Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24', 'removedCountries': ['Austria', 'Ireland']}, 'interventionBrowseModule': {'meshes': [{'id': 'C000594389', 'term': 'atezolizumab'}]}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'genentech@druginfo.com', 'phone': '800-821-8590', 'title': 'Medical Communications', 'organization': 'Hoffmann-La Roche'}, 'certainAgreement': {'otherDetails': "The Study being conducted under this Agreement is part of the Overall Study. Investigator is free to publish in reputable journals or to present at professional conferences the results of the Study, but only after the first publication or presentation that involves the Overall Study. The Sponsor may request that Confidential Information be deleted and/or the publication be postponed in order to protect the Sponsor's intellectual property rights.", 'restrictionType': 'OTHER', 'piSponsorEmployee': False, 'restrictiveAgreement': True}}, 'adverseEventsModule': {'timeFrame': 'From baseline up to approximately 42 months', 'description': 'Adverse Events reporting is for the Safety Evaluable Population, defined as patients who received any amount of any component of study treatment.', 'eventGroups': [{'id': 'EG000', 'title': 'COHORT 1', 'description': 'EWING SARCOMA', 'otherNumAtRisk': 11, 'deathsNumAtRisk': 11, 'otherNumAffected': 11, 'seriousNumAtRisk': 11, 'deathsNumAffected': 6, 'seriousNumAffected': 4}, {'id': 'EG001', 'title': 'COHORT 2', 'description': 'HODGKIN LYMPHOMA', 'otherNumAtRisk': 9, 'deathsNumAtRisk': 9, 'otherNumAffected': 8, 'seriousNumAtRisk': 9, 'deathsNumAffected': 5, 'seriousNumAffected': 3}, {'id': 'EG002', 'title': 'COHORT 3', 'description': 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'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MedDRA version 22.0'}, {'term': 'RASH MACULO-PAPULAR', 'stats': [{'groupId': 'EG000', 'numAtRisk': 11, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG001', 'numAtRisk': 9, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG002', 'numAtRisk': 11, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG003', 'numAtRisk': 3, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG004', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG005', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG006', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG007', 'numAtRisk': 10, 'numEvents': 1, 'numAffected': 1}, {'groupId': 'EG008', 'numAtRisk': 4, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG009', 'numAtRisk': 4, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG010', 'numAtRisk': 2, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG011', 'numAtRisk': 3, 'numEvents': 0, 'numAffected': 0}], 'organSystem': 'Skin and subcutaneous tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MedDRA version 22.0'}, {'term': 'TOXIC SKIN ERUPTION', 'stats': [{'groupId': 'EG000', 'numAtRisk': 11, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG001', 'numAtRisk': 9, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG002', 'numAtRisk': 11, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG003', 'numAtRisk': 3, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG004', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG005', 'numAtRisk': 10, 'numEvents': 1, 'numAffected': 1}, {'groupId': 'EG006', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG007', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG008', 'numAtRisk': 4, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG009', 'numAtRisk': 4, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG010', 'numAtRisk': 2, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG011', 'numAtRisk': 3, 'numEvents': 0, 'numAffected': 0}], 'organSystem': 'Skin and subcutaneous tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MedDRA version 22.0'}, {'term': 'SHOCK HAEMORRHAGIC', 'stats': [{'groupId': 'EG000', 'numAtRisk': 11, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG001', 'numAtRisk': 9, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG002', 'numAtRisk': 11, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG003', 'numAtRisk': 3, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG004', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG005', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG006', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG007', 'numAtRisk': 10, 'numEvents': 1, 'numAffected': 1}, {'groupId': 'EG008', 'numAtRisk': 4, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG009', 'numAtRisk': 4, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG010', 'numAtRisk': 2, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG011', 'numAtRisk': 3, 'numEvents': 0, 'numAffected': 0}], 'organSystem': 'Vascular disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MedDRA version 22.0'}, {'term': 'SUPERIOR VENA CAVA SYNDROME', 'stats': [{'groupId': 'EG000', 'numAtRisk': 11, 'numEvents': 1, 'numAffected': 1}, {'groupId': 'EG001', 'numAtRisk': 9, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG002', 'numAtRisk': 11, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG003', 'numAtRisk': 3, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG004', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG005', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG006', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG007', 'numAtRisk': 10, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG008', 'numAtRisk': 4, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG009', 'numAtRisk': 4, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG010', 'numAtRisk': 2, 'numEvents': 0, 'numAffected': 0}, {'groupId': 'EG011', 'numAtRisk': 3, 'numEvents': 0, 'numAffected': 0}], 'organSystem': 'Vascular disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT', 'sourceVocabulary': 'MedDRA version 22.0'}], 'frequencyThreshold': '5'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'PRIMARY', 'title': 'Percentage of Participants With an Objective Response (Complete Response [CR] or Partial Response [PR]) as Determined by the Investigator Using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) in Participants With Solid Tumors', 'denoms': [{'units': 'Participants', 'counts': [{'value': '11', 'groupId': 'OG000'}, {'value': '10', 'groupId': 'OG001'}, {'value': '10', 'groupId': 'OG002'}, {'value': '10', 'groupId': 'OG003'}, {'value': '10', 'groupId': 'OG004'}, {'value': '4', 'groupId': 'OG005'}, {'value': '4', 'groupId': 'OG006'}, {'value': '2', 'groupId': 'OG007'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 1', 'description': 'Participants with ewing sarcoma'}, {'id': 'OG001', 'title': 'Cohort 5', 'description': 'Participants with non-rhabdomyosarcoma soft tissue sarcoma'}, {'id': 'OG002', 'title': 'Cohort 6', 'description': 'Participants with osteosarcoma.'}, {'id': 'OG003', 'title': 'Cohort 7', 'description': 'Participants with rhabdomyosarcoma'}, {'id': 'OG004', 'title': 'Cohort 8', 'description': 'Participants with wilms tumor'}, {'id': 'OG005', 'title': 'Cohort 9', 'description': 'Participants with other tumor types with documented PD-L1 expression.'}, {'id': 'OG006', 'title': 'Cohort 10', 'description': 'Participants with other tumor types without documented PD-L1 expression.'}, {'id': 'OG007', 'title': 'Cohort 11', 'description': 'Participants with rhabdoid tumor.'}], 'classes': [{'categories': [{'measurements': [{'value': '0', 'groupId': 'OG000'}, {'value': '10.0', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}, {'value': '0', 'groupId': 'OG003'}, {'value': '0', 'groupId': 'OG004'}, {'value': '0', 'groupId': 'OG005'}, {'value': '0', 'groupId': 'OG006'}, {'value': '0', 'groupId': 'OG007'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'description': 'Note: In Cohort 5, the response was observed in a rhabdoid tumor. Participant was erroneously enrolled in the Non-rhabdomyosarcoma soft tissue sarcoma cohort.', 'unitOfMeasure': 'Percentage', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'PRIMARY', 'title': 'Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using Modified International Neuroblastoma Response Criteria (mINRC) in Participants With Neuroblastoma', 'denoms': [{'units': 'Participants', 'counts': [{'value': '11', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 3', 'description': 'Participants with neuroblastoma.'