Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24', 'removedCountries': ['Russia', 'Ukraine']}, 'conditionBrowseModule': {'meshes': [{'id': 'D008224', 'term': 'Lymphoma, Follicular'}, {'id': 'D008228', 'term': 'Lymphoma, Non-Hodgkin'}, {'id': 'D008223', 'term': 'Lymphoma'}, {'id': 'D009369', 'term': 'Neoplasms'}], 'ancestors': [{'id': 'D009370', 'term': 'Neoplasms by Histologic Type'}, {'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'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D000069283', 'term': 'Rituximab'}, {'id': 'D000077269', 'term': 'Lenalidomide'}], 'ancestors': [{'id': 'D058846', 'term': 'Antibodies, Monoclonal, Murine-Derived'}, {'id': 'D000911', 'term': 'Antibodies, Monoclonal'}, {'id': 'D000906', 'term': 'Antibodies'}, {'id': 'D007136', 'term': 'Immunoglobulins'}, {'id': 'D007162', 'term': 'Immunoproteins'}, {'id': 'D001798', 'term': 'Blood Proteins'}, {'id': 'D011506', 'term': 'Proteins'}, {'id': 'D000602', 'term': 'Amino Acids, Peptides, and Proteins'}, {'id': 'D012712', 'term': 'Serum Globulins'}, {'id': 'D005916', 'term': 'Globulins'}, {'id': 'D010797', 'term': 'Phthalimides'}, {'id': 'D010795', 'term': 'Phthalic Acids'}, {'id': 'D000146', 'term': 'Acids, Carbocyclic'}, {'id': 'D002264', 'term': 'Carboxylic Acids'}, {'id': 'D009930', 'term': 'Organic Chemicals'}, {'id': 'D010881', 'term': 'Piperidones'}, {'id': 'D010880', 'term': 'Piperidines'}, {'id': 'D006573', 'term': 'Heterocyclic Compounds, 1-Ring'}, {'id': 'D006571', 'term': 'Heterocyclic Compounds'}, {'id': 'D054833', 'term': 'Isoindoles'}, {'id': 'D006574', 'term': 'Heterocyclic Compounds, 2-Ring'}, {'id': 'D000072471', 'term': 'Heterocyclic Compounds, Fused-Ring'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 549}}, 'statusModule': {'overallStatus': 'ACTIVE_NOT_RECRUITING', 'startDateStruct': {'date': '2022-09-20', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-07', 'completionDateStruct': {'date': '2029-12', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-07-23', 'studyFirstSubmitDate': '2022-06-03', 'studyFirstSubmitQcDate': '2022-06-03', 'lastUpdatePostDateStruct': {'date': '2025-07-28', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2022-06-08', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2029-12', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Percentage of Participants Achieving Best Overall Response (BOR)', 'timeFrame': 'Up to approximately 5 years', 'description': 'BOR is defined as Complete Response (CR) or Partial Response (PR), determined by Lugano criteria, as assessed by an IRC.'}, {'measure': 'Progression-Free Survival (PFS)', 'timeFrame': 'Up to approximately 5 years', 'description': 'PFS is defined as duration from the date of randomization to the date of disease progression determined by Lugano criteria by independent review committee (IRC) or death (whichever occurs first).'}], 'secondaryOutcomes': [{'measure': 'Percentage of Participants Achieving CR', 'timeFrame': 'Up to approximately 5 years', 'description': 'Percentage of participants who achieve a CR determined per Lugano criteria, as assessed by the IRC prior to the initiation of subsequent anti-lymphoma therapy.'}, {'measure': 'Overall Survival (OS)', 'timeFrame': 'Up to approximately 8 years from randomization', 'description': "Overall survival is defined as the duration from the date of randomization to the date of the participant's death."}, {'measure': 'Percentage of Participants Achieving Minimal Residual Disease (MRD) Negativity', 'timeFrame': 'Up to approximately 5 years', 'description': 'MRD negativity rate is defined as the percentage of participants who achieve MRD negative status prior to the initiation of subsequent anti-lymphoma therapy.'