Raw JSON
{'hasResults': False, 'derivedSection': {'miscInfoModule': {'versionHolder': '2026-03-25'}, 'conditionBrowseModule': {'meshes': [{'id': 'D050177', 'term': 'Overweight'}, {'id': 'D009765', 'term': 'Obesity'}], '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'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'RANDOMIZED', 'maskingInfo': {'masking': 'QUADRUPLE', 'whoMasked': ['PARTICIPANT', 'CARE_PROVIDER', 'INVESTIGATOR', 'OUTCOMES_ASSESSOR'], 'maskingDescription': 'Sponsor staff involved in the clinical trial is masked according to company standard procedures.'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ESTIMATED', 'count': 1400}}, 'statusModule': {'overallStatus': 'NOT_YET_RECRUITING', 'startDateStruct': {'date': '2026-06-22', 'type': 'ESTIMATED'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2026-02', 'completionDateStruct': {'date': '2028-01-17', 'type': 'ESTIMATED'}, 'lastUpdateSubmitDate': '2026-02-24', 'studyFirstSubmitDate': '2026-01-21', 'studyFirstSubmitQcDate': '2026-01-21', 'lastUpdatePostDateStruct': {'date': '2026-02-25', 'type': 'ACTUAL'}, 'studyFirstPostDateStruct': {'date': '2026-01-22', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2027-11-29', 'type': 'ESTIMATED'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Relative change in body weight', 'timeFrame': 'From baseline (week 0) to end of treatment (week 44)', 'description': 'Measured in percentage (%).'}], 'secondaryOutcomes': [{'measure': 'Number of TEAEs (treatment emergent adverse events)', 'timeFrame': 'From baseline (week 0) to end of study (week 51)', 'description': 'Measured in count of events.'}, {'measure': 'Number of TESAEs (Treatment emergent serious adverse events)', 'timeFrame': 'From baseline (week 0) to end of study (week 51)', 'description': 'Measured in count of events.'}]}, 'oversightModule': {'oversightHasDmc': False, 'isFdaRegulatedDrug': True, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Overweight', 'Obesity']}, 'descriptionModule': {'briefSummary': 'This study is being done to find out how well a medicine called CagriSema helps people with overweight or obesity lose weight. CagriSema is still being tested in studies and is not yet available for doctors to prescribe. In this study the sponsor will compare two version of CagriSema injected by two different types of injection devices. Which treatment participants get is decided by chance using a computer program, so neither participants nor study staff will know which treatment is given. The study will last for about one year.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': 'Inclusion Criteria:\n\n* Male or female (sex at birth)\n* Age 18 years or above at the time of signing the informing consent.\n* Body Mass Index (BMI) is greater than or equal to (\\>= ) 30.0 kilograms per square metre (kg/m\\^2) or BMI \\>= 27.0 kg/m\\^2 with the presence of at least one obesity-related complication including, but not limited to, hypertension, dyslipidaemia, obstructive sleep apnoea or cardiovascular disease.\n\nExclusion Criteria:\n\n* Glycosylated haemoglobin (HbA1c) \\>= 6.5 % (48 millimoles per mole \\[mmol/mol\\]) as measured by the central laboratory at screening.\n* History of type 1 or type 2 diabetes.\n* Previous exposure to CagriSema in a clinical study.'}, 'identificationModule': {'nctId': 'NCT07357766', 'briefTitle': 'A Research Study to Compare Different Versions of Injectable CagriSema and Placebo in People With Excess Body Weight', 'organization': {'class': 'INDUSTRY', 'fullName': 'Novo Nordisk A/S'}, 'officialTitle': 'A Placebo-controlled Comparability Study to Compare Two Presentations of CagriSema in Participants With Overweight or Obesity', 'orgStudyIdInfo': {'id': 'NN9838-8166'}, 'secondaryIdInfos': [{'id': 'U1111-1317-0133', 'type': 'OTHER', 'domain': 'World Health Organization'}, {'id': '2024-520448-41', 'type': 'OTHER', 'domain': 'European Medical Agency (EMA)'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'CagriSema B in device 2 + Placebo in device 1', 'description': 'Participants will receive CagriSema B in device 2 followed by placebo matched to CagriSema in device 1 subcutaneously once weekly in a dose escalation manner for 16 weeks until the target maintenance dose and further continue to receive the same dose for up to 44 weeks.', 'interventionNames': ['Drug: Cagrisema']}, {'type': 'EXPERIMENTAL', 'label': 'CagriSema in device 1 + Placebo in device 2', 'description': 'Participants will receive CagriSema in device 1 followed by placebo matched to CagriSema B in device 2 subcutaneously once weekly in a dose escalation manner for 16 weeks until the target maintenance dose and further continue to receive the same dose for up to 44 weeks.', 'interventionNames': ['Drug: Cagrisema']}, {'type': 'PLACEBO_COMPARATOR', 'label': 'Placebo in device 1 + Placebo in device 2', 'description': 'Participants will receive placebo matched to Cagrisema in device 1 followed by placebo matched to CagriSema B in device 2 subcutaneously once weekly for up to 44 weeks.', 'interventionNames': ['Drug: Placebo CagriSema']}], 'interventions': [{'name': 'Cagrisema', 'type': 'DRUG', 'description': 'Cagrisema (Cagrilintide and Semaglutide) will be administered subcutaneously using device 1 or device 2.', 'armGroupLabels': ['CagriSema B in device 2 + Placebo in device 1', 'CagriSema in device 1 + Placebo in device 2']}, {'name': 'Placebo CagriSema', 'type': 'DRUG', 'description': 'Placebo matched to Cagrilintide and Placebo matched to Semaglutide will be administered subcutaneously using device 1 or device 2.', 'armGroupLabels': ['Placebo in device 1 + Placebo in device 2']}]}, 'contactsLocationsModule': {'locations': [{'zip': '35233', 'city': 'Birmingham', 'state': 'Alabama', 'country': 'United States', 'facility': 'Uni of Alabama at Birmingham', 'geoPoint': {'lat': 33.52066, 'lon': -86.80249}}, {'zip': '35124', 'city': 'Pelham', 'state': 'Alabama', 'country': 'United States', 'facility': 'Cahaba Research', 'geoPoint': {'lat': 33.28567, 'lon': -86.80999}}, {'zip': '90250', 'city': 'Hawthorne', 'state': 'California', 'country': 'United States', 'facility': 'Advanced Investigative Medicine, Inc.', 'geoPoint': {'lat': 33.9164, 'lon': -118.35257}}, {'zip': '92701', 'city': 'Santa Ana', 'state': 'California', 'country': 'United States', 'facility': 'Southern Cal Clinical Research', 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