Ignite Creation Date:
2025-12-25 @ 3:46 AM
Ignite Modification Date:
2025-12-26 @ 2:33 AM
Study NCT ID:
NCT05517902
Status:
COMPLETED
Last Update Posted:
2025-03-18
First Post:
2022-08-24
Is NOT Gene Therapy:
False
Has Adverse Events:
True
Brief Title:
StrataGraft Safety, Tolerability and Efficacy in Pediatric Subjects
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24', 'submissionTracking': {'firstMcpInfo': {'postDateStruct': {'date': '2025-02-05', 'type': 'ACTUAL'}}}}, 'conditionBrowseModule': {'meshes': [{'id': 'D002056', 'term': 'Burns'}], 'ancestors': [{'id': 'D014947', 'term': 'Wounds and Injuries'}]}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'medinfo@mnk.com', 'phone': '1-800-844-2830', 'title': 'Medical Information Call Center', 'organization': 'Mallinckrodt'}, 'certainAgreement': {'piSponsorEmployee': False, 'restrictiveAgreement': True}, 'limitationsAndCaveats': {'description': 'This study had low accrual and only 1 participant was enrolled.'}}, 'adverseEventsModule': {'timeFrame': 'Up to 12 months', 'description': 'Safety population included all participants who were enrolled and received StrataGraft.', 'eventGroups': [{'id': 'EG000', 'title': '2 to < 12 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.', 'otherNumAtRisk': 1, 'deathsNumAtRisk': 1, 'otherNumAffected': 1, 'seriousNumAtRisk': 1, 'deathsNumAffected': 0, 'seriousNumAffected': 0}, {'id': 'EG001', 'title': '12 to ≤ 17 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.', 'otherNumAtRisk': 0, 'deathsNumAtRisk': 0, 'otherNumAffected': 0, 'seriousNumAtRisk': 0, 'deathsNumAffected': 0, 'seriousNumAffected': 0}], 'otherEvents': [{'term': 'Atelectasis', 'stats': [{'groupId': 'EG000', 'numAtRisk': 1, 'numAffected': 1}, {'groupId': 'EG001', 'numAtRisk': 0, 'numAffected': 0}], 'organSystem': 'Respiratory, thoracic and mediastinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MedDRA 25.0'}, {'term': 'Bronchitis', 'stats': [{'groupId': 'EG000', 'numAtRisk': 1, 'numAffected': 1}, {'groupId': 'EG001', 'numAtRisk': 0, 'numAffected': 0}], 'organSystem': 'Infections and infestations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MedDRA 25.0'}, {'term': 'Pruritus', 'stats': [{'groupId': 'EG000', 'numAtRisk': 1, 'numAffected': 1}, {'groupId': 'EG001', 'numAtRisk': 0, 'numAffected': 0}], 'organSystem': 'Skin and subcutaneous tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MedDRA 25.0'}, {'term': 'Rash', 'stats': [{'groupId': 'EG000', 'numAtRisk': 1, 'numAffected': 1}, {'groupId': 'EG001', 'numAtRisk': 0, 'numAffected': 0}], 'organSystem': 'Skin and subcutaneous tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MedDRA 25.0'}, {'term': 'Wound infection', 'stats': [{'groupId': 'EG000', 'numAtRisk': 1, 'numAffected': 1}, {'groupId': 'EG001', 'numAtRisk': 0, 'numAffected': 0}], 'organSystem': 'Infections and infestations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MedDRA 25.0'}], 'frequencyThreshold': '0'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'PRIMARY', 'title': 'Percentage of Participants Who Achieved Confirmed Complete Closure of StrataGraft Treatment Sites Without Autograft Within 12 Weeks of StrataGraft Application', 'denoms': [{'units': 'Participants', 'counts': [{'value': '1', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': '2 to < 12 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}, {'id': 'OG001', 'title': '12 to ≤ 17 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}], 'classes': [{'categories': [{'measurements': [{'value': '100', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Up to Week 12', 'description': "Confirmed complete wound closure is defined as complete skin re-epithelialization confirmed at 2 consecutive visits at least 2 weeks apart, but no later than Week 20. Percentage of participants whose burn healed after StrataGraft treatment without needing the doctor to treat the burn with skin cut from other parts of the patient's own body were reported.", 'unitOfMeasure': 'percentage of participants', 'reportingStatus': 'POSTED', 'populationDescription': 'Safety population included all participants who were enrolled and received StrataGraft.'}, {'type': 'PRIMARY', 'title': 'Number of Participants With Treatment-emergent Adverse Events (TEAEs)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '1', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': '2 to < 12 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}, {'id': 'OG001', 'title': '12 to ≤ 17 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}], 'classes': [{'categories': [{'measurements': [{'value': '1', 'groupId': 'OG000'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'timeFrame': 'Up to Month 12', 'description': 'An adverse event (AE) is any untoward or undesirable medical occurrence in a participant who is administered a study treatment, which does not necessarily have to have a causal relationship with this treatment. TEAEs are AEs with an onset date on or after the start of StrataGraft treatment.', 'unitOfMeasure': 'Participants', 'reportingStatus': 'POSTED', 'populationDescription': 'Safety population included all participants who were enrolled and received StrataGraft.'