}, {'measure': 'Change in Functional Assessment of Cancer Therapy - Lymphoma (FACT-Lym)', 'timeFrame': 'Up to approximately 8 years', 'description': 'The objective of the FACT-Lym patient-reported outcome (PRO) is to address health-related quality of life issues for adult lymphoma patients. It utilizes a 5-point Like-type scale, with a higher score signifying a higher quality of life.'}, {'measure': 'PFS as Assessed by Investigator', 'timeFrame': 'Up to approximately 5 years', 'description': 'PFS is defined as duration from the date of randomization to the date of disease progression determined by Lugano criteria by investigator or death (whichever occurs first).'}, {'measure': 'Percentage of Participants Achieving BOR as Assessed by Investigator', 'timeFrame': 'Up to approximately 5 years', 'description': 'BOR is defined as CR PR, determined by Lugano criteria, as assessed by an investigator.'}, {'measure': 'Percentage of Participants Achieving CR as Assessed by Investigator', 'timeFrame': 'Up to approximately 5 years', 'description': 'Percentage of participants who achieve a CR determined per Lugano criteria, as assessed by the investigator prior to the initiation of subsequent anti-lymphoma therapy.'}, {'measure': 'Duration of Response (DOR)', 'timeFrame': 'Up to approximately 8 years', 'description': 'DOR is defined as the time from the first occurrence of response (CR or PR) to disease progression or death, whichever occurs first.'}, {'measure': 'Duration of Complete Response (DOCR)', 'timeFrame': 'Up to approximately 8 years', 'description': 'DOR is defined as the time from the first occurrence of CR to disease progression or death, whichever occurs first.'}, {'measure': 'Time to Progression (TTP)', 'timeFrame': 'Up to approximately 8 years', 'description': 'Time to progression is defined as the number of days from the date of study drug start to the date of the first documented disease progression or relapse.'}, {'measure': 'Time to Next Anti-Lymphoma Treatment (TTNLT)', 'timeFrame': 'Up to approximately 8 years', 'description': 'Time to next anti-lymphoma treatment is defined as the number of days from the date of the first documented disease progression or relapse to the date of next anti-lymphoma treatment.'}, {'measure': 'Percentage of Participants Achieving CR at the End of Treatment', 'timeFrame': 'Up to approximately 5 years', 'description': 'Percentage of participants who achieve a CR determined per Lugano criteria, as assessed by the IRC prior to the initiation of subsequent anti-lymphoma therapy.'}, {'measure': 'Time to Response (TTR)', 'timeFrame': 'Up to approximately 8 years', 'description': 'Time to response is defined for participants achieving a CR/PR as the time from starting therapy to first a CR/PR.'}, {'measure': 'Time to Complete Response (TTCR)', 'timeFrame': 'Up to approximately 8 years', 'description': 'Time to complete response is defined for participants achieving a CR/PR as the time from starting therapy to first a CR/PR.'}, {'measure': 'Event-Free Survival (EFS)', 'timeFrame': 'Up to approximately 8 years', 'description': 'EFS is defined as the duration from randomization to disease progression determined by Lugano criteria as assessed by the investigator, initiation of any non-protocol-specified new anti-lymphoma therapy for any reason, or death (whichever occurs first).'}, {'measure': 'Time to next anti-lymphoma treatment (TTNLT)', 'timeFrame': 'Up to approximately 8 years'}, {'measure': "Change in Patient's Global Impression of Severity (PGIS)", 'timeFrame': 'Up to approximately 8 years', 'description': "PGIS is a self-report measure PGIS reflects a participant's belief about their lymphoma symptoms over the past 7 days. The PGIS is a 5-point scale depicting a participant's rating of overall severity. Participants rate their lymphoma symptoms severity as none, mild, moderate, severe, or very severe."