[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"treatment-naive\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:treatment-naive":27},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,51],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":22,"briefSummary":24,"conditions":25,"keywords":28,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":39,"lastUpdatePostDateStruct":40,"startDateStruct":43,"completionDateStruct":45,"leadSponsor":47,"locationsCount":50},"100446902","phase-2-efficacy-of-venetoclax-in-combination-with-rituximab-in-waldenstrms-macroglobulinemia-100446902",false,"NCT05099471","Efficacy of Venetoclax in Combination With Rituximab in Waldenström's Macroglobulinemia","VIWA-1","Inclusion Criteria:\n\n* Proven clinicopathological diagnosis of WM as defined by consensus panel one of the Second International Workshop on WM (IWWM). Histopathology has to be perfomed before randomization but within the last 4 months before start of treatment. In addition, pathological specimens have to be sent to the national pathological reference center prior to randomization for the determination of the mutational status of MYD88 and CXCR4 prior to randomization if the mutational status hasn't been determined before. Pathological reference center must confirm the diagnosis of WM.\n* De novo WM independent of the genotype.\n* Patients must have at least one of the following criteria to start study treatment as partly defined by consensus panel criteria from the Seventh IWWM and ESMO Guideline:\n\n  * Recurrent fever, night sweats, weight loss, fatigue (at least one of them).\n  * Hyperviscosity.\n  * Lymphadenopathy which is either symptomatic or bulky (≥ 5 cm in maximum diameter).\n  * Symptomatic hepatomegaly and \u002F or splenomegaly.\n  * Symptomatic organomegaly and \u002F or organ or tissue infiltration.\n  * Peripheral neuropathy due to WM.\n  * Symptomatic cryoglobulinemia.\n  * Symptomatic Cold agglutinin anemia.\n  * Autoimmune hemolytic anemia and\u002For thrombocytopenia.\n  * Nephropathy related to WM.\n  * Amyloidosis related to WM.\n  * Hemoglobin ≤ 10 g\u002FdL (patients should not have received red blood cells transfusions for at least 7 days prior to obtaining the screening hemoglobin).\n  * Platelet count \\\u003C 100 x 109\u002FL (caused by bone marrow \\[BM\\] infiltration of the lymphoma).\n  * Serum monoclonal protein \\> 5 g\u002FdL, even with no overt clinical symptoms.\n  * IgM serum concentration ≥ 6 g\u002FdL.\n  * and other WM associated relevant symptoms\n* Subject must be ≥ 18 years of age.\n* Life expectancy \\> 3 months.\n* World Health Organization (WHO) \u002F ECOG performance status ≤ 2.\n* Left ventricular ejection fraction ≥ 40% as assessed by transthoracic echocardiogram (TTE).\n* Baseline platelet count ≥ 50x109\u002FL, absolute neutrophil count ≥ 0.75x109\u002FL (if not due to BM infiltration by the lymphoma).\n\n  . Adequate hepatic function per local laboratory reference range as follows:\n  * Aspartate transaminase (AST) and alanine transaminase (ALT) \\\u003C 3.0 x ULN.\n  * Bilirubin ≤1.5 x ULN (unless bilirubin rise is due to Gilbert's syndrome or of non-hepatic origin).\n* Subject must have adequate renal function as demonstrated by a creatinine clearance ≥ 30 mL\u002Fmin; calculated by the Cockcroft Gault formula or measured by 24 hours urine collection.\n* Women of childbearing potential (WCBP), i.e. fertile, following menarche and until becoming postmenopausal must have negative results for pregnancy test and must agree to use a highly effective method of birth control for the duration of the therapy up to 12 months after end of therapy\n* Men must agree not to father a child for the duration of therapy and 12 months after and must agree to advice their female partner to use a highly effective method of birth control. Males must refrain from sperm donation for the duration of treatment and at least 12 months after the last dose of study medication.\n* Each patient must voluntarily date and sign an informed consent form in the native language of the patient indicating that he or she understands the purpose of and procedures required for the study and are willing to participate in the study. Patients must be willing and able to adhere to the prohibitions and restrictions specified in this protocol.\n* Affiliation to a social security scheme (relevant for France only).