Viewing Study NCT06063967


Ignite Creation Date: 2025-12-25 @ 12:36 AM
Ignite Modification Date: 2025-12-25 @ 10:46 PM
Study NCT ID: NCT06063967
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2025-09-09
First Post: 2023-09-26
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: A Study to Assess Adverse Events and Change in Disease Activity of Risankizumab Subcutaneous Induction Treatment for Moderately to Severely Active Crohn's Disease.
Sponsor:
Organization:

Raw JSON

{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D003424', 'term': 'Crohn Disease'}], 'ancestors': [{'id': 'D015212', 'term': 'Inflammatory Bowel Diseases'}, {'id': 'D005759', 'term': 'Gastroenteritis'}, {'id': 'D005767', 'term': 'Gastrointestinal Diseases'}, {'id': 'D004066', 'term': 'Digestive System Diseases'}, {'id': 'D007410', 'term': 'Intestinal Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C000601773', 'term': 'risankizumab'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'TRIPLE', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SEQUENTIAL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 289}}, 'statusModule': {'overallStatus': 'ACTIVE_NOT_RECRUITING', 'startDateStruct': {'date': '2023-11-15', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-09', 'completionDateStruct': {'date': '2027-03', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-09-08', 'studyFirstSubmitDate': '2023-09-26', 'studyFirstSubmitQcDate': '2023-09-26', 'lastUpdatePostDateStruct': {'date': '2025-09-09', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2023-10-03', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2027-03', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': "Percentage of Participants With Crohn's Disease Activity Index (CDAI) Clinical Remission (CDAI < 150)", 'timeFrame': 'Week 12', 'description': "The CDAI consists of 8 components; 7 are based on participant diary entries, participant interviews, physical examinations, measurement of body weight and height and 1 is based on laboratory analysis. CDAI clinical remission of Crohn's disease is defined as CDAI \\< 150"}, {'measure': 'Percentage of Participants With Endoscopic Response', 'timeFrame': 'Week 12', 'description': "The Simple Endoscopic Score for Crohn's Disease (SES-CD) assesses endoscopic disease severity by evidence of active intestinal mucosal inflammation. Endoscopic response is defined as a decrease in SES-CD \\> 50% from Baseline (or for participants with isolated ileal disease and a Baseline SES-CD of 4, at least a 2-point reduction from Baseline)"}, {'measure': 'Number of Participants Experiencing Adverse Events', 'timeFrame': 'Up to approximately 96 weeks', 'description': 'An AE is defined as any untoward medical occurrence in a patient or clinical investigation participant administered a pharmaceutical product which does not necessarily have a causal relationship with this treatment.'}], 'secondaryOutcomes': [{'measure': 'Percentage of Participants With Clinical Remission', 'timeFrame': 'Week 12', 'description': 'Clinical remission is defined as using the average daily Stool Frequency (SF) ≤ 2.8 and not worse than Baseline AND average daily Abdominal Pain (AP) score ≤ 1 and not worse than Baseline.'}, {'measure': 'Percentage of Participants With Endoscopic Remission', 'timeFrame': 'Week 12', 'description': 'Endoscopic remission: SES-CD ≤ 4 and at least a 2 point reduction versus baseline and no subscore greater than 1 in any individual variable'}, {'measure': 'Percentage of Participants With Ulcer-Free Endoscopy', 'timeFrame': 'Week 12', 'description': 'Ulcer-free endoscopy: SES-CD ulcerated surface subscore of 0 in participants with SES-CD ulcerated surface subscore ≥ 1 at Baseline'}, {'measure': 'Change From Baseline of Functional Assessment of Chronic Illness Therapy (FACIT)-Fatigue', 'timeFrame': 'Week 12', 'description': "The FACIT-Fatigue scale is a 13-item tool that measures an individual's level of fatigue during their usual daily activities over the past 7 days. Each of the fatigue and impact of fatigue items are measured on a 5-point Likert scale. The FACIT Fatigue Scale is the sum of the individual 13 scores and ranges from 0 to 52 where higher scores indicate better the quality of life. A positive change from baseline indicates improvement."