[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100628605":3},{"organization":4,"armGroups":7,"interventions":32,"overallOfficials":194,"centralContacts":47,"locations":47,"responsibleParty":199,"collaborators":47,"id":201,"slug":202,"hasResults":203,"nctId":204,"briefTitle":205,"officialTitle":206,"acronym":47,"eligibilityCriteria":207,"healthyVolunteers":203,"sex":208,"minAge":209,"maxAge":47,"enrollmentInfo":210,"targetDuration":47,"studyType":213,"phases":214,"briefSummary":217,"conditions":218,"keywords":47,"overallStatus":221,"whyStopped":47,"lastUpdateSubmitDate":222,"lastUpdatePostDateStruct":223,"startDateStruct":226,"completionDateStruct":228,"leadSponsor":230,"locationsCount":47},{"fullName":5,"class":6},"National Cancer Institute (NCI)","NIH",[8,22,28],{"label":9,"type":10,"description":11,"interventionNames":12},"Arm D (carfilzomib, pomalidomide, dexamethasone)","ACTIVE_COMPARATOR","Patients receive carfilzomib IV on days 1, 2, 8, and 15 of cycle 1, on days 1, 8, and 15 of cycle 2, then on days 1 and 15 of subsequent cycles, pomalidomide PO QD on days 1-21 and dexamethasone PO or IV on days 1, 8, 15, and 22 of each cycle. Cycles repeat every 28 days in the absence of disease progression or unacceptable toxicity. Additionally, patients undergo urine and blood sample collection, FDG PET\u002FCT, and bone marrow biopsy and\u002For aspiration throughout the study.",[13,14,15,16,17,18,19,20,21],"Procedure: Biospecimen Collection","Procedure: Bone Marrow Aspiration","Procedure: Bone Marrow Biopsy","Drug: Carfilzomib","Procedure: Computed Tomography","Drug: Dexamethasone","Procedure: FDG-Positron Emission Tomography","Other: Fludeoxyglucose F-18","Drug: Pomalidomide",{"label":23,"type":24,"description":25,"interventionNames":26},"Arms A and B (teclistamab, pomalidomide)","EXPERIMENTAL","Patients teclistamab SC on days 1, 4, 7, 14, and 21 of cycle 1, days 1, 8, 15, and 22 of cycle 2, days 1 and 15 of cycles 3-6, then on day 1 of remaining cycles. Starting with cycle 2, patients receive pomalidomide PO QD on days 1-21 of each cycle. Cycles repeat every 28 days for up to 2 years in the absence of disease progression or unacceptable toxicity. Additionally, patients undergo urine and blood sample collection, FDG PET\u002FCT, and bone marrow biopsy and\u002For aspiration throughout the study.",[13,14,15,19,20,21,27],"Drug: Teclistamab",{"label":29,"type":24,"description":30,"interventionNames":31},"Arms C (teclistamab, pomalidomide)","Patients teclistamab SC on days 1, 4, 7, 14, and 21 of cycle 1, days 1, 8, 15, and 22 of cycle 2, days 1 and 15 of cycles 3-6, then on day 1 of subsequent cycles. Starting with cycle 2, patients receive pomalidomide PO QD on days 1-21 of subsequent cycles. Cycles repeat every 28 days for up to 2 years in the absence of disease progression or unacceptable toxicity. Additionally, patients undergo urine and blood sample collection, FDG PET\u002FCT, and bone marrow biopsy and\u002For aspiration throughout the study.",[13,14,15,17,19,20,21,27],[33,43,48,54,66,83,153,160,172,184],{"type":34,"name":35,"description":36,"armGroupLabels":37,"otherNames":38},"PROCEDURE","Biospecimen Collection","Undergo urine and blood sample collection",[9,23,29],[39,40,41,42],"Biological Sample Collection","Biospecimen Collected","Sample Collection","Specimen Collection",{"type":34,"name":44,"description":45,"armGroupLabels":46,"otherNames":47},"Bone Marrow Aspiration","Undergo bone marrow biopsy and\u002For aspiration",[9,23,29],null,{"type":34,"name":49,"description":45,"armGroupLabels":50,"otherNames":51},"Bone Marrow Biopsy",[9,23,29],[52,53],"Biopsy of Bone Marrow","Biopsy, Bone Marrow",{"type":55,"name":56,"description":57,"armGroupLabels":58,"otherNames":59},"DRUG","Carfilzomib","Given IV",[9],[60,61,62,63,64,65],"Carfilnat","CFZ","Kyprolis","PR 171","PR-171","PR171",{"type":34,"name":67,"description":68,"armGroupLabels":69,"otherNames":70},"Computed Tomography","Undergo FDG PET\u002FCT",[9,29],[71,72,73,74,75,76,77,78,79,80,81,82],"CAT","CAT Scan","Computed Axial Tomography","Computerized Axial Tomography","Computerized axial tomography (procedure)","Computerized Tomography","Computerized Tomography (CT) scan","CT","CT Scan","Diagnostic CAT Scan","Diagnostic CAT Scan Service Type","tomography",{"type":55,"name":84,"description":85,"armGroupLabels":86,"otherNames":87},"Dexamethasone","Given PO or