Viewing Study NCT04389632


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Study NCT ID: NCT04389632
Status: RECRUITING
Last Update Posted: 2025-12-09
First Post: 2020-05-12
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: A Study of Sigvotatug Vedotin in Advanced Solid Tumors
Sponsor:
Organization:

Raw JSON

{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D002289', 'term': 'Carcinoma, Non-Small-Cell Lung'}, {'id': 'D000077195', 'term': 'Squamous Cell Carcinoma of Head and Neck'}, {'id': 'D000077277', 'term': 'Esophageal Squamous Cell Carcinoma'}, {'id': 'C562730', 'term': 'Adenocarcinoma Of Esophagus'}, {'id': 'D010051', 'term': 'Ovarian Neoplasms'}, {'id': 'D001749', 'term': 'Urinary Bladder Neoplasms'}, {'id': 'D002583', 'term': 'Uterine Cervical Neoplasms'}, {'id': 'D013274', 'term': 'Stomach Neoplasms'}, {'id': 'D004938', 'term': 'Esophageal Neoplasms'}], 'ancestors': [{'id': 'D002283', 'term': 'Carcinoma, Bronchogenic'}, {'id': 'D001984', 'term': 'Bronchial Neoplasms'}, {'id': 'D008175', 'term': 'Lung Neoplasms'}, {'id': 'D012142', 'term': 'Respiratory Tract Neoplasms'}, {'id': 'D013899', 'term': 'Thoracic Neoplasms'}, {'id': 'D009371', 'term': 'Neoplasms by Site'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D008171', 'term': 'Lung Diseases'}, {'id': 'D012140', 'term': 'Respiratory Tract Diseases'}, {'id': 'D002294', 'term': 'Carcinoma, Squamous Cell'}, {'id': 'D002277', 'term': 'Carcinoma'}, {'id': 'D009375', 'term': 'Neoplasms, Glandular and Epithelial'}, {'id': 'D009370', 'term': 'Neoplasms by Histologic Type'}, {'id': 'D006258', 'term': 'Head and Neck Neoplasms'}, {'id': 'D018307', 'term': 'Neoplasms, Squamous Cell'}, {'id': 'D005770', 'term': 'Gastrointestinal Neoplasms'}, {'id': 'D004067', 'term': 'Digestive System Neoplasms'}, {'id': 'D004066', 'term': 'Digestive System Diseases'}, {'id': 'D004935', 'term': 'Esophageal Diseases'}, {'id': 'D005767', 'term': 'Gastrointestinal Diseases'}, {'id': 'D004701', 'term': 'Endocrine Gland Neoplasms'}, {'id': 'D010049', 'term': 'Ovarian Diseases'}, {'id': 'D000291', 'term': 'Adnexal Diseases'}, {'id': 'D005831', 'term': 'Genital Diseases, Female'}, {'id': 'D052776', 'term': 'Female Urogenital Diseases'}, {'id': 'D005261', 'term': 'Female Urogenital Diseases and Pregnancy Complications'}, {'id': 'D000091642', 'term': 'Urogenital Diseases'}, {'id': 'D005833', 'term': 'Genital Neoplasms, Female'}, {'id': 'D014565', 'term': 'Urogenital Neoplasms'}, {'id': 'D000091662', 'term': 'Genital Diseases'}, {'id': 'D004700', 'term': 'Endocrine System Diseases'}, {'id': 'D006058', 'term': 'Gonadal Disorders'}, {'id': 'D014571', 'term': 'Urologic Neoplasms'}, {'id': 'D001745', 'term': 'Urinary Bladder Diseases'}, {'id': 'D014570', 'term': 'Urologic Diseases'}, {'id': 'D052801', 'term': 'Male Urogenital Diseases'}, {'id': 'D014594', 'term': 'Uterine Neoplasms'}, {'id': 'D002577', 'term': 'Uterine Cervical Diseases'}, {'id': 'D014591', 'term': 'Uterine Diseases'}, {'id': 'D013272', 'term': 'Stomach Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C582435', 'term': 'pembrolizumab'}, {'id': 'D002945', 'term': 'Cisplatin'}, {'id': 'D016190', 'term': 'Carboplatin'}], 'ancestors': [{'id': 'D017606', 'term': 'Chlorine Compounds'}, {'id': 'D007287', 'term': 'Inorganic Chemicals'}, {'id': 'D017672', 'term': 'Nitrogen Compounds'}, {'id': 'D017671', 'term': 'Platinum Compounds'}, {'id': 'D056831', 'term': 'Coordination Complexes'}, {'id': 'D009930', 'term': 'Organic Chemicals'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SEQUENTIAL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 1006}}, 'statusModule': {'overallStatus': 'RECRUITING', 'startDateStruct': {'date': '2020-06-08', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-12', 