}, {'measure': 'Percentage of Participants with a CR-100 Clinical Response', 'timeFrame': 'Week 4', 'description': 'CR-100 defined as at least a 100-point reduction from Baseline in CDAI'}]}, 'oversightModule': {'isUsExport': True, 'oversightHasDmc': False, 'isFdaRegulatedDrug': True, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ["Risankizumab, Skyrizi, Crohn's Disease, ABBV-066"], 'conditions': ["Crohn's Disease"]}, 'referencesModule': {'seeAlsoLinks': [{'url': 'https://www.abbvieclinicaltrials.com/study/?id=M23-784', 'label': 'Related Info'}]}, 'descriptionModule': {'briefSummary': "Crohn's disease (CD) is a long-lasting disease that causes severe inflammation (redness, swelling), in the digestive tract, most often affecting the bowels. It can cause many different symptoms including abdominal pain, diarrhea, tiredness, and weight loss. This study will assess how safe and effective risankizumab subcutaneous (SC) induction treatment is in treating moderately to severely active CD in adult participants.\n\nRisankizumab is an approved drug for adults with CD. This study comprises of a Period A, a Period B, and a Period C. In Period A, participants are placed in 1 of 2 groups to receive either risankizumab SC Dose A or Placebo. In Period B, based on response, participants will receive risankizumab SC Dose B or Placebo. Participants who do not have improvement in CD symptoms at Week 12 will receive risankizumab SC Dose C and participants with worsening CD symptoms in period B will receive risankizumab SC. In Period C, eligible participants will receive open-label risankizumab SC Dose D. Approximately 276 adult participants with a diagnosis of moderately to severely active CD will be enrolled in approximately 250 sites globally.\n\nParticipants will receive SC induction treatment of risankizumab or matching placebo for up to 24 weeks in Period A and B followed by an open-label risankizumab extension in Period C for 52 weeks. The duration of the study will be approximately 93 weeks."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Biopsy-confirmed diagnosis of CD for at least 3 months prior to Baseline.\n* Participant meets the following disease activity criteria:\n\n 1. Moderate to severe CD as assessed by CDAI\n 2. Endoscopic evidence of mucosal inflammation as documented by a SES-CD\n* Participant has demonstrated intolerance, loss of response or inadequate response to conventional or advanced therapies for CD.\n\nExclusion Criteria:\n\n* Participants with a current diagnosis of ulcerative colitis or indeterminate colitis.\n* Participants with unstable doses of concomitant Crohn's disease therapy.\n* Participants with prior exposure to p19 inhibitors.\n* Participants with complications of Crohn's disease.\n* Participants having an ostomy or ileoanal pouch."