[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100492696":3},{"organization":4,"armGroups":7,"interventions":60,"overallOfficials":72,"centralContacts":91,"locations":98,"responsibleParty":202,"collaborators":205,"id":212,"slug":213,"hasResults":214,"nctId":215,"briefTitle":216,"officialTitle":217,"acronym":218,"eligibilityCriteria":219,"healthyVolunteers":214,"sex":220,"minAge":221,"maxAge":222,"enrollmentInfo":223,"targetDuration":72,"studyType":226,"phases":227,"briefSummary":229,"conditions":230,"keywords":72,"overallStatus":101,"whyStopped":72,"lastUpdateSubmitDate":232,"lastUpdatePostDateStruct":233,"startDateStruct":236,"completionDateStruct":238,"leadSponsor":240,"locationsCount":241},{"fullName":5,"class":6},"University of Heidelberg Medical Center","OTHER",[8,17,22,26,30,35,39,43,47,51,55],{"label":9,"type":10,"description":11,"interventionNames":12},"Arm A Tec-DRd Induction and Tec-D Maintenance","EXPERIMENTAL","Arm A participants will receive teclistamab as subcutaneous (SC) injection in combination with daratumumab SC, lenalidomide and dexamethasone in 6 cycles of induction therapy, followed by teclistamab SC injection in combination with daratumumab SC in maximum 18 cycles of maintenance therapy.",[13,14,15,16],"Drug: Teclistamab (Tec)","Drug: Daratumumab","Drug: Dexamethasone","Drug: Lenalidomide",{"label":18,"type":10,"description":19,"interventionNames":20},"Arm B Tec-DVRd Induction and Tec-D Maintenance","Arm B participants will receive teclistamab as subcutaneous (SC) injection in combination with daratumumab SC, lenalidomide, dexamethasone and bortezomib in 6 cycles of induction therapy, followed by teclistamab SC injection in combination with daratumumab SC in maximum 18 cycles of maintenance therapy.",[13,14,15,16,21],"Drug: Bortezomib",{"label":23,"type":10,"description":24,"interventionNames":25},"Arm C Tec-D Maintenance","Arm C participants will receive maximum 18 cycles of teclistamab SC injection in combination with daratumumab SC and lenalidomide as maintenance therapy.",[13,14],{"label":27,"type":10,"description":28,"interventionNames":29},"Arm A1 Tec-DRd Induction and Tec-D Maintenance","Arm A1 participants will receive teclistamab as subcutaneous (SC) injection in combination with daratumumab SC, lenalidomide and dexamethasone in 6 cycles of induction therapy, followed by teclistamab SC injection in combination with daratumumab SC in maximum 18 cycles of maintenance therapy.",[13,14,15,16],{"label":31,"type":10,"description":32,"interventionNames":33},"Arm C2 Tal-DR Maintenance","Arm C2 participants will receive maximum 18 cycles of talquetamab SC injection in combination with daratumumab SC and lenalidomide as maintenance therapy.",[14,16,34],"Drug: Talquetamab",{"label":36,"type":10,"description":37,"interventionNames":38},"Arm D Tec-DRd Induction and Tec-Tal following induction","Arm D participants will receive teclistamab as subcutaneous (SC) injection in combination with daratumumab SC, lenalidomide and dexamethasone in 6 cycles of induction therapy, followed by a combination of teclistamab and talquetamab SC injection in maximum 18 cycles of following induction therapy.",[13,14,15,16,34],{"label":40,"type":10,"description":41,"interventionNames":42},"Arm E Tal-DRd Induction and Tec-D Maintenance","Arm E participants will receive talquetamab as subcutaneous (SC) injection in combination with daratumumab SC, lenalidomide and dexamethasone in 6 cycles of induction therapy, followed by teclistamab SC injection in combination with daratumumab SC in maximum 18 cycles of maintenance therapy.",[13,14,15,16,34],{"label":44,"type":10,"description":45,"interventionNames":46},"Arm E1 Tal-DRd Induction and Tal-D Maintenance","Arm E1 participants will receive talquetamab as subcutaneous (SC) injection in combination with daratumumab SC, lenalidomide and dexamethasone in 6 cycles of induction therapy, followed by talquetamab SC injection in combination