}], 'classes': [{'categories': [{'measurements': [{'value': '0', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Percentage', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'PRIMARY', 'title': "Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using Revised Response Criteria for Malignant Lymphoma for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'denoms': [{'units': 'Participants', 'counts': [{'value': '9', 'groupId': 'OG000'}, {'value': '3', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 2', 'description': "Participants with Hodgkin's lymphoma"}, {'id': 'OG001', 'title': 'Cohort 4', 'description': "Participants with non-Hodgkin's lymphoma"}], 'classes': [{'categories': [{'measurements': [{'value': '22.2', 'groupId': 'OG000'}, {'value': '33.3', 'groupId': 'OG001'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Percentage', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'PRIMARY', 'title': 'Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using Response Assessment in Neuro-Oncology (RANO) Criteria in Participants With Atypical Teratoid Rhabdoid Tumor (ATRT)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '3', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 12', 'description': 'Participants with atypical teratoid rhabdoid tumor.'}], 'classes': [{'categories': [{'measurements': [{'value': '0', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Percentage', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'PRIMARY', 'title': 'Percentage of Participants With Clinical Benefit as Determined by the Investigator According to RECIST v1.1 Criteria in Participants With Osteosarcoma', 'denoms': [{'units': 'Participants', 'counts': [{'value': '10', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 6', 'description': 'Participants with osteosarcoma.'}], 'classes': [{'categories': [{'measurements': [{'value': '0', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Percentage', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population (defined as patients who received any amount of study drug), in the Osteosarcoma cohort as per protocol. (Objective response for the other cohorts are measured with different response criteria, and these are described in Outcome Measures 1, 2, 3, and 4).'}, {'type': 'PRIMARY', 'title': 'Progression-Free Survival (PFS) as Determined by the Investigator Using RECIST v1.1 in Participants With Solid Tumors', 'denoms': [{'units': 'Participants', 'counts': [{'value': '11', 'groupId': 'OG000'}, {'value': '10', 'groupId': 'OG001'}, {'value': '10', 'groupId': 'OG002'}, {'value': '10', 'groupId': 'OG003'}, {'value': '10', 'groupId': 'OG004'}, {'value': '4', 'groupId': 'OG005'}, {'value': '4', 'groupId': 'OG006'}, {'value': '2', 'groupId': 'OG007'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 1', 'description': 'Participants with ewing sarcoma.'}, {'id': 'OG001', 'title': 'Cohort 5', 'description': 'Participants with non-rhabdomyosarcoma soft tissue sarcoma'}, {'id': 'OG002', 'title': 'Cohort 6', 'description': 'Participants with osteosarcoma.'}, {'id': 'OG003', 'title': 'Cohort 7', 'description': 'Participants with rhabdomyosarcoma.'}, {'id': 'OG004', 'title': 'Cohort 8', 'description': 'Participants with wilms tumor.'}, {'id': 'OG005', 'title': 'Cohort 9', 'description': 'Participants with other tumor types with documented PD-L1 expression.'}, {'id': 'OG006', 'title': 'Cohort 10', 'description': 'Participant with other tumor types without documented PD-L1 expression.'}, {'id': 'OG007', 'title': 'Cohort 11', 'description': 'Participants with rhabdoid tumor.'}], 'classes': [{'categories': [{'measurements': [{'value': '1.2', 'groupId': 'OG000', 'lowerLimit': '0.6', 'upperLimit': '1.4'}, {'value': '1.3', 'groupId': 'OG001', 'lowerLimit': '1.1', 'upperLimit': '1.4'}, {'value': '1.2', 'groupId': 'OG002', 'lowerLimit': '0.7', 'upperLimit': '1.8'}, {'value': '1.1', 'groupId': 'OG003', 'lowerLimit': '0.8', 'upperLimit': '1.3'}, {'value': '1.3', 'groupId': 'OG004', 'lowerLimit': '1.1', 'upperLimit': '1.5'}, {'value': '1.2', 'groupId': 'OG005', 'lowerLimit': '0.7', 'upperLimit': '1.3'}, {'value': '1.2', 'groupId': 'OG006', 'lowerLimit': '1.1', 'upperLimit': '10.1'}, {'value': '0.7', 'groupId': 'OG007', 'lowerLimit': '0.3', 'upperLimit': '1.1'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until first documented occurrence of progressive disease, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'PRIMARY', 'title': 'PFS as Determined by the Investigator Using mINRC in Participants With Neuroblastoma', 'denoms': [{'units': 'Participants', 'counts': [{'value': '11', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 3', 'description': 'Participants with neuroblastoma.'}], 'classes': [{'categories': [{'measurements': [{'value': '2.6', 'groupId': 'OG000', 'lowerLimit': '1.2', 'upperLimit': '4.7'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until first documented occurrence of progressive disease, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'PRIMARY', 'title': "PFS as Determined by the Investigator Using Revised Response Criteria for Malignant Lymphoma for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'denoms': [{'units': 'Participants', 'counts': [{'value': '9', 'groupId': 'OG000'}, {'value': '3', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 2', 'description': "Participants with hodgkin's lymphoma."}, {'id': 'OG001', 'title': 'Cohort 4', 'description': "Participants with non-hodgkin's lymphoma."}], 'classes': [{'categories': [{'measurements': [{'value': '2.8', 'groupId': 'OG000', 'lowerLimit': '2.6', 'upperLimit': '4.4'}, {'value': '1.4', 'comment': 'More than 50% patient was censored.', 'groupId': 'OG001', 'lowerLimit': '1.1', 'upperLimit': 'NA'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until first documented occurrence of progressive disease, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'PRIMARY', 'title': 'PFS as Determined by the Investigator Using RANO Criteria in Participants With ATRT', 'denoms': [{'units': 'Participants', 'counts': [{'value': '3', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 12', 'description': 'Participants with atypical teratoid rhabdoid tumor.'}], 'classes': [{'categories': [{'measurements': [{'value': '1.4', 'groupId': 'OG000', 'lowerLimit': '1.4', 'upperLimit': '1.7'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until first documented occurrence of progressive disease, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'PRIMARY', 'title': 'Percentage of Participants Adverse Events, Serious Adverse Events and Adverse Events of Special Interest', 'denoms': [{'units': 'Participants', 'counts': [{'value': '87', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Atezolizumab', 'description': 'Participants received intravenous (IV) infusion of atezolizumab (maximum 1200 milligrams \\[mg\\]) on Day 1 of each 21-day cycle.'}], 'classes': [{'title': 'Adverse Events', 'categories': [{'measurements': [{'value': '97.7', 'groupId': 'OG000'}]}]}, {'title': 'Serious Adverse Events', 'categories': [{'measurements': [{'value': '37.9', 'groupId': 'OG000'}]}]}, {'title': 'Adverse Events of Special Interest', 'categories': [{'measurements': [{'value': '44.8', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'From baseline up to approximately 42 months', 'unitOfMeasure': 'Percentage', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'PRIMARY', 'title': 'Maximum Serum Concentration (Cmax) of Atezolizumab', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '26', 'groupId': 'OG001'}, {'value': '34', 'groupId': 'OG002'}, {'value': '18', 'groupId': 'OG003'}]}], 'groups': [{'id': 'OG000', 'title': '<2 Age (Years)', 'description': 'Participants \\<2 Age (Years)'}, {'id': 'OG001', 'title': '2 to <12 Age (Years)', 'description': 'Participants 2 to \\<12 Age (Years)'}, {'id': 'OG002', 'title': '12 to <18 Age (Years)', 'description': 'Participants 12 to \\<18 Age (Years)'}, {'id': 'OG003', 'title': '>=18 Age (Years)', 'description': 'Participants \\>=18 Age (Years)'}], 'classes': [{'title': 'Cycle 1', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '26', 'groupId': 'OG001'}, {'value': '34', 'groupId': 'OG002'}, {'value': '18', 'groupId': 'OG003'}]}], 'categories': [{'measurements': [{'value': '105', 'spread': '6.90', 'groupId': 'OG000'}, {'value': '312', 'spread': '28.7', 'groupId': 'OG001'}, {'value': '337', 'spread': '26.8', 'groupId': 'OG002'}, {'value': '424', 'spread': '26.9', 'groupId': 'OG003'}]}]}, {'title': 'Cycle 4', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '11', 'groupId': 'OG001'}, {'value': '16', 'groupId': 'OG002'}, {'value': '6', 'groupId': 'OG003'}]}], 'categories': [{'measurements': [{'value': '382', 'spread': '16.4', 'groupId': 'OG001'}, {'value': '373', 'spread': '78.9', 'groupId': 'OG002'}, {'value': '626', 'spread': '29.2', 'groupId': 'OG003'}]}]}], 'paramType': 'GEOMETRIC_MEAN', 'timeFrame': 'Predose (PRD; 0 hours [hr]), 0.5 hr post-infusion (P-I; infusion duration=30-60 minutes) on Day (D) 1 of Cycle (Cy) 1 and 4 (1 Cy=21 days)', 'unitOfMeasure': 'ug/mL', 'dispersionType': 'Geometric Coefficient of Variation', 'reportingStatus': 'POSTED', 'populationDescription': 'Included PK population, defined as patients who had received any amount of study drug and had at least one serum concentration result available at clinical data cutoff. In the "\\<2 Age (Years)" Arm/Group, 1 participant died after study entry with 1 cycle, and the other participant died after two cycles.'