Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24', 'removedCountries': ['China']}, 'conditionBrowseModule': {'meshes': [{'id': 'D016403', 'term': 'Lymphoma, Large B-Cell, Diffuse'}], 'ancestors': [{'id': 'D016393', 'term': 'Lymphoma, B-Cell'}, {'id': 'D008228', 'term': 'Lymphoma, Non-Hodgkin'}, {'id': 'D008223', 'term': 'Lymphoma'}, {'id': 'D009370', 'term': 'Neoplasms by Histologic Type'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D008232', 'term': 'Lymphoproliferative Disorders'}, {'id': 'D008206', 'term': 'Lymphatic Diseases'}, {'id': 'D006425', 'term': 'Hemic and Lymphatic Diseases'}, {'id': 'D007160', 'term': 'Immunoproliferative Disorders'}, {'id': 'D007154', 'term': 'Immune System Diseases'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 484}}, 'statusModule': {'overallStatus': 'ACTIVE_NOT_RECRUITING', 'startDateStruct': {'date': '2021-01-13', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'nctId': 'NCT05733650', 'statusForNctId': 'APPROVED_FOR_MARKETING', 'hasExpandedAccess': True}, 'statusVerifiedDate': '2025-12', 'completionDateStruct': {'date': '2028-04', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-12-01', 'studyFirstSubmitDate': '2020-11-09', 'studyFirstSubmitQcDate': '2020-11-09', 'lastUpdatePostDateStruct': {'date': '2025-12-02', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2020-11-13', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2025-10-13', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Overall Survival (OS)', 'timeFrame': 'Up to approximately 5 years'}], 'secondaryOutcomes': [{'measure': 'Progression Free Survival (PFS)', 'timeFrame': 'Up to approximately 5 years'}, {'measure': 'Overall Response Rate (ORR)', 'timeFrame': 'Up to approximately 5 years'}, {'measure': 'Complete Response (CR) Rate', 'timeFrame': 'Up to approximately 5 years'}, {'measure': 'Duration of Response (DOR)', 'timeFrame': 'Up to approximately 5 years'}, {'measure': 'Time to Response (TTR)', 'timeFrame': 'Up to approximately 5 years'}, {'measure': 'Duration of Minimal Residual Disease (MRD) Negative Status', 'timeFrame': 'Up to approximately 5 years'}, {'measure': 'Rate of MRD Negative Status', 'timeFrame': 'Up to approximately 5 years'}, {'measure': 'Time to Next Anti-lymphoma Therapy (TTNT)', 'timeFrame': 'Up to approximately 5 years'}, {'measure': 'Number of Participants with Adverse Events (AEs)', 'timeFrame': 'Up to approximately 5 years'}, {'measure': 'Number of Participants with Dose Interruptions and Delays', 'timeFrame': 'Up to approximately 5 years'}, {'measure': 'Number of Participants with an Anti-epcoritamab Antibody Response', 'timeFrame': 'Up to approximately 5 years'}, {'measure': 'Changes from Baseline in Lymphoma Symptoms as Measured by the Functional Assessment of Cancer Therapy - Lymphoma (FACT-Lym)', 'timeFrame': 'Baseline up to approximately 5 years'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': True, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['double-hit DLBCL', 'triple-hit DLBCL', 'follicular grade 3B', 'transformed DLBCL', 'T-cell histiocytes-rich large B cell lymphoma'], 'conditions': ['Diffuse Large B-cell Lymphoma']}, 'descriptionModule': {'briefSummary': "The purpose of this trial is to find out if epcoritamab, also known as EPKINLY™ and GEN3013, is safe and works well as treatment for participants with DLBCL that are not responding to treatment, have grown in size, or have come back following treatment with at least 1 prior systemic cancer therapy. All participants in this trial will be randomly assigned to receive either epcoritamab or a pre-specified investigator's choice (standard of care) chemotherapy (either rituximab + gemcitabine + oxaliplatin \\[R-GemOx\\], or bendamustine + rituximab \\[BR\\]). Participants must have failed or be ineligible to receive an autologous stem cell transplant (ASCT).