Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D006937', 'term': 'Hypercholesterolemia'}], 'ancestors': [{'id': 'D006949', 'term': 'Hyperlipidemias'}, {'id': 'D050171', 'term': 'Dyslipidemias'}, {'id': 'D052439', 'term': 'Lipid Metabolism Disorders'}, {'id': 'D008659', 'term': 'Metabolic Diseases'}, {'id': 'D009750', 'term': 'Nutritional and Metabolic Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'D000069438', 'term': 'Ezetimibe'}], 'ancestors': [{'id': 'D001384', 'term': 'Azetidines'}, {'id': 'D001385', 'term': 'Azetines'}, {'id': 'D006573', 'term': 'Heterocyclic Compounds, 1-Ring'}, {'id': 'D006571', 'term': 'Heterocyclic Compounds'}]}}, 'protocolSection': {'designModule': {'studyType': 'OBSERVATIONAL', 'designInfo': {'timePerspective': 'PROSPECTIVE', 'observationalModel': 'COHORT'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 5000}, 'patientRegistry': False}, 'statusModule': {'overallStatus': 'ACTIVE_NOT_RECRUITING', 'startDateStruct': {'date': '2021-01-15', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-11', 'completionDateStruct': {'date': '2026-10-30', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2025-11-14', 'studyFirstSubmitDate': '2020-10-01', 'studyFirstSubmitQcDate': '2020-10-01', 'lastUpdatePostDateStruct': {'date': '2025-11-18', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2020-10-08', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2026-10-30', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Summary of patient characteristics in patients with primary hypercholesterolemia or mixed dyslipidemia following treatment with bempedoic acid and/or its fixed-dose combination with ezetimibe', 'timeFrame': 'Baseline (date of signed informed consent) up to 1 year minimum or 2 year maximum follow up (depending on the availability of bempedoic acid in countries)'}], 'secondaryOutcomes': [{'measure': 'Overview of the cardiovascular risk of patients with primary hypercholesterolemia or mixed dyslipidemia following treatment with bempedoic acid/ and/or its fixed-dose combination with ezetimibe', 'timeFrame': 'Baseline (date of signed informed consent) up to 1 year minimum or 2 year maximum follow up (depending on the availability of bempedoic acid in countries)', 'description': 'Cardiovascular risk scores will be assessed using the Systematic Coronary Risk Estimation (SCORE) system, Second manifestations of arterial disease (SMART) and Framingham risk scores. The SMART risk score will estimate 10-year risk for very high-risk participants based on clinical patient characteristics. The gender-specific Framingham risk score will be used to estimate 10-year cardiovascular risk for high-risk participants.'}, {'measure': 'Summary of changes in plasma low-density lipoprotein cholesterol levels following treatment with bempedoic acid and/or its fixed-dose combination with ezetimibe in patients with primary hypercholesterolemia or mixed dyslipidemia', 'timeFrame': 'Baseline (date of signed informed consent) up to 1 year minimum or 2 year maximum follow up (depending on the availability of bempedoic acid in countries)'}, {'measure': 'Summary in changes in plasma levels of atherosclerotic cardiovascular disease-modifying cholesterol fragments following treatment with bempedoic acid and/or its fixed-dose combination with ezetimibe', 'timeFrame': 'Baseline (date of signed informed consent) up to 1 year minimum or 2 year maximum follow up (depending on the availability of bempedoic acid in countries)', 'description': 'Plasma levels of total cholesterol (TC), apolipoprotein B (apoB), high-density lipoprotein cholesterol (HDL-C), triglycerides (TGs) and lipoprotein a (Lp\\[a\\]) will be assessed.'