}, {'type': 'PRIMARY', 'title': 'Minimum Serum Concentration (Cmin) of Atezolizumab', 'denoms': [{'units': 'Participants', 'counts': [{'value': '1', 'groupId': 'OG000'}, {'value': '25', 'groupId': 'OG001'}, {'value': '32', 'groupId': 'OG002'}, {'value': '16', 'groupId': 'OG003'}]}], 'groups': [{'id': 'OG000', 'title': '<2 Age (Years)', 'description': 'Participants \\<2 Age (Years)'}, {'id': 'OG001', 'title': '2 to <12 Age (Years)', 'description': 'Participants 2 to \\<12 Age (Years)'}, {'id': 'OG002', 'title': '12 to <18 Age (Years)', 'description': 'Participants 12 to \\<18 Age (Years)'}, {'id': 'OG003', 'title': '>=18 Age (Years)', 'description': 'Participants \\>=18 Age (Years)'}], 'classes': [{'title': 'Cycle 2', 'denoms': [{'units': 'Participants', 'counts': [{'value': '1', 'groupId': 'OG000'}, {'value': '25', 'groupId': 'OG001'}, {'value': '32', 'groupId': 'OG002'}, {'value': '16', 'groupId': 'OG003'}]}], 'categories': [{'measurements': [{'value': '24.1', 'spread': 'NA', 'comment': 'Later cycles are NA because 1 participant died after study entry with 1 cycle, and the other participant died after two cycles.', 'groupId': 'OG000'}, {'value': '59.3', 'spread': '31.4', 'groupId': 'OG001'}, {'value': '56.5', 'spread': '50.4', 'groupId': 'OG002'}, {'value': '79.9', 'spread': '52.7', 'groupId': 'OG003'}]}]}, {'title': 'Cycle 3', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '13', 'groupId': 'OG001'}, {'value': '19', 'groupId': 'OG002'}, {'value': '8', 'groupId': 'OG003'}]}], 'categories': [{'measurements': [{'value': '58.9', 'spread': '234.4', 'groupId': 'OG001'}, {'value': '85.0', 'spread': '47.4', 'groupId': 'OG002'}, {'value': '148', 'spread': '48.9', 'groupId': 'OG003'}]}]}, {'title': 'Cycle 4', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '11', 'groupId': 'OG001'}, {'value': '16', 'groupId': 'OG002'}, {'value': '6', 'groupId': 'OG003'}]}], 'categories': [{'measurements': [{'value': '99.2', 'spread': '36.4', 'groupId': 'OG001'}, {'value': '113', 'spread': '41.1', 'groupId': 'OG002'}, {'value': '121', 'spread': '80.4', 'groupId': 'OG003'}]}]}, {'title': 'Cycle 8', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '4', 'groupId': 'OG001'}, {'value': '4', 'groupId': 'OG002'}, {'value': '2', 'groupId': 'OG003'}]}], 'categories': [{'measurements': [{'value': '166', 'spread': '19.8', 'groupId': 'OG001'}, {'value': '145', 'spread': '21.9', 'groupId': 'OG002'}, {'value': '209', 'spread': '8.10', 'groupId': 'OG003'}]}]}], 'paramType': 'GEOMETRIC_MEAN', 'timeFrame': 'PRD (0 hr) on D1 of Cy2,3,4,8, 12, 16 (1 Cy=21 days) and every 8 cycles thereafter; at any time during visit at study drug discontinuation visit, at least 90 days (maximum 150 days) after the last dose of study drug (up to approximately 42 months)', 'unitOfMeasure': 'ug/mL', 'dispersionType': 'Geometric Coefficient of Variation', 'reportingStatus': 'POSTED', 'populationDescription': 'Included PK population, defined as patients who had received any amount of study drug and had at least one serum concentration result available at clinical data cutoff. In the "\\<2 Age (Years)" Arm/Group, 1 participant died after study entry with 1 cycle, and the other participant died after two cycles.'}, {'type': 'PRIMARY', 'title': 'Atezolizumab Serum Concentration at Washout', 'denoms': [{'units': 'Participants', 'counts': [{'value': '17', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Atezolizumab', 'description': 'Participants received intravenous (IV) infusion of atezolizumab (maximum 1200 milligrams \\[mg\\]) on Day 1 of each 21-day cycle.'}], 'classes': [{'categories': [{'measurements': [{'value': '1.91', 'spread': '2815.1', 'groupId': 'OG000'}]}]}], 'paramType': 'GEOMETRIC_MEAN', 'timeFrame': 'At least 90 days (maximum 150 days) after last dose of study drug (up to approximately 42 months)', 'unitOfMeasure': 'ug/mL', 'dispersionType': 'Geometric Coefficient of Variation', 'reportingStatus': 'POSTED', 'populationDescription': 'Included PK population, defined as patients who had received any amount of study drug and had at least one serum concentration result available at clinical data cutoff.'}, {'type': 'PRIMARY', 'title': 'Area Under the Concentration-Time Curve (AUC) of Atezolizumab', 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '29', 'groupId': 'OG001'}, {'value': '38', 'groupId': 'OG002'}, {'value': '18', 'groupId': 'OG003'}]}], 'groups': [{'id': 'OG000', 'title': '<2 Age (Years)', 'description': 'Participants \\<2 Age (Years)'}, {'id': 'OG001', 'title': '2 to <12 Age (Years)', 'description': 'Participants 2 to \\<12 Age (Years)'}, {'id': 'OG002', 'title': '12 to <18 Age (Years)', 'description': 'Participants 12 to \\<18 Age (Years)'}, {'id': 'OG003', 'title': '>=18 Age (Years)', 'description': 'Participants \\>=18 Age (Years)'}], 'classes': [{'categories': [{'measurements': [{'value': '1130', 'spread': '5.28', 'groupId': 'OG000'}, {'value': '2209', 'spread': '21.3', 'groupId': 'OG001'}, {'value': '2816', 'spread': '17.7', 'groupId': 'OG002'}, {'value': '3579', 'spread': '28.4', 'groupId': 'OG003'}]}]}], 'paramType': 'GEOMETRIC_MEAN', 'timeFrame': 'PRD (0 hr), 0.5 hr P-I (infusion duration=30-60 minutes) on D1 of Cy1; at any time during visit on Cy1D8 (1 Cy=21 days)', 'unitOfMeasure': 'ugxday/mL', 'dispersionType': 'Geometric Coefficient of Variation', 'reportingStatus': 'POSTED', 'populationDescription': 'Included PK population, defined as patients who had received any amount of study drug and had at least one serum concentration result available at clinical data cutoff.'}, {'type': 'PRIMARY', 'title': 'Percentage of Participants With Anti-Therapeutic Antibodies (ATAs) to Atezolizumab', 'denoms': [{'units': 'Participants', 'counts': [{'value': '78', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Atezolizumab', 'description': 'Participants received intravenous (IV) infusion of atezolizumab (maximum 1200 milligrams \\[mg\\]) on Day 1 of each 21-day cycle.'}], 'classes': [{'title': 'Baseline', 'denoms': [{'units': 'Participants', 'counts': [{'value': '78', 'groupId': 'OG000'}]}], 'categories': [{'measurements': [{'value': '2.6', 'groupId': 'OG000'}]}]}, {'title': 'Post-baseline', 'denoms': [{'units': 'Participants', 'counts': [{'value': '77', 'groupId': 'OG000'}]}], 'categories': [{'measurements': [{'value': '14.3', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'PRD (0 hr) on D1 of Cy1,2,3,4,8,12,16 (1 Cy=21 days) & every 8 cycles thereafter; at any time during visit on Cy1D8, study drug discontinuation, at least 90 days (maximum 150 days) after last dose of study drug (up to approximately 42 months)', 'unitOfMeasure': 'Percentage', 'reportingStatus': 'POSTED', 'populationDescription': 'The baseline ADA-evaluable population included patients who had a baseline ADA result. The post-baseline ADA-evaluable population included patients who had at least one post-baseline ADA result and had received at least one dose of that study treatment. Patients never dosed and patients without valid ADA records were not included in the analysis.'}, {'type': 'SECONDARY', 'title': 'Duration of Response (DOR) as Determined by the Investigator Using RECIST v1.1 Criteria in Participants With Solid Tumors', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}, {'value': '0', 'groupId': 'OG003'}, {'value': '0', 'groupId': 'OG004'}, {'value': '0', 'groupId': 'OG005'}, {'value': '0', 'groupId': 'OG006'}, {'value': '0', 'groupId': 'OG007'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 1', 'description': 'Participants with ewing sarcoma'}, {'id': 'OG001', 'title': 'Cohort 5', 'description': 'Participants with non-rhabdomyosarcoma soft tissue sarcoma.'}, {'id': 'OG002', 'title': 'Cohort 6', 'description': 'Participants with osteosarcoma.'}, {'id': 'OG003', 'title': 'Cohort 7', 'description': 'Participants with rhabdomyosarcoma'}, {'id': 'OG004', 'title': 'Cohort 8', 'description': 'Participants with wilms tumor.'}, {'id': 'OG005', 'title': 'Cohort 9', 'description': 'Participants with other tumor types with documented PD-L1 expression.'}, {'id': 'OG006', 'title': 'Cohort 10', 'description': 'Participants with other tumor types without documented PD-L1 expression.'}, {'id': 'OG007', 'title': 'Cohort 11', 'description': 'Participants with rhabdoid tumor.'}], 'classes': [{'categories': [{'measurements': [{'value': '13.2', 'comment': 'There was only 1 participant.', 'groupId': 'OG001', 'lowerLimit': 'NA', 'upperLimit': 'NA'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': 'DOR as Determined by the Investigator Using mINRC in Participants With Neuroblastoma', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 3', 'description': 'Participants with neuroblastoma.'}], 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': "DOR as Determined by the Investigator Using Revised Response Criteria for Malignant Lymphoma for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'denoms': [{'units': 'Participants', 'counts': [{'value': '2', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 2', 'description': 'Participants with hodgkin lymphoma.'