'completionDateStruct': {'date': '2029-03-22', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-12-08', 'studyFirstSubmitDate': '2020-05-12', 'studyFirstSubmitQcDate': '2020-05-12', 'lastUpdatePostDateStruct': {'date': '2025-12-09', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2020-05-15', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2027-06-16', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Number of participants with adverse events (AEs)', 'timeFrame': 'Through 30-37 days following last dose of sigvotatug vedotin. For participants receiving pembrolizumab up to 90 days after last dose of pembrolizumab; up to 3 years', 'description': 'Any untoward medical occurrence in a clinical investigational participant administered a medicinal product and which does not necessarily have a causal relationship with this treatment.'}, {'measure': 'Number of patients with laboratory abnormalities', 'timeFrame': 'Through 30-37 days following last dose of sigvotatug vedotin; up to 3 years'}, {'measure': 'Number of participants with dose-limiting toxicities (DLTs)', 'timeFrame': 'Through 30-37 days following last dose of sigvotatug vedotin; up to 3 years'}], 'secondaryOutcomes': [{'measure': 'Confirmed objective response rate (ORR) per Response Evaluation Criteria in Solid Tumors (RECIST) v1.1 by investigator assessment', 'timeFrame': 'Up to approximately 3 years', 'description': 'The proportion of participants with complete response (CR) or partial response (PR) which is subsequently confirmed as assessed according to RECIST v1.1.'}, {'measure': 'Duration of objective response (DOR) per RECIST v1.1 by investigator assessment', 'timeFrame': 'Up to approximately 3 years', 'description': 'The time from the first documentation of objective response (CR or PR that is subsequently confirmed) to the first documentation of progressive disease (PD) or to death due to any cause'}, {'measure': 'Progression-free survival (PFS) per RECIST v1.1 by investigator assessment', 'timeFrame': 'Up to approximately 3 years', 'description': 'The time from the start of any study treatment to the first documentation of PD, or death due to any cause'}, {'measure': 'Overall survival (OS)', 'timeFrame': 'Up to approximately 3 years', 'description': 'The time from the start of any study treatment to the date of death due to any cause'}, {'measure': 'Area under the concentration-time curve (AUC)', 'timeFrame': 'Through 30-37 days following last dose of sigvotatug vedotin; up to 3 years', 'description': 'Pharmacokinetic (PK) endpoint'}, {'measure': 'Concentration at the end of infusion (Ceoi)', 'timeFrame': 'Through 30-37 days following last dose of sigvotatug vedotin; up to 3 years', 'description': 'PK endpoint'}, {'measure': 'Maximum observed concentration (Cmax)', 'timeFrame': 'Through 30-37 days following last dose of sigvotatug vedotin; up to 3 years', 'description': 'PK endpoint'}, {'measure': 'Time to maximum observed concentration (Tmax)', 'timeFrame': 'Through 30-37 days following last dose of sigvotatug vedotin; up to 3 years', 'description': 'PK endpoint'}, {'measure': 'Trough concentration (Ctrough)', 'timeFrame': 'Through 30-37 days following last dose of sigvotatug vedotin; up to 3 years', 'description': 'PK endpoint'}, {'measure': 'Apparent terminal elimination half-life (t1/2)', 'timeFrame': 'Through 30-37 days following last dose of sigvotatug vedotin; up to 3 years', 'description': 'PK endpoint'}, {'measure': 'Number of participants with antidrug antibodies (ADAs)', 'timeFrame': 'Through 30-37 days following last dose of sigvotatug vedotin; up to 3 years'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': True, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['NSCLC', 'HNSCC', 'cSCC', 'ESCC', 'EAC', 