\n\nExclusion Criteria:\n\n* Serious medical or psychiatric illness (especially undergoing treatment) likely to interfere with participation in this clinical study.\n* Subject is known to be positive for HIV.\n* Active severe infection\n* Congenital or acquired severe immunodeficiency not attributed to lymphoma (clinical appearance: recurrent infections, necessity of immunoglobulin substitution therapy, patients after transplantation)\n* Evidence of other clinically significant uncontrolled condition(s) including, but not limited to:\n\n  * Uncontrolled systemic infection (viral, bacterial or fungal).\n  * Chronic hepatitis B virus (HBV) or hepatitis C virus (HCV) infection requiring treatment. Note: subjects with serologic evidence of prior vaccination to HBV (i.e. hepatitis B surface (HBs) antigen negative-, anti-HBs antibody positive and anti-hepatitis B core (HBc) antibody negative) or positive anti-HBc antibody from intravenous immunoglobulins (IVIG) may participate\n* inadequate pulmonary function as demonstrated by DLCO ≤ 65% or FEV1 ≤ 65%.\n* Creatinine clearance ≥ 30 mL\u002Fmin to \\\u003C 45 ml\u002Fmin\n* Uncontrolled diabetes mellitus (as indicated by metabolic derangements and \u002F or severe diabetes mellitus related uncontrolled organ complications).\n* Uncontrolled hypertension.\n* Cardiac history of CHF requiring treatment or Ejection Fraction ≤ 50% or chronic stable angina.\n* Unstable angina pectoris, angioplasty, stenting, or myocardial infarction within 6 months prior to start therapy.\n* Clinically significant cardiac arrhythmia that is symptomatic or requires treatment, or asymptomatic sustained ventricular tachycardia.\n* Subject has a cardiovascular disability status of New York Heart Association Class \\> 2. Class 2 is defined as cardiac disease in which patients are comfortable at rest but ordinary physical activity results in fatigue, palpitations, dyspnea, or anginal pain.\n* History of stroke or intracranial haemorrhage within 6 months prior start of treatment\n* Known pericardial disease.\n* Known interstitial lung disease.\n* Infiltrative pulmonary disease, known pulmonary hypertension.\n* Prior history of malignancies unless the subject has been free of the disease for ≥ 3 years. Exceptions include the following:\n\n  * Basal cell carcinoma of the skin,\n  * Squamous cell carcinoma of the skin,\n  * Carcinoma in situ of the cervix,\n  * Carcinoma in situ of the breast,\n  * Incidental histologic finding of prostate cancer (TNM stage of T1a or T1b).\n* Known cirrhosis (meeting child-pugh stage C).\n* Chemotherapy with approved or investigational anticancer therapeutic within 21 days prior to start of therapy\n* Glucocorticoid therapy within 14 days prior to therapy that exceeds a cumulative dose of 160 mg of dexamethasone or equivalent dose of other corticosteroids given for anti-neoplastic intent.\n* Treatment with any of the following within 7 days prior to the first dose of study drug:\n\n  * moderate or strong cytochrome P450 3A (CYP3A) inhibitors (such as fluconazole, ketoconazole, and clarithromycin).\n  * moderate or strong CYP3A inducers (such as rifampin, carbamazepine, phenytoin, St. John's wort).\n* Contraindication to the active substances or any of the other excipients of the Investigational Medicinal Products as well as to any of the required concomitant drugs or supportive treatments, including hypersensitivity to antiviral drugs.\n* Vaccination with live attenuated vaccines within 4 weeks prior to start of therapy.\n* History or evidence of any other clinically significant disorder, condition or disease (with the exception of those outlined above) that, in the opinion of the investigator or sponsor, if consulted, would pose a risk to subject safely or interfere with the study evaluation, procedures or completion.\n* Women who are pregnant as well as women who are breast-feeding and do not consent to discontinue breast-feeding.\n* Participation in another clinical trial within four weeks before start of therapy in this study.\n* No consent for registration, storage and processing of the individual disease-characteristics.\n* Administration or consumption of any of the following within 3 days prior to the first dose of study drug:\n\n  * grapefruit or grapefruit products.\n  * Seville oranges (including marmalade containing Seville oranges).\n  * star fruit.