}, 'identificationModule': {'nctId': 'NCT06063967', 'acronym': 'AFFIRM', 'briefTitle': "A Study to Assess Adverse Events and Change in Disease Activity of Risankizumab Subcutaneous Induction Treatment for Moderately to Severely Active Crohn's Disease.", 'organization': {'class': 'INDUSTRY', 'fullName': 'AbbVie'}, 'officialTitle': "A Phase 3, Randomized, Placebo-Controlled, Double-Blind Study to Evaluate the Efficacy and Safety of Risankizumab Subcutaneous Induction Treatment in Subjects With Moderately to Severely Active Crohn's Disease", 'orgStudyIdInfo': {'id': 'M23-784'}, 'secondaryIdInfos': [{'id': '2024-516023-13-00', 'type': 'OTHER', 'domain': 'EU CT'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Period A: Risankizumab Dose A', 'description': 'Participants randomized to receive risankizumab Dose A administered by subcutaneous (SC) injection for up to 12 weeks during Period A.', 'interventionNames': ['Drug: Risankizumab SC']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Period A: Placebo', 'description': 'Participants randomized to receive placebo for risankizumab administered by Subcutaneous (SC) injection for up to 12 weeks during Period A.', 'interventionNames': ['Drug: Placebo for risankizumab']}, {'type': 'EXPERIMENTAL', 'label': 'Period B: Risankizumab Dose B', 'description': 'Participants randomized to receive risankizumab Dose A in Period A that achieved adequate response to receive risankizumab Dose B administered by subcutaneous (SC) injection for up to 12 weeks.', 'interventionNames': ['Drug: Risankizumab SC']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Period B: Placebo', 'description': 'Participants randomized to receive placebo risankizumab in Period A that achieved adequate response to continue to receive placebo for risankizumab administered by Subcutaneous (SC) injection for up to 12 weeks in Period B.', 'interventionNames': ['Drug: Placebo for risankizumab']}, {'type': 'EXPERIMENTAL', 'label': 'Period B: Risankizumab Dose C', 'description': 'Participants with inadequate response in Period A to receive Dose C administered by Subcutaneous (SC) injection for up to 12 weeks during Period B.', 'interventionNames': ['Drug: Risankizumab SC']}, {'type': 'EXPERIMENTAL', 'label': 'Period C: Open-Label Risankizumab Dose D', 'description': 'Participants who complete the Period B Week 24 visit to receive open-label risankizumab Dose D administered by subcutaneous (SC) injection for up to 52 weeks during Period C.', 'interventionNames': ['Drug: Risankizumab SC']}], 'interventions': [{'name': 'Risankizumab SC', 'type': 'DRUG', 'otherNames': ['ABBV-066', 'SKYRIZI'], 'description': 'subcutaneous (SC) injection', 'armGroupLabels': ['Period A: Risankizumab Dose A', 'Period B: Risankizumab Dose B', 'Period B: Risankizumab Dose C', 'Period C: Open-Label Risankizumab Dose D']}, {'name': 'Placebo for risankizumab', 'type': 'DRUG', 'description': 'subcutaneous (SC) injection', 'armGroupLabels': ['Period A: Placebo', 'Period B: Placebo']}]}, 'contactsLocationsModule': {'locations': [{'zip': '85351', 'city': 'Sun City', 'state': 'Arizona', 'country': 'United States', 'facility': 'Gi Alliance - Arizona Digestive Health - Sun City /ID# 268178', 'geoPoint': {'lat': 33.59754, 'lon': -112.27182}}, {'zip': '92879-3104', 'city': 'Corona', 'state': 'California', 'country': 'United States', 'facility': 'Kindred Medical Institute - Corona /ID# 262075', 'geoPoint': {'lat': 33.87529, 'lon': -117.56644}}, {'zip': '92118-1408', 'city': 'Coronado', 'state': 'California', 'country': 'United States', 'facility': 'Southern California Res. Ctr. /ID# 256612', 'geoPoint': {'lat': 32.68589, 'lon': -117.18309}}, {'zip': '91723', 'city': 'Covina', 'state': 'California', 'country': 'United States', 'facility': 'Valley Clinical Trials, LLC dba Flourish Research /ID# 256610', 'geoPoint': {'lat': 34.09001, 'lon': -117.89034}}, {'zip': '92648-5994', 'city': 'Huntington Beach', 'state': 'California', 'country': 'United States', 'facility': 'Newport Huntington Medical Group /ID# 256622', 'geoPoint': {'lat': 33.6603, 'lon': -117.99923}}, {'zip': '93534', 'city': 'Lancaster', 'state': 'California', 'country': 'United States', 'facility': 'Om Research LLC /ID# 259645', 'geoPoint': {'lat': 34.69804, 'lon': -118.13674}}, {'zip': '93534', 'city': 