\n\nEpcoritamab will be injected under the skin. Investigator's choice chemotherapy will be given intravenously.\n\nTrial details include:\n\n* The trial duration will be up to 5 years after last participant is randomized.\n* All trial participants have a 21-day screening period, a treatment period, and a follow-up period that continues until death.\n* The estimated trial duration for an individual participant depends upon the treatment arm assigned:\n\n * Participants who receive epcoritamab will have 28-day treatment cycles. Epcoritamab will be given once weekly for the first 3 months, then every other week for 6 months, then every 28 days until lymphoma progression or unacceptable adverse events.\n * Participants who receive investigator's choice (standard of care) chemotherapy will receive treatments either:\n\n * R-GemOx: On Day 1 (or Day 1 \\& Day 2), and Day 15 (or Day 15 \\& Day 16) every 28 days, for up to 4 months; or\n * BR: On Day 1 and Day 2 every 3 weeks for up to 4.5 months.", 'detailedDescription': "The trial is an open label, multi-center, global phase-3 randomized trial of epcoritamab. The goal of this randomized trial is to evaluate the efficacy of epcoritamab (GEN3013, DuoBody®-CD3xCD20) compared to investigator's choice of chemotherapy, in participants with relapsed, refractory DLBCL who have failed or are ineligible for high-dose chemotherapy and autologous stem cell transplant (HDT-ASCT). No change in chemotherapy is permitted for participants during the treatment phase of the trial.\n\nOverall Survival (OS) is the primary endpoint in USA and in China, with the analysis population including all randomized participants. OS/Progression Free Survival (PFS) are dual-primary endpoints for rest of the world (outside US and China), with the analysis population also including all participants randomized.\n\nThe China sub-study of GCT3013-05 is registered under NCT07226752."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Main Inclusion Criteria:\n\n1. Relapsed or refractory disease and previously treated with at least 1 line of systemic antineoplastic therapy including anti-CD20 monoclonal antibody (mAb)-containing combination chemotherapy since lymphoma diagnosis\n2. One of the confirmed histologies below with CD20-positivity:\n\n 1. DLBCL, not otherwise specified (NOS), including de novo or histologically transformed from follicular lymphoma (FL)\n 2. "Double-hit" or "triple-hit" DLBCL (technically classified in World Health Organization (WHO) 2016 as high-grade B-cell lymphoma (HGBCL), with MYC and BCL2 and/or BCL6 translocations), including de novo or histologically transformed from FL\n 3. FL Grade 3B\n 4. T-cell/histiocyte-rich large B-cell lymphoma\n3. Eastern Cooperative Oncology Group Performance Status (ECOG PS) score of 0-2\n4. Failed previous HDT-ASCT or not eligible for high-dose therapy autologous stem cell transplant (HDT-ASCT) at screening\n5. Participants must have detectable disease by positron emission tomography (PET) scan and measurable by computed tomography (CT) scan or magnetic resonance imaging (MRI)\n6. Acceptable renal and liver function\n7. Life expectancy \\>2 months on standard of care treatment\n\nMain Exclusion Criteria:\n\n1. Primary Central Nervous System (CNS) tumor or known CNS involvement\n2. Any prior therapy with a bispecific antibody targeting CD3 and CD20\n3. Major surgery within 4 weeks prior to randomization\n4. Chemotherapy and other non-investigational antineoplastic agents (except CD20 mAbs) within 4 weeks or 5 half-lives (whichever is shorter) prior to randomization\n5. Any investigational drug within 4 weeks or 5 half-lives, whichever is