}, {'type': 'SECONDARY', 'title': 'Percentage of StrataGraft Treatment Sites Per Participant Closed at Week 12 Without Autograft Placement', 'denoms': [{'units': 'Participants', 'counts': [{'value': '1', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': '2 to < 12 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}, {'id': 'OG001', 'title': '12 to ≤ 17 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}], 'classes': [{'categories': [{'measurements': [{'value': '100', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'At Week 12', 'description': 'Wound closure was evaluated through visual inspection by the investigator. Complete wound closure was defined as "complete re-epithelialization of the wound without drainage," confirmed at 2 consecutive visits at least 2 weeks apart.', 'unitOfMeasure': 'percentage of treatment sites', 'reportingStatus': 'POSTED', 'populationDescription': 'Safety population included all participants who were enrolled and received StrataGraft.'}, {'type': 'SECONDARY', 'title': 'Number of Confirmed Complete Wound Closures of the StrataGraft Treatment Sites on or Before Week 12 Without Autograft Placement', 'denoms': [{'units': 'Participants', 'counts': [{'value': '1', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': '2 to < 12 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}, {'id': 'OG001', 'title': '12 to ≤ 17 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}], 'classes': [{'categories': [{'measurements': [{'value': '1', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Up to Week 12', 'description': 'Complete wound closure was defined as "complete re-epithelialization of the wound without drainage," confirmed at two consecutive visits at least two weeks apart.', 'unitOfMeasure': 'number of complete wound closure', 'reportingStatus': 'POSTED', 'populationDescription': 'Safety population included all participants who were enrolled and received StrataGraft.'}, {'type': 'SECONDARY', 'title': 'Mean of Averaged Percent Area of StrataGraft Treatment Sites Per Participant Autografted by Week 12', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '0', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': '2 to < 12 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}, {'id': 'OG001', 'title': '12 to ≤ 17 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}], 'timeFrame': 'Up to Week 12', 'reportingStatus': 'POSTED', 'populationDescription': 'Safety population included all participants who were enrolled and received StrataGraft. None of the participant had StrataGraft treatment site that required autografting.'}]}, 'participantFlowModule': {'groups': [{'id': 'FG000', 'title': '2 to < 12 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% total body surface area (TBSA) on Day 1.'}, {'id': 'FG001', 'title': '12 to ≤ 17 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}], 'periods': [{'title': 'Overall Study', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '1'}, {'groupId': 'FG001', 'numSubjects': '0'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '1'}, {'groupId': 'FG001', 'numSubjects': '0'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '0'}]}]}], 'recruitmentDetails': 'Participant took part in the study at a single clinical site in the United States from 28 April 2023 to 9 May 2024.'}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '1', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}]}], 'groups': [{'id': 'BG000', 'title': '2 to < 12 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}, {'id': 'BG001', 'title': '12 to ≤ 17 Years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.'