[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100427350":3},{"organization":4,"armGroups":7,"interventions":23,"overallOfficials":38,"centralContacts":43,"locations":55,"responsibleParty":754,"collaborators":756,"id":759,"slug":760,"hasResults":761,"nctId":762,"briefTitle":763,"officialTitle":764,"acronym":765,"eligibilityCriteria":766,"healthyVolunteers":761,"sex":767,"minAge":768,"maxAge":769,"enrollmentInfo":770,"targetDuration":48,"studyType":773,"phases":774,"briefSummary":776,"conditions":777,"keywords":779,"overallStatus":71,"whyStopped":48,"lastUpdateSubmitDate":792,"lastUpdatePostDateStruct":793,"startDateStruct":796,"completionDateStruct":798,"leadSponsor":800,"locationsCount":801},{"fullName":5,"class":6},"Miltenyi Biomedicine GmbH","INDUSTRY",[8,14,17],{"label":9,"type":10,"description":11,"interventionNames":12},"Part I: CAR T-cell MB-CART2019.1","EXPERIMENTAL","Single infusion of 2.5 × 10\\^6 CAR-transduced autologous T cells per kg\u002Fbody weight.",[13],"Genetic: MB-CART2019.1",{"label":15,"type":10,"description":11,"interventionNames":16},"Part II: CAR T-cell MB-CART2019.1",[13],{"label":18,"type":19,"description":20,"interventionNames":21},"PART I: Standard of Care","ACTIVE_COMPARATOR","R-GemOx R-Pola",[22],"Drug: Standard of Care",[24,32],{"type":25,"name":26,"description":27,"armGroupLabels":28,"otherNames":29},"GENETIC","MB-CART2019.1","MB-CART2019.1 is designed to effectively target malignant B cells in patients suffering from late stage haematological B-cell malignancies. MB-CART2019.1 consists of autologous cluster of differentiation CD20\u002FCD19 chimeric antigen receptor (CAR) transduced CD4\u002FCD8 enriched T cells, derived from a leukapheresis and processed by using the CliniMACS Prodigy® device.",[9,15],[30,31],"Zamtocabtagene Autoleucel","Zamto-cel",{"type":33,"name":34,"description":34,"armGroupLabels":35,"otherNames":36},"DRUG","Standard of Care",[18],[37],"Rituximab, Gemcitabine, Oxaliplatin, Polatuzumab vedotin, Bendamustine, Rituximab",[39],{"name":40,"affiliation":41,"role":42},"Peter Borchmann, Prof. Dr.","University Hospital Cologne","PRINCIPAL_INVESTIGATOR",[44,50],{"name":45,"role":46,"phone":47,"phoneExt":48,"email":49},"Mark Hess, Dr.","CONTACT","+49 160 9897 0124",null,"mark.hess@miltenyi.com",{"name":51,"role":46,"phone":52,"phoneExt":53,"email":54},"Gregor Zadoyan, Dr.","+49 2204 8306","6639","gregor.zadoyan@miltenyi.com",[56,69,83,97,111,126,140,156,171,185,202,215,228,244,253,262,271,280,294,308,322,336,352,366,380,394,408,422,436,450,464,478,492,507,521,537,553,567,581,590,601,617,633,645,656,669,683,697,711,726,740],{"facility":57,"status":58,"city":59,"state":48,"zip":60,"country":61,"countryCode":62,"cosmosGeoPoint":63,"geoPoint":68,"contacts":48},"LKH - Medizinische Universitaet Graz","ACTIVE_NOT_RECRUITING","Graz","8036","Austria","AT",{"type":64,"coordinates":65},"Point",[66,67],15.44197,47.06733,{"lat":67,"lon":66},{"facility":70,"status":71,"city":72,"state":48,"zip":73,"country":61,"countryCode":62,"cosmosGeoPoint":74,"geoPoint":78,"contacts":79},"Universitatsklinikum Innsbruck Universitatsklinik fur Innere Medizin V","RECRUITING","Innsbruck","6020",{"type":64,"coordinates":75},[76,77],11.39454,47.26266,{"lat":77,"lon":76},[80],{"name":81,"role":46,"phone":48,"phoneExt":48,"email":82},"Norman Steiner, Dr.","normann.steiner@tirol-kliniken.at",{"facility":84,"status":71,"city":85,"state":48,"zip":86,"country":61,"countryCode":62,"cosmosGeoPoint":87,"geoPoint":91,"contacts":92},"Ordensklinikum Linz GmbH Elisabethinen","Linz","4020",{"type":64,"coordinates":88},[89,90],14.28611,48.30639,{"lat":90,"lon":89},[93],{"name":94,"role":46,"phone":95,"phoneExt":48,"email":96},"Veronika Buxhofer-Ausch, Dr.","+4373276764409","veronika.buxhofer@elisabethinen.or.at",{"facility":98,"status":71,"city":99,"state":48,"zip":100,"country":61,"countryCode":62,"cosmosGeoPoint":101,"geoPoint":105,"contacts":106},"Medizinische Universitaet Wien - Allgemeines Krankenhaus der Stadt Wien (AKH)","Vienna","1090",{"type":64,"coordinates":102},[103,104],16.37208,48.20849,{"lat":104,"lon":103},[107],{"name":108,"role":46,"phone":109,"phoneExt":48,"email":110},"Ulrich Jaeger, Prof.","+4314040044090","ulrich.jaeger@meduniwien.ac.at",{"facility":112,"status":71,"city":113,"state":48,"zip":114,"country":115,"countryCode":116,"cosmosGeoPoint":117,"geoPoint":121,"contacts":122},"Jules Bordet lnstitute","Anderlecht","1070","Belgium","BE",{"type":64,"coordinates":118},[119,120],4.31454,50.83619,{"lat":120,"lon":119},[123],{"name":124,"role":46,"phone":48,"phoneExt":48,"email":125},"Fulvio Massaro, Dr.","fulvio.massaro@hubruxelles.be",{"facility":127,"status":71,"city":128,"state":48,"zip":129,"country":115,"countryCode":116,"cosmosGeoPoint":130,"geoPoint":134,"contacts":135},"Universitaire Ziekenhuizen Leuven - Campus Gasthuisberg","Leuven","3000",{"type":64,"coordinates":131},[132,133],4.70093,50.87959,{"lat":133,"lon":132},[136],{"name":137,"role":46,"phone":138,"phoneExt":48,"email":139},"Peter Vandenberghe, Prof.","+32 16346889","peter.vandenberghe@uzleuven.be",{"facility":141,"status":71,"city":142,"state":48,"zip":143,"country":144,"countryCode":145,"cosmosGeoPoint":146,"geoPoint":150,"contacts":151},"University Hospital Center Zagreb","Zagreb","10000","Croatia","HR",{"type":64,"coordinates":147},[148,149],15.97798,45.81444,{"lat":149,"lon":148},[152],{"name":153,"role":46,"phone":154,"phoneExt":48,"email":155},"Igor Aurer, Prof.","+385 1238 8265","iaurer@kbc-zagreb.hr",{"facility":157,"status":71,"city":158,"state":48,"zip":159,"country":160,"countryCode":48,"cosmosGeoPoint":161,"geoPoint":165,"contacts":166},"University Hospital Hradec