with daratumumab SC in maximum 18 cycles of maintenance therapy.",[14,15,16,34],{"label":48,"type":10,"description":49,"interventionNames":50},"Arm F Tal-DVRd Induction and Tec-D Maintenance","Arm F participants will receive talquetamab as subcutaneous (SC) injection in combination with daratumumab SC, bortezomib, lenalidomide and dexamethasone in 6 cycles of induction therapy, followed by teclistamab SC injection in combination with daratumumab SC in maximum 18 cycles of maintenance therapy.",[13,14,15,16,21,34],{"label":52,"type":10,"description":53,"interventionNames":54},"Arm F1 Tal-DVRd Induction and Tal-D Maintenance","Arm F1 participants will receive talquetamab as subcutaneous (SC) injection in combination with daratumumab SC, bortezomib, lenalidomide and dexamethasone in 6 cycles of induction therapy, followed by talquetamab SC injection in combination with daratumumab SC in maximum 18 cycles of maintenance therapy.",[14,15,16,21,34],{"label":56,"type":10,"description":57,"interventionNames":58},"Arm-G JNJ-79635322-DRd induction - JNJ-79635322-D following ind","Arm G participants will receive six 28-day cycles of JNJ-79635322-DRd induction, followed byJNJ-79635322-D treatment for a maximum of eighteen 28-day cycles or until confirmed PD, death, intolerable toxicity, loss to follow-up, or consent withdrawal, whichever comes first. Tec-Tal or JNJ-79635322-D treatment can be discontinued when 12 months of sustained MRD negativity has been observed during the study.",[14,15,16,59],"Drug: JNJ-79635322",[61,68,73,77,81,85,88],{"type":62,"name":63,"description":64,"armGroupLabels":65,"otherNames":66},"DRUG","Teclistamab (Tec)","Subcutaneous administration of Teclistamab",[9,27,18,23,36,40,48],[67],"JNJ-64007957",{"type":62,"name":69,"description":70,"armGroupLabels":71,"otherNames":72},"Daratumumab","Subcutaneous administration of Daratumumab",[9,27,18,23,31,36,40,44,48,52,56],null,{"type":62,"name":74,"description":75,"armGroupLabels":76,"otherNames":72},"Dexamethasone","administered i.v. or orally",[9,27,18,36,40,44,48,52,56],{"type":62,"name":78,"description":79,"armGroupLabels":80,"otherNames":72},"Lenalidomide","Administration oral",[9,27,18,31,36,40,44,48,52,56],{"type":62,"name":82,"description":83,"armGroupLabels":84,"otherNames":72},"Bortezomib","Subcutaneous administration",[18,48,52],{"type":62,"name":86,"description":70,"armGroupLabels":87,"otherNames":72},"Talquetamab",[31,36,40,44,48,52],{"type":62,"name":89,"description":83,"armGroupLabels":90,"otherNames":72},"JNJ-79635322",[56],[92],{"name":93,"role":94,"phone":95,"phoneExt":96,"email":97},"Marc S Raab, Prof. Dr. med","CONTACT","+49 6221 56","8198","s.gmmg@med.uni-heidelberg.de",[99,112,121,130,139,148,157,163,176,185,194],{"facility":100,"status":101,"city":102,"state":72,"zip":103,"country":104,"countryCode":105,"cosmosGeoPoint":106,"geoPoint":111,"contacts":72},"Charité University Medicin Berlin","RECRUITING","Berlin","12203","Germany","DE",{"type":107,"coordinates":108},"Point",[109,110],13.41053,52.52437,{"lat":110,"lon":109},{"facility":113,"status":101,"city":114,"state":72,"zip":115,"country":104,"countryCode":105,"cosmosGeoPoint":116,"geoPoint":120,"contacts":72},"Clinic Chemnitz gGmbH","Chemnitz","09113",{"type":107,"coordinates":117},[118,119],12.92922,50.8357,{"lat":119,"lon":118},{"facility":122,"status":101,"city":123,"state":72,"zip":124,"country":104,"countryCode":105,"cosmosGeoPoint":125,"geoPoint":129,"contacts":72},"University Clinic Technical University Dresden","Dresden","01307",{"type":107,"coordinates":126},[127,128],13.73832,51.05089,{"lat":128,"lon":127},{"facility":131,"status":101,"city":132,"state":72,"zip":133,"country":104,"countryCode":105,"cosmosGeoPoint":134,"geoPoint":138,"contacts":72},"University Clinic Düsseldorf","Düsseldorf","40225",{"type":107,"coordinates":135},[136,137],6.77927,51.22319,{"lat":137,"lon":136},{"facility":140,"status":101,"city":141,"state":72,"zip":142,"country":104,"countryCode":105,"cosmosGeoPoint":143,"geoPoint":147,"contacts":72},"University