}, {'measure': "Change in Patient's Global Impression of Change (PGIC)", 'timeFrame': 'Up to approximately 8 years', 'description': "PGIS is a self-report measure PGIC reflects a participant's belief about the efficacy of treatment. The PGIC is a 7-point scale depicting a participant's rating of overall improvement since start of treatment. Participants rate their change as very much improved, much improved, minimally improved, no change, minimally worse, much worse, or very much worse."}, {'measure': 'Change in EuroQol 5-Dimension Questionnaire, 5-level (EQ-5D-5L)', 'timeFrame': 'Up to approximately 8 years', 'description': 'The EQ-5D-5L descriptive system measures health status and comprises 5 health aspects including mobility, self-care, usual activities, pain/discomfort, and anxiety/depression. Each parameter has 5 response levels: no problems, slight problems, moderate problems, severe problems, unable to/extreme problems. This instrument will not be administered during the Survival Follow-Up.'}]}, 'oversightModule': {'isUsExport': True, 'oversightHasDmc': True, 'isFdaRegulatedDrug': True, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Follicular Lymphoma (FL)', "Non-Hodgkin's lymphoma (NHL)", 'Lymphoma', 'Cancer', 'Epcoritamab', 'Rituximab', 'Lenalidomide', 'EPCORE FL-1', 'EPCORE'], 'conditions': ['Follicular Lymphoma (FL)']}, 'referencesModule': {'references': [{'pmid': '41371238', 'type': 'DERIVED', 'citation': 'Falchi L, Nijland M, Huang H, Linton KM, Seymour JF, Tao R, Kwiatek M, Costa A, Vassilakopoulos TP, Greil R, Jimenez-Ubieto A, Gangatharan SA, Benjamini O, Thieblemont C, Tucci A, Elinder-Camburn A, Illes A, Novak J, Pavlovsky MA, McDonald A, Yoon DH, Maruyama D, Sunkersett G, Mei JP, Mukherjee N, Zhu F, Alshreef A, Favaro E, Morschhauser F; EPCORE FL-1 Investigators. Epcoritamab, lenalidomide, and rituximab versus lenalidomide and rituximab for relapsed or refractory follicular lymphoma (EPCORE FL-1): a global, open-label, randomised, phase 3 trial. Lancet. 2025 Dec 7:S0140-6736(25)02360-8. doi: 10.1016/S0140-6736(25)02360-8. Online ahead of print.'}], 'seeAlsoLinks': [{'url': 'https://www.abbvieclinicaltrials.com/study/?id=M20-638', 'label': 'Related info'}]}, 'descriptionModule': {'briefSummary': 'Follicular Lymphoma (FL) is the second most common B-cell cancer and the most common type of cancer of lymphocytes. Unfortunately, this disease is incurable with conventional treatment and the disease recurs in almost all patients. This study will assess how safe and effective epcoritamab is in combination with lenalidomide and rituximab (R2) in treating adult participants with relapsed or refractory (R/R) FL. Adverse events and change in disease condition will be assessed.\n\nEpcoritamab is an investigational drug being developed for the treatment of FL. Study doctors put the participants in 1 of 3 groups, called treatment arms. Each group receives a different treatment. Enrollment to one of the groups is closed. Around 500 adult participants with R/R FL will be enrolled in approximately 300 sites across the world.\n\nParticipants will receive R2 (375 mg/m\\^2 intravenous infusion of rituximab up to 5 cycles and oral capsules of 20 mg lenalidomide for up to 12 cycles) alone or in combination with subcutaneous injections of epcoritamab for up to 12 cycles (each cycle is 28 days).\n\nThere may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, checking for side effects and completing questionnaires.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Eastern Cooperative Oncology Group (ECOG) performance status score 0 to 2.