'GEJ', 'HGSOC', 'Advanced HER2-Negative Breast Cancer', 'High Grade Serous Ovarian Cancer', 'Non-Small Cell Lung Cancer', 'Head and Neck Squamous Cell Cancer', 'Esophageal Cancer', 'Bladder Cancer', 'Cervical Cancer', 'Gastric Cancer', 'Seattle Genetics'], 'conditions': ['Carcinoma, Non-Small Cell Lung', 'Squamous Cell Carcinoma of Head and Neck', 'HER2 Negative Breast Neoplasms', 'Esophageal Squamous Cell Carcinoma', 'Esophageal Adenocarcinoma', 'Gastroesophageal Junction Adenocarcinoma', 'Ovarian Neoplasms', 'Cutaneous Squamous Cell Cancer', 'Exocrine Pancreatic Adenocarcinoma', 'Urinary Bladder Neoplasms', 'Uterine Cervical Neoplasms', 'Stomach Neoplasms']}, 'referencesModule': {'references': [{'pmid': '37619980', 'type': 'DERIVED', 'citation': 'Lyon RP, Jonas M, Frantz C, Trueblood ES, Yumul R, Westendorf L, Hale CJ, Stilwell JL, Yeddula N, Snead KM, Kumar V, Patilea-Vrana GI, Klussman K, Ryan MC. SGN-B6A: A New Vedotin Antibody-Drug Conjugate Directed to Integrin Beta-6 for Multiple Carcinoma Indications. Mol Cancer Ther. 2023 Dec 1;22(12):1444-1453. doi: 10.1158/1535-7163.MCT-22-0817.'}], 'seeAlsoLinks': [{'url': 'https://pmiform.com/clinical-trial-info-request?StudyID=SGNB6A-001', 'label': 'To obtain contact information for a study center near you, click here.'}]}, 'descriptionModule': {'briefSummary': 'This trial will look at a drug called sigvotatug vedotin (SGN-B6A) alone and with pembrolizumab, with or without chemotherapy, to find out whether it is safe for people who have solid tumors. It will study sigvotatug vedotin to find out what its side effects are. A side effect is anything the drug does besides treating cancer. It will also study whether sigvotatug vedotin works to treat solid tumors.\n\nThe study will have four parts.\n\n* Part A of the study will find out how much sigvotatug vedotin should be given to participants.\n* Part B will use the dose found in Part A to find out how safe sigvotatug vedotin is and if it works to treat solid tumors.\n* Part C of the study will find out how safe sigvotatug vedotin is in combination with these other drugs.\n* Part D will include people who have not received treatment. This part of the study will find out how safe sigvotatug vedotin is in combination with these other drugs and if these combinations work to treat solid tumors.\n* In Parts C and D, participants will receive sigvotatug vedotin with either:\n\n * Pembrolizumab or,\n * Pembrolizumab and carboplatin, or\n * Pembrolizumab and cisplatin.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Disease indication\n\n * Participants must have histologically or cytologically confirmed metastatic or unresectable solid malignancy within one of the tumor types listed below (dependent on study part).\n\n * Non-small cell lung cancer (NSCLC)\n * Head and neck squamous cell cancer (HNSCC)\n * Advanced HER2-negative breast cancer\n * Esophageal squamous cell carcinoma (ESCC)\n * Esophageal/Gastro-esophageal junction adenocarcinoma (EAC/GEJ)\n * Cutaneous squamous cell cancer (cSCC)\n * Exocrine pancreatic adenocarcinoma\n * Bladder cancer\n * Cervical cancer\n * Gastric cancer\n * High grade serous ovarian cancer (HGSOC)\n * Part A only: Participants must have disease that is relapsed or refractory or be intolerant to standard-of-care therapies and should have no appropriate standard-of-care therapeutic options.\n * Part B only: Participants must have disease that is relapsed or refractory or be intolerant to standard-of-care therapies. Participants must have received platinum-based therapy and a PD-1/PD-(L)1 inhibitor, if applicable and available.