[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"relapsed-b-cell-non-hodgkin-lymphoma\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:relapsed-b-cell-non-hodgkin-lymphoma":52},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,40,62],{"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":27,"whyStopped":4,"lastUpdateSubmitDate":28,"lastUpdatePostDateStruct":29,"startDateStruct":32,"completionDateStruct":34,"leadSponsor":36,"locationsCount":39},"100602619","phase-2-study-of-relapsed-refractory-b-cell-non--hodgkin-lymphoma-100602619",false,"NCT07125872","Study of Relapsed\u002F Refractory B-cell Non- Hodgkin Lymphoma","Open Label, Phase 2 Study of CD19 t-haNK and N-803 in Combination With Rituximab in Participants With Relapsed\u002F Refractory B-cell Non- Hodgkin Lymphoma","Inclusion Criteria:\n\n* 1- Age\\>18 years old 2- Able to understand and provide a signed informed consent that fulfills the relevant Human Research Ethics Committee( HRECC) or independent Ethics Committee( IEC) guidelines 3. Histologically or flow cytometry documented B-cell NHL, (excluding primary central nervous system \\[CNS\\] lymphoma, chronic lymphocytic leukemia \\[CLL\\], and Burkitt lymphoma) with the following specific criteria:\n\n  * Have completed ≥2 lines of cytotoxic chemotherapy.\n  * Have received rituximab or another anti-CD20 antibody.\n  * Have measurable disease by Lugano classification documented within 8 weeks of the time of consent, defined as nodal lesions \\>15 mm in the long axis or extranodal lesions \\>10 mm in long and short axis, or bone marrow involvement that is biopsy proven.\n\n    4\\. Eastern Cooperative Oncology Group (ECOG) performance status (Appendix 5) of 0 to 1.\n\n    5\\. Stated willingness to comply with study procedures. 6. Able to attend required study visits and return for adequate follow-up, as required by this protocol.\n\n    7\\. Agreement to practice effective contraception for female participants of childbearing potential and nonsterile males. Female participants of childbearing potential must agree to use effective contraception while on study and for at least 30 days after the last dose of study drug. Nonsterile male participants must agree to use a condom while on study and for up to 30 days after the last dose of study drug. Effective contraception includes orals, injectables, surgical sterilization (e.g., vasectomy, tubal ligation), two forms of barrier methods (e.g., condom, diaphragm) and implants such as intrauterine devices (IUDs).\n\nExclusion Criteria:\n\n* Participants with ANY of the following criteria are excluded from participation in the study:\n\n  1. Histologically documented primary CNS lymphoma, CLL, Burkitt, Burkitt-like lymphoma.\n  2. Known hypersensitivity or allergy to any component of the study medications, including sulfa-containing study medication(s) (e.g., albumin \\[human\\], dimethyl sulfoxide \\[DMSO\\]).\n  3. Inadequate organ function, evidenced by the following laboratory results:\n\n     1. ANC \\\u003C 1000 cells\u002Fmm3.\n     2. Platelet count \\\u003C 100,000 cells\u002Fmm3.\n     3. Total bilirubin ≥ 1.5 × the upper limit of normal (ULN; unless the participant has documented Gilbert's syndrome or indirect hyperbilirubinemia).\n     4. Aspartate aminotransferase (AST \\[SGOT\\])\u002FALT (SGPT) ≥ 2.5 × ULN.\n     5. Alkaline phosphatase (ALP) levels ≥ 2.5 × ULN (or ≥ 5 × ULN in participants with bone metastases).\n     6. Serum creatinine ≥ 160 µmol\u002FL. NOTE: Each study site should use its institutional ULN to determine eligibility.\n  4. Serious uncontrolled concomitant disease that would contraindicate the use of the investigational drug used in this study or that would put the participant at high risk for treatment-related complications.\n  5. History of significant autoimmune disease OR active, uncontrolled autoimmune phenomenon: such as systemic lupus erythematous, Wegner's glomerulonephritis, autoimmune hemolytic anemia, idiopathic thrombocytopenic purpura requiring steroid therapy defined as \\> 20 mg of prednisone or equivalent daily.\n  6. History of allogeneic hematopoietic stem-cell transplantation (HSCT) requiring ongoing systemic graft versus host disease (GvHD) therapy.