'Lancaster', 'state': 'California', 'country': 'United States', 'facility': 'Om Research LLC /ID# 267523', 'geoPoint': {'lat': 34.69804, 'lon': -118.13674}}, {'zip': '92868', 'city': 'Orange', 'state': 'California', 'country': 'United States', 'facility': 'Clinnova Research - Orange /ID# 270138', 'geoPoint': {'lat': 33.78779, 'lon': -117.85311}}, {'zip': '92868', 'city': 'Orange', 'state': 'California', 'country': 'United States', 'facility': 'University of California, Irvine Medical Center /ID# 259677', 'geoPoint': {'lat': 33.78779, 'lon': -117.85311}}, {'zip': '91730', 'city': 'Rancho Cucamonga', 'state': 'California', 'country': 'United States', 'facility': 'Prospective Research Innovations Inc. /ID# 267856', 'geoPoint': {'lat': 34.1064, 'lon': -117.59311}}, {'zip': '94158', 'city': 'San Francisco', 'state': 'California', 'country': 'United States', 'facility': 'University of California San Francisco - Mission Bay /ID# 267529', 'geoPoint': {'lat': 37.77493, 'lon': -122.41942}}, {'zip': '91355', 'city': 'Valencia', 'state': 'California', 'country': 'United States', 'facility': 'Amicis Research Center - Valencia /ID# 269158', 'geoPoint': {'lat': 34.44361, 'lon': -118.60953}}, {'zip': '92395', 'city': 'Victorville', 'state': 'California', 'country': 'United States', 'facility': 'OM Research LLC /ID# 268735', 'geoPoint': {'lat': 34.53611, 'lon': -117.29116}}, {'zip': '06810', 'city': 'Danbury', 'state': 'Connecticut', 'country': 'United States', 'facility': 'Danbury Hospital, Western Connecticut Health Network /ID# 261851', 'geoPoint': {'lat': 41.39482, 'lon': -73.45401}}, {'zip': '34711', 'city': 'Clermont', 'state': 'Florida', 'country': 'United States', 'facility': 'Novum Research /ID# 269223', 'geoPoint': {'lat': 28.54944, 'lon': -81.77285}}, {'zip': '33134-2442', 'city': 'Coral Gables', 'state': 'Florida', 'country': 'United States', 'facility': 'Research Associates of South Florida, LLC /ID# 261627', 'geoPoint': {'lat': 25.72149, 'lon': -80.26838}}, {'zip': '32610', 'city': 'Gainesville', 'state': 'Florida', 'country': 'United States', 'facility': 'University of Florida College of Medicine /ID# 261248', 'geoPoint': {'lat': 29.65163, 'lon': -82.32483}}, {'zip': '33813-4924', 'city': 'Lakeland', 'state': 'Florida', 'country': 'United States', 'facility': 'Auzmer Research /ID# 261437', 'geoPoint': {'lat': 28.03947, 'lon': -81.9498}}, {'zip': '32751-6108', 'city': 'Maitland', 'state': 'Florida', 'country': 'United States', 'facility': 'Cfagi Llc /Id# 262005', 'geoPoint': {'lat': 28.62778, 'lon': -81.36312}}, {'zip': '33063-5737', 'city': 'Margate', 'state': 'Florida', 'country': 'United States', 'facility': 'Atlantic Medical Research /ID# 256471', 'geoPoint': {'lat': 26.24453, 'lon': -80.20644}}, {'zip': '33032', 'city': 'Miami', 'state': 'Florida', 'country': 'United States', 'facility': 'Homestead Associates in Research /ID# 259643', 'geoPoint': {'lat': 25.77427, 'lon': -80.19366}}, {'zip': '33136', 'city': 'Miami', 'state': 'Florida', 'country': 'United States', 'facility': 'University of Miami /ID# 256587', 'geoPoint': {'lat': 25.77427, 'lon': -80.19366}}, {'zip': '33176-2302', 'city': 'Miami', 'state': 'Florida', 'country': 'United States', 'facility': 'JD Medical Group, LLC /ID# 262185', 'geoPoint': {'lat': 25.77427, 'lon': -80.19366}}, {'zip': '34102', 'city': 'Naples', 'state': 'Florida', 'country': 'United States', 'facility': 'Gastroenterology Group Naples /ID# 256566', 'geoPoint': {'lat': 26.14234, 'lon': -81.79596}}, {'zip': '34474', 'city': 'Ocala', 'state': 'Florida', 'country': 'United States', 'facility': 'Sarkis Clinical Trials - Ocala /ID# 267840', 'geoPoint': {'lat': 29.1872, 'lon': -82.14009}}, {'zip': '32803', 'city': 'Orlando', 'state': 'Florida', 'country': 'United States', 'facility': 'Endoscopic Research, Inc. /ID# 