\n * Part C only: For pembrolizumab combination cohorts, participants must be eligible for pembrolizumab per local standard of care. For pembrolizumab with cisplatin or carboplatin, participants must be eligible for both pembrolizumab and the platinum agent per local standard of care. Participants must be treatment naïve for locally advanced or metastatic systemic therapy (prior definitively intended or \\[neo\\]adjuvant therapy is allowed).\n * Part D only: Participants must be treatment naïve for locally advanced or metastatic systemic therapy.\n* Participants enrolled in the following study parts should have a tumor site accessible for biopsy and agree to biopsy as follows:\n\n * Disease-specific expansion cohorts (Part B and Part D): A baseline fresh tumor biopsy is required. An archival biopsy collected within 90 days prior to first dose of study drug may be used.\n * Biology expansion cohort: pretreatment biopsy and on-treatment (Cycle 1) biopsy\n* An Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 or 1\n* Measurable disease per the RECIST v1.1 at baseline\n\nExclusion Criteria\n\n* History of another malignancy within 3 years before first dose of study drug, or any evidence of residual disease from a previously diagnosed malignancy. Exceptions are malignancies with a negligible risk of metastasis or death.\n* Known active central nervous system metastases. Participants with previously treated brain metastases may participate provided they:\n\n * are clinically stable for at least 4 weeks prior to study entry after brain metastasis treatment,\n * have no new or enlarging brain metastases, and\n * are off of corticosteroids prescribed for symptoms associated with brain metastases for at least 7 days prior to first dose of study drug.\n * In Part D, participants with untreated, asymptomatic CNS metastases smaller than 1 cm may be enrolled without definitive treatment as long as they have no neurological symptoms, no or minimal surrounding edema, and no requirements for corticosteroids.\n* Carcinomatous meningitis\n* Previous receipt of an MMAE-containing agent or an agent targeting integrin beta-6\n* Pre-existing neuropathy Grade 1 or greater per the National Cancer Institute's Common Terminology Criteria for Adverse Events, version 5.0 (NCI CTCAE v5.0) for Parts C and D cohorts with cisplatin or carboplatin; Grade 2 or greater per the NCI CTCAE v5.0 for all other cohorts\n* Any uncontrolled Grade 3 or higher (per NCI CTCAE v5.0) viral, bacterial, or fungal infection within 2 weeks prior to the first dose of sigvotatug vedotin.\n\n * Routine antimicrobial prophylaxis is permitted\n* Grade ≥3 pulmonary disease unrelated to underlying malignancy. This includes clinically severe pulmonary function compromise resulting from clinically significant pulmonary illnesses\n* Part C and D: Prior therapy with a PD-1 inhibitor, anti-PD-(L)1, or anti PD-L2 agent or with an agent directed to another stimulatory or co-inhibitory T-cell receptor and was discontinued from that treatment due to a Grade 3 or higher immune-mediated adverse event (IMAE).\n* History of noninfectious interstitial lung disease (ILD) or pneumonitis that required steroids, current ILD or pneumonitis, or suspected ILD or pneumonitis that cannot be ruled out by imaging at screening\n* Known diffusing capacity of the lung for carbon monoxide (DLCO; adjusted for hemoglobin) \\<50% predicted\n* Investigator site staff directly involved in the conduct of the study and their family members, site staff otherwise supervised by the investigator, and sponsor and sponsor delegate employees directly involved in the conduct of the study and their family members."}, 'identificationModule': {'nctId': 'NCT04389632', 'briefTitle': 'A Study of Sigvotatug Vedotin in Advanced Solid Tumors', 'organization': {'class': 'INDUSTRY', 'fullName': 'Seagen Inc.'