Kralove","Hradec Králové","50005","Czechia",{"type":64,"coordinates":162},[163,164],15.83277,50.20923,{"lat":164,"lon":163},[167],{"name":168,"role":46,"phone":169,"phoneExt":48,"email":170},"David Belada, Dr.","+420 602128826","david.belada@seznam.cz",{"facility":172,"status":71,"city":173,"state":48,"zip":174,"country":160,"countryCode":48,"cosmosGeoPoint":175,"geoPoint":179,"contacts":180},"FNsP Ostrava","Ostrava","70852",{"type":64,"coordinates":176},[177,178],18.28204,49.83465,{"lat":178,"lon":177},[181],{"name":182,"role":46,"phone":183,"phoneExt":48,"email":184},"Michal Kascak, Dr.","+420 597 371 111","michal.kascak@fno.cz",{"facility":186,"status":187,"city":188,"state":48,"zip":189,"country":190,"countryCode":191,"cosmosGeoPoint":192,"geoPoint":196,"contacts":197},"Helsinki University Comprehensive Cancer Center","NOT_YET_RECRUITING","Helsinki","00029","Finland","FI",{"type":64,"coordinates":193},[194,195],24.93545,60.16952,{"lat":195,"lon":194},[198],{"name":199,"role":46,"phone":200,"phoneExt":48,"email":201},"Sirpa Leppa, Prof.","+358 5042 70820","sirpa.leppa@hus.fi",{"facility":203,"status":71,"city":204,"state":48,"zip":205,"country":190,"countryCode":191,"cosmosGeoPoint":206,"geoPoint":210,"contacts":211},"Oulu University Central Hospital","Oulu","90220",{"type":64,"coordinates":207},[208,209],25.46816,65.01236,{"lat":209,"lon":208},[212],{"name":213,"role":46,"phone":48,"phoneExt":48,"email":214},"Hanne Kuitunen, Dr.","hanne.kuitunen@ppshp.fi",{"facility":216,"status":71,"city":217,"state":48,"zip":218,"country":190,"countryCode":191,"cosmosGeoPoint":219,"geoPoint":223,"contacts":224},"Turku University Hospital","Turku","20520",{"type":64,"coordinates":220},[221,222],22.26869,60.45148,{"lat":222,"lon":221},[225],{"name":226,"role":46,"phone":48,"phoneExt":48,"email":227},"Juha Ranti, Dr","juha.ranti@varha.fi",{"facility":229,"status":71,"city":230,"state":48,"zip":231,"country":232,"countryCode":233,"cosmosGeoPoint":234,"geoPoint":238,"contacts":239},"Centre Hospitalier Universitaire (CHU) - Hopital Henri Mondor","Créteil","94010","France","FR",{"type":64,"coordinates":235},[236,237],2.46569,48.79266,{"lat":237,"lon":236},[240],{"name":241,"role":46,"phone":242,"phoneExt":48,"email":243},"Francois Lemmonier, Dr.","+33 1 49 81 21 71","Francois.LeMonnier@aphp.fr",{"facility":245,"status":58,"city":246,"state":48,"zip":247,"country":232,"countryCode":233,"cosmosGeoPoint":248,"geoPoint":252,"contacts":48},"CHRU de Lille - Hopital Claude Huriez","Lille","59000",{"type":64,"coordinates":249},[250,251],3.05512,50.63391,{"lat":251,"lon":250},{"facility":254,"status":58,"city":255,"state":48,"zip":256,"country":232,"countryCode":233,"cosmosGeoPoint":257,"geoPoint":261,"contacts":48},"Centre Hospitalier Lyon Sud, Hospices Civils de Lyon Groupement Hospitalier Sud","Lyon","69495",{"type":64,"coordinates":258},[259,260],4.84789,45.74906,{"lat":260,"lon":259},{"facility":263,"status":58,"city":264,"state":48,"zip":265,"country":232,"countryCode":233,"cosmosGeoPoint":266,"geoPoint":270,"contacts":48},"Centre Paoli Calmettes","Marseille","13273",{"type":64,"coordinates":267},[268,269],5.38107,43.29695,{"lat":269,"lon":268},{"facility":272,"status":58,"city":273,"state":48,"zip":274,"country":232,"countryCode":233,"cosmosGeoPoint":275,"geoPoint":279,"contacts":48},"Centre Hospitalier Universitaire de Nantes (CHU de Nantes) - Hopital Hotel Dieu","Nantes","44093",{"type":64,"coordinates":276},[277,278],-1.55336,47.21725,{"lat":278,"lon":277},{"facility":281,"status":71,"city":282,"state":48,"zip":283,"country":232,"countryCode":233,"cosmosGeoPoint":284,"geoPoint":288,"contacts":289},"Centre Hospitalier Universitaire de Bordeaux - Hopital Haut-Leveque","Pessac","33600",{"type":64,"coordinates":285},[286,287],-0.6324,44.80565,{"lat":287,"lon":286},[290],{"name":291,"role":46,"phone":292,"phoneExt":48,"email":293},"Francois-Xavier Gros, Dr.","+33 5 57 65 64 94","francois-xavier.gros@chu-bordeaux.fr",{"facility":295,"status":71,"city":296,"state":48,"zip":297,"country":232,"countryCode":233,"cosmosGeoPoint":298,"geoPoint":302,"contacts":303},"Centre Hospitalier Universitaire de Poitiers","Poitiers","86000",{"type":64,"coordinates":299},[300,301],0.34348,46.58261,{"lat":301,"lon":300},[304],{"name":305,"role":46,"phone":306,"phoneExt":48,"email":307},"Stephanie Guidez, Dr.","+33 5 49 44 46 89","stephanie.guidez@chu-poitiers.fr",{"facility":309,"status":71,"city":310,"state":48,"zip":311,"country":232,"countryCode":233,"cosmosGeoPoint":312,"geoPoint":316,"contacts":317},"Institut Universitaire du Cancer Service d´hématologie","Toulouse","31059",{"type":64,"coordinates":313},[314,315],1.44367,43.60426,{"lat":315,"lon":314},[318],{"name":319,"role":46,"phone":320,"phoneExt":48,"email":321},"Pierre Bories, Dr.","+33 531 1565 14","bories@onco-occitanie.fr",{"facility":323,"status":71,"city":324,"state":48,"zip":325,"country":232,"countryCode":233,"cosmosGeoPoint":326,"geoPoint":330,"contacts":331},"CHU de Nancy Hopitaux de Brabois","Vandœuvre-lès-Nancy","54500",{"type":64,"coordinates":327},[328,329],6.17114,48.66115,{"lat":329,"lon":328},[332],{"name":333,"role":46,"phone":334,"phoneExt":48,"email":335},"Pierre Feugier, Prof.","+33 383153282","p.feugier@chru-nancy.fr",{"facility":337,"status":71,"city":338,"state":48,"zip":339,"country":340,"countryCode":341,"cosmosGeoPoint":342,"geoPoint":346,"contacts":347},"Universitatsklinikum Augsburg","Augsburg","86156","Germany","DE",{"type":64,"coordinates":343},[344,345],10.89851,48.37154,{"lat":345,"lon":344},[348],{"name":349,"role":46,"phone":350,"phoneExt":48,"email":351},"Christoph Schmid, Dr.","+49 821 