256597', 'geoPoint': {'lat': 28.53834, 'lon': -81.37924}}, {'zip': '32804-5505', 'city': 'Orlando', 'state': 'Florida', 'country': 'United States', 'facility': 'AdventHealth Medical Group Blood & Marrow Transplant at Orlando /ID# 261811', 'geoPoint': {'lat': 28.53834, 'lon': -81.37924}}, {'zip': '33609', 'city': 'Tampa', 'state': 'Florida', 'country': 'United States', 'facility': 'GCP Clinical Research, LLC /ID# 260342', 'geoPoint': {'lat': 27.94752, 'lon': -82.45843}}, {'zip': '33613-1825', 'city': 'Tampa', 'state': 'Florida', 'country': 'United States', 'facility': 'Avita Clinical Research /ID# 261640', 'geoPoint': {'lat': 27.94752, 'lon': -82.45843}}, {'zip': '30322', 'city': 'Atlanta', 'state': 'Georgia', 'country': 'United States', 'facility': 'Winship Cancer Institute of Emory University /ID# 261877', 'geoPoint': {'lat': 33.749, 'lon': -84.38798}}, {'zip': '30328', 'city': 'Atlanta', 'state': 'Georgia', 'country': 'United States', 'facility': 'Mount Vernon Clinical Research /ID# 271813', 'geoPoint': {'lat': 33.749, 'lon': -84.38798}}, {'zip': '30033', 'city': 'Decatur', 'state': 'Georgia', 'country': 'United States', 'facility': 'Atlanta Ctr. for Gastro /ID# 261181', 'geoPoint': {'lat': 33.77483, 'lon': -84.29631}}, {'zip': '31201', 'city': 'Macon', 'state': 'Georgia', 'country': 'United States', 'facility': 'Gastroenterology Associates of Central Georgia, LLC /ID# 256611', 'geoPoint': {'lat': 32.84069, 'lon': -83.6324}}, {'zip': '30076-4913', 'city': 'Roswell', 'state': 'Georgia', 'country': 'United States', 'facility': 'Gastroenterology Consultants, P.C /ID# 260635', 'geoPoint': {'lat': 34.02316, 'lon': -84.36159}}, {'zip': '83404', 'city': 'Idaho Falls', 'state': 'Idaho', 'country': 'United States', 'facility': 'Grand Teton Research Group /ID# 267521', 'geoPoint': {'lat': 43.46658, 'lon': -112.03414}}, {'zip': '60637', 'city': 'Chicago', 'state': 'Illinois', 'country': 'United States', 'facility': 'Duplicate_The University of Chicago DCAM /ID# 256577', 'geoPoint': {'lat': 41.85003, 'lon': -87.65005}}, {'zip': '60026-8000', 'city': 'Glenview', 'state': 'Illinois', 'country': 'United States', 'facility': 'GI Alliance - Glenview /ID# 257744', 'geoPoint': {'lat': 42.06975, 'lon': -87.78784}}, {'zip': '60031-5711', 'city': 'Gurnee', 'state': 'Illinois', 'country': 'United States', 'facility': 'GI Alliance - Gurnee /ID# 257735', 'geoPoint': {'lat': 42.3703, 'lon': -87.90202}}, {'zip': '60453', 'city': 'Oak Lawn', 'state': 'Illinois', 'country': 'United States', 'facility': 'Southwest Gastroenterology /ID# 256619', 'geoPoint': {'lat': 41.71087, 'lon': -87.75811}}, {'zip': '46202-5149', 'city': 'Indianapolis', 'state': 'Indiana', 'country': 'United States', 'facility': 'IU Health University Hospital /ID# 259633', 'geoPoint': {'lat': 39.76838, 'lon': -86.15804}}, {'zip': '66160', 'city': 'Kansas City', 'state': 'Kansas', 'country': 'United States', 'facility': 'Univ Kansas Med Ctr /ID# 262551', 'geoPoint': {'lat': 39.11417, 'lon': -94.62746}}, {'zip': '66606', 'city': 'Topeka', 'state': 'Kansas', 'country': 'United States', 'facility': "Cotton O'Neil Clinical Research Center, Digestive Health /ID# 256592", 'geoPoint': {'lat': 39.04833, 'lon': -95.67804}}, {'zip': '40202', 'city': 'Louisville', 'state': 'Kentucky', 'country': 'United States', 'facility': 'University of Louisville Hospital /ID# 256569', 'geoPoint': {'lat': 38.25424, 'lon': -85.75941}}, {'zip': '71105-6800', 'city': 'Shreveport', 'state': 'Louisiana', 'country': 'United States', 'facility': 'Louisiana Research Center, LLC /ID# 256598', 'geoPoint': {'lat': 32.52515, 'lon': -93.75018}}, {'zip': '04102', 'city': 'Portland', 'state': 'Maine', 'country': 'United States', 'facility': 'Portland Gastroenterology Center - Portland - Congress Street /ID# 268428', 'geoPoint': {'lat': 