[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Amryt Pharma\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":139},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,5,0,[8,43,67,92,117],{"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":27,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":42},"100568288","phase-3-open-label-extension-study-to-evaluate-metreleptin-in-patients-with-partial-lipodystrophy-100568288",false,"NCT06679270","Open-label Extension Study to Evaluate Metreleptin in Patients With Partial Lipodystrophy","An Open-label Extension of APG-20 Study to Evaluate the Long-term Safety and Efficacy of Daily Subcutaneous Metreleptin Treatment in Subjects With Partial Lipodystrophy","Inclusion Criteria:\n\n1. Age ≥13 years of age, inclusive, at the time of signing the informed consent form (ICF).\n2. Subjects must have completed the Parent study APG-20 and, in the opinion of the Investigator and Sponsor, have been compliant with study procedures through Parent study Month 12 visit.\n3. Negative pregnancy test (urine or serum) for female subjects of childbearing potential\n4. Female subjects must be postmenopausal (defined as cessation of menses for at least 1 year), surgically sterile (hysterectomy, bilateral oophorectomy, or tubal ligation), or willing to use a highly effective method of contraception (such methods include combined \\[estrogen and progestogen containing\\] hormonal contraception associated with inhibition of ovulation: oral\u002Fintravaginal; transdermal\u002Fprogestogen-only hormonal contraception associated with inhibition of ovulation: oral\u002Finjectable; implantable\u002Fintrauterine device \\[IUD\\]\u002Fintrauterine hormone-releasing system \\[IUS\\]\u002Fbilateral tubal occlusion\u002Fvasectomized partner\u002Fsexual abstinence) for the duration of the study (from the time they sign an ICF, until 4 weeks after the last dose of study treatment). Hormonal contraception alone (including oral, injectable, transdermal, and implantable) is not acceptable; an additional barrier method must be used. Intravaginal hormonal contraception or IUS alone are allowed per Investigator's discretion. Subjects on oral contraceptives will not be required to discontinue medication. Subjects will not be permitted to commence oral contraceptives while taking study treatment during the study.\n5. Male subjects must be surgically sterile or willing to use an acceptable method of contraception for the duration of the study (from the time they sign an ICF), until 4 weeks after the last dose of study treatment. An acceptable method of contraception would be a barrier method, such as condoms, restraining from having sex, or a partner using the approved methods of contraception for female subjects as per Inclusion Criteria #4.\n6. Subjects who are blood\u002Fegg\u002Fsperm donors should be willing to halt donations during the study and for 4 weeks following their last dose of study treatment.\n7. Subjects who are willing to provide informed consent\u002Fassent prior to any study-specific procedures. If a minor, the subject has a parent or legal guardian able to read, understand, and sign the ICF and\u002For a Child Assent Form (if applicable), communicate with the Investigator, and understand and comply with the protocol requirements. Adolescent subjects must also read and understand the Child Assent Form.\n8. Subjects who are willing to follow the dietary restrictions recommended by the Investigator.\n\nExclusion Criteria:\n\n1. Severe hypersensitivity reactions to the study treatment of the Parent study APG-20.\n2. Known to have tested positive for human immunodeficiency virus (HIV) or known to be diagnosed with HIV-related LD. Positive HIV test in countries requiring HIV testing.\n3. Are immunocompromised or receiving immunomodulatory drugs.\n4. Estimated glomerular filtration rate (eGFR) \\\u003C30 mL\u002Fmin\u002F1.73m2 calculated by Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) for subjects ≥18 years of age and by Bedside Schwartz for subjects \\\u003C18 years of age.