}, {'measure': 'Summary of changes in plasma inflammatory marker hsCRP levels following treatment with bempedoic acid and/or its fixed-dose combination with ezetimibe in patients with primary hypercholesterolemia or mixed dyslipidemia', 'timeFrame': 'Baseline (date of signed informed consent) up to 1 year minimum or 2 year maximum follow up (depending on the availability of bempedoic acid in countries)', 'description': 'Inflammatory status was assessed using high-sensitive C-reactive protein.'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': False, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'keywords': ['Hypercholesterolemia', 'Mixed dyslipidemia', 'Bempedoic acid and/or its fixed-dose combination with ezetimibe'], 'conditions': ['Hypercholesterolemia', 'Mixed Dyslipidemia']}, 'descriptionModule': {'briefSummary': 'The primary objective is to describe in the real-world setting patient characteristics and outcomes of patients with primary hypercholesterolaemia (heterozygous familial and non-familial) or mixed dyslipidaemia using bempedoic acid and/or its fixed-dose combination with ezetimibe in managing plasma levels of low-density lipoprotein cholesterol (LDL-C).\n\nSecondary objectives are to document and evaluate as applicable:\n\n* Assessment of the cardiovascular risk of patients treated with bempedoic acid and/or its fixed-dose combination with ezetimibe using different risk scores (e.g. Systematic Coronary Risk Estimation (SCORE) system, SMART score for Very High Risk patients and Framingham risk score for High Risk patients. The scores will be re-calculated during the analysis and used as an analytical tool only).\n* Changes in low-density lipoprotein cholesterol (LDL-C) levels prior to treatment with bempedoic acid and/or its fixed-dose combination with ezetimibe compared to 1 year follow-up and subsequent data collection points, if applicable.\n* Characterize plasma levels of other potentially ASCVD-modifying cholesterol fragments, namely, LDL-C, total cholesterol (TC), apolipoprotein B (apoB), high-density lipoprotein cholesterol (HDL-C), non-HDL-C, triglycerides (TGs) and lipoprotein A (Lp\\[a\\]) compared to 1 year follow-up and subsequent data collection points, if applicable.\n* Changes in the levels of inflammatory marker hsCRP compared to 1 year follow-up and subsequent data collection points, if applicable.\n* Adverse Drug Reactions associated to bempedoic acid and/or its fixed-dose combination with ezetimibe.\n* Changes in uric acid levels compared to 1 year follow-up and subsequent data collection points, if applicable.\n* Relevant CV events:\n\n * Myocardial infarction\n * Unstable angina\n * Coronary artery bypass graft surgery (CABG)\n * Percutaneous transluminal coronary angioplasty (PTCA)\n * Stroke\n * Transient ischemic attack (TIA)\n * Acute peripheral arterial occlusion\n * All-cause death\n * Cardiovascular (CV)-death\n* Adverse effects associated with lipid-modifying treatment (LMT)\n\n * Laboratory abnormalities\n * Muscle-associated symptoms\n * New onset and/or worsening diabetes\n * Changes in the patients´ glycemic status over time\n* Site characteristics (sites and practitioners) caring for patients treated with bempedoic acid and/or its fixed-dose combination with ezetimibe.