}, {'id': 'BG002', 'title': 'Total', 'description': 'Total of all reporting groups'}], 'measures': [{'title': 'Age, Categorical', 'classes': [{'categories': [{'title': '<=18 years', 'measurements': [{'value': '1', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}]}, {'title': 'Between 18 and 65 years', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': '>=65 years', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'Male', 'measurements': [{'value': '1', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Ethnicity (NIH/OMB)', 'classes': [{'categories': [{'title': 'Hispanic or Latino', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'Not Hispanic or Latino', 'measurements': [{'value': '1', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}]}, {'title': 'Unknown or Not Reported', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Race (NIH/OMB)', 'classes': [{'categories': [{'title': 'American Indian or Alaska Native', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'Asian', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'Native Hawaiian or Other Pacific Islander', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'Black or African American', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'White', 'measurements': [{'value': '1', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}]}, {'title': 'More than one race', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}, {'title': 'Unknown or Not Reported', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}], 'populationDescription': 'Safety population included all participants who were enrolled and received StrataGraft.'}}, 'documentSection': {'largeDocumentModule': {'largeDocs': [{'date': '2023-09-26', 'size': 1352875, 'label': 'Study Protocol and Statistical Analysis Plan: Study Protocol and Statistical Analysis Plan', 'hasIcf': False, 'hasSap': True, 'filename': 'Prot_SAP_000.pdf', 'typeAbbrev': 'Prot_SAP', 'uploadDate': '2025-01-09T07:34', 'hasProtocol': True}, {'date': '2024-07-03', 'size': 1033476, 'label': 'Statistical Analysis Plan: Statistical Analysis Plan_Memo', 'hasIcf': False, 'hasSap': True, 'filename': 'SAP_001.pdf', 'typeAbbrev': 'SAP', 'uploadDate': '2025-01-09T07:40', 'hasProtocol': False}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE3'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NON_RANDOMIZED', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'PARALLEL'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 1}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2023-04-28', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2025-02', 'completionDateStruct': {'date': '2024-05-09', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2025-02-27', 'studyFirstSubmitDate': '2022-08-24', 'resultsFirstSubmitDate': '2025-01-09', 'studyFirstSubmitQcDate': '2022-08-24', 'lastUpdatePostDateStruct': {'date': '2025-03-18', 'type': 'ACTUAL'}, 'resultsFirstSubmitQcDate': '2025-02-27', 'studyFirstPostDateStruct': {'date': '2022-08-26', 'type': 'ACTUAL'}, 'resultsFirstPostDateStruct': {'date': '2025-03-18', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2024-05-09', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Percentage of Participants Who Achieved Confirmed Complete Closure of StrataGraft Treatment Sites Without Autograft Within 12 Weeks of StrataGraft Application', 'timeFrame': 'Up to Week 12', 'description': "Confirmed complete wound closure is defined as complete skin re-epithelialization confirmed at 2 consecutive visits at least 2 weeks apart, but no later than Week 20. Percentage of participants whose burn healed after StrataGraft treatment without needing the doctor to treat the burn with skin cut from other parts of the patient's own body were reported."}, {'measure': 'Number of Participants With Treatment-emergent Adverse Events (TEAEs)', 'timeFrame': 'Up to Month 12', 'description': 'An adverse event (AE) is any untoward or undesirable medical occurrence in a participant who is administered a study treatment, which does not necessarily have to have a causal relationship with this treatment. TEAEs are AEs with an onset date on or after the start of StrataGraft treatment.'}], 'secondaryOutcomes': [{'measure': 'Percentage of StrataGraft Treatment Sites Per Participant Closed at Week 12 Without Autograft Placement', 'timeFrame': 'At Week 12', 'description': 'Wound closure was evaluated through visual inspection by the investigator. Complete wound closure was defined as "complete re-epithelialization of the wound without drainage," confirmed at 2 consecutive visits at least 2 weeks apart.'}, {'measure': 'Number of Confirmed Complete Wound Closures of the StrataGraft Treatment Sites on or Before Week 12 Without Autograft Placement', 'timeFrame': 'Up to Week 12', 'description': 'Complete wound closure was defined as "complete re-epithelialization of the wound without drainage," confirmed at two consecutive visits at least two weeks apart.'}, {'measure': 'Mean of Averaged Percent Area of StrataGraft Treatment Sites Per Participant Autografted by Week 12', 'timeFrame': 'Up to Week 12'}]}, 'oversightModule': {'oversightHasDmc': True, 'isFdaRegulatedDrug': True, 'isFdaRegulatedDevice': False}, 'conditionsModule': {'conditions': ['Skin Wound', 'Burns', 'Trauma-related Wound']}, 'descriptionModule': {'briefSummary': "Autografting is a surgical procedure to transplant healthy skin (donor skin) from another part of the participant's own body (donor site) to the burned part. Autografting is the usual treatment for DPT burns.