\n  7. Anti-CD20 antibody treatment less than 2 weeks prior to cell infusion.\n  8. History of receiving allograft organ transplant requiring immunosuppression.\n  9. Participants post solid organ transplants who develop high grade lymphomas or leukemias.\n  10. Metastases to the CNS, including parenchyma or leptomeninges.\n  11. Nonmalignant CNS disease (e.g., stroke, epilepsy, vasculitis, or neurodegenerative disease).\n  12. History of active inflammatory bowel disease (e.g., Crohn's disease, ulcerative colitis).\n  13. Uncontrolled hypertension (systolic \\> 160 mm Hg and\u002For diastolic \\> 110 mm Hg) or clinically significant (i.e., active) cardiovascular disease, cerebrovascular accident\u002Fstroke, or myocardial infarction within 6 months prior to first study medication; unstable angina; congestive heart failure of New York Heart Association (Appendix 6) Class 2 or higher; or serious cardiac arrhythmia requiring medication.\n  14. Current chronic daily treatment (continuous for \\>3 months) with systemiccorticosteroids as defined as \\>20 mg of prednisone or equivalent daily, excluding inhaled steroids. Short-term steroid use to prevent IV contrast allergic reaction or anaphylaxis in participants who have known contrast allergies is allowed.\n  15. Currently taking any medication(s) (herbal or prescribed) known to have an adverse drug reaction with any of the study medications.\n  16. Tested positive for tuberculosis (TB) utilizing the QuantiFERON Gold TB test.\n  17. History of human immunodeficiency virus (HIV) with current CD4+ T-cell count \\\u003C 350 cells\u002FμL and a detectable HIV viral load.\n  18. Known carriers of hepatitis B virus (HBV) infection that is currently hepatitis B surface antigen (HBsAg) positive.\n  19. Concurrent active malignancy other than basal or squamous cell carcinomas of the skin.\n  20. Assessed by the Investigator to be unable or unwilling to comply with the requirements of the protocol.\n  21. Women who are pregnant or breastfeeding.","ALL","18 Years",{"count":19,"type":20},20,"ESTIMATED","INTERVENTIONAL",[23],"PHASE2","Open Label, Phase 2 Study of CD19 t-haNK and N-803 in Combination with Rituximab in subjects with Relapsed\u002F Refractory B-cell Non- Hodgkin Lymphoma. 40 Participant will be screened for 20 subjects enrollment.",[26],"Relapsed B-Cell Non Hodgkin Lymphoma","RECRUITING","2026-04-28",{"date":30,"type":31},"2026-05-04","ACTUAL",{"date":33,"type":31},"2025-11-11",{"date":35,"type":20},"2028-05-25",{"name":37,"class":38},"ImmunityBio, Inc.","INDUSTRY",2,{"id":41,"slug":42,"hasResults":11,"nctId":43,"briefTitle":44,"officialTitle":45,"acronym":4,"eligibilityCriteria":46,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":47,"enrollmentInfo":48,"targetDuration":4,"studyType":21,"phases":49,"briefSummary":50,"conditions":51,"keywords":4,"overallStatus":53,"whyStopped":4,"lastUpdateSubmitDate":54,"lastUpdatePostDateStruct":55,"startDateStruct":57,"completionDateStruct":59,"leadSponsor":61,"locationsCount":4},"100629645","phase-2-study-of-cd19-t-hank-and-nai-with-rituximab-in-participants-with-indolent-non-hodgkin-lymphoma-100629645","NCT07477366","Study of CD19 t-haNK and NAI With Rituximab in Participants With Indolent Non-Hodgkin Lymphoma","Open-Label, Phase 2 Chemotherapy-Free Study of CD19 t-haNK and NAI in Combination With Rituximab in Participants With Relapsed\u002FRefractory B-Cell Indolent Non-Hodgkin Lymphoma","Inclusion Criteria:\n\n1. Age ≥ 18 to ≤ 75 years old.\n2. Able to understand and provide a signed informed consent that fulfils the relevant Institutional Review Board (IRB) or Independent Ethics Committee (IEC) guidelines.\n3. Histologically or flow cytometry documented relapsed\u002Frefractory B-cell indolent NHL (iNHL) including but not limited to follicular lymphoma \\[FL\\]; lymphoplasmacytic lymphoma \\[LPL\\], also known as Waldenstrom macroglobulinemia \\[WM\\]; marginal zone lymphoma \\[MZL\\] with the following specific criteria:\n\n   1. Have completed ≥ 2 lines of cytotoxic chemotherapy.\n   2. Have received rituximab or another anti-CD20 antibody.