\n* Use of LMTs prior or concomitantly to receiving bempedoic acid and/or its fixed-dose combination with ezetimibe (therapies including combination treatments).\n* Bempedoic acid and/or its fixed-dose combination with ezetimibe treatment parameters such as treatment duration by therapy, dosage, prescription intervals, permanent discontinuations, switches and reasons for these, (concomitant medication, additional therapy/interventions).\n* Healthcare resource use especially consultation visits with specialist, nurse time and hospitalizations as well as patient-reported outcome using EQ-5D-5L and PAM-13.', 'detailedDescription': 'This non-interventional study will be conducted to characterize the risks and benefits of bempedoic acid and/or its fixed-dose combination with ezetimibe in a real-world clinical setting in adult patients with primary hypercholesterolaemia or mixed dyslipidaemia and to gain insight into the effectiveness (managing plasma levels of low-density lipoprotein cholesterol) as well as safety (clinical events associated with the treatment modalities). Real world evidence will be collected in 5000 participants, treated by specialized as well as non-specialized physicians in hospitals and office based centers.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'samplingMethod': 'NON_PROBABILITY_SAMPLE', 'studyPopulation': 'The study population will include participants with primary hypercholesterolemia or mixed dyslipidemia who are being treated with bempedoic acid and/or its fixed dose combination with ezetimibe.', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Written informed consent to participate\n* At least 18 years of age\n* Participants suffering from documented primary hypercholesterolemia or mixed dyslipidemia treated or intended to be treated with bempedoic acid and/or its fixed dose combination with ezetimibe at the discretion of the physician are appropriate for participation in the observation.\n* No contraindications exist according to the SmPC of bempedoic acid and/or its fixed-dose combination with ezetimibe\n* No concurrent participation in an interventional study (simultaneous participation in other non-interventional study is possible)\n* Life expectancy \\> 1 year\n\nExclusion Criteria:\n\n* As this is a non-interventional study, no explicit exclusion criteria are defined. The prescribing behavior will not be influenced. Only patients will be included where the decision has been made by the treating physician to treat the patients either with bempedoic acid and/or its fixed-dose combination with ezetimibe.'}, 'identificationModule': {'nctId': 'NCT04579367', 'acronym': 'MILOS', 'briefTitle': 'Treatment With Bempedoic Acid and/or Its Fixed-dose Combination With Ezetimibe in Primary Hypercholesterolemia or Mixed Dyslipidemia', 'organization': {'class': 'INDUSTRY', 'fullName': 'Daiichi Sankyo'}, 'officialTitle': 'Non-interventional Study on the Treatment With Bempedoic Acid and/or Its Fixed-dose Combination With Ezetimibe in Routine Clinical Practice in Patients With Primary Hypercholesterolemia or Mixed Dyslipidemia (MILOS)', 'orgStudyIdInfo': {'id': 'DSE-BMP-01-20-EU'}}, 'armsInterventionsModule': {'armGroups': [{'label': 'Bempedoic acid and/or fixed-dose combination with ezetimibe', 'description': 'Participants with primary hypercholesterolemia or mixed dyslipidemia who received bempedoic acid and/or its fixed-dose combination with ezetimibe.', 'interventionNames': ['Drug: Bempedoic acid and/or its fixed-dose combination with ezetimibe']}], 'interventions': [{'name': 'Bempedoic acid and/or its