\n* Participant has:\n\n * Fluorodeoxyglucose-positron emission tomography (FDG-PET) scan demonstrating positive lesion compatible with computed tomography (CT) or magnetic resonance image (MRI)-defined anatomical tumor sites AND\n * \\>= 1 measurable nodal lesion (long axis \\> 1.5 cm) or \\>= 1 measurable extra-nodal lesion (long axis \\> 1.0 cm) on CT scan or MRI.\n* Histologically confirmed classic follicular lymphoma (FL) \\[previously Grade 1 to 3a FL\\] stage II, III, or IV with no evidence of histologic transformation to an aggressive lymphoma and CD20+ disease on most recent representative tumor biopsy based on the pathology report.\n* Relapsed or refractory (R/R) disease to at least one prior systemic regimen that contained an anti-CD20 monoclonal antibody (mAb) in combination with chemotherapy. (Participant who received only prior anti-CD20 mAb monotherapy and/or radiation therapy is not eligible.)\n* Eligible to receive R2 per investigator determination.\n* Estimated Creatinine Clearance (CrCl) \\>= 50 mL/min.\n\nExclusion Criteria:\n\n* Documented refractoriness to lenalidomide.\n* Have lenalidomide exposure within 12 months prior to randomization.'}, 'identificationModule': {'nctId': 'NCT05409066', 'acronym': 'EPCORE FL-1', 'briefTitle': 'Study of Subcutaneous Epcoritamab in Combination With Intravenous Rituximab and Oral Lenalidomide (R2) to Assess Adverse Events and Change in Disease Activity in Adult Participants With Follicular Lymphoma', 'organization': {'class': 'INDUSTRY', 'fullName': 'Genmab'}, 'officialTitle': 'A Phase 3, Open-Label Study to Evaluate Safety and Efficacy of Epcoritamab in Combination With Rituximab and Lenalidomide (R2) Compared to R2 in Subjects With Relapsed or Refractory Follicular Lymphoma (EPCORE FL-1)', 'orgStudyIdInfo': {'id': 'M20-638'}, 'secondaryIdInfos': [{'id': '2023-505628-67', 'type': 'OTHER', 'domain': 'EU CT'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Epcoritamab Dose A in Combination With R2', 'description': 'Participants will receive epcoritamab Dose A in combination with lenalidomide and rituximab (R2) for 12 cycles (each cycle is 28 days).', 'interventionNames': ['Drug: Epcoritamab', 'Drug: Rituximab', 'Drug: Lenalidomide']}, {'type': 'EXPERIMENTAL', 'label': 'Epcoritamab Dose B in Combination With R2', 'description': 'Participants will receive epcoritamab Dose B in combination with lenalidomide and rituximab (R2) for 12 cycles (each cycle is 28 days). Enrollment is closed for this arm.', 'interventionNames': ['Drug: Epcoritamab', 'Drug: Rituximab', 'Drug: Lenalidomide']}, {'type': 'ACTIVE_COMPARATOR', 'label': 'Lenalidomide and Rituximab (R2)', 'description': 'Participants will receive lenalidomide and rituximab (R2) for 12 cycles (each cycle is 28 days).', 'interventionNames': ['Drug: Rituximab', 'Drug: Lenalidomide']}], 'interventions': [{'name': 'Epcoritamab', 'type': 'DRUG', 'description': 'Subcutaneous Injection', 'armGroupLabels': ['Epcoritamab Dose A in Combination With R2', 'Epcoritamab Dose B in Combination With R2']}, {'name': 'Rituximab', 'type': 'DRUG', 'description': 'Intravenous Infusion', 'armGroupLabels': ['Epcoritamab Dose A in Combination With R2', 'Epcoritamab Dose B in Combination With R2', 'Lenalidomide and Rituximab (R2)']}, {'name': 'Lenalidomide', 'type': 'DRUG', 'description': 'Oral Capsules', 'armGroupLabels': ['Epcoritamab Dose A in Combination With R2', 'Epcoritamab Dose B in Combination With R2', 'Lenalidomide and Rituximab (R2)']}]}, 'contactsLocationsModule': {'locations': [{'zip': '85719', 'city': 'Tucson', 'state': 'Arizona', 'country': 'United States', 'facility': 'The University of Arizona Cancer Center - North Campus /ID# 228862', 'geoPoint': {'lat': 32.22174, 'lon': -110.92648}}, {'zip': '72205', 'city': 'Little Rock', 'state': 'Arkansas', 'country': 'United States', 'facility': 'University of Arkansas for Medical Sciences /ID# 227198', 