[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100640656":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":26,"centralContacts":30,"locations":11,"responsibleParty":36,"collaborators":11,"id":38,"slug":39,"hasResults":40,"nctId":41,"briefTitle":42,"officialTitle":43,"acronym":11,"eligibilityCriteria":44,"healthyVolunteers":45,"sex":46,"minAge":47,"maxAge":48,"enrollmentInfo":49,"targetDuration":11,"studyType":52,"phases":53,"briefSummary":55,"conditions":56,"keywords":58,"overallStatus":61,"whyStopped":11,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":11},{"fullName":5,"class":6},"Regeneron Pharmaceuticals","INDUSTRY",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"REGN20934","EXPERIMENTAL",null,[13],"Drug: REGN20934",{"label":15,"type":16,"description":11,"interventionNames":17},"Placebo","PLACEBO_COMPARATOR",[18],"Drug: Placebo",[20,24],{"type":21,"name":9,"description":22,"armGroupLabels":23,"otherNames":11},"DRUG","Administered per the protocol",[9],{"type":21,"name":15,"description":22,"armGroupLabels":25,"otherNames":11},[15],[27],{"name":28,"affiliation":5,"role":29},"Clinical Trial Management","STUDY_DIRECTOR",[31],{"name":32,"role":33,"phone":34,"phoneExt":11,"email":35},"Clinical Trials Administrator","CONTACT","844-734-6643","clinicaltrials@regeneron.com",{"type":37,"investigatorFullName":11,"investigatorTitle":11,"investigatorAffiliation":11,"oldNameTitle":11,"oldOrganization":11},"SPONSOR","100640656","phase-1-safety-and-drug-concentrations-of-regn20934-in-adults-with-overweight-or-obesity-100640656",false,"NCT07594093","Safety and Drug Concentrations of REGN20934 in Adults With Overweight or Obesity","A Phase 1, Randomized, Double-Blind, Placebo-Controlled Study of the Safety, Tolerability, and Pharmacokinetics of Single Ascending Doses of REGN20934 in Adult Participants With Overweight or Obesity","Key Inclusion Criteria:\n\n1\\. Has a Body Mass Index (BMI) 25 to 35 kg\u002Fm\\^2\n\nKey Exclusion Criteria:\n\n1. A self-reported change of body weight \\>5 kg within approximately 90 days of visit 2\n2. History of type 1 or type 2 diabetes\n3. History of clinically significant cardiovascular, respiratory, hepatic, renal, gastrointestinal, endocrine, hematological, psychiatric, or neurological disease, as defined in the protocol\n\nNote: Other protocol defined inclusion\u002Fexclusion criteria apply",true,"ALL","18 Years","65 Years",{"count":50,"type":51},90,"ESTIMATED","INTERVENTIONAL",[54],"PHASE1","This study will test a study drug called REGN20934 to see how safe and well tolerated this drug is, as well as how the drug is processed in the body for participants with overweight or obesity.\n\nThe study is looking at:\n\n* What side effects REGN20934 might cause\n* How much REGN20934 is in the blood at different times\n* If the body makes antibodies to REGN20934",[57],"Overweight or Obesity",[59,60],"Overweight","Obesity or without diabetes","NOT_YET_RECRUITING","2026-05-11",{"date":64,"type":65},"2026-05-18","ACTUAL",{"date":67,"type":51},"2026-06-15",{"date":69,"type":51},"2027-02-22",{"name":5,"class":6}]