fixed-dose combination with ezetimibe', 'type': 'DRUG', 'description': 'This is a non-interventional study. No study medication will be provided to the patients. Medication will be prescribed by the treating physician in line with the clinical practice.', 'armGroupLabels': ['Bempedoic acid and/or fixed-dose combination with ezetimibe']}]}, 'contactsLocationsModule': {'locations': [{'zip': '6850', 'city': 'Dornbirn', 'country': 'Austria', 'facility': 'Dr. Armin Öhlinger Kardiologe & innere Medizin', 'geoPoint': {'lat': 47.41427, 'lon': 9.74195}}, {'zip': '6807', 'city': 'Feldkirch', 'country': 'Austria', 'facility': 'Landeskrankenhaus Feldkirch', 'geoPoint': {'lat': 47.23306, 'lon': 9.6}}, {'zip': '8036', 'city': 'Graz', 'country': 'Austria', 'facility': 'LKH-Univ. Klinikum Graz', 'geoPoint': {'lat': 47.06733, 'lon': 15.44197}}, {'zip': '8036', 'city': 'Graz', 'country': 'Austria', 'facility': 'Medizinische Universität Graz', 'geoPoint': {'lat': 47.06733, 'lon': 15.44197}}, {'zip': '4063', 'city': 'Hörsching', 'country': 'Austria', 'facility': 'Internist Dr. med. univ. Stefan Moser', 'geoPoint': {'lat': 48.22627, 'lon': 14.17786}}, {'zip': '6020', 'city': 'Innsbruck', 'country': 'Austria', 'facility': 'Medizinische Universität Innsbruck', 'geoPoint': {'lat': 47.26266, 'lon': 11.39454}}, {'zip': '9020', 'city': 'Klagenfurt', 'country': 'Austria', 'facility': 'KABEG Klinikum Klagenfurt am Wörthersee', 'geoPoint': {'lat': 46.62472, 'lon': 14.30528}}, {'zip': '4020', 'city': 'Linz', 'country': 'Austria', 'facility': 'Konventhospital der Barmherzigen Brüder Linz', 'geoPoint': {'lat': 48.30639, 'lon': 14.28611}}, {'zip': '4040', 'city': 'Linz', 'country': 'Austria', 'facility': 'Ordination Dr. Johannes Föchterle', 'geoPoint': {'lat': 48.30639, 'lon': 14.28611}}, {'zip': '7210', 'city': 'Mattersburg', 'country': 'Austria', 'facility': 'Ordination Frau Prof. Dr. Yvonne Winhofer-Stöckl', 'geoPoint': {'lat': 47.73333, 'lon': 16.4}}, {'zip': '5026', 'city': 'Salzburg', 'country': 'Austria', 'facility': 'Kompetenz-Zentrum Diabetes', 'geoPoint': {'lat': 47.79941, 'lon': 13.04399}}, {'zip': '3193', 'city': 'Sankt Aegyd am Neuwalde', 'country': 'Austria', 'facility': 'Ordination Universitätsdozent Dr. Alexander Kober', 'geoPoint': {'lat': 47.85383, 'lon': 15.56969}}, {'zip': '8511', 'city': 'Sankt Stefan ob Stainz', 'country': 'Austria', 'facility': 'Ordination Dr. med. univ. Evelyn Fließer-Görzer', 'geoPoint': {'lat': 46.92861, 'lon': 15.25889}}, {'zip': '1010', 'city': 'Vienna', 'country': 'Austria', 'facility': 'Ordination Dr. Thomas Maca', 'geoPoint': {'lat': 48.20849, 'lon': 16.37208}}, {'zip': '1030', 'city': 'Vienna', 'country': 'Austria', 'facility': 'Klinik Hietzing, Wiener Gesundheitsverbund', 'geoPoint': {'lat': 48.20849, 'lon': 16.37208}}, {'zip': '1060', 'city': 'Vienna', 'country': 'Austria', 'facility': 'Zentrum für Klinische Studien Dr. Hanusch GmbH', 'geoPoint': {'lat': 48.20849, 'lon': 16.37208}}, {'zip': '1090', 'city': 'Vienna', 'country': 'Austria', 'facility': 'Allgemeines Krankenhaus der Stadt Wien', 'geoPoint': {'lat': 48.20849, 'lon': 16.37208}}, {'zip': '1130', 'city': 'Vienna', 'country': 'Austria', 'facility': 'Univ.