[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100605432":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":11,"centralContacts":11,"locations":33,"responsibleParty":52,"collaborators":11,"id":54,"slug":55,"hasResults":56,"nctId":57,"briefTitle":58,"officialTitle":58,"acronym":11,"eligibilityCriteria":59,"healthyVolunteers":60,"sex":61,"minAge":62,"maxAge":11,"enrollmentInfo":63,"targetDuration":11,"studyType":66,"phases":67,"briefSummary":69,"conditions":70,"keywords":11,"overallStatus":36,"whyStopped":11,"lastUpdateSubmitDate":72,"lastUpdatePostDateStruct":73,"startDateStruct":76,"completionDateStruct":78,"leadSponsor":80,"locationsCount":81},{"fullName":5,"class":6},"Korea United Pharm. Inc.","INDUSTRY",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"Arm A","EXPERIMENTAL",null,[13,14],"Drug: treatment A","Drug: treatment C",{"label":16,"type":10,"description":11,"interventionNames":17},"Arm B",[18,14],"Drug: treatment B",[20,25,29],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":11},"DRUG","treatment A","UIC202502 1 Tab\u002Fday for 7 days",[9],{"type":21,"name":26,"description":27,"armGroupLabels":28,"otherNames":11},"treatment B","UIC202505 1 Tab\u002Fday for 7 days",[16],{"type":21,"name":30,"description":31,"armGroupLabels":32,"otherNames":11},"treatment C","UIC202502+UIC202505 2 Tab\u002Fday for 7 days",[9,16],[34],{"facility":35,"status":36,"city":37,"state":38,"zip":39,"country":40,"countryCode":11,"cosmosGeoPoint":41,"geoPoint":46,"contacts":47},"H plus Yangji Hospital","RECRUITING","Seoul","Gwanak-gu","08779","South Korea",{"type":42,"coordinates":43},"Point",[44,45],126.9784,37.566,{"lat":45,"lon":44},[48],{"name":49,"role":50,"phone":51,"phoneExt":11,"email":11},"Seung hyun Kang","CONTACT","1877-8875",{"type":53,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100605432","phase-1-a-two-arm-open-label-single-sequence-multiple-dose-cross-over-study-to-evaluate-the-pharmacokinetic-interaction-and-the-safety-of-uic202502-and-uic202505-in-healthy-adult-volunteers-100605432",false,"NCT07162441","A Two-arm, Open-label, Single-sequence, Multiple-dose, Cross-over Study to Evaluate the Pharmacokinetic Interaction and the Safety of UIC202502 and UIC202505 in Healthy Adult Volunteers","Inclusion Criteria:\n\n* Subjects aged 19 years or older at the time of screening.\n* Subjects with a body weight greater than 50 kg (≥45 kg for females) and a body mass index (BMI) between 18.0 and 30.0 kg\u002Fm² at screening.\n\n(BMI (kg\u002Fm²) = weight (kg) \u002F height (m)²)\n\n* Subjects with no clinically significant congenital or chronic diseases, pathological symptoms or findings at screening.\n* Subjects determined by the principal investigator to be suitable for diagnostic procedures and electrocardiogram assessments\n* Subjects who agree to use an effective method of contraception (excluding hormonal agents) recognized as appropriate in clinical trials from the first administration of the investigational drug until 14 days after the last administration, together with their spouse or partner.\n* Subjects who have provided written informed consent after receiving a full explanation and demonstrating an understanding of the purpose, procedures, and characteristics of this clinical trial and the investigational drug.\n\nExclusion Criteria:\n\n* Subjects with clinically significant diseases or a history of conditions involving the digestive, cardiovascular, endocrine, respiratory, hematologic\u002Foncologic infectious, renal\u002Fgenitourinary, psychiatric\u002Fneurologic, musculoskeletal, immune, otorhinolaryngologic, dermatologic, or ophthalmologic systems.\n* Subjects with a history of gastrointestinal surgery (excluding simple appendectomy or hernia repair) or gastrointestinal disease that may affect drug absorption.\n* Subjects who have taken drugs that induce or inhibit drug-metabolizing enzymes (e.g., barbiturates) within 1 month before the first dose, or drugs that may interfere with this clinical trial within 10 days before the first dose\n* Subjects who have participated in another clinical trial or bioequivalence study and received an investigational drug within 6 months before the first administration.\n* Subjects who have donated whole blood or blood components within 2 weeks, or received a blood transfusion within 4 weeks before the first administration.\n* Subjects who meet any of the following criteria within 1 month before the first dose:\n\n  * Average alcohol consumption exceeding 21 drinks\u002Fweek for men\n  * Average alcohol consumption exceeding 14 drinks\u002Fweek for women\n\n    (1 drink = 50 mL soju, 30 mL liquor, or 250 mL beer)\n  * Smoking more than 20 cigarettes\u002Fday on average\n* Subjects judged by the principal investigator to be unsuitable for participation in this clinical trial for any reason other than the above selection or exclusion criteria.\n* Female subjects who are pregnant, suspected of being pregnant, or lactating",true,"ALL","19 Years",{"count":64,"type":65},50,"ESTIMATED","INTERVENTIONAL",[68],"PHASE1","This study is open-label, multiple-dose, two-intervention group, single-sequence, crossover design to compare the safety and pharmacokinetics of UIC202502 and UIC202505 when administered alone or in combination.",[71],"Dyslipidemia","2025-08-31",{"date":74,"type":75},"2025-09-09","ACTUAL",{"date":77,"type":75},"2025-08-12",{"date":79,"type":65},"2026-03-01",{"name":5,"class":6},1]