}, {'id': 'OG001', 'title': 'Cohort 4', 'description': "Participants with non-hodgkin's lymphoma"}], 'classes': [{'categories': [{'measurements': [{'value': 'NA', 'comment': 'Kaplan-Meier median estimate not reached.', 'groupId': 'OG000', 'lowerLimit': '4.1', 'upperLimit': 'NA'}, {'value': 'NA', 'comment': 'Kaplan-Meier median estimate not reached.', 'groupId': 'OG001', 'lowerLimit': 'NA', 'upperLimit': 'NA'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': 'DOR as Determined by the Investigator Using RANO Criteria in Participants With ATRT', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 12', 'description': 'Participants with atypical teratoid rhabdoid tumor.'}], 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug. No participants had an objective response in this cohort.'}, {'type': 'SECONDARY', 'title': 'Overall Survival (OS)', 'denoms': [{'units': 'Participants', 'counts': [{'value': '87', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Atezolizumab', 'description': 'Participants received intravenous (IV) infusion of atezolizumab (maximum 1200 milligrams \\[mg\\]) on Day 1 of each 21-day cycle.'}], 'classes': [{'categories': [{'measurements': [{'value': '7.4', 'groupId': 'OG000', 'lowerLimit': '5.3', 'upperLimit': '9.6'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until death (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': 'Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using Immune-Modified RECIST v1.1 for Participants With Other Solid Tumors', 'denoms': [{'units': 'Participants', 'counts': [{'value': '11', 'groupId': 'OG000'}, {'value': '10', 'groupId': 'OG001'}, {'value': '10', 'groupId': 'OG002'}, {'value': '10', 'groupId': 'OG003'}, {'value': '10', 'groupId': 'OG004'}, {'value': '4', 'groupId': 'OG005'}, {'value': '4', 'groupId': 'OG006'}, {'value': '2', 'groupId': 'OG007'}, {'value': '3', 'groupId': 'OG008'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 1', 'description': 'Participants with ewing sarcoma.'}, {'id': 'OG001', 'title': 'Cohort 5', 'description': 'Participants with non-rhabdomyosarcoma.'}, {'id': 'OG002', 'title': 'Cohort 6', 'description': 'Participants with osteosarcoma.'}, {'id': 'OG003', 'title': 'Cohort 7', 'description': 'Participants with rhabdomyosarcoma.'}, {'id': 'OG004', 'title': 'Cohort 8', 'description': 'Participants with wilms tumor.'}, {'id': 'OG005', 'title': 'Cohort 9', 'description': 'Participants with other tumor types with documented PD-L1 expression.'}, {'id': 'OG006', 'title': 'Cohort 10', 'description': 'Participants with other tumor types without documented PD-L1 expression.'}, {'id': 'OG007', 'title': 'Cohort 11', 'description': 'Participants with rhabdoid tumor.'}, {'id': 'OG008', 'title': 'Cohort 12', 'description': 'Participants with atypical teratoid rhabdoid tumor.'}], 'classes': [{'categories': [{'measurements': [{'value': '0', 'groupId': 'OG000'}, {'value': '10', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}, {'value': '0', 'groupId': 'OG003'}, {'value': '0', 'groupId': 'OG004'}, {'value': '0', 'groupId': 'OG005'}, {'value': '0', 'groupId': 'OG006'}, {'value': '0', 'groupId': 'OG007'}, {'value': '0', 'groupId': 'OG008'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Percentage', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': 'Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using Immune-Related Response Criteria (irRC) for Participants With Neuroblastoma', 'denoms': [{'units': 'Participants', 'counts': [{'value': '11', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 3', 'description': 'Participants with neuroblastoma.'}], 'classes': [{'categories': [{'measurements': [{'value': '0', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Percentage', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': "Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using irRC for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'denoms': [{'units': 'Participants', 'counts': [{'value': '9', 'groupId': 'OG000'}, {'value': '3', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 2', 'description': "Participants with hodgkin's lymphoma."}, {'id': 'OG001', 'title': 'Cohort 4', 'description': 'Participants with non-hodgkin lymphoma.'}], 'classes': [{'categories': [{'measurements': [{'value': '33.3', 'groupId': 'OG000'}, {'value': '33.3', 'groupId': 'OG001'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Percentage', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': 'PFS as Determined by the Investigator Using Immune-Modified RECIST v1.1 for Participants With Other Solid Tumors', 'denoms': [{'units': 'Participants', 'counts': [{'value': '11', 'groupId': 'OG000'}, {'value': '10', 'groupId': 'OG001'}, {'value': '10', 'groupId': 'OG002'}, {'value': '10', 'groupId': 'OG003'}, {'value': '10', 'groupId': 'OG004'}, {'value': '4', 'groupId': 'OG005'}, {'value': '4', 'groupId': 'OG006'}, {'value': '2', 'groupId': 'OG007'}, {'value': '3', 'groupId': 'OG008'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 1', 'description': 'Participants with ewing sarcoma.'}, {'id': 'OG001', 'title': 'Cohort 5', 'description': 'Participants with non-rhabdomyosarcoma soft tissue sarcoma.'}, {'id': 'OG002', 'title': 'Cohort 6', 'description': 'Participants with osteosarcoma.'}, {'id': 'OG003', 'title': 'Cohort 7', 'description': 'Participants with rhabdomyosarcoma.'}, {'id': 'OG004', 'title': 'Cohort 8', 'description': 'Participants with wilms tumor.'}, {'id': 'OG005', 'title': 'Cohort 9', 'description': 'Participants with other tumor types with documented PD-L1 expression.'}, {'id': 'OG006', 'title': 'Cohort 10', 'description': 'Participants with other tumor types without documented PD-L1 expression.'}, {'id': 'OG007', 'title': 'Cohort 11', 'description': 'Participants with rhabdoid tumor.'}, {'id': 'OG008', 'title': 'Cohort 12', 'description': 'Participants with atypical teratoid rhabdoid tumor.'}], 'classes': [{'categories': [{'measurements': [{'value': '1.3', 'groupId': 'OG000', 'lowerLimit': '0.6', 'upperLimit': '1.4'}, {'value': '1.4', 'groupId': 'OG001', 'lowerLimit': '1.3', 'upperLimit': '3.7'}, {'value': '1.2', 'groupId': 'OG002', 'lowerLimit': '0.9', 'upperLimit': '1.8'}, {'value': '1.3', 'groupId': 'OG003', 'lowerLimit': '1.1', 'upperLimit': '1.8'}, {'value': '1.4', 'groupId': 'OG004', 'lowerLimit': '1.1', 'upperLimit': '2.8'}, {'value': '1.2', 'groupId': 'OG005', 'lowerLimit': '0.7', 'upperLimit': '1.3'}, {'value': '1.2', 'groupId': 'OG006', 'lowerLimit': '1.1', 'upperLimit': '10.1'}, {'value': '0.7', 'groupId': 'OG007', 'lowerLimit': '0.3', 'upperLimit': '1.1'}, {'value': '6.9', 'groupId': 'OG008', 'lowerLimit': '1.7', 'upperLimit': '9.3'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': 'PFS as Determined by the Investigator Using irRC for Participants With Neuroblastoma', 'denoms': [{'units': 'Participants', 'counts': [{'value': '11', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 3', 'description': 'Participants with neuroblastoma'}], 'classes': [{'categories': [{'measurements': [{'value': '6.9', 'groupId': 'OG000', 'lowerLimit': '2.6', 'upperLimit': '14.7'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': "PFS as Determined by the Investigator Using irRC for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'denoms': [{'units': 'Participants', 'counts': [{'value': '9', 'groupId': 'OG000'}, {'value': '3', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 2', 'description': 'Participants with hodgkin lymphoma'}, {'id': 'OG001', 'title': 'Cohort 4', 'description': "Participants with non-hodgkin's lymphoma"}], 'classes': [{'categories': [{'measurements': [{'value': '6.5', 'comment': 'More than 50% patient was censored.', 'groupId': 'OG000', 'lowerLimit': '2.6', 'upperLimit': 'NA'}, {'value': '3.7', 'comment': 'More than 50% patient was censored.', 'groupId': 'OG001', 'lowerLimit': '1.4', 'upperLimit': 'NA'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': 'DOR as Determined by the Investigator Using Immune-Modified RECIST v1.1 for Participants With Other Solid Tumors', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}, {'value': '0', 'groupId': 'OG002'}, {'value': '0', 'groupId': 'OG003'}, {'value': '0', 'groupId': 'OG004'}, {'value': '0', 'groupId': 'OG005'}, {'value': '0', 'groupId': 'OG006'}, {'value': '0', 'groupId': 'OG007'}, {'value': '0', 'groupId': 'OG008'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 1', 'description': 'Participants with ewing sarcoma.'}, {'id': 'OG001', 'title': 'Cohort 5', 'description': 'Participants with non-rhabdomyosarcoma soft tissue sarcoma.'}, {'id': 'OG002', 'title': 'Cohort 6', 'description': 'Participants with osteosarcoma.'}, {'id': 'OG003', 'title': 'Cohort 7', 'description': 'Participants with rhabdomyosarcoma.'}, {'id': 'OG004', 'title': 'Cohort 8', 'description': 'Participants with wilms tumor.'}, {'id': 'OG005', 'title': 'Cohort 9', 'description': 'Participants with other tumor types with documented PD-L1 expression.'