[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Sitryx Therapeutics Ltd\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":41},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":4,"eligibilityCriteria":14,"healthyVolunteers":15,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100635898",false,"NCT07558668","A 3-part Study of SYX-5219 in Healthy Volunteers and Participants With Atopic Dermatitis","A Multi-part, FiH Study in Healthy Participants and Participants With Atopic Dermatitis (AD) to Assess the Safety, Tolerability, Pharmacokinetics (PK) of Single & Multiple Ascending Doses and Selected Dose of SYX-5219 (AD Participants).","Inclusion Criteria:\n\nParts 1 \\& 2\n\n* Healthy male and female participant, between ≥ 18 to ≤ 65 years of age, inclusive, with a BMI of body mass index (BMI) of 18-32 kg\u002Fm2.\n* Female participant of non-childbearing potential or female of childbearing potential that is sexually abstinent.\n* No clinically significant abnormalities in laboratory, vital signs or ECG measurements.\n\nPart 3\n\n* Male and female participants with clinically confirmed diagnosis of active AD, between ≥ 18 to ≤ 65 years of age, inclusive, with a BMI of body mass index (BMI) of ≤40 kg\u002Fm2.\n* Meet minimum AD entry criteria;\n\n  * AD covering ≥10% of the body surface area (BSA) at screening and baseline.\n  * Eczema Area and Severity Index (EASI) score ≥16 at screening and baseline.\n  * Validated Investigator's Global Assessment (vIGA) score of ≥ 3 (moderate) at screening and baseline.\n  * Peak Pruritus NRS score of ≥ 4 at screening and baseline.\n\nExclusion Criteria:\n\nParts 1 \\& 2\n\n• Use of prescription or non-prescription drugs, including vitamins, herbal and dietary supplements within 35 days or 5 half-lives (whichever is longer) prior to the first dose of IMP.\n\nPart 3\n\n* Any clinically significant medical condition or physical\u002Flaboratory\u002FECG\u002Fvital signs abnormality that would, in the opinion of the Investigator, put the participant at undue risk.\n* Has medical history as stated in the main study exclusion criteria.\n* Received treatment(s) as stated in the main study exclusion criteria.",true,"ALL","18 Years","65 Years",{"count":20,"type":21},149,"ESTIMATED","INTERVENTIONAL",[24],"PHASE1","The purpose of this study is to evaluate the study drug, SYX-5219, in a multi-part First-in-Human (FiH) study to be conducted in healthy volunteers and participants with Atopic Dermatitis (AD). The objectives of this study are to determine the safety, tolerability and levels of SYX-5219 in the blood and urine when SYX-5219 is given in each part of the study (SAD, MAD, Food Effect and Participants with AD).\n\nThe study will be split into up to 3 parts as follows:\n\n* Part 1 - Single Ascending Dose (SAD) and Food Effect in healthy volunteers\n* Part 2 - Multiple Ascending Dose (MAD) in healthy volunteers\n* Part 3 - Multiple Dose in Participants with AD - enrolling up to 45 males and females with a confirmed diagnosis of AD of at least 6 months, evaluating multiple dose administrations of SYX-5219 or placebo daily over a period of 42 days.",[27],"Moderate to Severe Atopic Dermatitis","RECRUITING","2026-04-22",{"date":31,"type":32},"2026-04-30","ACTUAL",{"date":34,"type":32},"2025-02-26",{"date":36,"type":21},"2026-09-30",{"name":38,"class":39},"Sitryx Therapeutics Ltd","INDUSTRY",14,""]