IV",[9],[88,89,90,91,92,93,94,95,96,97,98,99,100,101,102,103,104,105,106,107,108,109,110,111,112,113,114,115,116,117,118,119,120,121,122,123,124,125,126,127,128,129,130,131,132,133,134,135,136,137,138,139,140,141,142,143,144,145,146,147,148,149,150,151,152],"Aacidexam","Adexone","Aknichthol Dexa","Alba-Dex","Alin","Alin Depot","Alin Oftalmico","Amplidermis","Anemul mono","Auricularum","Auxiloson","Baycadron","Baycuten","Baycuten N","Cortidexason","Cortisumman","Decacort","Decadrol","Decadron","Decadron DP","Decalix","Decameth","Decasone R.p.","Dectancyl","Dekacort","Deltafluorene","Deronil","Desamethasone","Desameton","Dexa-Mamallet","Dexa-Rhinosan","Dexa-Scheroson","Dexa-sine","Dexacortal","Dexacortin","Dexafarma","Dexafluorene","Dexalocal","Dexamecortin","Dexameth","Dexamethasone Intensol","Dexamethasonum","Dexamonozon","Dexapos","Dexinoral","Dexone","Dinormon","Dxevo","Fluorodelta","Fortecortin","Gammacorten","Hemady","Hexadecadrol","Hexadrol","LenaDex","Lokalison-F","Loverine","Methylfluorprednisolone","Millicorten","Mymethasone","Orgadrone","Spersadex","TaperDex","Visumetazone","ZoDex",{"type":34,"name":154,"description":68,"armGroupLabels":155,"otherNames":156},"FDG-Positron Emission Tomography",[9,23,29],[157,158,159],"FDG","FDG-PET","FDG-PET Imaging",{"type":161,"name":162,"description":163,"armGroupLabels":164,"otherNames":165},"OTHER","Fludeoxyglucose F-18","Given FDG",[9,23,29],[166,157,167,168,169,170,171],"18FDG","Fludeoxyglucose (18F)","fludeoxyglucose F 18","Fludeoxyglucose F18","Fluorine-18 2-Fluoro-2-deoxy-D-Glucose","Fluorodeoxyglucose F18",{"type":55,"name":173,"description":174,"armGroupLabels":175,"otherNames":176},"Pomalidomide","Given PO",[9,23,29],[177,178,179,180,181,182,183],"4-Aminothalidomide","Actimid","CC 4047","CC-4047","CC4047","Imnovid","Pomalyst",{"type":55,"name":185,"description":186,"armGroupLabels":187,"otherNames":188},"Teclistamab","Given SC",[23,29],[189,190,191,192,193],"JNJ 64007957","JNJ-64007957","JNJ64007957","Teclistamab-cqyv","Tecvayli",[195],{"name":196,"affiliation":197,"role":198},"Murali Janakiram","ECOG-ACRIN Cancer Research Group","PRINCIPAL_INVESTIGATOR",{"type":200,"investigatorFullName":47,"investigatorTitle":47,"investigatorAffiliation":47,"oldNameTitle":47,"oldOrganization":47},"SPONSOR","100628605","phase-1-testing-the-investigational-medication-combination-of-teclistamab-and-pomalidomide-compared-to-the-usual-treatment-carfilzomib-pomalidomide-and-dexamethasone-for-patients-with-multiple-myeloma-who-have-relapsed-shortly-after-treatment-100628605",false,"NCT07463807","Testing the Investigational Medication Combination of Teclistamab and Pomalidomide Compared to the Usual Treatment (Carfilzomib, Pomalidomide, and Dexamethasone) for Patients With Multiple Myeloma Who Have Relapsed Shortly After Treatment","Phase Ib\u002FII Fixed Duration Study of Teclistamab\u002FPomalidomide (TP) Versus Carfilzomib\u002FPomalidomide\u002FDexamethasone (KPd) in Early Relapse of Multiple Myeloma","Inclusion Criteria:\n\n* Patient must be ≥ 18 years of age\n* Patient must have an Eastern Cooperative Oncology Group (ECOG) performance status 0-2\n* Patient must have an identifiable dominant sequence (clonotype) established based on Adaptive Biotechnologies clonoSEQ® assay for Phase II only\n* Patient must have multiple myeloma and meet both of the following criteria for the original diagnosis of myeloma following the International Myeloma Working Group (IMWG) myeloma diagnostic criteria:\n\n  * Bone marrow plasmacytosis with ≥ 10% plasma cells or sheets of plasma cells or biopsy proven plasmacytoma.\n\n    * Tissue biopsy of any bone lesion or extramedullary plasmacytoma if applicable (positive\u002Fnegative for clonal plasma cells)\n  * Any one or more of the following symptomatic myeloma-defining events that prompted initiation of therapy as well as end-organ damage:\n\n    * Anemia (hemoglobin value of \\> 2 g\u002FdL below the lower limit of normal, or a hemoglobin value \\\u003C 10 g\u002FdL)\n    * Hypercalcemia (serum calcium \\> 1 mg\u002FdL higher than the upper limit of normal or \\> 11 mg\u002FdL)\n    * Bone disease (one or more osteolytic lesions on skeletal radiography, CT, or FDG-PET\u002FCT)\n    * Renal dysfunction (creatinine clearance \\\u003C 40 mL\u002Fmin or serum creatinine \\> 2 mg\u002FdL).