\n5. Diagnosis of clinically significant hematological abnormalities (including but not limited to clinically significant leukopenia, neutropenia, bone marrow abnormalities, leukemia or lymphoma, or clinically significant pathological lymphadenopathy).\n6. Malignancy that is ongoing\u002Fnot in remission or that currently requires or has required active treatment within the past year (with the exception of basal cell carcinoma of the skin, squamous cell carcinoma of the skin, or carcinoma in situ \\[e.g., breast carcinoma, cervical cancer in situ\\] that have undergone potentially curative therapy).\n7. For females only: currently pregnant (confirmed with a positive pregnancy test) or breastfeeding.\n8. Any condition where, in the opinion of the Investigator, participation in this study may pose a significant risk to the subject.","ALL","13 Years",{"count":19,"type":20},24,"ESTIMATED","INTERVENTIONAL",[23],"PHASE3","This Phase 3 study is an Open Label Extension of the APG-20 Study To Evaluate the Long-term Safety and Efficacy of Daily Subcutaneous Metreleptin Treatment in Subjects with Partial Lipodystrophy",[26],"Familial Partial Lipodystrophy",[28,29],"Metreleptin","familial partial lipodystrophy","RECRUITING","2026-01-30",{"date":33,"type":34},"2026-02-02","ACTUAL",{"date":36,"type":34},"2024-10-14",{"date":38,"type":20},"2028-12",{"name":40,"class":41},"Amryt Pharma","INDUSTRY",7,{"id":44,"slug":45,"hasResults":11,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":4,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":50,"enrollmentInfo":51,"targetDuration":4,"studyType":21,"phases":53,"briefSummary":54,"conditions":55,"keywords":57,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":66},"100554738","phase-3-open-label-study-to-evaluate-metreleptin-in-children-under-6-years-of-age-with-generalised-lipodystrophy-100554738","NCT06502990","Open-label Study to Evaluate Metreleptin in Children Under 6 Years of Age With Generalised Lipodystrophy","Open-label, Phase 3b Study to Evaluate Effectiveness, Safety and Pharmacokinetic Parameters of Metreleptin in Patients Under 6 Years of Age With Generalised Lipodystrophy and Associated Diabetes Mellitus and\u002For Hypertriglyceridaemia","Inclusion Criteria:\n\n* Confirmed diagnosis of Generalised Lipodystrophy\n* Metreleptin treatment naive\n\nExclusion Criteria:\n\n* Weight \\\u003C9 kg at Screening (Visit 1)","5 Years",{"count":52,"type":20},15,[23],"This is an open-label, Phase 3b study to evaluate effectiveness, safety and pharmacokinetic parameters of metreleptin in patients under 6 years of age with generalised lipodystrophy and associated diabetes mellitus and\u002For hypertriglyceridaemia",[56],"Generalized Lipodystrophy",[28],"2026-01-16",{"date":60,"type":34},"2026-01-20",{"date":62,"type":34},"2025-05-23",{"date":64,"type":20},"2026-09-30",{"name":40,"class":41},12,{"id":68,"slug":69,"hasResults":11,"nctId":70,"briefTitle":71,"officialTitle":71,"acronym":72,"eligibilityCriteria":73,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":74,"targetDuration":76,"studyType":77,"phases":4,"briefSummary":78,"conditions":79,"keywords":82,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":85,"startDateStruct":86,"completionDateStruct":88,"leadSponsor":90,"locationsCount":91},"100234123","measure-metreleptin-effectiveness-and-safety-registry-100234123","NCT02325674","MEASuRE: Metreleptin Effectiveness And Safety Registry","MEASuRE","Inclusion Criteria:\n\n* Patients treated with metreleptin through commercial supply at the time or before enrolment into registry\n* Patients who provide a written consent\n* Patient coming off metreleptin clinical studies and continuing or restarting treatment with metreleptin through commercial supply\n\nExclusion Criteria:\n\n• Patients currently treated with an investigational agent as part of a clinical trial",{"count":75,"type":20},100,"10 Years","OBSERVATIONAL","The study is a post-authorization, prospective, voluntary