\n* Person of legal age who is incapable of comprehending the nature, significance and implications of the clinical trial and of determining his\u002Fher will in the light of these facts","ALL","18 Years",{"count":19,"type":20},80,"ESTIMATED","INTERVENTIONAL",[23],"PHASE2","In Waldenström's macroglobulinemia (WM) chemotherapy induces only low CR\u002FVGPR rates and response duration is limited. In addition, WM patients are often elderly, partly not tolerating chemotherapy related toxicities. Thus, innovative approaches are needed which combine excellent activity and tolerability in WM. Chemotherapy-free approaches are highly attractive for this patient group. Based on its high activity and favorable toxicity profile in indolent B-NHL such as CLL, Venetoclax was approved for the treatment of this diseases by the FDA and the European Medicines Agency (EMA). First data in relapsed\u002Frefractory WM have documented high activity and low toxicity of Venetoclax also in WM, including patients with prior Ibrutinib treatment or patients carrying CXCR4 mutations. Ibrutinib itself has high activity and a relatively low toxicity profile in WM, but has also major disadvantages: the main disadvantage is the need to apply this drug continuously. Furthermore, Ibrutinib efficacy depends largely on the genotype with a substantial drop in major responses and PFS in the presence of CXCR4 mutations and non-mutated MYD88. In particular the need of continuous treatment for Ibrutinib has prevented that Ibrutinib has become the standard of care outcompeting conventional Rituximab\u002Fchemotherapy. This is reflected in current guidelines such as the NCCN and the ESMO guidelines, which still see immunochemotherapy as a backbone of treatment, largely because of the advantage of a timely fixed application. Data in CLL in the relapsed as well as in the first line setting have convincingly shown that in contrast to Ibrutinib Venetoclax is highly efficient also when used in a timely defined application scheme over 12 months in combination with the anti-CD20 antibody Rituximab. Data documented deep responses including molecular responses and a highly significant advantage over immunochemotherapy in large international Phase III trials, changing the standard of care in this disease.\n\nBased on this the hypothesis is that timely fixed application of the combination of Venetoclax and Rituximab induces significantly superior treatment outcomes compared to chemotherapy and Rituximab (DRC) in patients with treatment naïve WM, regardless of the genotype. A first indication for this assumption in the proposed trial will allow the performance of confirmatory phase 3 trials that might change the standard of care in WM.",[26,27],"Waldenstrom Macroglobulinemia","Treatment Naive",[29,30,31,32,33,34,35,36,37],"Hematology","Oncology","Venetoclax","Rituximab","DRC","Lymphoma","NHL","indolent","monoclonal IgM","RECRUITING","2026-04-28",{"date":41,"type":42},"2026-05-05","ACTUAL",{"date":44,"type":42},"2025-03-21",{"date":46,"type":20},"2033-03",{"name":48,"class":49},"Christian Buske","OTHER",14,{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":58,"enrollmentInfo":59,"targetDuration":4,"studyType":21,"phases":61,"briefSummary":63,"conditions":64,"keywords":66,"overallStatus":38,"whyStopped":4,"lastUpdateSubmitDate":71,"lastUpdatePostDateStruct":72,"startDateStruct":74,"completionDateStruct":76,"leadSponsor":78,"locationsCount":80},"100602681","fixed-duration-zanubrutinib-bendamustine-and-obinutuzumab-zbg-in-treatment-nave-advanced-stage-follicular-lymphoma-100602681","NCT07126678","Fixed-Duration Zanubrutinib, Bendamustine, and Obinutuzumab (ZBG) in Treatment-Naïve Advanced Stage Follicular Lymphoma","Prospective Exploratory Study of Fixed-Duration Zanubrutinib, Bendamustine, and Obinutuzumab (ZBG) in Treatment-Naïve Advanced Stage Follicular Lymphoma","Inclusion Criteria:\n\n1. Voluntary participation with signed informed consent;\n2. Age ≥18 years and ≤75 years, regardless of gender;\n3. Life expectancy ≥3 months;\n4. ECOG performance status 0-2; patients with ECOG 3 may be enrolled only if their decline in performance status is disease-related and the investigator judges they may benefit from treatment;\n5. Histologically confirmed diagnosis of grade I, II, or IIIa follicular lymphoma (FL), treatment-naïve, stage III-IV disease, and meeting treatment criteria (GELF criteria);\n6. Measurable and\u002For evaluable lymphoma lesions;\n7. Adequate bone marrow reserve: absolute neutrophil count (ANC) \\>1.0×10⁹\u002FL or platelets \\>75×10⁹\u002FL, unless cytopenia is deemed related to bone marrow infiltration by lymphoma and the investigator believes it may recover;\n8. Liver function: AST (SGOT), ALT (SGPT) ≤2.5×ULN (without liver involvement) or ≤5×ULN (with liver involvement); total bilirubin (TBIL) ≤ULN; serum creatinine (CRE) ≤1.5×ULN;\n9. Creatinine clearance ≥30 mL\u002Fmin (calculated by Cockcroft-Gault formula);\n10. Ability to comply with study visit schedules and other protocol requirements;\n11. All patients of childbearing potential must agree to use effective contraception during the study and for 24 months after treatment cessation; women of childbearing potential must have a negative urine pregnancy test before treatment initiation.