\n    * Clonal bone marrow plasma cells (BMPCs) ≥ 60%\n    * Involved\u002Funinvolved serum free light chain ratio ≥ 100\n    * \\> 1 focal lesions on magnetic resonance imaging (MRI) studies ≥ 5 mm\n  * NOTE: Patients with smoldering myeloma (serum m protein ≥ 3 gm\u002FdL or bone marrow plasma cells ≥ 10% or greater plus no evidence of anemia, hypercalcemia, lytic bone lesions or renal dysfunction) and monoclonal gammopathy of undetermined significance (serum m protein \\\u003C 3 gm\u002FdL and bone marrow plasma cells \\\u003C 10% or greater plus no evidence of anemia, hypercalcemia, lytic bone lesions or renal dysfunction) are not eligible\n* Patient must have experienced early relapse disease defined as relapse after one line of lenalidomide therapy including single agent lenalidomide or lenalidomide\u002Fdexamethasone or CD38 antibody\u002Flenalidomide +\u002F- dexamethasone. The relapse can be progressive disease as determined by the treating clinician and meeting measurable disease criteria\n* Patient must have received no more than two lines of IMWG defined therapy (induction +\u002F- transplant + maintenance is considered a single line of therapy)\n* Patient must not receive non-protocol concurrent chemotherapy for the study disease, or any ancillary therapy considered investigational while participating in the study\n* Patient must have received an immunomodulatory drug (lenalidomide) and a CD38 antibody (daratumumab or isatuximab)\n* Patient must have measurable disease as defined by having one or more of the following, obtained within 28 days prior to registration\u002Frandomization:\n\n  * ≥ 0.5 g\u002FdL monoclonal protein (M-protein) on serum protein electrophoresis\n  * ≥ 200 mg\u002F24 hrs of monoclonal protein (M-protein) on a 24-hour urine protein electrophoresis\n  * Involved free light chain ≥ 10 mg\u002FdL AND abnormal serum immunoglobulin kappa to lambda free light chain ratio (\\\u003C 0.26 or \\> 1.65)\n  * Exception: patients without measurable disease in the serum or urine, but with bone or soft tissue plasmacytoma(s) ≥ 2 cm or who have bone marrow plasma cells ≥ 30% are eligible on study\n  * NOTE: Urine protein electrophoresis (UPEP) (on a 24 hour collection) is required, no substitute method is acceptable. Urine must be followed monthly if the baseline urine M-spike is ≥ 200 mg\u002F24 hr. Please note that if both serum and urine m-components are present, both must be followed in order to evaluate response.\n* Patient must not be known to be refractory to carfilzomib or pomalidomide\n* Patient must not have received a prior BCMA therapy\n* Patient must not be pregnant due to the potential harm to an unborn fetus with the treatment regimens being used\n\n  * All patients of childbearing potential must have a blood test or urine study within 14 days prior to registration\u002Frandomization to rule out pregnancy. Patients must also agree to a second pregnancy test completed within 24 hours prior to the first dose of pomalidomide and teclistamab and agree to ongoing pregnancy testing while on protocol treatment\n  * A patient of childbearing potential is defined as anyone, regardless of whether they have undergone tubal ligation, who meets the following criteria:\n\n    * Has achieved menarche at some point\n    * Has not undergone a hysterectomy or bilateral oophorectomy\n    * Has not been naturally postmenopausal (amenorrhea following cancer therapy does not rule out childbearing potential) for at least 24 consecutive months (i.e., has had menses at any time in the preceding 24 consecutive months)\n* Patient must not expect to conceive or father children by using accepted and effective method(s) of contraception or by abstaining from sexual intercourse for the duration of their participation in the study and for 6 months after the last dose of protocol treatment for patients on Arms A, B, and C and for 1 month after the last dose of protocol treatment for patients on Arm D. In addition, all patients must also agree to register to the mandatory Risk Evaluation and Mitigation Strategies (REMS)® program and be willing and able to comply with the requirements of the REMS® program\n* Patient must agree to not breastfeed while on protocol treatment due to the potential risk for adverse events in nursing infants, and must agree to continue not breastfeeding for an additional 5 months after the last dose of Arm A, B, or C protocol treatment and for an additional 28 days after the last dose of Arm D protocol treatment\n* Patient must agree to abstain for donating eggs (ova, oocytes) while on study treatment and for 6 months after the last dose of Arm