[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100652353":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":25,"centralContacts":32,"locations":37,"responsibleParty":54,"collaborators":25,"id":56,"slug":57,"hasResults":58,"nctId":59,"briefTitle":60,"officialTitle":61,"acronym":25,"eligibilityCriteria":62,"healthyVolunteers":63,"sex":64,"minAge":65,"maxAge":66,"enrollmentInfo":67,"targetDuration":25,"studyType":70,"phases":71,"briefSummary":73,"conditions":74,"keywords":25,"overallStatus":76,"whyStopped":25,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"Boehringer Ingelheim","INDUSTRY",[8,16],{"label":9,"type":10,"description":11,"interventionNames":12},"Treatment sequence 1","EXPERIMENTAL","Sequence:\n\n1. \\- Reference treatment (BI 3000202)\n2. \\- Test treatment 1 (BI 3000202 + Ciclosporin)\n3. \\- Test treatment 2 (BI 3000202 + Itraconazole)",[13,14,15],"Drug: BI 3000202","Drug: Ciclosporin","Drug: Itraconazole",{"label":17,"type":10,"description":18,"interventionNames":19},"Treatment sequence 2","Sequence:\n\n1. \\- Test treatment 1 (BI 3000202 + Ciclosporin)\n2. \\- Reference treatment (BI 3000202)\n3. \\- Test treatment 2 (BI 3000202 + Itraconazole)",[13,14,15],[21,26,29],{"type":22,"name":23,"description":23,"armGroupLabels":24,"otherNames":25},"DRUG","BI 3000202",[9,17],null,{"type":22,"name":27,"description":27,"armGroupLabels":28,"otherNames":25},"Ciclosporin",[9,17],{"type":22,"name":30,"description":30,"armGroupLabels":31,"otherNames":25},"Itraconazole",[9,17],[33],{"name":5,"role":34,"phone":35,"phoneExt":25,"email":36},"CONTACT","18002430127","clintriage.rdg@boehringer-ingelheim.com",[38],{"facility":39,"status":25,"city":40,"state":25,"zip":41,"country":42,"countryCode":43,"cosmosGeoPoint":44,"geoPoint":49,"contacts":50},"Humanpharmakologisches Zentrum Biberach","Biberach","88397","Germany","DE",{"type":45,"coordinates":46},"Point",[47,48],8.03333,48.33333,{"lat":48,"lon":47},[51],{"name":5,"role":34,"phone":52,"phoneExt":25,"email":53},"08007234742","deutschland@bitrialsupport.com",{"type":55,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR","100652353","phase-1-a-study-in-healthy-men-to-find-out-how-blocking-certain-transport-proteins-affects-the-amount-of-bi-3000202-in-the-blood-100652353",false,"NCT07774325","A Study in Healthy Men to Find Out How Blocking Certain Transport Proteins Affects the Amount of BI 3000202 in the Blood","The Effects of P-gp Inhibition and OATP Inhibition on the Pharmacokinetics of a Single Oral Dose of BI 3000202 in Healthy Male Trial Participants (an Open-label, Three-period, Two-sequence Crossover Trial, With Period 3 as Fixed Treatment)","Inclusion Criteria:\n\n1. Healthy male trial participant according to the assessment of the investigator, as based on a complete medical history, physical examination, vital signs (Blood pressure, Pulse rate), 12-lead Electrocardiogram, and clinical laboratory tests\n2. Age of 18 to 55 years (inclusive)\n3. Body mass index of 18.5 to 29.9 kg\u002Fm² (inclusive). Additionally, a minimum body weight of at least 60 kg is required\n4. Signed and dated written informed consent in accordance with International Council for Harmonisation-Good Clinical Practice and local legislation prior to admission to the trial\n\nExclusion Criteria:\n\n1. Any finding in the medical examination (including Blood pressure, Pulse rate or Electrocardiogram) deviating from normal and assessed as clinically relevant by the investigator\n2. Repeated measurement of systolic blood pressure outside the range of 90 to 140 mmHg, diastolic blood pressure outside the range of 50 to 90 mmHg, or pulse rate outside the range of 45 to 90 bpm\n3. Any laboratory value outside the reference range that the investigator considers to be of clinical relevance\n4. Any evidence of a concomitant disease assessed as clinically relevant by the investigator\n5. Further exclusion criteria apply.",true,"MALE","18 Years","55 Years",{"count":68,"type":69},16,"ESTIMATED","INTERVENTIONAL",[72],"PHASE1","The main objective of this trial is to investigate the effects of multiple doses of Itraconazole and multiple doses of Ciclosporin on the pharmacokinetics of BI 3000202 in plasma following a single oral dose in healthy male trial participants.",[75],"Healthy","NOT_YET_RECRUITING","2026-08-17",{"date":79,"type":80},"2026-08-19","ACTUAL",{"date":82,"type":69},"2026-09-01",{"date":84,"type":69},"2026-10-26",{"name":5,"class":6},1]