-Prof. Dr. Thomas Stulnig', 'geoPoint': {'lat': 48.20849, 'lon': 16.37208}}, {'zip': '1180', 'city': 'Vienna', 'country': 'Austria', 'facility': 'Herz Zentrum Währing', 'geoPoint': {'lat': 48.20849, 'lon': 16.37208}}, {'zip': '1210', 'city': 'Vienna', 'country': 'Austria', 'facility': 'Karl Landsteiner Institut für kardiovaskuläre und intensivmedizinische Forschung', 'geoPoint': {'lat': 48.20849, 'lon': 16.37208}}, {'zip': '9300', 'city': 'Aalst', 'country': 'Belgium', 'facility': 'ASZ', 'geoPoint': {'lat': 50.93604, 'lon': 4.0355}}, {'zip': 'B-5005', 'city': 'Bouge', 'country': 'Belgium', 'facility': 'Clinique Saint-Luc Bouge Namur', 'geoPoint': {'lat': 50.47193, 'lon': 4.89218}}, {'zip': 'B-7301', 'city': 'Boussu', 'country': 'Belgium', 'facility': 'Epicura Hornu', 'geoPoint': {'lat': 50.43417, 'lon': 3.7944}}, {'zip': 'B-2930', 'city': 'Brasschaat', 'country': 'Belgium', 'facility': 'A.Z. KLINA Brasschaat', 'geoPoint': {'lat': 51.2912, 'lon': 4.49182}}, {'zip': 'B-1000', 'city': 'Brussels', 'country': 'Belgium', 'facility': 'Clinique Saint-Jean Bruxelles', 'geoPoint': {'lat': 50.85045, 'lon': 4.34878}}, {'zip': 'B-1020', 'city': 'Brussels', 'country': 'Belgium', 'facility': 'CHU Brugman', 'geoPoint': {'lat': 50.85045, 'lon': 4.34878}}, {'zip': 'B-1070', 'city': 'Brussels', 'country': 'Belgium', 'facility': 'CUB-Hôpital Erasme', 'geoPoint': {'lat': 50.85045, 'lon': 4.34878}}, {'zip': 'B-1090', 'city': 'Brussels', 'country': 'Belgium', 'facility': 'UZ Brussel', 'geoPoint': {'lat': 50.85045, 'lon': 4.34878}}, {'zip': 'B-1180', 'city': 'Brussels', 'country': 'Belgium', 'facility': "Clinique de l'Europe Saint Elisabeth", 'geoPoint': {'lat': 50.85045, 'lon': 4.34878}}, {'zip': 'B-1200', 'city': 'Brussels', 'country': 'Belgium', 'facility': 'UCL Saint-Luc Woluwé Bruxelles', 'geoPoint': {'lat': 50.85045, 'lon': 4.34878}}, {'zip': 'B-5590', 'city': 'Ciney', 'country': 'Belgium', 'facility': 'Private Practice', 'geoPoint': {'lat': 50.29449, 'lon': 5.10015}}, {'zip': '9200', 'city': 'Dendermonde', 'country': 'Belgium', 'facility': 'Az Sint Blazius', 'geoPoint': {'lat': 51.02869, 'lon': 4.10106}}, {'zip': 'B-2650', 'city': 'Edegem', 'country': 'Belgium', 'facility': 'UZ Antwerpen', 'geoPoint': {'lat': 51.15662, 'lon': 4.44504}}, {'zip': 'B-3600', 'city': 'Genk', 'country': 'Belgium', 'facility': 'Z.O.L - Campus St. Jan', 'geoPoint': {'lat': 50.965, 'lon': 5.50082}}, {'zip': 'B-9000', 'city': 'Ghent', 'country': 'Belgium', 'facility': 'AZ St-Lucas & Volkskliniek', 'geoPoint': {'lat': 51.05, 'lon': 3.71667}}, {'zip': 'B-9000', 'city': 'Ghent', 'country': 'Belgium', 'facility': 'UZ Gent', 'geoPoint': {'lat': 51.05, 'lon': 3.71667}}, {'zip': 'B-6060', 'city': 'Gilly', 'country': 'Belgium', 'facility': 'GHDC Charleroi - Site Hôpital Saint-Joseph', 'geoPoint': {'lat': 50.42449, 'lon': 4.4789}}, {'zip': 'B-6887', 'city': 'Gribomont', 'country': 'Belgium', 'facility': 'Private Practice', 'geoPoint': {'lat': 49.82166, 'lon': 5.3243}}, {'zip': 'B-7100', 'city': 'Haine-Saint-Paul', 'country': 'Belgium', 'facility': 'Pôle hospitalier Jolimont', 'geoPoint': {'lat': 50.45544, 'lon': 4.1885}}, {'zip': 'B-3545', 'city': 'Halen', 'country': 'Belgium', 'facility': 'BVBA Med Kab', 'geoPoint': {'lat': 50.94837, 'lon': 5.11096}}, {'zip': 'B-3500', 'city': 'Hasselt', 'country': 'Belgium', 'facility': 'Jessa Ziekenhuis', 'geoPoint': {'lat': 50.93106, 'lon': 5.33781}}, {'zip': 'B-4500', 'city': 'Huy', 'country': 'Belgium', 'facility': 'CHR Huy', 'geoPoint': {'lat': 50.51894, 'lon': 5.23284}}, {'zip': 'B-9800', 'city': 'Ieper', 'country': 'Belgium', 'facility': 'JAN YPERMAN Ziekenhuis', 'geoPoint': {'lat': 50.85114, 'lon': 2.88569}}, {'zip': 'B-8500', 'city': 'Kortrijk', 'country': 'Belgium', 'facility': 'AZ Groeninge Kortrijk', 'geoPoint': {'lat': 50.82803, 'lon': 3.26487}}, {'zip': 'B-7100', 'city': 'La Louvière', 'country': 