}, {'id': 'OG006', 'title': 'Cohort 10', 'description': 'Participants with other tumor types without documented PD-L1 expression.'}, {'id': 'OG007', 'title': 'Cohort 11', 'description': 'Participants with rhabdoid tumor.'}, {'id': 'OG008', 'title': 'Cohort 12', 'description': 'Participants with atypical teratoid rhabdoid tumor.'}], 'classes': [{'categories': [{'measurements': [{'value': '13.2', 'comment': 'There was only 1 participant with response.', 'groupId': 'OG001', 'lowerLimit': 'NA', 'upperLimit': 'NA'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': 'DOR as Determined by the Investigator Using irRC for Participants With Neuroblastoma', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 3', 'description': 'Participants with neuroblastoma'}], 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug. No participants had response therefore no participants analyzed.'}, {'type': 'SECONDARY', 'title': "DOR as Determined by the Investigator Using irRC for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'denoms': [{'units': 'Participants', 'counts': [{'value': '3', 'groupId': 'OG000'}, {'value': '1', 'groupId': 'OG001'}]}], 'groups': [{'id': 'OG000', 'title': 'Cohort 2', 'description': 'Participants with Hodgkin lymphoma.'}, {'id': 'OG001', 'title': 'Cohort 4', 'description': "Participants with non-hodgkin's lymphoma"}], 'classes': [{'categories': [{'measurements': [{'value': 'NA', 'comment': 'Kaplan-Meier median estimate not reached.', 'groupId': 'OG000', 'lowerLimit': '7.3', 'upperLimit': 'NA'}, {'value': 'NA', 'comment': 'Kaplan-Meier median estimate not reached.', 'groupId': 'OG001', 'lowerLimit': 'NA', 'upperLimit': 'NA'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'unitOfMeasure': 'Months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Included safety-evaluable population, defined as patients who received any amount of study drug.'}, {'type': 'SECONDARY', 'title': 'Optimal Dose of Atezolizumab in Pediatric Adult Participants', 'denoms': [{'units': 'Participants', 'counts': [{'value': '69', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': '<18 Age (Years)', 'description': 'Participants \\<18 Age (Years)'}], 'classes': [{'categories': [{'measurements': [{'value': '15', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'From baseline up to approximately 42 months', 'description': 'Atezolizumab was administered on Day 1 only for a cycle duration of 3 weeks.', 'unitOfMeasure': 'mg/kg', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Optimal Dose of Atezolizumab in Young Adult Participants', 'denoms': [{'units': 'Participants', 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'COHORT 7', 'description': 'RHABDOMYOSARCOMA'}, {'id': 'FG007', 'title': 'COHORT 8', 'description': 'WILMS TUMOR'}, {'id': 'FG008', 'title': 'COHORT 9', 'description': 'OTHER TUMOR TYPES WITH DOCUMENTED PD-L1 EXPRESSION'}, {'id': 'FG009', 'title': 'COHORT 10', 'description': 'OTHER TUMOR TYPES WITHOUT DOCUMENTED PD-L1 EXPRESSION'}, {'id': 'FG010', 'title': 'COHORT 11', 'description': 'RHABDOID TUMOR'}, {'id': 'FG011', 'title': 'COHORT 12', 'description': 'ATYPICAL TERATOID RHABDOID TUMOR'}], 'periods': [{'title': 'Overall Study', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '11'}, {'groupId': 'FG001', 'numSubjects': '9'}, {'groupId': 'FG002', 'numSubjects': '11'}, {'groupId': 'FG003', 'numSubjects': '3'}, {'groupId': 'FG004', 'numSubjects': '10'}, {'groupId': 'FG005', 'numSubjects': '10'}, {'groupId': 'FG006', 'numSubjects': '10'}, {'groupId': 'FG007', 'numSubjects': '10'}, {'groupId': 'FG008', 'numSubjects': '4'}, {'groupId': 'FG009', 'numSubjects': '4'}, {'groupId': 'FG010', 'numSubjects': '2'}, {'groupId': 'FG011', 'numSubjects': '3'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '0'}, {'groupId': 'FG002', 'numSubjects': '0'}, {'groupId': 'FG003', 'numSubjects': '0'}, {'groupId': 'FG004', 'numSubjects': '0'}, {'groupId': 'FG005', 'numSubjects': '0'}, {'groupId': 'FG006', 'numSubjects': '0'}, {'groupId': 'FG007', 'numSubjects': '0'}, {'groupId': 'FG008', 'numSubjects': '0'}, {'groupId': 'FG009', 'numSubjects': '0'}, {'groupId': 'FG010', 'numSubjects': '0'}, {'groupId': 'FG011', 'numSubjects': '0'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '11'}, {'groupId': 'FG001', 'numSubjects': '9'}, {'groupId': 'FG002', 'numSubjects': '11'}, {'groupId': 'FG003', 'numSubjects': '3'}, {'groupId': 'FG004', 'numSubjects': '10'}, {'groupId': 'FG005', 'numSubjects': '10'}, {'groupId': 'FG006', 'numSubjects': '10'}, {'groupId': 'FG007', 'numSubjects': '10'}, {'groupId': 'FG008', 'numSubjects': '4'}, {'groupId': 'FG009', 'numSubjects': '4'}, {'groupId': 'FG010', 'numSubjects': '2'}, {'groupId': 'FG011', 'numSubjects': '3'}]}], 'dropWithdraws': [{'type': 'Death', 'reasons': [{'groupId': 'FG000', 'numSubjects': '6'}, {'groupId': 'FG001', 'numSubjects': '5'}, {'groupId': 'FG002', 'numSubjects': '7'}, {'groupId': 'FG003', 'numSubjects': '2'}, {'groupId': 'FG004', 'numSubjects': '9'}, {'groupId': 'FG005', 'numSubjects': '8'}, {'groupId': 'FG006', 'numSubjects': '9'}, {'groupId': 'FG007', 'numSubjects': '9'}, {'groupId': 'FG008', 'numSubjects': '3'}, {'groupId': 'FG009', 'numSubjects': '4'}, {'groupId': 'FG010', 'numSubjects': '2'}, {'groupId': 'FG011', 'numSubjects': '3'}]}, {'type': 'Lost to Follow-up', 'reasons': [{'groupId': 'FG000', 'numSubjects': '2'}, {'groupId': 'FG001', 'numSubjects': '0'}, {'groupId': 'FG002', 'numSubjects': '1'}, {'groupId': 'FG003', 'numSubjects': '0'}, {'groupId': 'FG004', 'numSubjects': '0'}, {'groupId': 'FG005', 'numSubjects': '1'}, {'groupId': 'FG006', 'numSubjects': '1'}, {'groupId': 'FG007', 'numSubjects': '0'}, {'groupId': 'FG008', 'numSubjects': '0'}, {'groupId': 'FG009', 'numSubjects': '0'}, {'groupId': 'FG010', 'numSubjects': '0'}, {'groupId': 'FG011', 'numSubjects': '0'}]}, {'type': 'Withdrawal by Subject', 'reasons': [{'groupId': 'FG000', 'numSubjects': '2'}, {'groupId': 'FG001', 'numSubjects': '0'}, {'groupId': 'FG002', 'numSubjects': '1'}, {'groupId': 'FG003', 'numSubjects': '0'}, {'groupId': 'FG004', 'numSubjects': '1'}, {'groupId': 'FG005', 'numSubjects': '1'}, {'groupId': 'FG006', 'numSubjects': '0'}, {'groupId': 'FG007', 'numSubjects': '0'}, {'groupId': 'FG008', 'numSubjects': '1'}, {'groupId': 'FG009', 'numSubjects': '0'}, {'groupId': 'FG010', 'numSubjects': '0'}, {'groupId': 'FG011', 'numSubjects': '0'}]}, {'type': 'Study Terminated by Sponsor', 'reasons': [{'groupId': 'FG000', 'numSubjects': '1'}, {'groupId': 'FG001', 'numSubjects': '4'}, {'groupId': 'FG002', 'numSubjects': '2'}, {'groupId': 'FG003', 'numSubjects': '1'}, {'groupId': 'FG004', 'numSubjects': '0'}, {'groupId': 'FG005', 'numSubjects': '0'}, {'groupId': 'FG006', 'numSubjects': '0'}, {'groupId': 'FG007', 'numSubjects': '0'}, {'groupId': 'FG008', 'numSubjects': '0'}, {'groupId': 'FG009', 'numSubjects': '0'}, {'groupId': 'FG010', 'numSubjects': '0'}, {'groupId': 'FG011', 'numSubjects': '0'}]}, {'type': 'Medical condition may jeopardize safety', 'reasons': [{'groupId': 'FG000', 'numSubjects': '0'}, {'groupId': 'FG001', 'numSubjects': '0'}, {'groupId': 'FG002', 'numSubjects': '0'}, {'groupId': 'FG003', 'numSubjects': '0'}, {'groupId': 'FG004', 'numSubjects': '0'}, {'groupId': 'FG005', 'numSubjects': '0'}, {'groupId': 'FG006', 'numSubjects': '0'}, {'groupId': 'FG007', 'numSubjects': '1'}, {'groupId': 'FG008', 'numSubjects': '0'}, {'groupId': 'FG009', 'numSubjects': '0'}, {'groupId': 'FG010', 'numSubjects': '0'}, {'groupId': 'FG011', 'numSubjects': '0'}]}]}]}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '11', 'groupId': 'BG000'}, {'value': '9', 'groupId': 'BG001'}, {'value': '11', 'groupId': 'BG002'}, {'value': '3', 'groupId': 'BG003'}, {'value': '10', 'groupId': 'BG004'}, {'value': '10', 'groupId': 'BG005'}, {'value': '10', 'groupId': 'BG006'}, {'value': '10', 'groupId': 'BG007'}, {'value': '4', 'groupId': 'BG008'}, {'value': '4', 'groupId': 'BG009'}, {'value': '2', 'groupId': 'BG010'}, {'value': '3', 'groupId': 'BG011'}, {'value': '87', 'groupId': 'BG012'}]}], 'groups': [{'id': 'BG000', 'title': 'COHORT 1', 'description': 'EWING SARCOMA'}, {'id': 'BG001', 'title': 'COHORT 2', 'description': 'HODGKIN LYMPHOMA'}, {'id': 'BG002', 'title': 'COHORT 3', 'description': 'NEUROBLASTOMA'}, {'id': 'BG003', 'title': 'COHORT 4', 'description': 'NON HODGKIN LYMPHOMA'}, {'id': 'BG004', 'title': 'COHORT 5', 'description': 'NON-RHABDOMYOSARCOMA SOFT TISSUE SARCOMA;'}, {'id': 'BG005', 'title': 'COHORT 6', 'description': 'OSTEOSARCOMA'}, {'id': 'BG006', 'title': 'COHORT 7', 'description': 'RHABDOMYOSARCOMA'}, {'id': 'BG007', 'title': 'COHORT 8', 'description': 'WILMS TUMOR'}, {'id': 'BG008', 'title': 'COHORT 9', 'description': 'OTHER TUMOR TYPES WITH DOCUMENTED PD-L1 EXPRESSION'}, {'id': 'BG009', 'title': 'COHORT 10', 'description': 'OTHER TUMOR TYPES WITHOUT DOCUMENTED PD-L1 EXPRESSION'}, {'id': 'BG010', 'title': 'COHORT 11', 'description': 'RHABDOID TUMOR'}, {'id': 'BG011', 'title': 