[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100546067":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":22,"centralContacts":26,"locations":27,"responsibleParty":50,"collaborators":26,"id":52,"slug":53,"hasResults":54,"nctId":55,"briefTitle":56,"officialTitle":57,"acronym":58,"eligibilityCriteria":59,"healthyVolunteers":54,"sex":60,"minAge":61,"maxAge":62,"enrollmentInfo":63,"targetDuration":26,"studyType":66,"phases":67,"briefSummary":69,"conditions":70,"keywords":26,"overallStatus":74,"whyStopped":75,"lastUpdateSubmitDate":76,"lastUpdatePostDateStruct":77,"startDateStruct":79,"completionDateStruct":81,"leadSponsor":84,"locationsCount":85},{"fullName":5,"class":6},"Ferring Pharmaceuticals","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Nadofaragene Firadenovec","EXPERIMENTAL","Eligible subjects will receive nadofaragene firadenovec. This will be instilled quarterly in the bladder followed by quarterly disease assessments.",[13],"Drug: nadofaragene firadenovec",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DRUG","nadofaragene firadenovec","The investigational medicinal product dose, concentration, and assessments are aligned with nadofaragene firadenovec US prescribing information.",[9],[21],"Adstiladrin",[23],{"name":24,"affiliation":5,"role":25},"Global Clinical Compliance","STUDY_DIRECTOR",null,[28,41],{"facility":29,"status":26,"city":30,"state":31,"zip":32,"country":33,"countryCode":34,"cosmosGeoPoint":35,"geoPoint":40,"contacts":26},"Ferring Investigational Site","Little Rock","Arkansas","72211","United States","US",{"type":36,"coordinates":37},"Point",[38,39],-92.28959,34.74648,{"lat":39,"lon":38},{"facility":29,"status":26,"city":42,"state":43,"zip":44,"country":33,"countryCode":34,"cosmosGeoPoint":45,"geoPoint":49,"contacts":26},"Atlanta","Georgia","30328",{"type":36,"coordinates":46},[47,48],-84.38798,33.749,{"lat":48,"lon":47},{"type":51,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR","100546067","phase-4-a-trial-to-evaluate-efficacy-of-reinduction-with-nadofaragene-firadenovec-in-subjects-with-cis--high-grade-tat1-and-no-complete-response-to-first-nadofaragene-firadenovec-dose-100546067",false,"NCT06390111","A Trial to Evaluate Efficacy of Reinduction With Nadofaragene Firadenovec in Subjects With CIS ± High-grade Ta\u002FT1 and no Complete Response to First Nadofaragene Firadenovec Dose.","A Phase 4, Multi-center, Open Label Trial to Evaluate Efficacy of Reinduction With Nadofaragene Firadenovec in Subjects With CIS ± High-grade Ta\u002FT1 and no Complete Response to First Nadofaragene Firadenovec Dose.","ABLE-42","Inclusion Criteria:\n\n* Diagnosed, as documented, with CIS ± high-grade disease Ta\u002FT1 and absence of progression after first dose of nadofaragene firadenovec within the last 5 months from instillation.\n* Diagnosed, as documented, with:\n\n  * Low risk of disease progression as assessed at the discretion of the investigator\n  * Previous Bacillus Calmette Guerin (BCG) therapy (BCG exposed) with no maximum limit to the amount of BCG administered\n\nExclusion Criteria:\n\n* Current or previous evidence of muscle-invasive (muscularis propria) or metastatic disease presented at the screening visit. Examples of increased risk of muscle-invasive include but are not limited to:\n\n  * Presence of lymphovascular invasion and \u002F or micropapillary disease as shown in the histology of the biopsy sample\n  * Subjects with T1 disease accompanied by the presence of hydronephrosis secondary to the primary tumor\n* Current and prior systemic or local therapy for bladder cancer since first dose of nadofaragene firadenovec\n* Current or prior investigational treatment for BCG-unresponsive NMIBC or any other investigational drug (drug used in a clinical trial, i.e drug used in a Ferring sponsored non-interventional study does not apply) since first dose of nadofaragene firadenovec\n* Clinically significant and unexplained elevated liver or renal function tests\n* History of malignancy of other organ system within past 5 years, except treated basal cell carcinoma or squamous cell carcinoma of the skin and ≤pT2 upper tract urothelial carcinoma at least 24 months after nephroureterectomy. Also subjects with genitourinary cancers other than urothelial cancer or prostate cancer that are under active surveillance are excluded","ALL","18 Years","99 Years",{"count":64,"type":65},0,"ACTUAL","INTERVENTIONAL",[68],"PHASE4","In this phase 4 trial (000439), subjects with NMIBC CIS (± high-grade Ta\u002FT1) who have not responded to their first dose of nadofaragene firadenovec (commercial ADSTILADRIN received before trial entry) will be offered reinduction when entering the trial.",[71,72,73],"Bladder Cancer","Ta\u002FT1","CIS","WITHDRAWN","Ferring decided to prioritize collection of ADSTILADRIN re-induction data in patients with HR BCG-unresponsive NMIBC who did not have a CR to the initial dose of ADSTILADRIN through data sources within the clinical setting including ABLE-22 and -41.","2024-11-20",{"date":78,"type":65},"2024-11-22",{"date":80,"type":65},"2024-06-17",{"date":82,"type":83},"2026-07-31","ESTIMATED",{"name":5,"class":6},2]