4003714","christoph.schmid@klinikum-augsburg.de",{"facility":353,"status":71,"city":354,"state":48,"zip":355,"country":340,"countryCode":341,"cosmosGeoPoint":356,"geoPoint":360,"contacts":361},"Universitaetsklinikum Knappschaftskrankenhaus Bochum der Ruhr-Universitat Bochum","Bochum","44892",{"type":64,"coordinates":357},[358,359],7.21648,51.48165,{"lat":359,"lon":358},[362],{"name":363,"role":46,"phone":364,"phoneExt":48,"email":365},"Roland Schroers, Prof.","+49 2342993447","roland.schroers@rub.de",{"facility":367,"status":71,"city":368,"state":48,"zip":369,"country":340,"countryCode":341,"cosmosGeoPoint":370,"geoPoint":374,"contacts":375},"Universitaetsklinikum Koeln","Cologne","50937",{"type":64,"coordinates":371},[372,373],6.95,50.93333,{"lat":373,"lon":372},[376],{"name":377,"role":46,"phone":378,"phoneExt":48,"email":379},"Peter Borchmann, Prof.","+49 221 478 88159","peter.borchmann@uk-koeln.de",{"facility":381,"status":71,"city":382,"state":48,"zip":383,"country":340,"countryCode":341,"cosmosGeoPoint":384,"geoPoint":388,"contacts":389},"Klinikum Erlangen der Friedrich-Alexander-Universitaet Erlangen-Nuernberg","Erlangen","91054",{"type":64,"coordinates":385},[386,387],11.00783,49.59099,{"lat":387,"lon":386},[390],{"name":391,"role":46,"phone":392,"phoneExt":48,"email":393},"Andreas Mackensen, Prof. Dr.","+49 9131 85-35954","andreas.mackensen@uk-erlangen.de",{"facility":395,"status":71,"city":396,"state":48,"zip":397,"country":340,"countryCode":341,"cosmosGeoPoint":398,"geoPoint":402,"contacts":403},"Universitaetsklinikum Essen","Essen","45147",{"type":64,"coordinates":399},[400,401],7.01228,51.45657,{"lat":401,"lon":400},[404],{"name":405,"role":46,"phone":406,"phoneExt":48,"email":407},"Bastian Von Tresckow, Dr.","+49 2017233136","bastian.vontresckow@uk-essen.de",{"facility":409,"status":71,"city":410,"state":48,"zip":411,"country":340,"countryCode":341,"cosmosGeoPoint":412,"geoPoint":416,"contacts":417},"University Medical Center Hamburg-Eppendorf","Hamburg","20246",{"type":64,"coordinates":413},[414,415],9.99302,53.55073,{"lat":415,"lon":414},[418],{"name":419,"role":46,"phone":420,"phoneExt":48,"email":421},"Francis Ayuk, Prof. Dr.","+49 40741054850","ayuketan@uke.de",{"facility":423,"status":71,"city":424,"state":48,"zip":425,"country":340,"countryCode":341,"cosmosGeoPoint":426,"geoPoint":430,"contacts":431},"Universitaetsklinikum Heidelberg","Heidelberg","69120",{"type":64,"coordinates":427},[428,429],8.69079,49.40768,{"lat":429,"lon":428},[432],{"name":433,"role":46,"phone":434,"phoneExt":48,"email":435},"Peter Dreger, Prof. Dr.","+49 6221568008","peter.dreger@med.uni-heidelberg.de",{"facility":437,"status":71,"city":438,"state":48,"zip":439,"country":340,"countryCode":341,"cosmosGeoPoint":440,"geoPoint":444,"contacts":445},"Universitätsklinikum Leipzig","Leipzig","04103",{"type":64,"coordinates":441},[442,443],12.37129,51.33962,{"lat":443,"lon":442},[446],{"name":447,"role":46,"phone":448,"phoneExt":48,"email":449},"Vladan Vucinic, Dr. med.","+49 341 97 13050","Vladan.Vucinic@medizin.uni-leipzig.de",{"facility":451,"status":71,"city":452,"state":48,"zip":453,"country":340,"countryCode":341,"cosmosGeoPoint":454,"geoPoint":458,"contacts":459},"Klinikum der Universitat München, Studienzentrale fur Hematologie der Medizinischen Klinik II","München","81377",{"type":64,"coordinates":455},[456,457],13.31243,51.60698,{"lat":457,"lon":456},[460],{"name":461,"role":46,"phone":462,"phoneExt":48,"email":463},"Veit Bücklein, Dr.","+49 8944000","veit.buecklein@med.uni-muenchen.de",{"facility":465,"status":71,"city":466,"state":48,"zip":467,"country":340,"countryCode":341,"cosmosGeoPoint":468,"geoPoint":472,"contacts":473},"University Hospital Regensburg","Regensburg","93053",{"type":64,"coordinates":469},[470,471],12.10161,49.01513,{"lat":471,"lon":470},[474],{"name":475,"role":46,"phone":476,"phoneExt":48,"email":477},"Matthias Edinger, Prof. Dr.","+49 94 9445580","matthias.edinger@ukr.de",{"facility":479,"status":71,"city":480,"state":48,"zip":481,"country":340,"countryCode":341,"cosmosGeoPoint":482,"geoPoint":486,"contacts":487},"University Hospital of Tuebingen","Tübingen","72076",{"type":64,"coordinates":483},[484,485],9.05222,48.52266,{"lat":485,"lon":484},[488],{"name":489,"role":46,"phone":490,"phoneExt":48,"email":491},"Wolfgang Bethge, Prof. Dr.","+49 70712983176","wolfgang.bethge@med.uni-tuebingen.de",{"facility":493,"status":71,"city":494,"state":48,"zip":495,"country":496,"countryCode":497,"cosmosGeoPoint":498,"geoPoint":502,"contacts":503},"Del-Pesti Centrumkorhaz - Orszagos Hematologiai es Infektologiai Intezet","Budapest","1097","Hungary","HU",{"type":64,"coordinates":499},[500,501],19.04045,47.49835,{"lat":501,"lon":500},[504],{"name":505,"role":46,"phone":48,"phoneExt":48,"email":506},"Laszlo Gopcsa, Dr.","gopcsa.laszlo@dpckorhaz.hu",{"facility":508,"status":71,"city":509,"state":48,"zip":510,"country":496,"countryCode":497,"cosmosGeoPoint":511,"geoPoint":515,"contacts":516},"Debreceni Egyetem - Orvos es Egeszsegtudomanyi Centrum (DEOEC) (University of Debrecen Medical and Health Science Center)","Debrecen","4032",{"type":64,"coordinates":512},[513,514],21.62444,47.53167,{"lat":514,"lon":513},[517],{"name":518,"role":46,"phone":519,"phoneExt":48,"email":520},"Arpad Illes, Prof. Dr.","+36 52255601","illesarpaddr@gmail.com",{"facility":522,"status":71,"city":523,"state":48,"zip":524,"country":525,"countryCode":526,"cosmosGeoPoint":527,"geoPoint":531,"contacts":532},"Azienda Ospedaliera San Giovanni Battista Di Torino","Torino","10126","Italy","IT",{"type":64,"coordinates":528},[529,530],11.99138,44.88856,{"lat":530,"lon":529},[533],{"name":534,"role":46,"phone":535,"phoneExt":48,"email":536},"Barbara