43.65737, 'lon': -70.2589}}, {'zip': '02114', 'city': 'Boston', 'state': 'Massachusetts', 'country': 'United States', 'facility': 'Massachusetts General Hospital /Id# 261051', 'geoPoint': {'lat': 42.35843, 'lon': -71.05977}}, {'zip': '48047', 'city': 'Chesterfield', 'state': 'Michigan', 'country': 'United States', 'facility': 'Clin Res Inst of Michigan, LLC /ID# 256609', 'geoPoint': {'lat': 42.66281, 'lon': -82.84242}}, {'zip': '48047', 'city': 'Chesterfield', 'state': 'Michigan', 'country': 'United States', 'facility': 'Clin Res Inst of Michigan, LLC /ID# 261017', 'geoPoint': {'lat': 42.66281, 'lon': -82.84242}}, {'zip': '49519', 'city': 'Wyoming', 'state': 'Michigan', 'country': 'United States', 'facility': 'Gastroenterology Associates of Western Michigan, PLC d.b.a. West Michigan Clinic /ID# 256568', 'geoPoint': {'lat': 42.91336, 'lon': -85.70531}}, {'zip': '55905-0001', 'city': 'Rochester', 'state': 'Minnesota', 'country': 'United States', 'facility': 'Mayo Clinic - Rochester /ID# 256594', 'geoPoint': {'lat': 44.02163, 'lon': -92.4699}}, {'zip': '64111', 'city': 'Kansas City', 'state': 'Missouri', 'country': 'United States', 'facility': 'Saint Lukes Hospital of Kansas City /ID# 271816', 'geoPoint': {'lat': 39.09973, 'lon': -94.57857}}, {'zip': '07631-4152', 'city': 'Englewood', 'state': 'New Jersey', 'country': 'United States', 'facility': 'Allied Health Clinical Research Organization, LLC /ID# 261618', 'geoPoint': {'lat': 40.89288, 'lon': -73.97264}}, {'zip': '11235-3919', 'city': 'Brooklyn', 'state': 'New York', 'country': 'United States', 'facility': 'NY Scientific /ID# 261209', 'geoPoint': {'lat': 40.6501, 'lon': -73.94958}}, {'zip': '10032-3729', 'city': 'New York', 'state': 'New York', 'country': 'United States', 'facility': 'Columbia University Medical Center /ID# 261879', 'geoPoint': {'lat': 40.71427, 'lon': -74.00597}}, {'zip': '10075', 'city': 'New York', 'state': 'New York', 'country': 'United States', 'facility': 'New York Gastroenterology Associates /ID# 257730', 'geoPoint': {'lat': 40.71427, 'lon': -74.00597}}, {'zip': '27514-4220', 'city': 'Chapel Hill', 'state': 'North Carolina', 'country': 'United States', 'facility': 'Univ NC Chapel Hill /ID# 256368', 'geoPoint': {'lat': 35.9132, 'lon': -79.05584}}, {'zip': '27834', 'city': 'Greenville', 'state': 'North Carolina', 'country': 'United States', 'facility': 'Carolina Research /ID# 261435', 'geoPoint': {'lat': 35.61266, 'lon': -77.36635}}, {'zip': '27804', 'city': 'Rocky Mount', 'state': 'North Carolina', 'country': 'United States', 'facility': 'Boice-Willis Clinic, P.A. /ID# 262209', 'geoPoint': {'lat': 35.93821, 'lon': -77.79053}}, {'zip': '58104-5925', 'city': 'Fargo', 'state': 'North Dakota', 'country': 'United States', 'facility': 'Plains Clinical Research Center, LLC /ID# 256602', 'geoPoint': {'lat': 46.87719, 'lon': -96.7898}}, {'zip': '43235', 'city': 'Columbus', 'state': 'Ohio', 'country': 'United States', 'facility': 'Optimed Research, Ltd. /ID# 256573', 'geoPoint': {'lat': 39.96118, 'lon': -82.99879}}, {'zip': '43210', 'city': 'Hilliard', 'state': 'Ohio', 'country': 'United States', 'facility': 'The Ohio State University - Hilliard /ID# 256623', 'geoPoint': {'lat': 40.0334, 'lon': -83.15825}}, {'zip': '73102', 'city': 'Oklahoma City', 'state': 'Oklahoma', 'country': 'United States', 'facility': 'Hightower Clinical /ID# 256613', 'geoPoint': {'lat': 35.46756, 'lon': -97.51643}}, {'zip': '74104', 'city': 'Tulsa', 'state': 'Oklahoma', 'country': 'United States', 'facility': 'Options Health Research /ID# 271243', 'geoPoint': {'lat': 36.15398, 'lon': -95.99277}}, {'zip': '38018', 'city': 'Cordova', 'state': 'Tennessee', 'country': 'United States', 'facility': 'Gastro One /ID# 256614', 'geoPoint': {'lat': 35.15565, 'lon': 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