[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100635415":3},{"organization":4,"armGroups":7,"interventions":27,"overallOfficials":11,"centralContacts":41,"locations":47,"responsibleParty":62,"collaborators":11,"id":64,"slug":65,"hasResults":66,"nctId":67,"briefTitle":68,"officialTitle":69,"acronym":11,"eligibilityCriteria":70,"healthyVolunteers":66,"sex":71,"minAge":72,"maxAge":11,"enrollmentInfo":73,"targetDuration":11,"studyType":76,"phases":77,"briefSummary":79,"conditions":80,"keywords":11,"overallStatus":50,"whyStopped":11,"lastUpdateSubmitDate":83,"lastUpdatePostDateStruct":84,"startDateStruct":87,"completionDateStruct":89,"leadSponsor":91,"locationsCount":92},{"fullName":5,"class":6},"Hanlim Pharm. Co., Ltd.","INDUSTRY",[8,14,18,23],{"label":9,"type":10,"description":11,"interventionNames":12},"Test group","EXPERIMENTAL",null,[13],"Drug: Test group",{"label":15,"type":10,"description":11,"interventionNames":16},"Exploratory test group",[17],"Drug: Exploratory test group",{"label":19,"type":20,"description":11,"interventionNames":21},"Control group 1","PLACEBO_COMPARATOR",[22],"Drug: Control group 1",{"label":24,"type":20,"description":11,"interventionNames":25},"Control group 2",[26],"Drug: Control group 2",[28,32,35,38],{"type":29,"name":9,"description":30,"armGroupLabels":31,"otherNames":11},"DRUG","HL1113T2 + placebo of HL1113T1, HL1113R1, HL1113R2, once daily, administered for 12 weeks",[9],{"type":29,"name":15,"description":33,"armGroupLabels":34,"otherNames":11},"HL1113T1 + placebo of HL1113T2, HL1113R1, HL1113R2, once daily, administered for 12 weeks",[15],{"type":29,"name":19,"description":36,"armGroupLabels":37,"otherNames":11},"HL1113R1 + placebo of HL1113T1, HL1113T2, HL1113R2, once daily, administered for 12 weeks",[19],{"type":29,"name":24,"description":39,"armGroupLabels":40,"otherNames":11},"HL1113R2 + placebo of HL1113T1, HL1113T2, HL1113R1, once daily, administered for 12 weeks",[24],[42],{"name":43,"role":44,"phone":45,"phoneExt":11,"email":46},"Kang","CONTACT","82234896198","kyliekang@hanlim.com",[48],{"facility":49,"status":50,"city":51,"state":11,"zip":11,"country":52,"countryCode":11,"cosmosGeoPoint":53,"geoPoint":58,"contacts":59},"The Catholic University of Korea Bucheon St. Mary's Hospital","RECRUITING","Seoul","South Korea",{"type":54,"coordinates":55},"Point",[56,57],126.9784,37.566,{"lat":57,"lon":56},[60],{"name":61,"role":44,"phone":11,"phoneExt":11,"email":11},"Lim",{"type":63,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100635415","phase-3-clinical-trial-to-evaluate-the-efficacy-and-safety-of-monotherapy-group-of-hl1113r1-or-hl1113r2-versus-hl1113-fixed-dose-combination-in-patients-with-essential-hypertension-and-type-ii-diabetes-mellitus-100635415",false,"NCT07552389","Clinical Trial to Evaluate the Efficacy and Safety of Monotherapy Group of HL1113R1 or HL1113R2 Versus HL1113 (Fixed Dose Combination) in Patients With Essential Hypertension and Type II Diabetes Mellitus","A Randomized, Active Controlled, Double Blind, Parallel, Multi Center, Phase 3 Study to Evaluate the Efficacy and Safety of Monotherapy Group of HL1113R1 or HL1113R2 Versus HL1113 (Fixed Dose Combination) in Patients With Essential Hypertension and Type II Diabetes Mellitus","Inclusion Criteria:\n\n* Adult male or female subjects aged ≥19 years at the time of written informed consent.\n* Subjects diagnosed with essential hypertension accompanied by type 2 diabetes mellitus.\n* etc.\n\nExclusion Criteria:\n\n* Subjects whose blood pressure measured in the selected arm at both screening and randomization meets the following criterion: MSDBP ≥ 110 mmHg\n* Subjects whose blood pressure measured three consecutive times in each arm at intervals of at least 2 minutes at screening shows a difference of ≥20 mmHg in SBP and ≥10 mmHg in DBP.\n* etc.","ALL","19 Years",{"count":74,"type":75},228,"ESTIMATED","INTERVENTIONAL",[78],"PHASE3","This clinical trial is a randomized, active controlled, double blind, parallel, multi center, phase 3 study to evaluate the efficacy and safety of monotherapy group of HL1113R1 or HL1113R2 versus HL1113 (Fixed dose combination) in patients with essential hypertension and type II diabetes mellitus",[81,82],"Hypertension","Diabete Type 2","2026-04-20",{"date":85,"type":86},"2026-04-27","ACTUAL",{"date":88,"type":86},"2025-12-18",{"date":90,"type":75},"2028-12",{"name":5,"class":6},1]