Clinic Freiburg","Freiburg im Breisgau","79106",{"type":107,"coordinates":144},[145,146],7.85222,47.9959,{"lat":146,"lon":145},{"facility":149,"status":101,"city":150,"state":72,"zip":151,"country":104,"countryCode":105,"cosmosGeoPoint":152,"geoPoint":156,"contacts":72},"Hamburg University Clinic Eppendorf","Hamburg","20246",{"type":107,"coordinates":153},[154,155],9.99302,53.55073,{"lat":155,"lon":154},{"facility":158,"status":101,"city":150,"state":72,"zip":159,"country":104,"countryCode":105,"cosmosGeoPoint":160,"geoPoint":162,"contacts":72},"Asklepios Clinic Hamburg Altona","22763",{"type":107,"coordinates":161},[154,155],{"lat":155,"lon":154},{"facility":164,"status":101,"city":165,"state":72,"zip":166,"country":104,"countryCode":105,"cosmosGeoPoint":167,"geoPoint":171,"contacts":172},"University Hospital Heidelberg","Heidelberg","69120",{"type":107,"coordinates":168},[169,170],8.69079,49.40768,{"lat":170,"lon":169},[173],{"name":174,"role":175,"phone":72,"phoneExt":72,"email":72},"Marc S Raab","PRINCIPAL_INVESTIGATOR",{"facility":177,"status":101,"city":178,"state":72,"zip":179,"country":104,"countryCode":105,"cosmosGeoPoint":180,"geoPoint":184,"contacts":72},"University Clinic Schleswig-Holstein Campus Kiel","Kiel","24105",{"type":107,"coordinates":181},[182,183],10.13489,54.32133,{"lat":183,"lon":182},{"facility":186,"status":101,"city":187,"state":72,"zip":188,"country":104,"countryCode":105,"cosmosGeoPoint":189,"geoPoint":193,"contacts":72},"Technical University Munich","Munich","81675",{"type":107,"coordinates":190},[191,192],11.57549,48.13743,{"lat":192,"lon":191},{"facility":195,"status":101,"city":196,"state":72,"zip":72,"country":104,"countryCode":105,"cosmosGeoPoint":197,"geoPoint":201,"contacts":72},"University Würzburg","Würzburg",{"type":107,"coordinates":198},[199,200],9.95121,49.79391,{"lat":200,"lon":199},{"type":175,"investigatorFullName":203,"investigatorTitle":204,"investigatorAffiliation":5,"oldNameTitle":72,"oldOrganization":72},"Marc Raab","Prof. Dr. med.",[206,209],{"name":207,"class":208},"Janssen Research & Development, LLC","INDUSTRY",{"name":210,"class":211},"Deutsche Studiengruppe Multiples Myelom (DSMM)","UNKNOWN","100492696","phase-2-gmmg-hd10--dsmm-xx--64007957mmy2003-majestec-5-100492696",false,"NCT05695508","GMMG-HD10 \u002F DSMM-XX \u002F 64007957MMY2003, MajesTEC-5","A Phase 2 Study to Evaluate Safety and Efficacy of Teclistamab-, Talquetamab-, and JNJ-79635322-based Combination Regimens in Participants With Newly Diagnosed Transplant Eligible Multiple Myeloma","HD10\u002FDSMMXX","Inclusion Criteria:\n\n\\- 18 years of age to 70 years of age, inclusive\n\n* Have an ECOG performance status score of 0 to 2 at screening\n* Have an ECOG performance status score of 0 to 2 at screening and immediately prior to the start of administration of study treatment\n\nParticipants in Arms A, A1, B, D, E, E1, F, F1 and G must also satisfy all of the following criteria to be enrolled in the study:\n\n1\\. Documented multiple myeloma requiring treatment as defined by the criteria below:\n\n1. Multiple myeloma diagnosis according to the IMWG diagnostic criteria\n2. Measurable disease at screening as defined by any of the following:\n\n   1\\. Serum M-protein level ≥1.0 g\u002FdL or 2. Urine M-protein level ≥200 mg\u002F24 hours or 3. Serum immunoglobulin free light chain level ≥10 mg\u002FdL and abnormal serum free light chain ratio 2. Newly diagnosed participants for whom HDT and ASCT is part of the intended treatment plan (except Arm D and G participants).\n\n   Participants Arm C and C2 must also satisfy all of the following criteria:\n   1. Newly diagnosed multiple myeloma according to IMWG criteria.