Botto, Dr.","+39 116335967","bbotto@cittadellasalute.to.it",{"facility":538,"status":71,"city":539,"state":48,"zip":540,"country":541,"countryCode":542,"cosmosGeoPoint":543,"geoPoint":547,"contacts":548},"Amsterdam Universitaire Medische Centra (UMC) - locatie Amsterdam Medisch Centrum (AMC)","Amsterdam","1105 AZ","Netherlands","NL",{"type":64,"coordinates":544},[545,546],4.88969,52.37403,{"lat":546,"lon":545},[549],{"name":550,"role":46,"phone":551,"phoneExt":48,"email":552},"Marie Kersten, Dr.","+31 20566 5955","m.j.kersten@amsterdamumc.nl",{"facility":554,"status":71,"city":555,"state":48,"zip":556,"country":541,"countryCode":542,"cosmosGeoPoint":557,"geoPoint":561,"contacts":562},"University Medical Center Groningen","Groningen","9713 GZ",{"type":64,"coordinates":558},[559,560],6.56667,53.21917,{"lat":560,"lon":559},[563],{"name":564,"role":46,"phone":565,"phoneExt":48,"email":566},"Tom van Meerten, Dr.","+31 503616161","t.van.meerten@umcg.nl",{"facility":568,"status":71,"city":569,"state":48,"zip":570,"country":541,"countryCode":542,"cosmosGeoPoint":571,"geoPoint":575,"contacts":576},"Leiden University Medical Center (LUMC)","Leiden","2333 ZA",{"type":64,"coordinates":572},[573,574],4.49306,52.15833,{"lat":574,"lon":573},[577],{"name":578,"role":46,"phone":579,"phoneExt":48,"email":580},"Aniko Sijs Szabo, Dr.","+31 71 5296524","a.sijs-szabo@lumc.nl",{"facility":582,"status":58,"city":583,"state":48,"zip":584,"country":541,"countryCode":542,"cosmosGeoPoint":585,"geoPoint":589,"contacts":48},"Erasmus University Medical Center","Rotterdam","3015 GC",{"type":64,"coordinates":586},[587,588],4.47917,51.9225,{"lat":588,"lon":587},{"facility":591,"status":58,"city":592,"state":48,"zip":593,"country":594,"countryCode":595,"cosmosGeoPoint":596,"geoPoint":600,"contacts":48},"Uniwersytecki Szpital Kliniczny - Klinika Hematologii, Terapii Komorkowych i Chorob Wewnetrznych","Wroclaw","50367","Poland","PL",{"type":64,"coordinates":597},[598,599],17.03006,51.10286,{"lat":599,"lon":598},{"facility":602,"status":187,"city":603,"state":48,"zip":604,"country":605,"countryCode":606,"cosmosGeoPoint":607,"geoPoint":611,"contacts":612},"Instituto Portugues de Oncologia do Porto Francisco Gentil E.P.E","Porto","4200-072","Portugal","PT",{"type":64,"coordinates":608},[609,610],-8.61097,41.1485,{"lat":610,"lon":609},[613],{"name":614,"role":46,"phone":615,"phoneExt":48,"email":616},"Jose Mario Mariz, Dr.","+351 2250 84000","mariz@ipoporto.min-saude.pt",{"facility":618,"status":71,"city":619,"state":48,"zip":620,"country":621,"countryCode":622,"cosmosGeoPoint":623,"geoPoint":627,"contacts":628},"Hospital Universitari Vall d'Hebron","Barcelona","08035","Spain","ES",{"type":64,"coordinates":624},[625,626],2.15899,41.38879,{"lat":626,"lon":625},[629],{"name":630,"role":46,"phone":631,"phoneExt":48,"email":632},"Gloria Iacoboni Garcia-Calvo, Dr.","+34 680522422","giacoboni@vhio.net",{"facility":634,"status":71,"city":619,"state":48,"zip":635,"country":621,"countryCode":622,"cosmosGeoPoint":636,"geoPoint":638,"contacts":639},"Hospital Clinic de Barcelona (Hospital Clinic i Provincial)","08036",{"type":64,"coordinates":637},[625,626],{"lat":626,"lon":625},[640],{"name":641,"role":46,"phone":642,"phoneExt":643,"email":644},"Ana Triguero, Dr.","+34 93 227 43 53","4366","atriguero@clinic.cat",{"facility":646,"status":71,"city":619,"state":48,"zip":647,"country":621,"countryCode":622,"cosmosGeoPoint":648,"geoPoint":650,"contacts":651},"Catalan Institute of Oncology (ICO) Hospitalet","08907",{"type":64,"coordinates":649},[625,626],{"lat":626,"lon":625},[652],{"name":653,"role":46,"phone":654,"phoneExt":48,"email":655},"Anna Sureda Balari, Dr.","+34 935565649","asureda@iconcologia.net",{"facility":657,"status":71,"city":658,"state":48,"zip":659,"country":621,"countryCode":622,"cosmosGeoPoint":660,"geoPoint":664,"contacts":665},"Hospital Clínico San Carlos (HCSC)","Madrid","28040",{"type":64,"coordinates":661},[662,663],-3.70256,40.4165,{"lat":663,"lon":662},[666],{"name":667,"role":46,"phone":48,"phoneExt":48,"email":668},"Daniel Morillo Giles, Dr.","dmorillo@startmadrid.com",{"facility":670,"status":71,"city":671,"state":48,"zip":672,"country":621,"countryCode":622,"cosmosGeoPoint":673,"geoPoint":677,"contacts":678},"Hospital Universitario Virgen De La Arrixaca (Huva)","Murcia","30120",{"type":64,"coordinates":674},[675,676],-1.13004,37.98704,{"lat":676,"lon":675},[679],{"name":680,"role":46,"phone":681,"phoneExt":48,"email":682},"Antonio Salar Silvestre, Dr.","+34 932483343","antonio.salar2@carm.es",{"facility":684,"status":71,"city":685,"state":48,"zip":686,"country":621,"countryCode":622,"cosmosGeoPoint":687,"geoPoint":691,"contacts":692},"Clinica Universidad de Navarra","Pamplona","31008",{"type":64,"coordinates":688},[689,690],-1.64323,42.81687,{"lat":690,"lon":689},[693],{"name":694,"role":46,"phone":695,"phoneExt":48,"email":696},"Carlos Grande Garcia, Dr.","+34 913 531 920","cgrandeg@unav.es",{"facility":698,"status":71,"city":699,"state":48,"zip":700,"country":621,"countryCode":622,"cosmosGeoPoint":701,"geoPoint":705,"contacts":706},"Hospital Clinico Universitario de Salamanca","Salamanca","37007",{"type":64,"coordinates":702},[703,704],-5.66388,40.96882,{"lat":704,"lon":703},[707],{"name":708,"role":46,"phone":709,"phoneExt":48,"email":710},"Alejandro Martin Garcia-Sancho, Dr.","+34 923291384","amartingar@usal.es",{"facility":712,"status":187,"city":713,"state":48,"zip":714,"country":715,"countryCode":48,"cosmosGeoPoint":716,"geoPoint":720,"contacts":721},"Dr. Abdurrahman Yurtaslan Ankara Oncology Training and Research Hospital","Ankara","06200","Turkey (Türkiye)",{"type":64,"coordinates":717},[718,719],32.85427,39.91987,{"lat":719,"lon":718},[722],{"name":723,"role":46,"phone":724,"phoneExt":48,"email":725},"Fevzi Altuntas, Prof. Dr.","+90 532 658 80 50","fevzi.altuntas1@saglik.go.tr",{"facility":727,"status":187,"city":728,"state":48,"zip":729,"country":715,"countryCode":48,"cosmosGeoPoint":730,"geoPoint":734,"contacts":735},"American Hospital","Şişli","34365",{"type":64,"coordinates":731},[732,733],28.98717,41.06046,{"lat":733,"lon":732},[736],{"name":737,"role":46,"phone":738,"phoneExt":48,"email":739},"Burhan Ferhanoglu, Prof. Dr.","+90 2122 335336","burhanf@amerikanhastanesi.org",{"facility":741,"status":187,"city":742,"state":48,"zip":743,"country":715,"countryCode":48,"cosmosGeoPoint":744,"geoPoint":748,"contacts":749},"Koc Universitesi Hastanesi (Koc University Hospital)","Zeytinburnu","34010",{"type":64,"coordinates":745},[746,747],28.90417,40.99441,{"lat":747,"lon":746},[750],{"name":751,"role":46,"phone":752,"phoneExt":48,"email":753},"Sinem Civriz Bozdag, Prof.","+90 5057 658142","sbozdag@kuh.ku.edu.tr",{"type":755,"investigatorFullName":48,"investigatorTitle":48,"investigatorAffiliation":48,"oldNameTitle":48,"oldOrganization":48},"SPONSOR",[757],{"name":758,"class":6},"ICON plc","100427350","phase-2-efficacy-and-safety-of-mb-cart20191-vs-soc-in-lymphoma-patients-100427350",false,"NCT04844866","Efficacy and Safety of MB-CART2019.1 vs. SoC in Lymphoma Patients","A Pivotal Phase II Randomised, Multi-centre, Open-label Study to Evaluate the Efficacy and Safety of MB-CART2019.1 Compared to SoC Therapy in Participants With r\u002Fr DLBCL, Who Are Not Eligible for HDC and ASCT","DALY 2-EU","Part I:\n\n1. Histologically proven DLBCL and associated subtypes, according to the World Health Organization (WHO) 2016 classification including:\n\n   * DLBCL not otherwise specified (NOS).\n   * High-grade B-cell lymphoma (HGBL) with MYC and BCL2 and\u002For BCL6 rearrangements with DLBCL\u002Fblastoid\u002Fintermediate histology or HGBL with MYC and BCL2 and\u002For BCL6 rearrangements (double hit lymphoma\u002Ftriple hit lymphoma).\n   * High-grade BCL, NOS.\n   * Primary (thymic) large mediastinal BCL.\n   * Disease transformed from an earlier diagnosis of low-grade lymphoma (e.g. an indolent pathology such as follicular lymphoma, marginal zone lymphoma) into DLBCL with DLBCL disease progression subsequent to DLBCL-directed systemic treatment.\n   * Follicular lymphoma Grade 3B.\n2. Relapsed or refractory disease after first-line chemoimmunotherapy:\n\n   * Refractory disease defined as no CR to first-line therapy (e.g. R-CHOP \\[rituximab, cyclophosphamide, daunorubicin, vincristine and prednisone\\]).\n\n     * Progressive disease (PD) after at least 2 full cycles of first-line therapy.\n     * Stable disease (SD) after 4 cycles of first-line therapy.\n     * PR as best response after at least 6 cycles of first-line therapy and biopsy-proven persistent disease (except where prohibited due to comorbidities) within ≤ 24 months from the start of the first-line therapy.\n   * Relapsed disease defined as complete remission to first-line therapy followed by biopsy-proven disease progression (except where prohibited due to comorbidities) within ≤ 24 months from the start of the first-line therapy.\n3. Participants must have received adequate first-line therapy containing at least the combination of an anthracycline-based regimen and rituximab (anti-CD20 monoclonal antibody). Local therapies (e.g. radiotherapies) will not be considered as line of therapy if performed during the same line of treatment.\n4. Archival paraffin-embedded tumour tissue acquired ≤ 2 years (preferred: ≤ 2 months) prior to screening for the central pathology review to confirm DLBCL diagnosis must be made available for participation in this study. If archival paraffin-embedded tumour tissue is not available, fresh tumour tissue sample (preferred) or core-needle biopsy must be made available for the central pathology review.\n5. Participants deemed ineligible to receive HDC followed by ASCT based on the treating physician's assessment and meeting the following criteria:\n\n   EITHER\n   * Age ≥ 18 years and\n\n     * Prior ASCT (as first-line consolidation) or\n     * Haematopoietic cell transplantation-specific comorbidity index (HCT-CI) \\> 3. OR\n   * Age ≥ 65 years and ≥ 1of the criteria below:\n\n     * Impaired cardiac function (left ventricular ejection fraction \\[LVEF\\] \\\u003C 50%), or\n     * Impaired renal function (estimated glomerular filtration rate \\[eGFR\\] \\\u003C 60 mL\u002Fmin) calculated according to the modified Modification of Diet in Renal Disease (MDRD) formula, or\n     * Impaired pulmonary function (diffusing capacity for carbon monoxide or forced expiratory volume in 1 second \\\u003C 80%) or dyspnoea on slight activity, or\n     * Eastern Cooperative Oncology Group (ECOG) performance status \\> 1. OR\n   * Age ≥ 70 years. Documentation of the reason for ineligibility for ASCT must be present in the participant's source data.\n\n   In addition, all participants must fulfil the following criteria:\n6. Age ≥ 18 years.\n7. Measurable disease according to Lugano criteria. The lesion must be measurable (nodes \\> 1.5 cm in the long axis; extranodal lesions \\> 1 cm in the long axis) and positive on a positron emission tomography scan.\n8. Estimated life expectancy of \\> 3 months for other reasons than the primary disease.