'COHORT 12', 'description': 'ATYPICAL TERATOID RHABDOID TUMOR'}, {'id': 'BG012', 'title': 'Total', 'description': 'Total of all reporting groups'}], 'measures': [{'title': 'Age, Continuous', 'classes': [{'categories': [{'measurements': [{'value': '13.6', 'spread': '3.3', 'groupId': 'BG000'}, {'value': '14.2', 'spread': '3.0', 'groupId': 'BG001'}, {'value': '12.8', 'spread': '9.4', 'groupId': 'BG002'}, {'value': '19.0', 'spread': '6.6', 'groupId': 'BG003'}, {'value': '14.5', 'spread': '6.5', 'groupId': 'BG004'}, {'value': '17.1', 'spread': '4.1', 'groupId': 'BG005'}, {'value': '13.0', 'spread': '8.5', 'groupId': 'BG006'}, {'value': '12.6', 'spread': '6.8', 'groupId': 'BG007'}, {'value': '14.8', 'spread': '1.0', 'groupId': 'BG008'}, {'value': '11.3', 'spread': '0.5', 'groupId': 'BG009'}, {'value': '0.5', 'spread': '0.7', 'groupId': 'BG010'}, {'value': '7.3', 'spread': '4.6', 'groupId': 'BG011'}, {'value': '13.5', 'spread': '6.4', 'groupId': 'BG012'}]}]}], 'paramType': 'MEAN', 'unitOfMeasure': 'Years', 'dispersionType': 'STANDARD_DEVIATION'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '5', 'groupId': 'BG000'}, {'value': '6', 'groupId': 'BG001'}, {'value': '4', 'groupId': 'BG002'}, {'value': '0', 'groupId': 'BG003'}, {'value': '5', 'groupId': 'BG004'}, {'value': '4', 'groupId': 'BG005'}, {'value': '4', 'groupId': 'BG006'}, {'value': '6', 'groupId': 'BG007'}, {'value': '0', 'groupId': 'BG008'}, {'value': '4', 'groupId': 'BG009'}, {'value': '1', 'groupId': 'BG010'}, {'value': '1', 'groupId': 'BG011'}, {'value': '40', 'groupId': 'BG012'}]}, {'title': 'Male', 'measurements': [{'value': '6', 'groupId': 'BG000'}, {'value': '3', 'groupId': 'BG001'}, {'value': '7', 'groupId': 'BG002'}, {'value': '3', 'groupId': 'BG003'}, {'value': '5', 'groupId': 'BG004'}, {'value': '6', 'groupId': 'BG005'}, {'value': '6', 'groupId': 'BG006'}, {'value': '4', 'groupId': 'BG007'}, {'value': '4', 'groupId': 'BG008'}, {'value': '0', 'groupId': 'BG009'}, {'value': '1', 'groupId': 'BG010'}, {'value': '2', 'groupId': 'BG011'}, {'value': '47', 'groupId': 'BG012'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Ethnicity (NIH/OMB)', 'classes': [{'categories': [{'title': 'Hispanic or Latino', 'measurements': [{'value': '2', 'groupId': 'BG000'}, {'value': '1', 'groupId': 'BG001'}, {'value': '2', 'groupId': 'BG002'}, {'value': '1', 'groupId': 'BG003'}, {'value': '1', 'groupId': 'BG004'}, {'value': '2', 'groupId': 'BG005'}, {'value': '3', 'groupId': 'BG006'}, {'value': '1', 'groupId': 'BG007'}, {'value': '2', 'groupId': 'BG008'}, {'value': '0', 'groupId': 'BG009'}, {'value': '0', 'groupId': 'BG010'}, {'value': '1', 'groupId': 'BG011'}, {'value': '16', 'groupId': 'BG012'}]}, {'title': 'Not Hispanic or Latino', 'measurements': [{'value': '7', 'groupId': 'BG000'}, {'value': '5', 'groupId': 'BG001'}, {'value': '7', 'groupId': 'BG002'}, {'value': '2', 'groupId': 'BG003'}, {'value': '5', 'groupId': 'BG004'}, {'value': '6', 'groupId': 'BG005'}, {'value': '6', 'groupId': 'BG006'}, {'value': '6', 'groupId': 'BG007'}, {'value': '2', 'groupId': 'BG008'}, {'value': '3', 'groupId': 'BG009'}, {'value': '2', 'groupId': 'BG010'}, {'value': '0', 'groupId': 'BG011'}, {'value': '51', 'groupId': 'BG012'}]}, {'title': 'Unknown or Not Reported', 'measurements': [{'value': '2', 'groupId': 'BG000'}, {'value': '3', 'groupId': 'BG001'}, {'value': '2', 'groupId': 'BG002'}, {'value': '0', 'groupId': 'BG003'}, {'value': '4', 'groupId': 'BG004'}, {'value': '2', 'groupId': 'BG005'}, {'value': '1', 'groupId': 'BG006'}, {'value': '3', 'groupId': 'BG007'}, {'value': '0', 'groupId': 'BG008'}, {'value': '1', 'groupId': 'BG009'}, {'value': '0', 'groupId': 'BG010'}, {'value': '2', 'groupId': 'BG011'}, {'value': '20', 'groupId': 'BG012'}]}]}], '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'}, {'value': '0', 'groupId': 'BG003'}, {'value': '0', 'groupId': 'BG004'}, {'value': '0', 'groupId': 'BG005'}, {'value': '0', 'groupId': 'BG006'}, {'value': '0', 'groupId': 'BG007'}, {'value': '0', 'groupId': 'BG008'}, {'value': '0', 'groupId': 'BG009'}, {'value': '0', 'groupId': 'BG010'}, {'value': '0', 'groupId': 'BG011'}, {'value': '0', 'groupId': 'BG012'}]}, {'title': 'Asian', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}, {'value': '0', 'groupId': 'BG003'}, {'value': '0', 'groupId': 'BG004'}, {'value': '1', 'groupId': 'BG005'}, {'value': '0', 'groupId': 'BG006'}, {'value': '0', 'groupId': 'BG007'}, {'value': '1', 'groupId': 'BG008'}, {'value': '0', 'groupId': 'BG009'}, {'value': '0', 'groupId': 'BG010'}, {'value': '1', 'groupId': 'BG011'}, {'value': '3', 'groupId': 'BG012'}]}, {'title': 'Native Hawaiian or Other Pacific Islander', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '0', 'groupId': 'BG002'}, {'value': '0', 'groupId': 'BG003'}, {'value': '0', 'groupId': 'BG004'}, {'value': '0', 'groupId': 'BG005'}, {'value': '0', 'groupId': 'BG006'}, {'value': '0', 'groupId': 'BG007'}, {'value': '0', 'groupId': 'BG008'}, {'value': '0', 'groupId': 'BG009'}, {'value': '0', 'groupId': 'BG010'}, {'value': '0', 'groupId': 'BG011'}, {'value': '0', 'groupId': 'BG012'}]}, {'title': 'Black or African American', 'measurements': [{'value': '0', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}, {'value': '1', 'groupId': 'BG003'}, {'value': '0', 'groupId': 'BG004'}, {'value': '1', 'groupId': 'BG005'}, {'value': '0', 'groupId': 'BG006'}, {'value': '1', 'groupId': 'BG007'}, {'value': '1', 'groupId': 'BG008'}, {'value': '1', 'groupId': 'BG009'}, {'value': '0', 'groupId': 'BG010'}, {'value': '0', 'groupId': 'BG011'}, {'value': '6', 'groupId': 'BG012'}]}, {'title': 'White', 'measurements': [{'value': '8', 'groupId': 'BG000'}, {'value': '5', 'groupId': 'BG001'}, {'value': '5', 'groupId': 'BG002'}, {'value': '2', 'groupId': 'BG003'}, {'value': '6', 'groupId': 'BG004'}, {'value': '6', 'groupId': 'BG005'}, {'value': '8', 'groupId': 'BG006'}, {'value': '5', 'groupId': 'BG007'}, {'value': '1', 'groupId': 'BG008'}, {'value': '2', 'groupId': 'BG009'}, {'value': '2', 'groupId': 'BG010'}, {'value': '0', 'groupId': 'BG011'}, {'value': '50', 'groupId': 'BG012'}]}, {'title': 'More than one race', 'measurements': [{'value': '1', 'groupId': 'BG000'}, {'value': '0', 'groupId': 'BG001'}, {'value': '1', 'groupId': 'BG002'}, {'value': '0', 'groupId': 'BG003'}, {'value': '0', 'groupId': 'BG004'}, {'value': '0', 'groupId': 'BG005'}, {'value': '0', 'groupId': 'BG006'}, {'value': '0', 'groupId': 'BG007'}, {'value': '0', 'groupId': 'BG008'}, {'value': '0', 'groupId': 'BG009'}, {'value': '0', 'groupId': 'BG010'}, {'value': '0', 'groupId': 'BG011'}, {'value': '2', 'groupId': 'BG012'}]}, {'title': 'Unknown or Not Reported', 'measurements': [{'value': '2', 'groupId': 'BG000'}, {'value': '4', 'groupId': 'BG001'}, {'value': '4', 'groupId': 'BG002'}, {'value': '0', 'groupId': 'BG003'}, {'value': '4', 'groupId': 'BG004'}, {'value': '2', 'groupId': 'BG005'}, {'value': '2', 'groupId': 'BG006'}, {'value': '4', 'groupId': 'BG007'}, {'value': '1', 'groupId': 'BG008'}, {'value': '1', 'groupId': 'BG009'}, {'value': '0', 'groupId': 'BG010'}, {'value': '2', 'groupId': 'BG011'}, {'value': '26', 'groupId': 'BG012'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}]}}, 'documentSection': {'largeDocumentModule': {'largeDocs': [{'date': '2016-10-21', 'size': 1381854, 'label': 'Study Protocol and Statistical Analysis Plan', 'hasIcf': False, 'hasSap': True, 'filename': 'Prot_SAP_000.pdf', 'typeAbbrev': 'Prot_SAP', 'uploadDate': '2020-01-06T14:20', 'hasProtocol': True}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE1', 'PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 87}}, 'statusModule': {'whyStopped': 'Sponsor decision to terminate because limited investigational agent activity was observed.', 'overallStatus': 'TERMINATED', 'startDateStruct': {'date': '2015-11-30', 'type': 'ACTUAL'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2020-02', 'completionDateStruct': {'date': '2019-06-06', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2020-02-24', 'studyFirstSubmitDate': '2015-08-18', 'resultsFirstSubmitDate': '2019-11-11', 'studyFirstSubmitQcDate': '2015-09-03', 'lastUpdatePostDateStruct': {'date': '2020-02-25', 'type': 'ACTUAL'}, 'resultsFirstSubmitQcDate': '2020-02-24', 'studyFirstPostDateStruct': {'date': '2015-09-04', 'type': 'ESTIMATED'}, 'resultsFirstPostDateStruct': {'date': '2020-02-25', 'type': 'ACTUAL'}, 'primaryCompletionDateStruct': {'date': '2019-06-06', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Percentage of Participants With an Objective Response (Complete Response [CR] or Partial Response [PR]) as Determined by the Investigator Using Response Evaluation Criteria in Solid Tumors Version 1.1 (RECIST v1.1) in Participants With Solid Tumors', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)', 'description': 'Note: In Cohort 5, the response was observed in a rhabdoid tumor. Participant was erroneously enrolled in the Non-rhabdomyosarcoma soft tissue sarcoma cohort.'