}, 'officialTitle': 'A Phase 1 Study of Sigvotatug Vedotin in Advanced Solid Tumors', 'orgStudyIdInfo': {'id': 'SGNB6A-001'}, 'secondaryIdInfos': [{'id': 'C5751001', 'type': 'OTHER', 'domain': 'Alias Study Number'}, {'id': '2023-508469-34-00', 'type': 'REGISTRY', 'domain': 'CTIS (EU)'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Part A: Dose escalation', 'description': 'sigvotatug vedotin monotherapy', 'interventionNames': ['Drug: sigvotatug vedotin']}, {'type': 'EXPERIMENTAL', 'label': 'Part B: Dose expansion', 'description': 'sigvotatug vedotin monotherapy', 'interventionNames': ['Drug: sigvotatug vedotin']}, {'type': 'EXPERIMENTAL', 'label': 'Part C: sigvotatug vedotin combination therapy in NSCLC, HNSCC, ESCC', 'description': 'sigvotatug vedotin + pembrolizumab +/- (carboplatin or cisplatin)', 'interventionNames': ['Drug: sigvotatug vedotin', 'Drug: pembrolizumab', 'Drug: cisplatin', 'Drug: carboplatin']}, {'type': 'EXPERIMENTAL', 'label': 'Part D: sigvotatug vedotin combination therapy in 1L NSCLC', 'description': 'sigvotatug vedotin + pembrolizumab +/- (carboplatin)', 'interventionNames': ['Drug: sigvotatug vedotin', 'Drug: pembrolizumab', 'Drug: carboplatin']}, {'type': 'EXPERIMENTAL', 'label': 'Part D: sigvotatug vedotin combination therapy in 1L HNSCC', 'description': 'sigvotatug vedotin + pembrolizumab +/- (carboplatin or cisplatin)', 'interventionNames': ['Drug: sigvotatug vedotin', 'Drug: pembrolizumab', 'Drug: cisplatin', 'Drug: carboplatin']}], 'interventions': [{'name': 'sigvotatug vedotin', 'type': 'DRUG', 'otherNames': ['SGN-B6A', 'PF-08046047'], 'description': 'Administered into the vein (IV; intravenously)', 'armGroupLabels': ['Part A: Dose escalation', 'Part B: Dose expansion', 'Part C: sigvotatug vedotin combination therapy in NSCLC, HNSCC, ESCC', 'Part D: sigvotatug vedotin combination therapy in 1L HNSCC', 'Part D: sigvotatug vedotin combination therapy in 1L NSCLC']}, {'name': 'pembrolizumab', 'type': 'DRUG', 'otherNames': ['Keytruda'], 'description': '200mg every 3 weeks or 400mg every 6 weeks, given by IV', 'armGroupLabels': ['Part C: sigvotatug vedotin combination therapy in NSCLC, HNSCC, ESCC', 'Part D: sigvotatug vedotin combination therapy in 1L HNSCC', 'Part D: sigvotatug vedotin combination therapy in 1L NSCLC']}, {'name': 'cisplatin', 'type': 'DRUG', 'description': '75 mg/m2 every 3 weeks, given by IV', 'armGroupLabels': ['Part C: sigvotatug vedotin combination therapy in NSCLC, HNSCC, ESCC', 'Part D: sigvotatug vedotin combination therapy in 1L HNSCC']}, {'name': 'carboplatin', 'type': 'DRUG', 'description': 'AUC 5 mg/mL per min every 3 weeks, given by IV', 'armGroupLabels': ['Part C: sigvotatug vedotin combination therapy in NSCLC, HNSCC, ESCC', 'Part D: sigvotatug vedotin combination therapy in 1L HNSCC', 'Part D: sigvotatug vedotin combination therapy in 1L NSCLC']}]}, 'contactsLocationsModule': {'locations': [{'zip': '99508', 'city': 'Anchorage', 'state': 'Alaska', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Alaska Oncology and Hematology', 'geoPoint': {'lat': 61.21806, 'lon': -149.90028}}, {'zip': '72703', 'city': 'Fayetteville', 'state': 'Arkansas', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Highlands Oncology Group', 'geoPoint': {'lat': 36.06258, 'lon': -94.15743}}, {'zip': '72758', 'city': 'Rogers', 'state': 'Arkansas', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Highlands Oncology Group', 'geoPoint': {'lat': 36.33202, 'lon': -94.11854}}, {'zip': '72762', 'city': 'Springdale', 'state': 'Arkansas', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Highlands Oncology Group', 'geoPoint': {'lat': 36.18674, 'lon': -94.12881}}, {'zip': '92805', 'city': 'Anaheim', 'state': 'California', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Providence Medical Foundation', 'geoPoint': {'lat': 