\n   3. Have measurable disease by Lugano classification documented within 8 weeks of the time of consent, defined as nodal lesions \\> 15 mm in the long axis or extranodal lesions \\> 10 mm in long and short axis, or bone marrow involvement that is biopsy proven.\n4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1.\n5. Stated willingness to comply with study procedures.\n6. Able to attend required study visits and return for adequate follow-up, as required by this protocol.\n7. Agreement to practice effective contraception for female participants of childbearing potential and nonsterile males. Female participants of childbearing potential are defined as any female who has experienced menarche and who is NOT permanently sterile or postmenopausal. Postmenopausal is defined as 12 consecutive months with no menses without an alternative medical cause. Female participants of childbearing potential must have a negative pregnancy test and adhere to using a highly effective method of contraception (eg, tubal ligation, approved hormonal contraceptive, or an intrauterine device \\[IUD\\]) prior to screening and agree to continue its use during the study or be surgically sterilized (eg, hysterectomy) while on study and for 12 months post last dose of study drug. Male participants must agree to use barrier methods of birth control while on study and for 12 months post last dose of study drug).\n\nExclusion Criteria:\n\n1. Histologically documented large B-cell lymphomas (eg, diffuse large B-cell lymphoma \\[DLBCL\\], anaplastic large cell lymphoma \\[ALCL\\], follicular large cell lymphoma, mantle cell lymphoma), primary central nervous system (CNS) lymphoma, chronic lymphocytic leukemia (CLL), Burkitt and Burkitt-like lymphoma.\n2. Known hypersensitivity or allergy to any component of the study medications, including sulfa containing study medication(s) (eg, albumin \\[human\\], dimethyl sulfoxide \\[DMSO\\]).\n3. Inadequate organ function, evidenced by the following laboratory results:\n\n   1. ANC \\\u003C 1000 cells\u002Fmm3.\n   2. Platelet count \\\u003C 100,000 cells\u002Fmm3.\n   3. Total bilirubin ≥ 1.5 × the upper limit of normal (ULN; unless the participant has documented Gilbert's syndrome or indirect hyperbilirubinemia).\n   4. Aspartate aminotransferase (AST \u002FALT ≥ 2.5 × ULN.\n   5. Alkaline phosphatase (ALP) levels ≥ 2.5 × ULN (or ≥ 5 × ULN in participants with bone metastases).\n   6. Serum creatinine ≥ 2 mg\u002FdL. NOTE: Each study site should use its institutional ULN to determine eligibility\n4. Serious uncontrolled concomitant disease that would contraindicate the use of the investigational drug used in this study or that would put the participant at high risk for treatment-related complications.\n5. History of significant autoimmune disease OR active, uncontrolled autoimmune phenomenon: such as systemic lupus erythematous, Wegner's glomerulonephritis, autoimmune hemolytic anemia, idiopathic thrombocytopenic purpura requiring steroid therapy defined as \\> 20 mg of prednisone or equivalent daily.\n6. History of allogeneic hematopoietic stem cell transplantation (HSCT) requiring ongoing systemic graft versus host disease (GvHD) therapy.\n7. Anti-CD20 antibody treatment less than 2 weeks prior to cell infusion.\n8. History of receiving allograft organ transplant requiring immunosuppression.\n9. Participants that underwent a solid organ transplant who develop high grade lymphomas or leukemias.\n10. Metastases to the CNS, including the parenchyma or leptomeninges.\n11. Nonmalignant CNS disease (eg, stroke, epilepsy, vasculitis, or neurodegenerative disease).\n12. History of or active inflammatory bowel disease (eg, Crohn's disease, ulcerative colitis).\n13. Uncontrolled hypertension (systolic \\> 160 mm Hg and\u002For diastolic \\> 110 mm Hg) or clinically significant (ie, active) cardiovascular disease, cerebrovascular accident\u002Fstroke, or myocardial infarction within 6 months prior to first study medication; unstable angina; congestive heart failure of New York Heart Association Class 2 or higher; or serious cardiac arrhythmia requiring medication.\n14. Current chronic daily treatment (continuous for \\> 3 months) with systemic corticosteroids as defined as \\> 20 mg of prednisone or equivalent daily, excluding inhaled steroids. Short-term steroid use to prevent IV contrast allergic reaction or anaphylaxis in participants who have known contrast allergies is allowed.