longer, prior to randomization\n6. Autologous stem cell transplant (ASCT) within 100 days of randomization\n7. Treatment with chimeric antigen receptor T-cell (CAR-T) therapy within 100 days prior to randomization\n8. Seizure disorder requiring anti-epileptic therapy\n9. Clinically significant cardiac disease'}, 'identificationModule': {'nctId': 'NCT04628494', 'acronym': 'EPCORE DLBCL-1', 'briefTitle': "A Phase 3 Trial of Epcoritamab vs Investigator's Choice Chemotherapy in Relapsed/Refractory (R/R) Diffuse Large B-cell Lymphoma (DLBCL)", 'organization': {'class': 'INDUSTRY', 'fullName': 'Genmab'}, 'officialTitle': "A Randomized, Open-Label, Phase 3 Trial of Epcoritamab vs Investigator's Choice Chemotherapy in Relapsed/Refractory Diffuse Large B-cell Lymphoma (R/R DLBCL)", 'orgStudyIdInfo': {'id': 'GCT3013-05'}, 'secondaryIdInfos': [{'id': '2023-504830-23-00', 'type': 'CTIS'}, {'id': '2020-003016-27', 'type': 'EUDRACT_NUMBER'}, {'id': 'jRCT2021220017', 'type': 'REGISTRY', 'domain': 'Japan Registry for Clinical Trials (jRCT)'}, {'id': 'CTR20221558', 'type': 'REGISTRY', 'domain': 'ChinaDrugTrials.org.cn'}, {'id': 'MOH_2021-01-18_009672', 'type': 'REGISTRY', 'domain': 'Clinical Research Site - mytrial'}, {'id': 'NL75079.056.20', 'type': 'REGISTRY', 'domain': 'CCMO (the Netherlands)'}, {'id': '286972', 'type': 'OTHER', 'domain': 'IRAS ID; UK Research Summaries Database'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Epcoritamab (GEN3013; DuoBody®CD3xCD20)', 'description': 'Epcoritamab will be administered in Cycles of 28 days until any of the discontinuation criteria is met', 'interventionNames': ['Biological: Epcoritamab']}, {'type': 'ACTIVE_COMPARATOR', 'label': "Investigator's choice of chemotherapy", 'description': 'R-GemOx will be administrated in Cycles of 28 days until maximum cycles completion or any of the discontinuation criteria is met\n\nBR will be administrated in Cycles of 21 days until maximum cycles completion or any of the discontinuation criteria is met', 'interventionNames': ["Drug: Investigator's Choice Chemotherapy"]}], 'interventions': [{'name': 'Epcoritamab', 'type': 'BIOLOGICAL', 'otherNames': ['GEN3013', 'DuoBody®-CD3xCD20', 'EPKINLY™'], 'description': 'Following mandatory pre-medication, participants will be administered epcoritamab as a subcutaneous injection.', 'armGroupLabels': ['Epcoritamab (GEN3013; DuoBody®CD3xCD20)']}, {'name': "Investigator's Choice Chemotherapy", 'type': 'DRUG', 'otherNames': ['BR or R-GemOx'], 'description': 'Following mandatory pre-medication, participants will be administered intravenously either BR or R-GemOx.', 'armGroupLabels': ["Investigator's choice of chemotherapy"]}]}, 'contactsLocationsModule': {'locations': [{'zip': '46237', 'city': 'Indianapolis', 'state': 'Indiana', 'country': 'United States', 'facility': 'Indiana Blood and Marrow Transplantation', 'geoPoint': {'lat': 39.76838, 'lon': -86.15804}}, {'zip': '46250', 'city': 'Indianapolis', 'state': 'Indiana', 'country': 'United States', 'facility': 'Community Health Network Cancer Center North', 'geoPoint': {'lat': 39.76838, 'lon': -86.15804}}, {'zip': '40536', 'city': 'Lexington', 'state': 'Kentucky', 'country': 'United States', 'facility': 'University of Kentucky Markey Cancer Center', 'geoPoint': {'lat': 37.98869, 'lon': -84.47772}}, {'zip': '49201', 'city': 'Jackson', 'state': 'Michigan', 'country': 'United States', 'facility': 'Henry Ford Health System', 'geoPoint': {'lat': 42.24587, 'lon': -84.40135}}, {'zip': '55416', 'city': 'Saint Louis Park', 'state': 'Minnesota', 'country': 'United States', 'facility': 'MMCORC Attn Delaney Anderson', 'geoPoint': {'lat': 44.9483, 'lon': -93.34801}}, {'zip': '08103', 'city': 'Camden', 'state': 'New Jersey', 'country': 'United States', 'facility': 