\n\nIt works to close the wound, but can cause other problems:\n\n* Donor sites are painful, can become infected or scarred, or can even become full thickness (FT) wounds themselves\n* Treatment problems can require more grafting\n* Additional surgery increases the risk of medical problems caused by the treatment\n\nStratatech is trying to find a safe and effective alternative to autografting to promote the healing of severe burns. The purpose of this study was to evaluate whether StrataGraft treatment eliminates or reduces the need for autografting and promotes wound closure in a pediatric population with thermal burns that contain intact dermal elements and for which autografting is clinically indicated (DPT burns).\n\nParticipants were enrolled into one of two age-based cohorts: 2 to \\< 12 years and 12 to ≤ 17 years to receive a single application of StrataGraft, in up to 3 non-contiguous DPT burn areas located on the same extremity or plane of the torso."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD'], 'maximumAge': '17 Years', 'minimumAge': '2 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Written informed consent provided by the parent(s) or legal guardian(s) and assent from the child when appropriate\n* Have enough healthy skin to reserve as donor site(s), in case autografting becomes necessary\n* Thermal burns of no more than a total of 30% TBSA\n* Study treatment sites that are DPT in depth and which are clinically indicated for excision and autografting, and located on the torso or extremities\n* Study treatment area(s) totaling 0.5% to 10% TBSA and may be composed of up to 3 non-contiguous areas located on the same extremity or plane of the torso\n* Sufficient healthy skin available and reserved as a donor site in the event that the StrataGraft treatment site requires autografting\n\nExclusion Criteria:\n\n* Is pregnant or breastfeeding\n* Receiving treatment to suppress the immune system and/or systemic corticosteroids (inhaled corticosteroids are permitted)\n* A known history of malignancy\n* Pre-admission insulin-dependent diabetes\n* Concurrent trauma, conditions, and/or personal situations that, in the opinion of the investigator, may compromise the participant's safety or the study objectives\n* A burn injury that occurred ≥ 14 days prior to planned StrataGraft application Is expected to survive less than 12 months\n* Is participating in another interventional trial, or did within 90 days before enrollment\n* A proposed study treatment site that has been previously excised or autografted; located adjacent to an undebrided/unexcised burn area; demonstrates signs and symptoms of wound infection, per judgement of the clinical investigator; lies across joints or is located on the feet (i.e., distal to the malleolus), hands (distal to the wrist), face, neck, buttocks, perineum, or genitalia"}, 'identificationModule': {'nctId': 'NCT05517902', 'acronym': 'StrataSTEPS', 'briefTitle': 'StrataGraft Safety, Tolerability and Efficacy in Pediatric Subjects', 'organization': {'class': 'INDUSTRY', 'fullName': 'Mallinckrodt'}, 'officialTitle': 'A Phase 3 Multicenter, Single-Arm, Open-Label Study Evaluating the Safety, Tolerability and Efficacy of StrataGraft® Construct in Pediatric Subjects With Deep Partial Thickness (DPT) Thermal Burns', 'orgStudyIdInfo': {'id': 'MNK15011001'}}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': '2 to < 12 years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% total body surface area (TBSA) on Day 1.', 'interventionNames': ['Biological: StrataGraft']}, {'type': 'EXPERIMENTAL', 'label': '12 to ≤ 17 years Age Group Cohort', 'description': 'Single application of StrataGraft to 0.5% to 10% TBSA on Day 1.', 'interventionNames': ['Biological: StrataGraft']}], 'interventions': [{'name': 'StrataGraft', 'type': 'BIOLOGICAL', 'description': 'StrataGraft® Construct', 'armGroupLabels': ['12 to ≤ 17 years Age Group Cohort', '2 to < 12 years Age Group Cohort']}]}, 'contactsLocationsModule': {'locations': [{'zip': '53715', 'city': 'Madison', 'state': 'Wisconsin', 'country': 'United States', 'facility': 'Research Site', 'geoPoint': {'lat': 43.07305, 'lon': -89.40123}}], 'overallOfficials': [{'name': 'Clinical Team Leader', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Stratatech, a Mallinckrodt Company'}]}, 'ipdSharingStatementModule': {'ipdSharing': 'NO'}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Stratatech, a Mallinckrodt Company', 'class': 'INDUSTRY'}, 'collaborators': [{'name': 'Biomedical Advanced Research and Development Authority', 'class': 'FED'}], 'responsibleParty': {'type': 'SPONSOR'}}}}