registry of patients treated with commercial metreleptin including, but not limited to, patients in the US and EEA.",[80,81],"Generalised Lipodystrophy","Partial Lipodystrophy",[83,84],"Lipodystrophy","Metreleptin Registry",{"date":60,"type":34},{"date":87,"type":34},"2016-10-11",{"date":89,"type":20},"2031-10-31",{"name":40,"class":41},28,{"id":93,"slug":94,"hasResults":11,"nctId":95,"briefTitle":96,"officialTitle":97,"acronym":98,"eligibilityCriteria":99,"healthyVolunteers":11,"sex":16,"minAge":4,"maxAge":4,"enrollmentInfo":100,"targetDuration":4,"studyType":77,"phases":4,"briefSummary":102,"conditions":103,"keywords":106,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":109,"lastUpdatePostDateStruct":110,"startDateStruct":112,"completionDateStruct":114,"leadSponsor":116,"locationsCount":5},"100548636","a-study-to-assess-the-incidence-of-skin-cancers-in-patients-with-epidermolysis-bullosa-receiving-filsuvez-100548636","NCT06423573","A Study to Assess the Incidence of Skin Cancers in Patients With Epidermolysis Bullosa Receiving Filsuvez","A Long-term Non-interventional Study to Assess the Incidence of Skin Malignancies in Patients With Dystrophic and Junctional Epidermolysis Bullosa Receiving Treatment With Filsuvez","FOSteR","Inclusion Criteria:\n\n* Patients with a confirmed diagnosis of dystrophic EB or junctional EB\n\nExclusion Criteria:\n\n* None",{"count":101,"type":20},580,"In patients with epidermolysis bullosa (EB), collagen does not form properly, so their skin is very fragile and blisters easily. Such patients are also at greatly increased risk of developing skin cancers. Filsuvez is a topical gel used to promote healing of skin lesions in patients with certain types of EB. In this observational study, patients with either dystrophic EB (DEB) or junctional EB (JEB) will receive standard of care treatment, whether Filsuvez or something else, and will be followed for up to 5 years. The main purpose is to see if the use of Filsuvez affects the likelihood of developing skin malignancies in these patient populations.",[104,105],"Epidermolysis Bullosa, Dystrophic","Epidermolysis Bullosa, Junctional",[107,108],"Filsuvez","Birch bark extract","2025-09-18",{"date":111,"type":34},"2025-09-19",{"date":113,"type":34},"2024-12-18",{"date":115,"type":20},"2032-08-01",{"name":40,"class":41},{"id":118,"slug":119,"hasResults":11,"nctId":120,"briefTitle":121,"officialTitle":122,"acronym":4,"eligibilityCriteria":123,"healthyVolunteers":11,"sex":16,"minAge":124,"maxAge":4,"enrollmentInfo":125,"targetDuration":4,"studyType":21,"phases":126,"briefSummary":128,"conditions":129,"keywords":130,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":131,"lastUpdatePostDateStruct":132,"startDateStruct":134,"completionDateStruct":136,"leadSponsor":138,"locationsCount":66},"100553344","phase-4-open-label-study-to-evaluate-metreleptin-in-patients-with-partial-lipodystrophy-100553344","NCT06484868","Open-label Study to Evaluate Metreleptin in Patients With Partial Lipodystrophy","A 24-Month, Multi-Centre, Open Label Phase IV Post Authorisation Efficacy Study to Evaluate the Efficacy, Safety and Immunogenicity of Daily Subcutaneous Metreleptin Treatment in Patients With Partial Lipodystrophy","Inclusion Criteria:\n\n* Confirmed diagnosis of familial or acquired partial lipodystrophy\n\nExclusion Criteria:\n\n* Treatment with any Investigational Medicinal Product (IMP) within 6 months or 5 times the terminal half-life of the corresponding IMP, whichever is longer, before the screening visit.\n\nOther protocol defined inclusion\u002Fexclusion criteria apply","12 Years",{"count":66,"type":20},[127],"PHASE4","This is an Open Label, Phase IV, Post Authorisation Study to Evaluate the Efficacy, Safety and Immunogenicity of Daily Subcutaneous Metreleptin Treatment in people with Partial Lipodystrophy",[81],[28],"2025-07-02",{"date":133,"type":34},"2025-07-03",{"date":135,"type":34},"2024-02-08",{"date":137,"type":20},"2028-02",{"name":40,"class":41},""]