'geoPoint': {'lat': 34.74648, 'lon': -92.28959}}, {'zip': '94705', 'city': 'Berkeley', 'state': 'California', 'country': 'United States', 'facility': 'Alta Bates Summit Medical Center for Research /ID# 229428', 'geoPoint': {'lat': 37.87159, 'lon': -122.27275}}, {'zip': '90211', 'city': 'Beverly Hills', 'state': 'California', 'country': 'United States', 'facility': 'Beverly Hills Cancer Center /ID# 231535', 'geoPoint': {'lat': 34.07362, 'lon': -118.40036}}, {'zip': '90806-1701', 'city': 'Long Beach', 'state': 'California', 'country': 'United States', 'facility': 'Long Beach Memorial Medical Ct /ID# 228997', 'geoPoint': {'lat': 33.76696, 'lon': -118.18923}}, {'zip': '90033', 'city': 'Los Angeles', 'state': 'California', 'country': 'United States', 'facility': 'University of Southern California /ID# 227195', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '90067', 'city': 'Los Angeles', 'state': 'California', 'country': 'United States', 'facility': 'Valkyrie Clinical Trials /ID# 268502', 'geoPoint': {'lat': 34.05223, 'lon': -118.24368}}, {'zip': '30322-1013', 'city': 'Atlanta', 'state': 'Georgia', 'country': 'United States', 'facility': 'Duplicate_Emory University /ID# 227299', 'geoPoint': {'lat': 33.749, 'lon': -84.38798}}, {'zip': '96813-4920', 'city': 'Honolulu', 'state': 'Hawaii', 'country': 'United States', 'facility': 'Hawaii Cancer Care - Waterfront Plaza /ID# 262448', 'geoPoint': {'lat': 21.30694, 'lon': -157.85833}}, {'zip': '60611-2927', 'city': 'Chicago', 'state': 'Illinois', 'country': 'United States', 'facility': 'Northwestern University Feinberg School of Medicine /ID# 227248', 'geoPoint': {'lat': 41.85003, 'lon': -87.65005}}, {'zip': '46526', 'city': 'Goshen', 'state': 'Indiana', 'country': 'United States', 'facility': 'Goshen Center for Cancer Care /ID# 227189', 'geoPoint': {'lat': 41.58227, 'lon': -85.83444}}, {'zip': '46250-2042', 'city': 'Indianapolis', 'state': 'Indiana', 'country': 'United States', 'facility': 'Community Health Network, Inc. /ID# 259756', 'geoPoint': {'lat': 39.76838, 'lon': -86.15804}}, {'zip': '70808', 'city': 'Baton Rouge', 'state': 'Louisiana', 'country': 'United States', 'facility': 'Our Lady Of The Lake Regional Medical Center /ID# 251393', 'geoPoint': {'lat': 30.44332, 'lon': -91.18747}}, {'zip': '21201', 'city': 'Baltimore', 'state': 'Maryland', 'country': 'United States', 'facility': 'University of Maryland, Baltimore /ID# 227191', 'geoPoint': {'lat': 39.29038, 'lon': -76.61219}}, {'zip': '02114', 'city': 'Boston', 'state': 'Massachusetts', 'country': 'United States', 'facility': 'Massachusetts General Hospital /ID# 245233', 'geoPoint': {'lat': 42.35843, 'lon': -71.05977}}, {'zip': '01605', 'city': 'Worcester', 'state': 'Massachusetts', 'country': 'United States', 'facility': 'UMass Memorial Medical Center /ID# 227323', 'geoPoint': {'lat': 42.26259, 'lon': -71.80229}}, {'zip': '48202', 'city': 'Detroit', 'state': 'Michigan', 'country': 'United States', 'facility': 'Henry Ford Hospital /ID# 227250', 'geoPoint': {'lat': 42.33143, 'lon': -83.04575}}, {'zip': '63017', 'city': 'Chesterfield', 'state': 'Missouri', 'country': 'United States', 'facility': "St. Luke's Hospital - Chesterfield /ID# 247817", 'geoPoint': {'lat': 38.66311, 'lon': -90.57707}}, {'zip': '59102', 'city': 'Billings', 'state': 'Montana', 'country': 'United States', 'facility': 'Intermountain Health St. Vincent Regional Hospital - Cancer Centers of Montana /ID# 251220', 'geoPoint': {'lat': 45.78329, 'lon': -108.50069}}, {'zip': '07960-6136', 'city': 'Morristown', 'state': 'New Jersey', 'country': 'United States', 'facility': 'Morristown Medical Center /ID# 231427', 'geoPoint': {'lat': 40.79677, 'lon': -74.48154}}, {'zip': '14263', 'city': 'Buffalo', 'state': 'New York', 'country': 'United States', 'facility': 