A, B or C protocol treatment\n* Patient must agree to abstain from donating sperm while on study treatment and for 3 months after the last dose of protocol treatment even if they have had a successful vasectomy\n* Patient must agree to abstain from donating blood during study participation and for at least 28 days after the last dose of protocol treatment\n* Patient must not receive non-protocol concurrent chemotherapy, or any ancillary therapy considered investigational while participating in the study\n\n  * NOTE: Bisphosphonates are considered supportive care rather than therapy and are thus allowed while on protocol treatment\n* Patient must not have peripheral neuropathy \\> grade 2 on clinical examination at the time of registration\u002Frandomization\n* Patient must not have known uncontrolled congestive heart failure (CHF), New York Heart Association (NYHA) class III or IV, uncontrolled hypertension as defined as systolic \\> 180 and\u002For diastolic \\> 100, uncontrolled atrial (A) fib, or left ventricular ejection fraction (LVEF) \\\u003C 40% within 6 months prior to registration\u002Frandomization\n* Patient must not have known allergies, hypersensitivity, or intolerance to corticosteroids, monoclonal antibodies or human proteins, or their excipients, or known sensitivity to mammalian-derived products\n* Patient must have the ability to understand and the willingness to sign a written informed consent document. Patients with impaired decision-making capacity (IDMC) who have a legally authorized representative (LAR) or caregiver and\u002For family member available will also be considered eligible\n* Absolute neutrophil count (ANC) ≥ 1,500\u002FuL (≤ 14 days prior to registration\u002Frandomization)\n* Platelets ≥ 100,000\u002FuL (≤ 14 days prior to registration\u002Frandomization)\n* Total bilirubin ≤ 3 x institutional upper limit of normal (ULN) (≤ 14 days prior to registration\u002Frandomization)\n* Aspartate aminotransferase (AST)(serum glutamic oxaloacetic transaminase \\[SGOT\\]) and alanine aminotransferase (ALT)(serum glutamic pyruvic transaminase \\[SGPT\\]) ≤ 3.0 x institutional ULN (≤ 14 days prior to registration\u002Frandomization)\n* Calculated creatinine clearance ≥ 30 mL\u002Fmin (≤ 14 days prior to registration\u002Frandomization)\n* Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months of registration\u002Frandomization are eligible for this trial\n* For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated\n* Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load\n* Patients with past central nervous system (CNS) involvement are eligible if there is no current CNS involvement\n* Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial","ALL","18 Years",{"count":211,"type":212},162,"ESTIMATED","INTERVENTIONAL",[215,216],"PHASE1","PHASE2","This phase Ib\u002FII trial compares the effect of teclistamab and pomalidomide to standard treatment with carfilzomib, pomalidomide and dexamethasone in treating patients with multiple myeloma that has come back after a period of improvement (relapsed). Teclistamab is a bispecific antibody that can bind to two different antigens at the same time. Teclistamab binds to B-cell maturation antigen (BCMA), a protein found on some B-cells and myeloma cells, and CD3 on T-cells (a type of white blood cell) and may interfere with the ability of cancer cells to grow and spread. Pomalidomide is in a class of medications called immunomodulatory agents. It works by helping the immune system kill cancer cells and by helping the bone marrow to produce normal blood cells. Carfilzomib blocks the action of enzymes called proteasomes, which may help keep cancer cells from growing and may kill them. It is a type of proteasome inhibitor. Dexamethasone is in a class of medications called corticosteroids. It is used to reduce inflammation and lower the body's immune response to help lessen the side effects of chemotherapy drugs. Giving teclistamab and pomalidomide may be safe, tolerable and improve response by lowering myeloma cells to undetectable levels when compared to standard treatment with carfilzomib, pomalidomide and dexamethasone in treating patients with relapsed multiple myeloma.",[219,220],"Recurrent Multiple Myeloma","Refractory Multiple Myeloma","NOT_YET_RECRUITING","2026-06-26",{"date":224,"type":225},"2026-06-29","ACTUAL",{"date":227,"type":212},"2026-07-24",{"date":229,"type":212},"2026-08-31",{"name":5,"class":6}]