Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24'}, 'conditionBrowseModule': {'meshes': [{'id': 'D009765', 'term': 'Obesity'}, {'id': 'D050177', 'term': 'Overweight'}, {'id': 'D003924', 'term': 'Diabetes Mellitus, Type 2'}], 'ancestors': [{'id': 'D044343', 'term': 'Overnutrition'}, {'id': 'D009748', 'term': 'Nutrition Disorders'}, {'id': 'D009750', 'term': 'Nutritional and Metabolic Diseases'}, {'id': 'D001835', 'term': 'Body Weight'}, {'id': 'D012816', 'term': 'Signs and Symptoms'}, {'id': 'D013568', 'term': 'Pathological Conditions, Signs and Symptoms'}, {'id': 'D003920', 'term': 'Diabetes Mellitus'}, {'id': 'D044882', 'term': 'Glucose Metabolism Disorders'}, {'id': 'D008659', 'term': 'Metabolic Diseases'}, {'id': 'D004700', 'term': 'Endocrine System Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C000729680', 'term': 'orforglipron'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'DOUBLE', 'whoMasked': ['PARTICIPANT', 'INVESTIGATOR']}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 1613}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2023-06-05', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-09', 'completionDateStruct': {'date': '2025-08-08', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2025-09-17', 'studyFirstSubmitDate': '2023-05-15', 'studyFirstSubmitQcDate': '2023-05-15', 'lastUpdatePostDateStruct': {'date': '2025-09-18', 'type': 'ESTIMATED'}, 'studyFirstPostDateStruct': {'date': '2023-05-24', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2025-08-08', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Mean Percent Change from Baseline in Body Weight', 'timeFrame': 'Baseline, Week 72'}], 'secondaryOutcomes': [{'measure': 'Mean Change from Baseline in Waist Circumference', 'timeFrame': 'Baseline, Week 72'}, {'measure': 'Mean Change from Baseline in Hemoglobin A1c (HbA1c) %', 'timeFrame': 'Baseline, Week 72'}, {'measure': 'Mean Change from Baseline in Fasting Glucose', 'timeFrame': 'Baseline, Week 72'}, {'measure': 'Mean Change from Baseline in Systolic Blood Pressure (SBP)', 'timeFrame': 'Baseline, Week 72'}, {'measure': 'Mean Change from Baseline in Fasting Triglycerides', 'timeFrame': 'Baseline, Week 72'}, {'measure': 'Mean Percent Change from Baseline in Fasting non-High-Density Lipoprotein (HDL) Cholesterol', 'timeFrame': 'Baseline, Week 72'}, {'measure': 'Mean Percent Change from Baseline in Fasting Insulin', 'timeFrame': 'Baseline, Week 72'}, {'measure': 'Mean Change from Baseline in Diastolic Blood Pressure (DBP)', 'timeFrame': 'Baseline, Week 72'}, {'measure': 'Mean Change from Baseline in Short Form 36 Version 2 Health Survey Acute Form (SF-36v2) Domain Scores', 'timeFrame': 'Baseline, Week 72'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': True, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Obesity', 'Overweight', 'Type 2 Diabetes']}, 'referencesModule': {'references': [{'pmid': '41275875', 'type': 'DERIVED', 'citation': 'Horn DB, Ryan DH, Kis SG, Alves B, Mu Y, Kim SG, Aberle J, Bain SC, Allen S, Sarker E, Wu Q, Stefanski A, Jouravskaya I; ATTAIN-2 Trial Investigators. Orforglipron, an oral small-molecule GLP-1 receptor agonist, for the treatment of obesity in people with type 2 diabetes (ATTAIN-2): a phase 3, double-blind, randomised, multicentre, placebo-controlled trial. Lancet. 2025 Nov 20:S0140-6736(25)02165-8. doi: 10.1016/S0140-6736(25)02165-8. Online ahead of print.'}], 'seeAlsoLinks': [{'url': 'https://trials.lilly.com/en-US/trial/404300', 'label': 'A Study of Orforglipron in Adult Participants With Obesity or Overweight and Type 2 Diabetes (ATTAIN-2)'}]}, 'descriptionModule': {'briefSummary': 'This study will investigate the safety and efficacy of once daily oral treatment with orforglipron compared with placebo on body weight in adult participants with obesity or overweight and type 2 diabetes. The study will last about 77 weeks and may include up to 22 visits.