\n9. Women of childbearing potential (WOCBP) must agree to use highly effective contraceptive measures (Pearl index \\\u003C 1) or practice true sexual abstinence from any heterosexual intercourse (True abstinence is only acceptable if it is in line with the preferred and usual life style of the participant.) or must have a vasectomised partner as the sole sexual partner (The vasectomised partner must have received medical assessment of the surgical success.) for at least 1 month before the study start, during the study and in the 12 months following the last dose of study treatment. A woman is considered a WOCBP, i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile. Highly effective methods of contraception include hormonal contraceptives associated with inhibition of ovulation (oral, intravaginal, transdermal, injectable, implantable) and intrauterine devices or systems (e.g. hormonal and non-hormonal) and bilateral tubal occlusion. Permanent sterilisation methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy. A post-menopausal state is defined as no menses for 12 months without an alternative medical cause. WOCBP who want to become pregnant after completing treatment should seek advice about oocyte cryoconservation prior to treatment because of possible irreversible infertility. WOCBP must refrain from egg donation throughout the study until 12 months after the last dose of study treatment.\n\n   Men with non-pregnant WOCBP partners must agree to use highly effective contraceptive measures (Pearl index \\\u003C 1, e.g. spermicide and condom or other highly effective contraceptive measures (Pearl index \\\u003C 1) taken by their WOCBP partner) or practice true sexual abstinence from any heterosexual intercourse (True abstinence is only acceptable if it is in line with the preferred and usual life style of the participant.), unless they are surgically sterile (meaning at least 2 consecutive analyses following vasectomy demonstrate absence of sperms in the ejaculate), during the study and in the 12 months following the last dose of study treatment. Men should seek advice about sperm conservation prior to treatment because of possible irreversible infertility. Men must furthermore refrain from sperm donation throughout the study until 12 months after the last administration of study treatment.\n10. In the opinion of the investigator, the participant must be able to comply with all study-related procedures, medication use and evaluations.\n11. Mental capacity and legal ability to consent to participation in the clinical study.\n\nCriteria for Exclusion:\n\n1. Contraindications for R-GemOx, BR plus polatuzumab vedotin, cyclophosphamide and fludarabine as judged by the treating physician.\n2. Prior chimeric antigen receptor therapy or other genetically modified T-cell therapy.\n3. Participants who have received more than one line of treatment for DLBCL or associated subtypes.\n4. Prior haematopoietic stem cell transplantation (HSCT; as first-line consolidation) \\\u003C 3 months at the time of leukapheresis.\n5. ECOG performance status \\> 2.\n6. Absolute neutrophil count \\\u003C 1,000\u002FμL (unless secondary to bone marrow involvement by DLBCL as demonstrated by bone marrow biopsy).\n7. Platelet count \\\u003C 50,000\u002FμL (unless secondary to bone marrow involvement by DLBCL as demonstrated by bone marrow biopsy).\n8. Absolute lymphocyte count \\\u003C 100\u002FμL.\n9. Participants who have central nervous system (CNS) lymphoma involvement in present or past medical history.\n10. Participants with the requirement for urgent therapy due to tumour mass effects.\n11. Infection with human immunodeficiency virus.\n12. Presence of active or prior hepatitis B or C as indicated by serology (for detailed criteria see Section 10.2.7.10). Treated infection with hepatitis B or C virus unless confirmed to be polymerase chain reaction negative.\n13. Active infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).\n14. Active, severe systemic fungal, viral or bacterial infection.\n15. Known history or evidence of severely immunocompromised state, i.e. corticosteroid treatment \\> 10 mg\u002Fday for more than 6 months.\n16. Has received vaccination with live virus vaccines 6 weeks prior to randomisation.\n17. Prior CD19-targeted therapy.\n18. Known history or presence of seizure activities or on active anti-seizure medications within the previous 12 months.\n19. History or presence of non-malignant CNS disease that, in the judgement of the investigator, may impair the ability to evaluate neurotoxicity.\n20. Known history or presence of autoimmune CNS disease, such as multiple sclerosis, optic neuritis or other immunologic or inflammatory disease.\n21. Known history or presence of cerebral vascular accident (CVA) within 12 months prior to randomisation.\n\n    Note: In case of history of CVA \\> 12 months prior to leukapheresis, then the participant must not have any unstable or life-threatening neurological deficits.\n22. Participants with Richter's transformation or Richter's syndrome.\n23. Participants who are concurrently on any other experimental treatments or during the previous 4 weeks or 5 half-lives.\n24. Clinical heart failure with New York Heart Association class ≥ 2 or LVEF \\\u003C 30% or severe cardiac arrhythmias or QT prolongation (resting QTcF ≥ 450 msec \\[male\\] or ≥ 460 msec \\[female\\] at screening) that would (according to the evaluation of the investigator) face an uncontrollable risk by receiving the medications administered in the trial.\n25. Resting peripheral oxygen saturation \\\u003C 90% on room air.\n26. Liver dysfunction as indicated by total bilirubin \\> 2.5 × institutional upper limit of normal (ULN), aspartate aminotransferase and\u002For alanine aminotransferase \\> 5 × ULN or typical symptoms like jaundice.