'Roswell Park Cancer Institute /ID# 239128', 'geoPoint': {'lat': 42.88645, 'lon': -78.87837}}, {'zip': '11501', 'city': 'Mineola', 'state': 'New York', 'country': 'United States', 'facility': 'NYU Langone Hospital - Long Island /ID# 253343', 'geoPoint': {'lat': 40.74927, 'lon': -73.64068}}, {'zip': '10016', 'city': 'New York', 'state': 'New York', 'country': 'United States', 'facility': 'NYU Laura and Isaac Perlmutter Cancer Center /ID# 227322', 'geoPoint': {'lat': 40.71427, 'lon': -74.00597}}, {'zip': '10029', 'city': 'New York', 'state': 'New York', 'country': 'United States', 'facility': 'Icahn School of Medicine at Mount Sinai /ID# 227181', 'geoPoint': {'lat': 40.71427, 'lon': -74.00597}}, {'zip': '10065-6007', 'city': 'New York', 'state': 'New York', 'country': 'United States', 'facility': 'Memorial Sloan Kettering Cancer Center-Koch Center /ID# 227193', 'geoPoint': {'lat': 40.71427, 'lon': -74.00597}}, {'zip': '27834', 'city': 'Greenville', 'state': 'North Carolina', 'country': 'United States', 'facility': 'East Carolina University - Brody School of Medicine /ID# 227192', 'geoPoint': {'lat': 35.61266, 'lon': -77.36635}}, {'zip': '73104-5418', 'city': 'Oklahoma City', 'state': 'Oklahoma', 'country': 'United States', 'facility': 'University of Oklahoma, Stephenson Cancer Center /ID# 227325', 'geoPoint': {'lat': 35.46756, 'lon': -97.51643}}, {'zip': '75246', 'city': 'Dallas', 'state': 'Texas', 'country': 'United States', 'facility': 'Baylor Sammons Cancer Center /ID# 261584', 'geoPoint': {'lat': 32.78306, 'lon': -96.80667}}, {'zip': '75702', 'city': 'Tyler', 'state': 'Texas', 'country': 'United States', 'facility': 'Texas Oncology - Northeast Texas /ID# 265890', 'geoPoint': {'lat': 32.35126, 'lon': -95.30106}}, {'zip': '84143', 'city': 'Salt Lake City', 'state': 'Utah', 'country': 'United States', 'facility': 'Intermountain Healthcare LDS Hospital /ID# 259948', 'geoPoint': {'lat': 40.76078, 'lon': -111.89105}}, {'zip': '23219', 'city': 'Richmond', 'state': 'Virginia', 'country': 'United States', 'facility': 'Virginia Commonwealth University Medical Center Main Hospital /ID# 227211', 'geoPoint': {'lat': 37.55376, 'lon': -77.46026}}, {'zip': '1114', 'city': 'Ciudad Autonoma de Buenos Aire', 'state': 'Buenos Aires F.D.', 'country': 'Argentina', 'facility': 'Fundaleu /Id# 229700'}, {'zip': '1431', 'city': 'Ciudad Autonoma de Buenos Aire', 'state': 'Buenos Aires F.D.', 'country': 'Argentina', 'facility': 'Duplicate_CEMIC /ID# 229697'}, {'zip': '5016', 'city': 'Córdoba', 'state': 'Córdoba Province', 'country': 'Argentina', 'facility': 'Hospital Privado Universitario - Hospital Privado Centro Medico de Cordoba S.A. /ID# 229701', 'geoPoint': {'lat': -31.40648, 'lon': -64.18853}}, {'zip': '3000', 'city': 'Santa Fe', 'state': 'Santa Fe Province', 'country': 'Argentina', 'facility': 'Clinica de Nefrologia, Urologia y Enfermedades Cardiovasculares /ID# 232124', 'geoPoint': {'lat': -31.64881, 'lon': -60.70868}}, {'zip': '2050', 'city': 'Camperdown', 'state': 'New South Wales', 'country': 'Australia', 'facility': 'Royal Prince Alfred Hospital /ID# 239272', 'geoPoint': {'lat': -33.88965, 'lon': 151.17642}}, {'zip': '2747', 'city': 'Kingswood', 'state': 'New South Wales', 'country': 'Australia', 'facility': 'Nepean Hospital /ID# 239093', 'geoPoint': {'lat': -33.75614, 'lon': 150.72346}}, {'zip': '4814', 'city': 'Douglas', 'state': 'Queensland', 'country': 'Australia', 'facility': 'Townsville University Hospital /ID# 231124', 'geoPoint': {'lat': -19.32394, 'lon': 146.75234}}, {'zip': '3199', 'city': 'Frankston', 'state': 'Victoria', 'country': 'Australia', 'facility': 'Peninsula Private Hospital /ID# 238796', 'geoPoint': {'lat': -38.14458, 'lon': 145.12291}}, {'zip': '6150', 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