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Have a body mass index (BMI) ≥27.0 kilogram/square meter (kg/m²).\n* Have a history of at least 1 self-reported unsuccessful dietary effort to lose body weight.\n* Have a diagnosis of Type 2 Diabetes (T2D), with HbA1c ≥7% (≥53 mmol/mol) to ≤10% (86 mmol/mol) and are on stable treatment for T2D for at least 90 days prior to screening, consisting of:\n\n * either diet/exercise alone or\n * up to 3 oral antihyperglycemic medications (excluding dipeptidyl peptidase IV inhibitors (DPP-4i) or glucagon-like peptide-1 (GLP-1) receptor agonists (RA).\n\nExclusion Criteria:\n\n* Have Type 1 Diabetes (T1D), history of ketoacidosis or hyperosmolar state/coma, or any other types of diabetes except T2D.\n* Have a self-reported change in body weight \\>5 kg (11 pounds) within 90 days prior to screening.\n* Are currently receiving or planning to receive treatment for diabetic retinopathy and/or macular edema (for example, laster photocoagulation or intravitreal injections of anti-vascular endothelial growth factor inhibitors).\n* Have family (first-degree relative) or personal history of medullary thyroid cancer (MTC) or multiple endocrine neoplasia 2 (MEN2) syndrome.\n* Have had a history of chronic or acute pancreatitis.'}, 'identificationModule': {'nctId': 'NCT05872620', 'acronym': 'ATTAIN-2', 'briefTitle': 'A Study of Orforglipron in Adult Participants With Obesity or Overweight and Type 2 Diabetes', 'organization': {'class': 'INDUSTRY', 'fullName': 'Eli Lilly and Company'}, 'officialTitle': 'A Phase 3, Randomized, Double-Blind Study to Investigate the Efficacy and Safety of Once-Daily Oral LY3502970 Compared With Placebo in Adult Participants With Obesity or Overweight and Type 2 Diabetes (ATTAIN-2)', 'orgStudyIdInfo': {'id': '18560'}, 'secondaryIdInfos': [{'id': 'J2A-MC-GZGQ', 'type': 'OTHER', 'domain': 'Eli Lilly and Company'}, {'id': '2022-502837-24-00', 'type': 'OTHER', 'domain': 'Eli Lilly and Company'}, {'id': 'U1111-1289-8799', 'type': 'OTHER', 'domain': 'UTN Number'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Orforglipron Dose 1', 'description': 'Participants will receive orforglipron administered orally.', 'interventionNames': ['Drug: Orforglipron']}, {'type': 'EXPERIMENTAL', 'label': 'Orforglipron Dose 2', 'description': 'Participants will receive orforglipron administered orally.', 'interventionNames': ['Drug: Orforglipron']}, {'type': 'EXPERIMENTAL', 'label': 'Orforglipron Dose 3', 'description': 'Participants will receive orforglipron administered orally.', 'interventionNames': ['Drug: Orforglipron']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Placebo', 'description': 'Participants will receive placebo', 'interventionNames': ['Drug: Placebo']}], 'interventions': [{'name': 'Orforglipron', 'type': 'DRUG', 'otherNames': ['LY3502970'], 'description': 'Administered orally', 'armGroupLabels': ['Orforglipron Dose 1', 'Orforglipron Dose 2', 'Orforglipron Dose 3']}, {'name': 'Placebo', 'type': 'DRUG', 'description': 'Administered orally', 'armGroupLabels': ['Placebo']}]}, 'contactsLocationsModule': {'locations': [{'zip': '35124', 'city': 'Pelham', 'state': 'Alabama', 'country': 'United States', 'facility': 'Cahaba Research - Pelham', 'geoPoint': {'lat': 33.28567, 'lon': -86.80999}}, {'zip': '85741', 'city': 'Tucson', 'state': 'Arizona', 'country': 'United States', 'facility': 'Novak Clinical Research - Tucson - North La Cholla Boulevard', 'geoPoint': {'lat': 32.22174, 'lon': -110.92648}}, {'zip': '85364', 'city': 'Yuma', 'state': 'Arizona', 'country': 'United States', 'facility': 'Yuma Clinical Trials', 'geoPoint': {'lat': 32.72532, 'lon': -114.6244}}, {'zip': '92025', 'city': 'Escondido', 'state': 'California', 'country': 'United 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