\n27. Serum creatinine ≥ 2.0 × ULN or eGFR \\\u003C 30 mL\u002Fmin calculated according to the modified MDRD formula.\n28. Pregnant or breast-feeding women.\n29. Prior history of malignancies other than DLBCL. Exceptions include participants who have been free of the disease for ≥ 3 years prior to screening and participants with adequately treated and removed basal cell carcinoma of the skin, squamous cell carcinoma of the skin, carcinoma in situ of the cervix, carcinoma in situ of the breast, carcinoma in situ of the bladder or incidental histological finding of untreated localised (T1a, T1b or T1c) prostate cancer under surveillance.\n30. History of severe immediate hypersensitivity to any investigational medicinal product (IMP), auxiliary medicinal product (AxMP), premedication or rescue medication or its excipients that is scheduled to be given during study participation.\n31. Major surgery less than 30 days before start of treatment.\n32. Any medical condition likely to interfere with assessment of safety or efficacy of study treatment.\n\nPart II:\n\n1. Histologically proven DLBCL and associated subtypes, according to the WHO 2016 classification including:\n\n   * DLBCL, NOS.\n   * HGBL with MYC and BCL2 and\u002For BCL6 rearrangements with DLBCL\u002Fblastoid\u002Fintermediate histology or HGBL with MYC and BCL2 and\u002For BCL6 rearrangements (double hit lymphoma\u002Ftriple hit lymphoma).\n   * High-grade BCL, NOS.\n   * Primary (thymic) large mediastinal BCL.\n   * Disease transformed from an earlier diagnosis of low-grade lymphoma (e.g., an indolent pathology such as follicular lymphoma, marginal zone lymphoma) into DLBCL with DLBCL disease progression subsequent to DLBCL-directed systemic treatment.\n   * Follicular lymphoma Grade 3B.\n2. Relapsed or refractory disease after first-line chemoimmunotherapy:\n\n   * Refractory disease defined as no CR to first-line therapy (e.g., R-CHOP).\n\n     * PD after at least 2 full cycles of first-line therapy.\n     * SD after 4 cycles of first-line therapy.\n     * PR as best response after at least 6 cycles of first-line therapy and biopsy-proven persistent disease (except where prohibited due to comorbidities) within ≤ 12 months after completion of first-line treatment.\n   * Relapsed disease defined as complete remission to first-line therapy followed by biopsy-proven disease progression (except where prohibited due to comorbidities) within ≤ 12 months after completion of first-line treatment.\n3. Participant must have received adequate first-line therapy containing at least the combination of an anthracycline-based regimen and rituximab (anti-CD20 monoclonal antibody). Local therapies (e.g., radiotherapies) will not be considered as line of therapy if performed during the same line of treatment.\n4. Archival paraffin-embedded tumour tissue acquired ≤ 2 years (preferred: ≤ 2 months) prior to screening for the central pathology review to confirm DLBCL diagnosis must be made available for participation in this study. If archival paraffin-embedded tumour tissue is not available, fresh tumour tissue sample (preferred) or core-needle biopsy must be made available for the central pathology review.\n5. Measurable disease according to Lugano criteria. The lesion must be measurable (nodes \\> 1.5 cm in the long axis; extranodal lesions \\> 1 cm in the long axis) and positive on a positron emission tomography scan.\n6. Approved treatment options not suitable according to investigator's assessment.\n\n   In addition, all participants must fulfil the following criteria:\n7. Age ≥ 18 and ≤ 70 years.\n8. Estimated life expectancy of \\> 3 months for other reasons than the primary disease.\n9. ECOG 0-1.\n10. Adequate bone marrow function, defined as:\n\n    * Absolute neutrophil count ≥ 1,000\u002FμL (unless secondary to bone marrow involvement by DLBCL as demonstrated by bone marrow biopsy).\n    * Platelet count ≥ 50,000\u002FμL (unless secondary to bone marrow involvement by DLBCL as demonstrated by bone marrow biopsy).\n    * Absolute lymphocyte count ≥ 100\u002FμL.\n11. Adequate organ function, defined as:\n\n    * New York Heart Association class \\\u003C 2 or LVEF ≥ 50%.\n    * No severe cardiac arrhythmias or QT prolongation (resting QTcF \\\u003C 450 msec \\[male\\] or \\\u003C 460 msec \\[female\\] at screening).\n    * No clinically relevant pleural effusion or pericardial effusion.\n    * Resting peripheral oxygen saturation ≥ 92% on room air.\n    * Total bilirubin ≤ 2.0 × ULN, AST and\u002For ALT ≤ 5 × ULN\n    * Serum creatinine \\\u003C 1.0 × ULN or eGFR (according to modified MDRD formula) ≥ 60 mL\u002Fmin.\n12. WOCBP must agree to use highly effective contraceptive measures (Pearl index \\\u003C 1) or practice true sexual abstinence from any heterosexual intercourse (True abstinence is only acceptable if it is in line with the preferred and usual life style of the participant.) or must have a vasectomised partner as the sole sexual partner (The vasectomised partner must have received medical assessment of the surgical success.) for at least 1 month before the study start, during the study and in the 12 months following the last dose of study treatment. A woman is considered a WOCBP, i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile. Highly effective methods of contraception include hormonal contraceptives associated with inhibition of ovulation (oral, intravaginal, transdermal, injectable, implantable) and intrauterine devices or systems (e.g., hormonal and non-hormonal) and bilateral tubal occlusion. Permanent sterilisation methods include hysterectomy, bilateral salpingectomy, and bilateral oophorectomy. A post-menopausal state is defined as no menses