[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100636492":3},{"organization":4,"armGroups":7,"interventions":40,"overallOfficials":51,"centralContacts":55,"locations":61,"responsibleParty":87,"collaborators":46,"id":89,"slug":90,"hasResults":91,"nctId":92,"briefTitle":93,"officialTitle":94,"acronym":46,"eligibilityCriteria":95,"healthyVolunteers":91,"sex":96,"minAge":97,"maxAge":98,"enrollmentInfo":99,"targetDuration":46,"studyType":102,"phases":103,"briefSummary":105,"conditions":106,"keywords":46,"overallStatus":64,"whyStopped":46,"lastUpdateSubmitDate":109,"lastUpdatePostDateStruct":110,"startDateStruct":113,"completionDateStruct":115,"leadSponsor":117,"locationsCount":118},{"fullName":5,"class":6},"Novo Nordisk A\u002FS","INDUSTRY",[8,14,18,22,26,30,34],{"label":9,"type":10,"description":11,"interventionNames":12},"Cohort 1 NNC0113-5840","EXPERIMENTAL","Participants will be randomized to receive NNC0113-5840 single dose level 1 subcutaneously.",[13],"Drug: NNC0113-5840",{"label":15,"type":10,"description":16,"interventionNames":17},"Cohort 2 NNC0113-5840","Participants will be randomized to receive NNC0113-5840 single dose level 2 subcutaneously.",[13],{"label":19,"type":10,"description":20,"interventionNames":21},"Cohort 3 NNC0113-5840","Participants will be randomized to receive NNC0113-5840 single dose level 3 subcutaneously.",[13],{"label":23,"type":10,"description":24,"interventionNames":25},"Cohort 4 NNC0113-5840","Participants will be randomized to receive NNC0113-5840 single dose level 4 subcutaneously.",[13],{"label":27,"type":10,"description":28,"interventionNames":29},"Cohort 5 NNC0113-5840","Participants will be randomized to receive NNC0113-5840 single dose level 5 subcutaneously.",[13],{"label":31,"type":10,"description":32,"interventionNames":33},"Cohort 6 NNC0113-5840","Participants will be randomized to receive NNC0113-5840 single dose level 6 subcutaneously.",[13],{"label":35,"type":36,"description":37,"interventionNames":38},"Placebo matching NNC0113-5840","PLACEBO_COMPARATOR","Participants will receive placebo matched to NNC0113-5840 subcutaneously.",[39],"Drug: Placebo",[41,47],{"type":42,"name":43,"description":44,"armGroupLabels":45,"otherNames":46},"DRUG","NNC0113-5840","NNC0113-5840 will be administered subcutaneously using needle and syringe in a lifted fold of the abdominal skin.",[9,15,19,23,27,31],null,{"type":42,"name":48,"description":49,"armGroupLabels":50,"otherNames":46},"Placebo","Placebo matched to NNC0113-5840 will be administered subcutaneously using needle and syringe in a lifted fold of the abdominal skin.",[35],[52],{"name":53,"affiliation":5,"role":54},"Clinical Transparency (dept. 2834)","STUDY_DIRECTOR",[56],{"name":57,"role":58,"phone":59,"phoneExt":46,"email":60},"Novo Nordisk","CONTACT","(+1) 866-867-7178","clinicaltrials@novonordisk.com",[62,76],{"facility":63,"status":64,"city":65,"state":66,"zip":67,"country":68,"countryCode":69,"cosmosGeoPoint":70,"geoPoint":75,"contacts":46},"PAREXEL Glendale\u002FLA EPCU","RECRUITING","Glendale","California","91206","United States","US",{"type":71,"coordinates":72},"Point",[73,74],-118.25508,34.14251,{"lat":74,"lon":73},{"facility":77,"status":78,"city":79,"state":80,"zip":81,"country":68,"countryCode":69,"cosmosGeoPoint":82,"geoPoint":86,"contacts":46},"PAREXEL Intl - EPCU-Baltimore","NOT_YET_RECRUITING","Baltimore","Maryland","21225",{"type":71,"coordinates":83},[84,85],-76.61219,39.29038,{"lat":85,"lon":84},{"type":88,"investigatorFullName":46,"investigatorTitle":46,"investigatorAffiliation":46,"oldNameTitle":46,"oldOrganization":46},"SPONSOR","100636492","phase-1-a-research-study-investigating-how-a-new-medicine-nnc0113-5840-works-in-people-with-overweight-or-obesity-100636492",false,"NCT07566390","A Research Study Investigating How a New Medicine NNC0113-5840 Works in People With Overweight or Obesity","A First in Human Dose Study Investigating the Safety, Tolerability and Pharmacokinetics of Single Ascending Doses of NNC0113-5840 in Participants With Overweight or Obesity","Inclusion Criteria:\n\n1. Male or female\n2. Age 18-55 years (both inclusive) at the time of signing the informed consent.\n3. Body mass index (BMI) between 25.0 and 34.9 kilogram per meter square (kg\u002Fm2) (both inclusive) at screening. Overweight should be due to excess adipose tissue, as judged by the investigator.\n4. Considered eligible based on the medical history, physical examination, and the results of vital signs, electrocardiogram and clinical laboratory tests performed during the screening visit and visit 2, day -1, as judged by the investigator.\n\nExclusion Criteria:\n\n1. Known or suspected hypersensitivity to study intervention(s) or related products.\n2. Any condition, which in the investigator's opinion might jeopardise participant's safety or compliance with the protocol.\n3. Glycosylated haemoglobin (HbA1c) more than or equal to (≥) 6.5 percent (%) \\[48 millimole per mole (mmol\u002Fmol)\\] at screening.","ALL","18 Years","55 Years",{"count":100,"type":101},48,"ESTIMATED","INTERVENTIONAL",[104],"PHASE1","The purpose of this clinical study is to find out if NNC0113-5840 is safe for treating people with excess body weight. There are 2 study treatments in this study, participants will get either NNC0113-5840 (the product being tested) or Placebo (treatment that has no active medicine in it), Which treatment participants get is decided by chance.",[107,108],"Obesity","Overweight","2026-08-03",{"date":111,"type":112},"2026-08-04","ACTUAL",{"date":114,"type":112},"2026-05-01",{"date":116,"type":101},"2026-12-26",{"name":5,"class":6},2]