'MD Anderson Cancer Center at Cooper', 'geoPoint': {'lat': 39.92595, 'lon': -75.11962}}, {'zip': '27157', 'city': 'Winston-Salem', 'state': 'North Carolina', 'country': 'United States', 'facility': 'Wake Forest Baptist Health', 'geoPoint': {'lat': 36.09986, 'lon': -80.24422}}, {'zip': '45229', 'city': 'Cincinnati', 'state': 'Ohio', 'country': 'United States', 'facility': 'The Christ Hospital Cancer Center', 'geoPoint': {'lat': 39.12711, 'lon': -84.51439}}, {'zip': '45247', 'city': 'Cincinnati', 'state': 'Ohio', 'country': 'United States', 'facility': 'TriHealth Cancer Institute- Good Samaritan Hospital', 'geoPoint': {'lat': 39.12711, 'lon': -84.51439}}, {'zip': '78234', 'city': 'Fort Sam Houston', 'state': 'Texas', 'country': 'United States', 'facility': 'Brooke Army Medical Center', 'geoPoint': {'lat': 29.45303, 'lon': -98.4417}}, {'zip': '84405', 'city': 'Ogden', 'state': 'Utah', 'country': 'United States', 'facility': 'Community Cancer Trials of Utah', 'geoPoint': {'lat': 41.223, 'lon': -111.97383}}, {'zip': '84143', 'city': 'Salt Lake City', 'state': 'Utah', 'country': 'United States', 'facility': 'LDS Hospital', 'geoPoint': {'lat': 40.76078, 'lon': -111.89105}}, {'zip': '23298', 'city': 'Richmond', 'state': 'Virginia', 'country': 'United States', 'facility': 'Virginia Commonwealth University (VCU) Massey Cancer Center', 'geoPoint': {'lat': 37.55376, 'lon': -77.46026}}, {'zip': '98902', 'city': 'Yakima', 'state': 'Washington', 'country': 'United States', 'facility': 'North Star Lodge Cancer Center', 'geoPoint': {'lat': 46.60207, 'lon': -120.5059}}, {'zip': '53188', 'city': 'Waukesha', 'state': 'Wisconsin', 'country': 'United States', 'facility': 'Waukesha Memorial Hospital', 'geoPoint': {'lat': 43.01168, 'lon': -88.23148}}, {'city': 'Bedford Park', 'country': 'Australia', 'facility': 'Flinders Medical Centre', 'geoPoint': {'lat': -35.02204, 'lon': 138.56815}}, {'city': 'Concord', 'country': 'Australia', 'facility': 'Concord Repatriation General Hospital', 'geoPoint': {'lat': -33.84722, 'lon': 151.10381}}, {'city': 'Frankston', 'country': 'Australia', 'facility': 'Peninsula Private Hospital Clinical Trials Unit', 'geoPoint': {'lat': -38.14458, 'lon': 145.12291}}, {'city': 'South Brisbane', 'country': 'Australia', 'facility': 'Icon Cancer Centre Corporate Office', 'geoPoint': {'lat': -27.48034, 'lon': 153.02049}}, {'city': 'Waratah', 'country': 'Australia', 'facility': 'Calvary Mater Newcastle', 'geoPoint': 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{'city': 'Ghent', 'country': 'Belgium', 'facility': 'Universitair Ziekenhuis Gent', 'geoPoint': {'lat': 51.05, 'lon': 3.71667}}, {'city': 'Jette', 'country': 'Belgium', 'facility': 'UZ Brussel', 'geoPoint': {'lat': 50.87309, 'lon': 4.33419}}, {'city': 'La Louvière', 'country': 'Belgium', 'facility': 'Hôpital de Jolimont', 'geoPoint': {'lat': 50.48657, 'lon': 4.18785}}, {'city': 'Leuven', 'country': 'Belgium', 'facility': 'Universitair Ziekenhuis gasthuisberg Leuven', 'geoPoint': {'lat': 50.87959, 'lon': 4.70093}}, {'city': 'Sint-Niklaas', 'country': 'Belgium', 'facility': 'AZ Nikolaas- Verenigde Ziekenhuizen van Waas en Durme', 'geoPoint': {'lat': 51.16509, 'lon': 4.1437}}, {'city': 'Turnhout', 'country': 'Belgium', 'facility': 'AZ Turnhout, Campus Sint-Elisabeth', 'geoPoint': {'lat': 51.32254, 'lon': 4.94471}}, {'city': 'Québec', 'country': 'Canada', 'facility': 'CHU de Quebec-Universite Laval', 'geoPoint': {'lat': 46.81228, 'lon': -71.21454}}, {'city': 'Aalborg', 'country': 'Denmark', 'facility': 'Aalborg Universitetshospital', 'geoPoint': {'lat': 57.048, 'lon': 9.9187}}, {'city': 'Aarhus', 'country': 'Denmark', 'facility': 'Aarhus University Hospital, Department of Hematology, Clinical Research Unit C116', 'geoPoint': {'lat': 56.15674, 'lon': 