'Belgium', 'facility': 'CHU Tivoli', 'geoPoint': {'lat': 50.48657, 'lon': 4.18785}}, {'zip': 'B-3000', 'city': 'Leuven', 'country': 'Belgium', 'facility': 'UZ Leuven', 'geoPoint': {'lat': 50.87959, 'lon': 4.70093}}, {'zip': 'B-4000', 'city': 'Liège', 'country': 'Belgium', 'facility': 'CHR Citadelle de Liège', 'geoPoint': {'lat': 50.63373, 'lon': 5.56749}}, {'zip': 'B-4000', 'city': 'Liège', 'country': 'Belgium', 'facility': 'CHU Liège', 'geoPoint': {'lat': 50.63373, 'lon': 5.56749}}, {'zip': 'B-6042', 'city': 'Lodelinsart', 'country': 'Belgium', 'facility': 'CHU Charleroi Hopital civil Marie-Curie', 'geoPoint': {'lat': 50.43138, 'lon': 4.44886}}, {'zip': 'B-7000', 'city': 'Mons', 'country': 'Belgium', 'facility': 'CHU Mons Ambroise Paré', 'geoPoint': {'lat': 50.45413, 'lon': 3.95229}}, {'zip': 'B-8400', 'city': 'Ostend', 'country': 'Belgium', 'facility': 'AZ Sint Jan', 'geoPoint': {'lat': 51.21551, 'lon': 2.927}}, {'zip': 'B-8800', 'city': 'Roeselare', 'country': 'Belgium', 'facility': 'AZ Delta', 'geoPoint': {'lat': 50.94653, 'lon': 3.12269}}, {'zip': 'B-9600', 'city': 'Ronse', 'country': 'Belgium', 'facility': 'AZ Glorieux', 'geoPoint': {'lat': 50.74574, 'lon': 3.6005}}, {'zip': 'B-3800', 'city': 'Sint-Truiden', 'country': 'Belgium', 'facility': 'Sint Trudo', 'geoPoint': {'lat': 50.81679, 'lon': 5.18647}}, {'zip': 'B-8700', 'city': 'Tielt', 'country': 'Belgium', 'facility': 'Sint-Andriesziekenhuis Tielt', 'geoPoint': {'lat': 50.99931, 'lon': 3.32707}}, {'zip': 'B-5530', 'city': 'Yvoir', 'country': 'Belgium', 'facility': 'CHU UCL Mont-Godinne', 'geoPoint': {'lat': 50.3279, 'lon': 4.88059}}, {'zip': '52062', 'city': 'Aachen', 'country': 'Germany', 'facility': 'Downtown Clinic Aachen', 'geoPoint': {'lat': 50.77664, 'lon': 6.08342}}, {'zip': '52078', 'city': 'Aachen', 'country': 'Germany', 'facility': 'Praxis Delonge', 'geoPoint': {'lat': 50.77664, 'lon': 6.08342}}, {'zip': '92224', 'city': 'Amberg', 'country': 'Germany', 'facility': 'Praxis Osterziel', 'geoPoint': {'lat': 49.44287, 'lon': 11.86267}}, {'zip': '08280', 'city': 'Aue', 'country': 'Germany', 'facility': 'MVZ Helios Aue', 'geoPoint': {'lat': 50.59034, 'lon': 12.70657}}, {'zip': '08645', 'city': 'Bad Elster', 'country': 'Germany', 'facility': 'Kardiologische Praxis Enders', 'geoPoint': {'lat': 50.28192, 'lon': 12.2343}}, {'zip': '74177', 'city': 'Bad Friedrichshall', 'country': 'Germany', 'facility': 'SLK-Klinikum am Plattenwald'}, {'zip': '61348', 'city': 'Bad Homburg', 'country': 'Germany', 'facility': 'Herzcarre Praxis', 'geoPoint': {'lat': 50.22683, 'lon': 8.61816}}, {'zip': '61348', 'city': 'Bad Homburg', 'country': 'Germany', 'facility': 'Kardiologische Praxis', 'geoPoint': {'lat': 50.22683, 'lon': 8.61816}}, {'zip': '61348', 'city': 'Bad Homburg', 'country': 'Germany', 'facility': 'Zentrum für klinische Forschung', 'geoPoint': {'lat': 50.22683, 'lon': 8.61816}}, {'zip': '79189', 'city': 'Bad Krozingen', 'country': 'Germany', 'facility': 'Universitätsklinikum Freiburg - Universitäts-Herzzentrum', 'geoPoint': {'lat': 47.91667, 'lon': 7.7}}, {'zip': '23795', 'city': 'Bad Segeberg', 'country': 'Germany', 'facility': 'Praxis am Landratspark', 'geoPoint': {'lat': 53.93775, 'lon': 10.30745}}, {'zip': '72270', 'city': 'Baiersbronn', 'country': 'Germany', 'facility': 'Hausärzte am Spritzenhaus', 'geoPoint': {'lat': 48.50318, 'lon': 8.37699}}, {'zip': '96049', 'city': 'Bamberg', 'country': 'Germany', 'facility': 'CIMS Studienzentrum Bamberg GmbH Drs. 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