant or breastfeeding.\n15. Any condition that, in the opinion of the study team contraindicates participation in this study.","ALL","16 Years","120 Years",{"count":20,"type":21},15,"ESTIMATED","INTERVENTIONAL",[24],"PHASE2","Background:\n\nAutoimmune lymphoproliferative syndrome (ALPS) is a rare disorder of the immune system caused by a mutation in the FAS gene. In ALPS, the body stores too many germ-fighting cells called lymphocytes. This can lead to an enlarged spleen and lymph nodes. Current treatments for ALPS can have many adverse effects. Better treatments for ALPS are needed.\n\nObjective:\n\nTo test a study drug (soquelitinib) in people with ALPS.\n\nEligibility:\n\nPeople aged 16 years and older with ALPS.\n\nDesign:\n\nParticipants will have 8 clinic visits and 6 remote visits within 1 year.\n\nParticipants will be screened. They will have a physical exam with blood and urine tests. Some may have tests of their lung function.\n\nSoquelitinib is a tablet taken by mouth twice a day. Participants will record their doses and any symptoms on a paper or online form.\n\nBlood tests and other procedures will be repeated during study visits. Three visits will include imaging scans. Participants will lie on a table that slides through a doughnut-shaped machine while X-rays capture pictures of the inside of their body.\n\nSome participants may be able to remain in the study for a second year.",[27],"Autoimmune Lymphoproliferative Syndrome",[27,29,30,31,32,33,34],"Fas","Hypersplenism","Lymphoproliferation","Interleukin-2 Inducible T-cell Kinase","Soquelitinib","Targeted Treatment","RECRUITING","2026-06-10",{"date":38,"type":39},"2026-06-11","ACTUAL",{"date":41,"type":39},"2025-03-10",{"date":43,"type":21},"2026-12-01",{"name":45,"class":46},"National Institute of Allergy and Infectious Diseases (NIAID)","NIH",3,{"id":49,"slug":50,"hasResults":11,"nctId":51,"briefTitle":52,"officialTitle":52,"acronym":53,"eligibilityCriteria":54,"healthyVolunteers":11,"sex":16,"minAge":55,"maxAge":56,"enrollmentInfo":57,"targetDuration":4,"studyType":59,"phases":4,"briefSummary":60,"conditions":61,"keywords":4,"overallStatus":35,"whyStopped":4,"lastUpdateSubmitDate":81,"lastUpdatePostDateStruct":82,"startDateStruct":84,"completionDateStruct":86,"leadSponsor":88,"locationsCount":91},"100431799","conception-of-a-diagnosis-prognosis-and-therapeutic-decision-tool-for-patients-with-autoimmunity-and-inflammation-100431799","NCT04902807","Conception of a Diagnosis, Prognosis and Therapeutic Decision Tool for Patients With Autoimmunity and Inflammation","ATRACTion","Inclusion Criteria for controls (patients relatives and unrelated subjects):\n\n* Individuals aged\\\u003C18 y\u002Fo.\n* Individuals \\> 6 kg\n* Individuals not affected by an immune-related disease or not affected by cancer\n* Individuals whose parents have signed an enlightened consent.\n\nInclusion criteria for patients\n\n* Individuals with health insurance.\n* Patients treated at Necker hospital with PIDs and autoimmunity\u002Finflammation related to known genetic defects (cytopenia, Enteropathy Inflammatory bowel disease (IBD), Systemic Lupus Erythematosus (SLE), Juvenile Idiopathic Arthritis (JIA), Familial Hemophagocytic Lymphohistiocytosis (FHL), chronic EBV infection associated (Ca-EBV) with EBV-infected T and\u002For Natural Killer (NK) cells and with a high risk to develop macrophage activation syndrome similar to FHL. See table below for diagnosis inclusion criteria.\n* Individuals aged\\\u003C18 y\u002Fo.\n* Individuals \\> 9 kg\n* Patients whose parents have signed an enlightened consent.\n\nExclusion Criteria:\n\n* Intake of antibiotics within 2 weeks prior inclusion\n* Absence of parent's or child consent form\n* Cytotoxic cancer treatments\n* antiviral treatments (HIV, hepatitis …)\n* Short term life-threatening conditions\n* Individuals placed under judicial protection","1 Year","18 Years",{"count":58,"type":21},500,"OBSERVATIONAL","The main objective of this study is to generate diagnosis and therapeutic-decision tools through the identification of molecular causes of PIDs with autoimmunity\u002Finflammation and the variability in disease outcome at the transcriptional level using a combination of omics signatures (transcriptomics, epigenomics, proteomics, metagenomics, metabolomics and lipidomics).",[27,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80],"Autoimmune Cytopenia","Autoimmune Diseases","Autoimmune Anemia","Autoimmune Thrombocytopenia","Autoimmune Hepatitis","Autoimmune Diabetes","Autoimmune Rheumatologic Disease","Systemic Lupus Erythematosus","Juvenile Idiopathic Arthritis","Hemophagocytic Lymphohistiocytoses","EBV Lymphoproliferation","RAS-Associated Autoimmune Leucoproliferative Disease","Primary Immunodeficiency","APECED","IPEX","BENTA","Enteropathy, Autoimmune","Combined Immunodeficiency","IBD","2025-09-02",{"date":83,"type":39},"2025-09-08",{"date":85,"type":39},"2021-09-07",{"date":87,"type":21},"2026-06",{"name":89,"class":90},"Institut National de la Santé Et de la Recherche Médicale, France","OTHER_GOV",1]