33.83529, 'lon': -117.9145}}, {'zip': '92835', 'city': 'Fullerton', 'state': 'California', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Providence Medical Foundation', 'geoPoint': {'lat': 33.87029, 'lon': -117.92534}}, {'zip': '92835', 'city': 'Fullerton', 'state': 'California', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Providence St. Jude Medical Center Virginia K Crosson and Infusion Center', 'geoPoint': {'lat': 33.87029, 'lon': -117.92534}}, {'zip': '90720', 'city': 'Los Alamitos', 'state': 'California', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Cancer and Blood Research Center, LLC', 'geoPoint': {'lat': 33.80307, 'lon': -118.07256}}, {'zip': '90720', 'city': 'Los Alamitos', 'state': 'California', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Cancer and Blood Specialty 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'state': 'California', 'status': 'NOT_YET_RECRUITING', 'country': 'United States', 'facility': 'Cancer AND Blood Specialty Clinic', 'geoPoint': {'lat': 33.83585, 'lon': -118.34063}}, {'zip': '33913', 'city': 'Fort Myers', 'state': 'Florida', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'American Oncology Partners, PA. a Florida professional service corporation, d/b/a Vista Oncology', 'geoPoint': {'lat': 26.62168, 'lon': -81.84059}}, {'zip': '33916', 'city': 'Fort Myers', 'state': 'Florida', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Florida Cancer Specialists & Research Institute, LLC', 'geoPoint': {'lat': 26.62168, 'lon': -81.84059}}, {'zip': '33916', 'city': 'Fort Myers', 'state': 'Florida', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Florida cancer Specialists', 'geoPoint': {'lat': 26.62168, 'lon': -81.84059}}, {'zip': '33021', 'city': 'Hollywood', 'state': 'Florida', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Memorial Cancer Institute', 'geoPoint': {'lat': 26.0112, 'lon': -80.14949}}, {'zip': '33021', 'city': 'Hollywood', 'state': 'Florida', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Memorial Healthcare System', 'geoPoint': {'lat': 26.0112, 'lon': -80.14949}}, {'zip': '32827', 'city': 'Orlando', 'state': 'Florida', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Florida cancer Specialists', 'geoPoint': {'lat': 28.53834, 'lon': -81.37924}}, {'zip': '33028', 'city': 'Pembroke Pines', 'state': 'Florida', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Memorial Cancer Institute at Memorial Hospital West', 'geoPoint': {'lat': 26.00315, 'lon': -80.22394}}, {'zip': '33028', 'city': 'Pembroke Pines', 'state': 'Florida', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Memorial Hospital West', 'geoPoint': {'lat': 26.00315, 'lon': -80.22394}}, {'zip': '60409', 'city': 'Calumet City', 'state': 'Illinois', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'Ingalls Family Care Center', 'geoPoint': {'lat': 41.61559, 'lon': -87.52949}}, {'zip': '60611', 'city': 'Chicago', 'state': 'Illinois', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'UChicago Medicine - River East', 'geoPoint': {'lat': 41.85003, 'lon': -87.65005}}, {'zip': '60637', 'city': 'Chicago', 'state': 'Illinois', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'The University Of Chicago', 'geoPoint': {'lat': 41.85003, 'lon': -87.65005}}, {'zip': '60637', 'city': 'Chicago', 'state': 'Illinois', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'University of Chicago Medical Center', 'geoPoint': {'lat': 41.85003, 'lon': -87.65005}}, {'zip': '60422', 'city': 'Flossmoor', 'state': 'Illinois', 'status': 'RECRUITING', 'country': 'United States', 'facility': 'UChicago Medicine at Ingalls - Flossmoor', 'geoPoint': {'lat': 41.54281, 'lon': -87.68477}}, {'zip': '60426', 'city': 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