[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"lymphoma-diffuse-large-b-cell\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:lymphoma-diffuse-large-b-cell":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":30,"lastUpdatePostDateStruct":31,"startDateStruct":34,"completionDateStruct":36,"leadSponsor":38,"locationsCount":41},"100610381","phase-1-a-study-of-ly4584180-in-adult-participants-with-previously-treated-blood-cancers-100610381",false,"NCT07226843","A Study of LY4584180 in Adult Participants With Previously Treated Blood Cancers","NOVA-BCL6-1, A First-in-Human, Multicenter Phase 1a\u002F1b Study to Investigate Safety, Tolerability, Pharmacokinetics, and Efficacy of LY4584180 in Adult Participants With Previously Treated Hematologic Malignancies","Inclusion Criteria:\n\n* Has been treated for the following blood cancers and has received at least 2 prior lines of systemic therapy or not eligible for available therapy:\n\n  * Diffuse large B-cell lymphoma - not otherwise specified\n  * High-grade B-cell lymphoma\n  * Diffuse large B-cell lymphoma - transformed from indolent lymphomas\n  * Follicular large B-cell lymphoma\n  * Follicular lymphoma\n  * Other non-Hodgkin lymphoma\n* Has measurable disease\n* Has discontinued all previous treatments for cancer and has recovered from the immediate effects of therapy\n\nExclusion Criteria:\n\n* Has an active second cancer\n* Has known central nervous system (CNS) involvement by systemic lymphoma. Patients with previous treatment for CNS involvement who are neurologically stable and without evidence of active CNS disease may be eligible and enrolled if a compelling clinical rationale is provided by the Investigator and with documented Sponsor approval.\n* Has known Cytomegalovirus infection. Participants with negative status are eligible\n* Has known hepatitis B or C infection or uncontrolled HIV\n* Has known significant heart disease","ALL","18 Years",{"count":19,"type":20},460,"ESTIMATED","INTERVENTIONAL",[23],"PHASE1","The main purpose of this study is to evaluate safety and efficacy, and measure how much LY4584180 gets into the bloodstream and how long it takes the body to eliminate it in patients with previously treated blood cancers. For each participant, the study could last about 9 months or possibly longer including screening.",[26,27,28],"Lymphoma, Non-Hodgkin's","Lymphoma, Diffuse Large B-Cell","Follicular Lymphoma","RECRUITING","2026-06-22",{"date":32,"type":33},"2026-06-23","ACTUAL",{"date":35,"type":33},"2026-04-17",{"date":37,"type":20},"2030-02",{"name":39,"class":40},"Eli Lilly and Company","INDUSTRY",46,{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":48,"eligibilityCriteria":49,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":50,"targetDuration":4,"studyType":21,"phases":52,"briefSummary":54,"conditions":55,"keywords":4,"overallStatus":29,"whyStopped":4,"lastUpdateSubmitDate":60,"lastUpdatePostDateStruct":61,"startDateStruct":63,"completionDateStruct":65,"leadSponsor":67,"locationsCount":69},"100614810","phase-1-study-of-allo-quadcar01-t-an-allogeneic-car-t-targeting-cd19cd20-in-patients-with-relapsed-or-refractory-b-cell-malignancies-100614810","NCT07284433","Study of Allo-QuadCAR01-T, an Allogeneic CAR-T Targeting CD19\u002FCD20, in Patients With Relapsed or Refractory B-Cell Malignancies","A Single-arm, Multicenter, Open-label, Phase I\u002FII Trial of Allo-QuadCAR01-T, an Allogeneic CAR-T-cell Therapy Targeting CD19 and CD20, for the Treatment of Relapsed or Refractory B-cell Malignancies","QUADvance","Inclusion Criteria:\n\n* Adults 18 years or older.\n* Diagnosed with relapsed or refractory B-cell non-Hodgkin lymphoma (B-NHL) or chronic lymphocytic leukemia (CLL).\n* Must have received at least 2 prior lines of therapy.\n* ECOG performance status 0-1 (able to carry out daily activities).\n* Adequate organ function (heart, liver, kidneys).\n* HLA B\u002FC match with donor cells.\n* No active uncontrolled infections.\n\nExclusion Criteria:\n\n* Active CNS involvement (including PCNSL) in dose escalation cohorts; may be allowed in later cohorts with Sponsor approval.\n* Prior CAR-T within 3 months of screening, or ≥Grade 3 ICAHT from prior CAR-T.\n* Autologous stem cell transplant within 3 months.\n* Prior allogeneic stem cell transplant or solid organ transplant.\n* Prior therapy with dual CD19\u002FCD20 CAR-T.\n* Severe hypersensitivity to trial agents or similar compounds.\n* History of GvHD or post-transplant lymphoproliferative disorder.\n* Presence of La\u002FSS-B autoantibodies or related autoimmune diseases.\n* Other malignancy that may interfere with trial, except:\n\n  * Curatively treated basal\u002Fsquamous skin cancer or cervical carcinoma in situ\n  * Low-grade, early-stage prostate cancer (Gleason ≤6, Stage 1-2) with no therapy needed\n  * Adjuvant endocrine therapy for non-metastatic breast cancer (≥2 years)\n  * Any other curatively treated malignancy in remission ≥2 years\n* Active viral infection within 1 week of screening, or serious bacterial\u002Ffungal infection.\n* Hemorrhagic cystitis.\n* Active neuro-autoimmune disease (e.g., MS, Guillain-Barré, ALS).\n* Active or residual HBV, HCV, or syphilis.\n* Active HIV. History of HIV may be eligible with Sponsor approval if:\n* Neurological disorders within 6 months (e.g., stroke, dementia, Parkinson's, cerebellar disease, CNS autoimmune disease).\n* Significant cardiac disease within 6 months (e.g., MI, stent, unstable angina).\n* Primary immunodeficiency or autoimmune disease requiring systemic treatment within 1 year (unless stable and Sponsor-approved).\n* Unresolved ≥Grade 2 non-hematologic toxicity from prior therapy (except neuropathy up to Grade 2).\n* Systemic immunosuppression within 28 days.\n* Last systemic lymphoma\u002FCLL therapy (standard or investigational) within 28 days or 5 half-lives.\n* Major surgery within 14 days.\n* Local radiation within 28 days.\n* Live vaccination within 28 days.\n* Pregnant or breastfeeding.",{"count":51,"type":20},178,[23,53],"PHASE2","This study is testing Allo-QuadCAR01-T, a new off-the-shelf CAR-T therapy for people with hard-to-treat B-cell cancers. Unlike current CAR-T treatments that use a patient's own cells, this therapy uses donor cells that are ready to use, which can save time and reduce costs. It targets two proteins, CD19 and CD20, to lower the chance of relapse and uses gene editing to make it safer. The trial has three parts: first to find a safe dose, then to confirm it, and finally to test how well it works in patients with diffuse large B-cell lymphoma (DLBCL). Patients will get one infusion after chemotherapy to prepare their body. The main goal is to check safety and see how many patients have a complete response by Week 13. About 160 patients will take part, and researchers will follow them for up to 15 years.",[56,57,58,59],"Lymphoma Diffuse Large B-cell","Leukemia and Lymphoma","Leukemia Relapse","Lymphoma Receiving CAR-T Therapy","2026-04-01",{"date":62,"type":33},"2026-04-02",{"date":64,"type":33},"2026-01-06",{"date":66,"type":20},"2029-11-02",{"name":68,"class":40},"AvenCell Therapeutics, Inc.",13]