\n   2. Must have received 4 to 6 28-day cycles of 3 or 4 drug-induction therapy that includes a proteasome inhibitor and\u002For an IMiD with or without anti-CD38 monoclonal antibody and a single or tandem ASCT. Post-ASCT consolidation is permitted for up to 2 cycles as long as the total number of induction plus consolidation cycles does not exceed 6.\n\n   3 Must have received only one line of therapy and achieved at least a PR as per IMWG 2016 response criteria based on the investigator's assessment. Participants with plasmacytomas at the time of diagnosis must meet IMWG 2016 response criteria for ≥PR based on repeat imaging utilizing the same modality 4. Must have received HDT and ASCT within 12 months of the start of induction therapy and be within 6 months of the last ASCT (7 months for participants who received consolidation) at the time of enrollment.\n\n   Exclusion Criteria:\n\n   \\- CNS involvement or clinical signs of meningeal involvement of multiple myeloma.\n\n   \\- Stroke or seizure within 6 months prior study start Cycle1 Day1.\n\n   \\- History of transplantations requiring immunosuppressive therapy.\n\n   \\- Seropositive for HIV, HEP B, Active Hep C infection (details see protocol).\n\n   \\- COPD with a FEV1 \\\u003C50% of predicted normal.\n\n   \\- Moderate \u002Fsevere persistent asthma within the past 2 years or any uncontrolled asthma. Exclude if FEV1 \\\u003C50% of predicted normal.\n\n   \\- Concurrent medical or psychiatric condition or disease that is likely to interfere with study procedures, or that in the investigators opinion would constitute a hazard for participants.\n\n   \\- Contraindications or life-threatening allergies, hypersensitivity, or intolerance to any study drug\u002Fexcipients.\n\n   \\- Pregnant, breastfeeding, or planning to become pregnant while enrolled in this study or within 6 months after the last dose of any study treatment regimen.\n\n   \\- Plans to father a child while enrolled in this study or within 100 days after the last dose of any component of the study treatment regimen.\n\n   Arm A, A1, B, D, E, E1, F, F1\n   * Prior or current systemic therapy or stem cell transplant for any plasma cell dyscrasia, with the exception of emergency use of a short course (equivalent of dexamethasone 40 mg\u002Fday for a maximum 4 days) of corticosteroids before treatment.\n   * Arm B only: Peripheral neuropathy or neuropathic pain Grade 2 or higher as defined by the NCI-CTCAE Version 5.\n\n   Due to a potential interaction with bortezomib, received a strong CYP3A4 inducer within 5 half-lives prior to enrollment\n\n   Arm C and C2\n\n   \\- Discontinued treatment due to any AE related to lenalidomide as determined by the investigator.\n   * Progressed on multiple myeloma therapy at any time prior to screening.\n   * Received a cumulative dose of corticosteroids equivalent to ≥40 mg of dexamethasone within the 14 day period before the start of study treatment administration.\n   * Intolerant to the starting dose of lenalidomide (10 mg).\n\n   For further details on inclusion\u002Fexclusion criteria please refer to the study protocol.","ALL","18 Years","70 Years",{"count":224,"type":225},160,"ESTIMATED","INTERVENTIONAL",[228],"PHASE2","A Phase 2 Study to Evaluate Safety and Efficacy of Teclistamab-, Talquetamab-, and JNJ-79635322-based Combination Regimens in Participants with Newly Diagnosed Transplant Eligible Multiple Myeloma\n\nOBJECTIVES:\n\nTo evaluate the safety and tolerability of teclistamab-, talquetamab-, and JNJ-79635322-based combination regimens over the entire treatment phase for each arm, in participants with ND-TEMM\n\nTo evaluate the efficacy of teclistamab- and talquetamab-based combination regimens as induction and post-transplant maintenance treatments; JNJ-79635322-based combinations as induction and as replacement for HDT+ASCT following induction; and teclistamab in combination with talquetamab",[231],"Multiple Myeloma","2025-12-17",{"date":234,"type":235},"2025-12-24","ACTUAL",{"date":237,"type":235},"2022-12-01",{"date":239,"type":225},"2029-09-15",{"name":5,"class":6},11]