[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100645068":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":32,"centralContacts":36,"locations":46,"responsibleParty":65,"collaborators":41,"id":68,"slug":41,"hasResults":69,"nctId":70,"briefTitle":71,"officialTitle":71,"acronym":72,"eligibilityCriteria":73,"healthyVolunteers":69,"sex":74,"minAge":75,"maxAge":41,"enrollmentInfo":76,"targetDuration":41,"studyType":79,"phases":80,"briefSummary":82,"conditions":83,"keywords":87,"overallStatus":49,"whyStopped":41,"lastUpdateSubmitDate":93,"lastUpdatePostDateStruct":94,"startDateStruct":97,"completionDateStruct":99,"leadSponsor":101,"locationsCount":102},{"fullName":5,"class":6},"Instituto Mexicano del Seguro Social","OTHER_GOV",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Dual therapy: darunavir\u002Fcobicistat + lamivudine","ACTIVE_COMPARATOR","Darunavir\u002Fcobicistat 800\u002F150 mg + lamivudine 300 mg. This arm is the active comparator one, with dual therapy, 2 drugs: darunavir\u002Fcobicistat 800\u002F150 mg plus lamivudine 300 mg",[13],"Drug: Dual therapy: darunavir\u002Fcobicistat + lamivudine",{"label":15,"type":16,"description":17,"interventionNames":18},"Triple therapy: darunavir\u002Fcobicistat plus tenofovir alafenamide\u002Femtricitabine","EXPERIMENTAL","Darunavir\u002Fcobicistat 800\u002F150 mg + tenofovir alafenamide\u002Femtricitabine 10\u002F200 mg. This treatment is the commonly used or standard 3-drug therapy, this arm is the active comparator one consisting of darunavir\u002Fcobicistat 800\u002F150 mg, plus tenofovir alafenamide\u002Femtricitabine 10\u002F200 mg.",[19],"Drug: Triple therapy: darunavir\u002Fcobicistat plus tenofovir alafenamide\u002Femtricitabine",[21,27],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"DRUG","The intervention group will receive dual therapy with DRV\u002FC 800\u002F150 mg + 3TC 300 mg, which will be compared to standard 3-drug therapy: DRV\u002FC 800\u002F150 mg + TAF\u002FFTC 10\u002F200 mg.",[9],[26],"DRV\u002FC+3TC",{"type":22,"name":15,"description":28,"armGroupLabels":29,"otherNames":30},"The intervention group will receive triple therapy: DRV\u002FC 800\u002F150 mg + TAF\u002FFTC 10\u002F200 mg.which will be compared to dual therapy with DRV\u002FC 800\u002F150 mg + 3TC 300 mg.",[15],[31],"DRV\u002Fc+TAF\u002FFTC",[33],{"name":34,"affiliation":5,"role":35},"Sandra Patricia Ramírez Eguia","PRINCIPAL_INVESTIGATOR",[37,43],{"name":38,"role":39,"phone":40,"phoneExt":41,"email":42},"José Antonio Mata Marín, Master","CONTACT","+524428518215",null,"sandrarmzeg@gmail.com",{"name":44,"role":39,"phone":45,"phoneExt":41,"email":42},"Jóse Antonio Mata Marin, Master","4428518215",[47],{"facility":48,"status":49,"city":50,"state":50,"zip":51,"country":52,"cosmosGeoPoint":53,"geoPoint":58,"contacts":59},"Hospital de Infectología \"Dr Daniel Méndez Hernández\" National Medical Center \"La Raza\", Instituto Mexicano del Seguro Social","RECRUITING","Mexico City","02990","Mexico",{"type":54,"coordinates":55},"Point",[56,57],-99.12766,19.42847,{"lat":57,"lon":56},[60,62,64],{"name":61,"role":39,"phone":45,"phoneExt":41,"email":42},"Jóse Antonio Mata Marin",{"name":63,"role":39,"phone":45,"phoneExt":41,"email":42},"Jóse Antonio Mata Marín",{"name":34,"role":35,"phone":41,"phoneExt":41,"email":41},{"type":35,"investigatorFullName":66,"investigatorTitle":67,"investigatorAffiliation":5,"oldNameTitle":41,"oldOrganization":41},"José Antonio Mata Marín","Effectiveness and safety of darunavir\u002Fcobicistat plus lamivudine compared with darunavir\u002Fcobicistat plus tenofovir alafenamide\u002Femtricitabine in virologically suppressed people living with HIV at 24 and 48 weeks of follow-up","100645068",false,"NCT07678268","Effectiveness and Safety of Darunavir\u002FCobicistat Plus Lamivudine Compared With Darunavir\u002FCobicistat Plus Tenofovir Alafenamide\u002FEmtricitabine in Virologically Suppressed People Living With HIV at 24 and 48 Weeks of Follow-up","TLALOC-2","Inclusion Criteria:\n\n* Virologically suppressed men living with HIV, transitioning from a DRV\u002Fc (800 mg\u002F150 mg) + TDF\u002FFTC (300 mg\u002F200 mg) regimen for at least 48 weeks prior to the study\n* Viral suppression for 48 weeks prior to the study\n* Agree to participate in the study by signing a written informed consent form\n* Age ≥18 years\n* Glomerular filtration rate (GFR) by CDK-EPI ≥60 mL\u002Fmin\n* Beneficiaries of the Mexican Social Security Institute (IMSS) treated at the Infectious Diseases Hospital of the \"La Raza\" National Medical Center\n\nExclusion Criteria:\n\n* Withdrawal of informed consent\n* Loss of coverage\n* Failure to attend sample collection within the required timeframe","MALE","18 Years",{"count":77,"type":78},78,"ESTIMATED","INTERVENTIONAL",[81],"PHASE4","A single-center, open-label, randomized pilot clinical trial between March 2025 and March 2026 at the Hospital de Infectología \"La Raza\" National Medical Center in Mexico City. Eligible participants were adult males (≥18 years) with HIV-1 infection who had maintained virological suppression (HIV-1 RNA \\\u003C50 copies\u002FmL) for 48 weeks on either DRV\u002Fc + 3TC or DRV\u002Fc + TDF\u002FFTC prior to enrollment (TLALOC-1 trial), and had an estimated glomerular filtration rate (eGFR) by CKD-EPI ≥60 mL\u002Fmin\u002F1.73 m². The primary endpoints were virological efficacy and safety at 24 weeks.",[84,85,86],"HIV Infection","Antiretroviral Therapy","Lentivirus Infections",[88,89,90,91,92],"HIV infection","antiretroviral therapy","two drugs regimen","renal safety","neuropsychiatric adverse events","2026-06-25",{"date":95,"type":96},"2026-07-01","ACTUAL",{"date":98,"type":96},"2025-07-10",{"date":100,"type":78},"2026-12-10",{"name":5,"class":6},1]