\n\nExclusion Criteria:\n\n1. Grade IIIb FL or transformed FL;\n2. Received lymphoma-directed therapy within 2 weeks prior to enrollment;\n3. Any severe medical condition, including but not limited to:\n\n   * Poorly controlled hypertension (defined as failure to achieve control despite lifestyle modifications and treatment with at least 3 maximally tolerated antihypertensive drugs \\[including diuretics\\] for ≥4 weeks, or requiring ≥4 antihypertensive drugs for adequate control);\n   * Uncontrolled congestive heart failure (NYHA class 3 \\[moderate\\] or 4 \\[severe\\]) within 6 months prior to screening;\n   * Left ventricular ejection fraction (LVEF) \\\u003C50%;\n   * Symptomatic coronary artery disease (e.g., chest pain, palpitations, fatigue) or requiring medication;\n   * Severe bradycardia (heart rate \\\u003C40 bpm), hypotension, dizziness, or syncope; patients with arrhythmia history require cardiac evaluation;\n   * Active bacterial, viral, fungal, or other infections (except for nail fungal infections) or major infections within 2 weeks before the first dose of study drug;\n   * Moderate to severe liver disease (Child-Pugh B or C);\n   * Active bleeding within 2 months before screening or clinically significant bleeding tendency per investigator judgment;\n   * Pulmonary conditions impairing function (e.g., pulmonary fibrosis, drug-induced pneumonitis) deemed intolerable by the investigator;\n   * Any psychiatric or cognitive impairment that may compromise understanding of informed consent, protocol compliance, or study adherence;\n4. Known active hepatitis C virus (HCV) infection; other acquired\u002Fcongenital immunodeficiency disorders, including HIV infection;\n5. Central nervous system (CNS) involvement by lymphoma;\n6. Diagnosis or treatment for malignancies other than lymphoma, except:\n\n   * Malignancies treated with curative intent and no evidence of disease for ≥5 years before enrollment;\n   * Adequately treated basal cell carcinoma (excluding melanoma) with no evidence of disease;\n   * Adequately treated cervical carcinoma in situ with no evidence of disease;\n7. Hypersensitivity to any study drug;\n8. Pregnant or breastfeeding women;\n9. History of stroke or intracranial hemorrhage within 6 months before enrollment;\n10. Requiring anticoagulation with warfarin or equivalent vitamin K antagonists;\n11. Requiring chronic use of strong CYP3A inhibitors;\n12. Administration of live attenuated vaccines within 4 weeks before study entry.","75 Years",{"count":60,"type":20},15,[62],"NA","This study investigates a fixed-duration regimen of zanubrutinib, bendamustine, and obinutuzumab (ZBG) in the treatment of treatment-naïve patients with advanced-stage follicular lymphoma.\n\nPatients will receive combination therapy with zanubrutinib, bendamustine, and obinutuzumab over 6 cycles, with each cycle lasting 28 days. The specific dosing schedule is as follows: Bendamustine 70 mg\u002Fm²: administered intravenously on Days 2-3 of Cycle 1, and on Days 1-2 of Cycles 2-6. Obinutuzumab 1000 mg: administered intravenously on Days 1, 8, and 15 of Cycle 1, and on Day 1 of Cycles 2-6 (every 28-day cycle). Zanubrutinib 160 mg orally twice daily (bid), continuously throughout Cycles 1-6.\n\nTreatment is discontinued after 6 cycles, with no subsequent maintenance therapy.\n\nPrimary endpoint is 2-year PFS. Secondary endpoints include: CR rate after 6 cycles, ORR after 3 and 6 cycles MRD-negative rate after 3 and 6 cycles, OS, safety and tolerability.",[65,27],"Follicular Lymphoma",[67,68,69,70,27],"Follicular lymphoma","fixed-duration","zanubrutinib","ZBG","2025-08-15",{"date":73,"type":42},"2025-08-17",{"date":75,"type":42},"2025-07-15",{"date":77,"type":20},"2028-12-30",{"name":79,"class":49},"The First Affiliated Hospital with Nanjing Medical University",1]