}, {'measure': 'Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using Modified International Neuroblastoma Response Criteria (mINRC) in Participants With Neuroblastoma', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': "Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using Revised Response Criteria for Malignant Lymphoma for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using Response Assessment in Neuro-Oncology (RANO) Criteria in Participants With Atypical Teratoid Rhabdoid Tumor (ATRT)', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'Percentage of Participants With Clinical Benefit as Determined by the Investigator According to RECIST v1.1 Criteria in Participants With Osteosarcoma', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'Progression-Free Survival (PFS) as Determined by the Investigator Using RECIST v1.1 in Participants With Solid Tumors', 'timeFrame': 'Baseline until first documented occurrence of progressive disease, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'PFS as Determined by the Investigator Using mINRC in Participants With Neuroblastoma', 'timeFrame': 'Baseline until first documented occurrence of progressive disease, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': "PFS as Determined by the Investigator Using Revised Response Criteria for Malignant Lymphoma for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'timeFrame': 'Baseline until first documented occurrence of progressive disease, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'PFS as Determined by the Investigator Using RANO Criteria in Participants With ATRT', 'timeFrame': 'Baseline until first documented occurrence of progressive disease, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'Percentage of Participants Adverse Events, Serious Adverse Events and Adverse Events of Special Interest', 'timeFrame': 'From baseline up to approximately 42 months'}, {'measure': 'Maximum Serum Concentration (Cmax) of Atezolizumab', 'timeFrame': 'Predose (PRD; 0 hours [hr]), 0.5 hr post-infusion (P-I; infusion duration=30-60 minutes) on Day (D) 1 of Cycle (Cy) 1 and 4 (1 Cy=21 days)'}, {'measure': 'Minimum Serum Concentration (Cmin) of Atezolizumab', 'timeFrame': 'PRD (0 hr) on D1 of Cy2,3,4,8, 12, 16 (1 Cy=21 days) and every 8 cycles thereafter; at any time during visit at study drug discontinuation visit, at least 90 days (maximum 150 days) after the last dose of study drug (up to approximately 42 months)'}, {'measure': 'Atezolizumab Serum Concentration at Washout', 'timeFrame': 'At least 90 days (maximum 150 days) after last dose of study drug (up to approximately 42 months)'}, {'measure': 'Area Under the Concentration-Time Curve (AUC) of Atezolizumab', 'timeFrame': 'PRD (0 hr), 0.5 hr P-I (infusion duration=30-60 minutes) on D1 of Cy1; at any time during visit on Cy1D8 (1 Cy=21 days)'}, {'measure': 'Percentage of Participants With Anti-Therapeutic Antibodies (ATAs) to Atezolizumab', 'timeFrame': 'PRD (0 hr) on D1 of Cy1,2,3,4,8,12,16 (1 Cy=21 days) & every 8 cycles thereafter; at any time during visit on Cy1D8, study drug discontinuation, at least 90 days (maximum 150 days) after last dose of study drug (up to approximately 42 months)'}], 'secondaryOutcomes': [{'measure': 'Duration of Response (DOR) as Determined by the Investigator Using RECIST v1.1 Criteria in Participants With Solid Tumors', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'DOR as Determined by the Investigator Using mINRC in Participants With Neuroblastoma', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': "DOR as Determined by the Investigator Using Revised Response Criteria for Malignant Lymphoma for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'DOR as Determined by the Investigator Using RANO Criteria in Participants With ATRT', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'Overall Survival (OS)', 'timeFrame': 'Baseline until death (up to approximately 42 months)'}, {'measure': 'Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using Immune-Modified RECIST v1.1 for Participants With Other Solid Tumors', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using Immune-Related Response Criteria (irRC) for Participants With Neuroblastoma', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': "Percentage of Participants With an Objective Response (CR or PR) as Determined by the Investigator Using irRC for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'PFS as Determined by the Investigator Using Immune-Modified RECIST v1.1 for Participants With Other Solid Tumors', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'PFS as Determined by the Investigator Using irRC for Participants With Neuroblastoma', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': "PFS as Determined by the Investigator Using irRC for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'DOR as Determined by the Investigator Using Immune-Modified RECIST v1.1 for Participants With Other Solid Tumors', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'DOR as Determined by the Investigator Using irRC for Participants With Neuroblastoma', 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': "DOR as Determined by the Investigator Using irRC for Participants With Hodgkin's Lymphoma or Non-Hodgkin's Lymphoma", 'timeFrame': 'Baseline until disease progression, or death from any cause, whichever occurs first (up to approximately 42 months)'}, {'measure': 'Optimal Dose of Atezolizumab in Pediatric Adult Participants', 'timeFrame': 'From baseline up to approximately 42 months', 'description': 'Atezolizumab was administered on Day 1 only for a cycle duration of 3 weeks.'}, {'measure': 'Optimal Dose of Atezolizumab in Young Adult Participants', 'timeFrame': 'From baseline up to approximately 42 months', 'description': 'Atezolizumab was administered on Day 1 only for a cycle duration of 3 weeks.'}]}, 'oversightModule': {'oversightHasDmc': True}, 'conditionsModule': {'conditions': ['Solid Tumor']}, 'referencesModule': {'references': [{'pmid': '37038005', 'type': 'DERIVED', 'citation': 'Nabbi A, Danesh A, Espin-Garcia O, Pedersen S, Wellum J, Fu LH, Paulson JN, Geoerger B, Marshall LV, Trippett T, Rossato G, Pugh TJ, Hutchinson KE. Multimodal immunogenomic biomarker analysis of tumors from pediatric patients enrolled to a phase 1-2 study of single-agent atezolizumab. Nat Cancer. 2023 Apr;4(4):502-515. doi: 10.1038/s43018-023-00534-x. Epub 2023 Apr 10.'}, {'pmid': '31780255', 'type': 'DERIVED', 'citation': 'Geoerger B, Zwaan CM, Marshall LV, Michon J, Bourdeaut F, Casanova M, Corradini N, Rossato G, Farid-Kapadia M, Shemesh CS, Hutchinson KE, Donaldson F, Liao M, Caron H, Trippett T. Atezolizumab for children and young adults with previously treated solid tumours, non-Hodgkin lymphoma, and Hodgkin lymphoma (iMATRIX): a multicentre phase 1-2 study. Lancet Oncol. 2020 Jan;21(1):134-144. doi: 10.1016/S1470-2045(19)30693-X. Epub 2019 Nov 25.'}, {'pmid': '31753029', 'type': 'DERIVED', 'citation': 'Shemesh CS, Chanu P, Jamsen K, Wada R, Rossato G, Donaldson F, Garg A, Winter H, Ruppel J, Wang X, Bruno R, Jin J, Girish S. Population pharmacokinetics, exposure-safety, and immunogenicity of atezolizumab in pediatric and young adult patients with cancer. J Immunother Cancer. 2019 Nov 21;7(1):314. doi: 10.1186/s40425-019-0791-x.'}]}, 'descriptionModule': {'briefSummary': 'This early phase, multicenter, open-label, single-arm study evaluated the safety, tolerability, pharmacokinetics, immunogenicity, and preliminary efficacy of atezolizumab in pediatric and young adult participants with solid tumors for which prior treatment was proven to be ineffective.'}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['CHILD', 'ADULT'], 'maximumAge': '30 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Pediatric solid tumor (including Hodgkin's and Non-Hodgkin's lymphoma), for which prior treatment had proven to be ineffective (that is, relapsed or refractory) or intolerable\n* Disease that is measurable as defined by RECIST v1.1, mINRC, Revised Response Criteria for Malignant Lymphoma, RANO criteria (as appropriate) or evaluable by nuclear medicine techniques, immunocytochemistry techniques, tumor markers, or other reliable measures\n* Archival tumor tissue block or 15 freshly cut, unstained, serial slides available for submission, or willingness to undergo a core or excisional biopsy prior to enrollment (fine-needle aspiration, brush biopsy, and lavage samples are not acceptable).