[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100644741":3},{"organization":4,"armGroups":7,"interventions":10,"overallOfficials":15,"centralContacts":19,"locations":27,"responsibleParty":42,"collaborators":10,"id":44,"slug":10,"hasResults":45,"nctId":46,"briefTitle":47,"officialTitle":48,"acronym":49,"eligibilityCriteria":50,"healthyVolunteers":45,"sex":51,"minAge":52,"maxAge":10,"enrollmentInfo":53,"targetDuration":10,"studyType":56,"phases":10,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":29,"whyStopped":10,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},{"fullName":5,"class":6},"Centre Hospitalier Princesse Grace","OTHER",[8,12],{"label":9,"type":10,"description":11,"interventionNames":10},"JAK inhibitor morning then evening",null,"JAK inhibitor intake every morning during 3 months then every evening during 3 months",{"label":13,"type":10,"description":14,"interventionNames":10},"JAK inhibitor evening then morning","JAK inhibitor intake every evening during 3 months then every morning during 3 months",[16],{"name":17,"affiliation":5,"role":18},"Olivier BROCQ, MD","PRINCIPAL_INVESTIGATOR",[20,25],{"name":17,"role":21,"phone":22,"phoneExt":23,"email":24},"CONTACT","97 98 99 00","+377","recherche.clinique@chpg.mc",{"name":26,"role":21,"phone":22,"phoneExt":23,"email":24},"Nicolas RIJO",[28],{"facility":5,"status":29,"city":30,"state":10,"zip":31,"country":30,"countryCode":32,"cosmosGeoPoint":33,"geoPoint":38,"contacts":39},"RECRUITING","Monaco","98000","MC",{"type":34,"coordinates":35},"Point",[36,37],7.42145,43.73718,{"lat":37,"lon":36},[40,41],{"name":26,"role":21,"phone":22,"phoneExt":23,"email":24},{"name":17,"role":18,"phone":10,"phoneExt":10,"email":10},{"type":43,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100644741",false,"NCT07674134","Comparison of Oral Administration of a JAK Inhibitor in Rheumatoid Arthritis","Comparison of Morning Versus Evening Oral Administration of a JAK Inhibitor in Rheumatoid Arthritis","JAK-INHI","Inclusion Criteria:\n\n* Patient aged over 18 years\n* Patient with Rheumatoid Arthritis according to the 2010 ACR\u002FEULAR criteria\n* Patient meeting the criteria for initiation of a JAK inhibitor according to the marketing authorization and international recommendations\n* Patient capable of providing informed, written, dated, and signed consent before the start of any trial-related procedure.\n\nExclusion Criteria:\n\n* No contraindication to a bDMARD\n* Not stable dose of corticosteroids in the 4 weeks preceding enrollment\n* Not stable dose of maintenance therapy (methotrexate, leflunomide, hydroxychloroquine, cyclosporine, gold salts) in the 4 weeks preceding enrollment\n* Prior treatment with a JAK inhibitor\n* Patient unable to be followed-up in the study during 6 months\n* Minors or adults under guardianship or curatorship, or deprived of their liberty\n* Pregnant or breastfeeding patient\n* Patient refusing to use an effective method of contraception for the duration of the study\n* Person not affiliated with a social security scheme.","ALL","18 Years",{"count":54,"type":55},90,"ESTIMATED","OBSERVATIONAL","The aim of this study is to offer patients two treatment options: morning or evening administration of a JAK inhibitor prescribed within the framework of its marketing authorization, according to the EULAR response.\n\nThe objective is to determine whether evening administration in our patients with rheumatoid arthritis provides greater efficacy than morning administration in our patients taking JAK inhibitors once daily.",[59],"Rheumatoid Arthritis (RA)",[61],"JAK inhibitor","2026-06-23",{"date":64,"type":65},"2026-06-29","ACTUAL",{"date":67,"type":65},"2024-04-23",{"date":69,"type":55},"2026-11",{"name":5,"class":6},1]