for 12 months without an alternative medical cause. WOCBP who want to become pregnant after completing treatment should seek advice about oocyte cryoconservation prior to treatment because of possible irreversible infertility. WOCBP must refrain from egg donation throughout the study until 12 months after the last dose of study treatment. Men with non-pregnant WOCBP partners must agree to use highly effective contraceptive measures (Pearl index \\\u003C 1, e.g., spermicide and condom or other highly effective contraceptive measures (Pearl index \\\u003C 1) taken by their WOCBP partner) or practice true sexual abstinence from any heterosexual intercourse (True abstinence is only acceptable if it is in line with the preferred and usual life style of the participant.), unless they are surgically sterile (meaning at least 2 consecutive analyses following vasectomy demonstrate absence of sperms in the ejaculate), during the study and in the 12 months following the last dose of study treatment. Men should seek advice about sperm conservation prior to treatment because of possible irreversible infertility. Men must furthermore refrain from sperm donation throughout the study until 12 months after the last administration of study treatment.\n13. In the opinion of the investigator, the participant must be able to comply with all study-related procedures, medication use and evaluations.\n14. Mental capacity and legal ability to consent to participation in the clinical study.\n\nCriteria for Exclusion:\n\n1. Contraindications for cyclophosphamide and fludarabine as judged by the treating physician.\n2. Prior chimeric antigen receptor therapy or other genetically modified T-cell therapy.\n3. Participants who have received more than one line of prior therapy for DLBCL or associated subtypes.\n4. Prior HSCT (as first-line consolidation) \\\u003C 3 months at the time of leukapheresis.\n5. Participants who have CNS lymphoma involvement in present or past medical history.\n6. Participants with the requirement for urgent therapy due to tumour mass effects.\n7. Infection with human immunodeficiency virus.\n8. Presence of active or prior hepatitis B or C as indicated by serology. Treated infection with hepatitis B or C virus unless confirmed to be polymerase chain reaction negative.\n9. Infection with Treponema pallidum (pathogen causing syphilis).\n10. Infection with human T-lymphotropic virus 1.\n11. Active infection with SARS-CoV-2.\n12. Active, severe systemic fungal, viral, or bacterial infection.\n13. Known history or evidence of severely immunocompromised state, i.e. corticosteroid treatment \\> 10 mg\u002Fday for more than 6 months.\n14. Has received vaccination with live virus vaccines within 6 weeks prior to randomisation.\n15. Prior CD19-targeted therapy.\n16. Known history or presence of seizure activities or on active anti-seizure medications within the previous 12 months.\n17. History or presence of non-malignant CNS disease that, in the judgement of the investigator, may impair the ability to evaluate neurotoxicity.\n18. Known history or presence of autoimmune CNS disease, such as multiple sclerosis, optic neuritis or other immunologic or inflammatory disease.\n19. Known history or presence of CVA within 12 months prior to randomisation. Note: In case of history of CVA \\> 12 months prior to leukapheresis, then the participant must not have any unstable or life-threatening neurological deficits.\n20. Participants with Richter's transformation or Richter's syndrome.\n21. Participants who are concurrently on any other experimental treatments or during the previous 4 weeks or 5 half-lives.\n22. Pregnant or breastfeeding woman.\n23. Prior history of malignancies other than DLBCL. Exceptions include participants who have been free of the disease for ≥ 3 years prior to screening and participants with adequately treated and removed basal cell carcinoma of the skin, squamous cell carcinoma of the skin, carcinoma in situ of the cervix, carcinoma in situ of the breast, carcinoma in situ of the bladder or incidental histological finding of untreated localised (T1a, T1b or T1c) prostate cancer under surveillance.\n24. History of severe immediate hypersensitivity to any IMP, AxMP, premedication or rescue medication or its excipients that is scheduled to be given during study participation.\n25. Major surgery less than 30 days before start of treatment.\n26. Any medical condition likely to interfere with assessment of safety or efficacy of study treatment.","ALL","18 Years","70 Years",{"count":771,"type":772},213,"ESTIMATED","INTERVENTIONAL",[775],"PHASE2","In the current protocol version, there are two parts. Part I is a pivotal Phase II randomised, multi-centre, open-label study to evaluate the efficacy and safety of MB-CART2019.1 compared to standard of care therapy in participants with relapsed\u002Frefractory diffuse large B-cell lymphoma, who are not eligible for high-dose chemotherapy and autologous stem cell transplantation.\n\nPart II is a Phase II single-arm, open-label, multi-centre study evaluating the efficacy and safety of MB-CART2019.1 in younger, fit participants with R-R DLBCL. Part II will start after completion of enrolment in Part I.",[778],"Diffuse Large B-cell Lymphoma",[780,781,26,782,783,784,778,785,786,787,788,789,790,791],"CAR T cells","chimeric antigen receptor","CD20","CD19","relapsed refractory","DLBCL","Non-Hodgkin Lymphoma","NHL","zamtocabtagene autoleucel","blood cancer","LBCL","Follicular Lymphoma 3B","2026-06-08",{"date":794,"type":795},"2026-06-10","ACTUAL",{"date":797,"type":795},"2021-08-18",{"date":799,"type":772},"2031-09-30",{"name":5,"class":6},51]