\n15. Currently taking any medication(s) (herbal or prescribed) known to have an adverse drug reaction with any of the study medications.\n16. History of human immunodeficiency virus (HIV) with current CD4+ T-cell count \\\u003C 350 cells\u002FμL and\u002For a detectable HIV viral load.\n17. Known carriers of hepatitis B virus (HBV) infection that is currently hepatitis B surface antigen (HBsAg) positive.\n18. Concurrent active malignancy other than basal or squamous cell carcinomas of the skin.\n19. Assessed by the Investigator to be unable or unwilling to comply with the requirements of the protocol.\n20. Women who are pregnant or breastfeeding.","75 Years",{"count":19,"type":20},[23],"Open-Label, Phase 2 Chemotherapy-Free Study ofCD19 t-haNK and NAI in Combination With Rituximab in Participants With Relapsed\u002FRefractory B-Cell Indolent Non-Hodgkin Lymphoma. 40 Participant will be screened for 20 subjects enrollment.",[52],"Relapsed B-Cell Non-Hodgkin Lymphoma","NOT_YET_RECRUITING","2026-03-13",{"date":56,"type":31},"2026-03-17",{"date":58,"type":20},"2026-04",{"date":60,"type":20},"2028-12",{"name":37,"class":38},{"id":63,"slug":64,"hasResults":11,"nctId":65,"briefTitle":66,"officialTitle":67,"acronym":4,"eligibilityCriteria":68,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":69,"targetDuration":4,"studyType":21,"phases":71,"briefSummary":73,"conditions":74,"keywords":77,"overallStatus":27,"whyStopped":4,"lastUpdateSubmitDate":80,"lastUpdatePostDateStruct":81,"startDateStruct":83,"completionDateStruct":85,"leadSponsor":87,"locationsCount":5},"100540216","phase-1-a-study-of-lucar-20sp-in-subjects-with-relapsedrefractory-b-cell-non-hodgkin-lymphoma-100540216","NCT06313957","A Study of LUCAR-20SP in Subjects With Relapsed\u002FRefractory B-cell Non-Hodgkin Lymphoma","A Phase I Clinical Study to Evaluate the Safety, Tolerability, and Efficacy of LUCAR-20SP, an Allogenic Chimeric Antigen Receptor(CAR)-T Cell Therapy Targeting CD20 in Subjects With Relapsed\u002FRefractory B-cell Non-Hodgkin Lymphoma","Inclusion Criteria:\n\n* Subjects voluntarily participate in clinical research;\n* Age ≥18 years old;\n* Eastern Cooperative Oncology Group (ECOG) score 0-1;\n* Histologically confirmed large B-cell lymphoma, follicular lymphoma, mantle cell lymphoma, histologically indolent lymphoma to diffuse large B-cell lymphoma; CD20 positive;\n* At least one measurable tumor lesion according to the Lugano 2014.\n* Expected survival ≥3 months;\n* Clinical laboratory values in the screening period meet criteria.\n* Effective contraception.\n\nExclusion Criteria:\n\n* Prior antitumor therapy with insufficient washout period.\n* Previous treatment with allogeneic cell and gene therapy (such as CAR-T); Except subjects with evidence that previous allogeneic cell and gene therapy products (such as CAR-positive T cells and CAR transgenes) in the subject have been below the lower limit of detection;\n* Previously received allogeneic hematopoietic stem cell transplantation;\n* Previously received gene therapy;\n* Donor specific antibody (DSA) positive subjects will be excluded;\n* Severe underlying diseases;\n* Hepatitis B virus deoxyribonucleic acid (HBV DNA), hepatitis C virus ribonucleic acid (HCV RNA) or human immunodeficiency virus antibody (HIV-Ab) positive;\n* Presence of other serious pre-existing medical conditions that may limit patient participation in the study. Any condition that, in the investigator's judgment, will make the subject unsuitable for participation in this study.",{"count":70,"type":20},42,[72],"PHASE1","This is a prospective, single-arm, open-label, exploratory clinical study of LUCAR-20SP in adult subjects with relapsed\u002Frefractory B-cell non-Hodgkin lymphoma.",[75,76],"Relapsed B-cell Non-Hodgkin Lymphoma","Refractory B-cell Non-Hodgkin Lymphoma",[78,79],"Relapsed B-cell non-Hodgkin lymphoma","Refractory B-cell non-Hodgkin lymphoma","2025-03-20",{"date":82,"type":31},"2025-03-25",{"date":84,"type":31},"2024-03-14",{"date":86,"type":20},"2028-09",{"name":88,"class":89},"Peking University Cancer Hospital & Institute","OTHER"]