10.21076}}, {'city': 'Roskilde', 'country': 'Denmark', 'facility': 'Clinical Research Unit, Roskilde Sygehus', 'geoPoint': {'lat': 55.64152, 'lon': 12.08035}}, {'city': 'Vejle', 'country': 'Denmark', 'facility': 'Vejle Hospital', 'geoPoint': {'lat': 55.70927, 'lon': 9.5357}}, {'city': 'Helsinki', 'country': 'Finland', 'facility': 'HUS Cancer Center/ Clinical Trial Unit', 'geoPoint': {'lat': 60.16952, 'lon': 24.93545}}, {'city': 'Oulu', 'country': 'Finland', 'facility': 'Oulu university hospital, Department of hematology', 'geoPoint': {'lat': 65.01236, 'lon': 25.46816}}, {'city': 'Amiens', 'country': 'France', 'facility': 'Audrey ALEME', 'geoPoint': {'lat': 49.9, 'lon': 2.3}}, {'city': 'Bayonne', 'country': 'France', 'facility': 'Centre Hospitalier de la Côte Basque', 'geoPoint': {'lat': 43.49316, 'lon': -1.473}}, {'city': 'Brest', 'country': 'France', 'facility': 'CHRU de Brest - Hospital Morvan', 'geoPoint': {'lat': 48.39029, 'lon': -4.48628}}, {'city': 'Caen', 'country': 'France', 'facility': 'CHU Caen - IHBN', 'geoPoint': {'lat': 49.18585, 'lon': -0.35912}}, {'city': 'La Rochelle', 'country': 'France', 'facility': 'Groupe Hospitalier de La Rochelle', 'geoPoint': {'lat': 46.16308, 'lon': -1.15222}}, {'city': 'Limoges', 'country': 'France', 'facility': 'CHU de LIMOGES', 'geoPoint': {'lat': 45.83362, 'lon': 1.24759}}, {'city': 'Lyon', 'country': 'France', 'facility': 'Centre Léon Bérard', 'geoPoint': {'lat': 45.74906, 'lon': 4.84789}}, {'city': 'Marseille', 'country': 'France', 'facility': 'Hopital de la Conception APHM', 'geoPoint': {'lat': 43.29695, 'lon': 5.38107}}, {'city': 'Nantes', 'country': 'France', 'facility': 'CHU de Nantes - Hôtel Dieu', 'geoPoint': {'lat': 47.21725, 'lon': -1.55336}}, {'city': 'Nice', 'country': 'France', 'facility': 'Centre Antoine Lacassagne', 'geoPoint': {'lat': 43.70313, 'lon': 7.26608}}, {'city': 'Paris', 'country': 'France', 'facility': 'Clinique Victor Hugo', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'city': 'Paris', 'country': 'France', 'facility': 'Hôpital Saint-Louis', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'city': 'Pessac', 'country': 'France', 'facility': 'CHU de Bordeaux Hôpital Haut-Lévêque', 'geoPoint': {'lat': 44.80565, 'lon': -0.6324}}, {'city': 'Pierre-Bénite', 'country': 'France', 'facility': 'Centre Hospitalier Lyon Sud', 'geoPoint': {'lat': 45.70359, 'lon': 4.82424}}, {'city': 'Poitiers', 'country': 'France', 'facility': 'CHU de Poitiers - Hôpital la Milétrie', 'geoPoint': {'lat': 46.58261, 'lon': 0.34348}}, {'city': 'Pontoise', 'country': 'France', 'facility': 'Centre Hospitalier Rene Dubos', 'geoPoint': {'lat': 49.05, 'lon': 2.1}}, {'city': 'Quimper', 'country': 'France', 'facility': 'Ch Cornouaille', 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Institute of Oncology', 'geoPoint': {'lat': 47.49835, 'lon': 19.04045}}, {'city': 'Budapest', 'country': 'Hungary', 'facility': 'Semmelweis Egyetem Belgyógyászati és Onkológiai Klinika', 'geoPoint': {'lat': 47.49835, 'lon': 19.04045}}, {'city': 'Debrecen', 'country': 'Hungary', 'facility': 'Debreceni Egyetem Klinikai Kozpont, Belgyogyaszati Klinika, Hematologia', 'geoPoint': {'lat': 47.53167, 'lon': 21.62444}}, {'city': 'Eger', 'country': 'Hungary', 'facility': 'Belgyógyászati osztály Markhot Ferenc Kórház', 'geoPoint': {'lat': 47.90265, 'lon': 20.37329}}, {'city': 'Győr', 'country': 'Hungary', 'facility': 'Petz Aladar Egyetemi Oktato Korhaz', 'geoPoint': {'lat': 47.68333, 'lon': 17.63512}}, {'city': 'Nyíregyháza', 'country': 'Hungary', 'facility': 'Josa Andras Teaching Hospital, Hematology Dept', 'geoPoint': {'lat': 47.95539, 'lon': 21.71671}}, {'city': 'Pécs', 'country': 'Hungary', 'facility': 'University of Pecs 1st. 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