\n\nParticipants with fewer than 15 slides available may be eligible for study entry following discussion with Medical Monitor\n\n* Lansky Performance Status (participants less than \\[\\<\\] 16 years old) or Karnofsky Performance Status (participants greater than or equal to \\[\\>=\\] 16 years old) \\>=50\n* Life expectancy \\>=3 months, in the investigator's judgment\n* Adequate hematologic and end organ function, confirmed by laboratory results obtained within 28 days prior to initiation of study drug\n\nExclusion Criteria:\n\n* Known primary central nervous system (CNS) malignancy or symptomatic CNS metastases, except ATRT\n* Treatment with high-dose chemotherapy and hematopoietic stem-cell rescue within 3 months prior to initiation of study drug\n* Prior allogeneic hematopoietic stem-cell transplantation or prior solid-organ transplantation\n* Treatment with chemotherapy (other than high-dose chemotherapy as described above) or differentiation therapy (such as retinoic acid) or immunotherapy (such as anti-GD2 antibody treatment) within 3 weeks prior to initiation of study drug or, if treatment included nitrosoureas, within 6 weeks prior to initiation of study drug\n* Treatment with thoracic or mediastinal radiotherapy within 3 weeks prior to initiation of study drug\n* Treatment with hormonal therapy (except hormone replacement therapy or oral contraceptives) or biologic therapy within 4 weeks or 5 half-lives, whichever is shorter, prior to initiation of study drug. This requirement may be waived at the investigator's request if the participant has recovered from therapeutic toxicity to the degree specified in the protocol, with approval of the Medical Monitor\n* Treatment with a long-acting hematopoietic growth factor within 2 weeks prior to initiation of study drug or a short-acting hematopoietic growth factor within 1 week prior to initiation of study drug\n* Treatment with investigational therapy (with the exception of cancer therapies as described above) within 4 weeks prior to initiation of study drug\n* Treatment with a live vaccine or a live, attenuated vaccine (e.g., nasal spray of live attenuated influenza vaccine or FluMist®) within 4 weeks prior to initiation of study drug or anticipation that such treatment will be required during the study or within 5 months after the final dose of study drug\n* Treatment with herbal cancer therapy within 1 week prior to initiation of study drug\n* Prior treatment with cluster of differentiation 137 (CD137) agonists or immune checkpoint blockade therapies, including anti-cytotoxic T-lymphocyte-associated protein 4 (anti-CTLA4), anti-programmed death-1 (PD-1), or anti-PD-L1 therapeutic antibodies\n* Treatment with systemic immunostimulatory agents (including but not limited to interferons or interleukin 2 \\[IL-2\\]) within 6 weeks or five drug elimination half-lives prior to Day 1 of Cycle 1, whichever is longer\n* Treatment with systemic corticosteroids or other systemic immunosuppressive medications (including but not limited to prednisone, dexamethasone, cyclophosphamide, azathioprine, methotrexate, thalidomide, and anti-tumor necrosis factor \\[TNF\\] agents) at the time of initiation of study drug, or anticipated requirement for systemic immunosuppressive medications during the study\n* Current treatment with therapeutic anticoagulants\n* Any non-hematologic toxicity (excluding alopecia) from prior treatment that has not resolved to Grade less than or equal to (\\<=) 1 (per National Cancer Institute Common Terminology Criteria for Adverse Events \\[NCI CTCAE\\] version 4.0) at screening\n* Known hypersensitivity to biopharmaceuticals produced in Chinese hamster ovary cells or any component of the atezolizumab formulation"}, 'identificationModule': {'nctId': 'NCT02541604', 'briefTitle': 'A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Immunogenicity, and Preliminary Efficacy of Atezolizumab (Anti-Programmed Death-Ligand 1 [PD-L1] Antibody) in Pediatric and Young Adult Participants With Solid Tumors', 'organization': {'class': 'INDUSTRY', 'fullName': 'Hoffmann-La Roche'}, 'officialTitle': 'An Early-Phase, Multicenter, Open-Label Study of the Safety and Pharmacokinetics of Atezolizumab (MPDL3280A) In Pediatric and Young Adult Patients With Previously Treated Solid Tumors', 'orgStudyIdInfo': {'id': 'GO29664'}, 'secondaryIdInfos': [{'id': '2014-004697-41', 'type': 'EUDRACT_NUMBER'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Atezolizumab', 'description': 'Participants received intravenous (IV) infusion of atezolizumab (maximum 1200 milligrams \\[mg\\]) on Day 1 of each 21-day cycle.', 'interventionNames': ['Drug: Atezolizumab']}], 'interventions': [{'name': 'Atezolizumab', 'type': 'DRUG', 'otherNames': ['RO5541267; MPDL3280A; Tecentriq'], 'description': 'Atezolizumab was administered as IV infusion (maximum 1200 mg) on Day 1 of each 21-day cycle.', 'armGroupLabels': ['Atezolizumab']}]}, 'contactsLocationsModule': {'locations': [{'zip': '72202', 'city': 'Little Rock', 'state': 'Arkansas', 'country': 'United States', 'facility': "Arkansas Children'S Hospital", 'geoPoint': {'lat': 34.74648, 'lon': -92.28959}}, {'zip': '94304', 'city': 'Palo Alto', 'state': 'California', 'country': 'United States', 'facility': "Stanford University/Lucile Packard Children's Hospital", 'geoPoint': {'lat': 37.44188, 'lon': -122.14302}}, {'zip': '02215', 'city': 'Boston', 'state': 'Massachusetts', 'country': 'United States', 'facility': 'Dana Farber Cancer Institute', 'geoPoint': {'lat': 42.35843, 'lon': -71.05977}}, {'zip': '10065', 'city': 'New York', 'state': 'New York', 'country': 'United States', 'facility': 'Memorial Sloan Kettering Cancer Center', 'geoPoint': {'lat': 40.71427, 'lon': -74.00597}}, {'zip': '17033', 'city': 'Hershey', 'state': 'Pennsylvania', 'country': 'United States', 'facility': 'Penn State Milton S. Hershey Medical Center', 'geoPoint': {'lat': 40.28592, 'lon': -76.65025}}, {'zip': '77030', 'city': 'Houston', 'state': 'Texas', 'country': 'United States', 'facility': 'MD Anderson Cancer Center', 'geoPoint': {'lat': 29.76328, 'lon': -95.36327}}, {'zip': '78229', 'city': 'San Antonio', 'state': 'Texas', 'country': 'United States', 'facility': 'University of Texas Health Science Center at San Antonio', 'geoPoint': {'lat': 29.42412, 'lon': -98.49363}}, {'zip': 'T3B 6A8', 'city': 'Calgary', 'state': 'Alberta', 'country': 'Canada', 'facility': "Alberta Children'S Hospital", 'geoPoint': {'lat': 51.05011, 'lon': -114.08529}}, {'zip': '2100', 'city': 'København Ø', 'country': 'Denmark', 'facility': 'Rigshospitalet; BØRNEUNGEKLINIKKEN, Ambulatoriet for kræft- og Blodsygdomme hos børn og unge', 'geoPoint': {'lat': 55.70968, 'lon': 12.56862}}, {'zip': '69373', 'city': 'Lyon', 'country': 'France', 'facility': "Centre Léon Bérard, Institut d'Hémato-Oncologie Pédiatrique", 'geoPoint': {'lat': 45.74906, 'lon': 4.84789}}, {'zip': '75231', 'city': 'Paris', 'country': 'France', 'facility': 'Institut Curie, Oncologie Pédiatrique', 'geoPoint': {'lat': 48.85341, 'lon': 2.3488}}, {'zip': '94805', 'city': 'Villejuif', 'country': 'France', 'facility': 'Institut Gustave Roussy; Service Pediatrique', 'geoPoint': {'lat': 48.7939, 'lon': 2.35992}}, {'zip': '60590', 'city': 'Frankfurt', 'country': 'Germany', 'facility': 'Klinik Johann Wolfgang von Goethe Uni', 'geoPoint': {'lat': 49.68333, 'lon': 10.53333}}, {'zip': '49100', 'city': 'Petah Tikva', 'country': 'Israel', 'facility': "Schneider Children's Medical Center", 'geoPoint': {'lat': 32.08707, 'lon': 34.88747}}, {'zip': '00165', 'city': 'Rome', 'state': 'Lazio', 'country': 'Italy', 'facility': 'Ospedale Pediatrico Bambino Gesù - IRCCS; Dipartimento di Onco-Ematologia Pediatrica', 'geoPoint': {'lat': 41.89193, 'lon': 12.51133}}, {'zip': '16147', 'city': 'Genoa', 'state': 'Liguria', 'country': 'Italy', 'facility': 'IRCCS Istituto Giannina Gaslini; Unità Operativa Oncologica Pediatrica', 'geoPoint': {'lat': 44.40478, 'lon': 8.94439}}, {'zip': '20133', 'city': 'Milan', 'state': 'Lombardy', 'country': 'Italy', 'facility': 'Fondazione IRCCS Istituto Nazionale dei Tumori; Struttura Complessa di Pediatria Oncologica', 'geoPoint': {'lat': 45.46427, 'lon': 9.18951}}, {'zip': '10126', 'city': 'Turin', 'state': 'Piedmont', 'country': 'Italy', 'facility': 'Azienda Ospedaliera Universitaria Città della Salute e della Scienza di Torino', 'geoPoint': {'lat': 45.07049, 'lon': 7.68682}}, {'zip': '35128', 'city': 'Padua', 'state': 'Veneto', 'country': 'Italy', 'facility': 'Azienda Ospedaliera di Padova; Clinica di Onco-ematologia pediatrica', 'geoPoint': {'lat': 45.40797, 'lon': 11.88586}}, {'zip': '3015 GJ', 'city': 'Rotterdam', 'country': 'Netherlands', 'facility': 'Erasmus MC / location Sophia Kinderziekenhuis', 'geoPoint': {'lat': 51.9225, 'lon': 4.47917}}, {'zip': '08950', 'city': 'Esplugues de Llobregas', 'state': 'Barcelona', 'country': 'Spain', 'facility': 'Hospital Sant Joan De Deu'}, {'zip': '08035', 'city': 'Barcelona', 'country': 'Spain', 'facility': "Hospital Universitari Vall d'Hebron", 'geoPoint': {'lat': 41.38879, 'lon': 2.15899}}, {'zip': '28009', 'city': 'Madrid', 'country': 'Spain', 'facility': 'Hospital Infantil Universitario Nino Jesus', 'geoPoint': {'lat': 40.4165, 'lon': -3.70256}}, {'zip': '46026', 'city': 'Valencia', 'country': 'Spain', 'facility': 'Hospital Universitari i Politecnic La Fe de Valencia', 'geoPoint': {'lat': 39.47391, 'lon': -0.37966}}, {'zip': '8032', 'city': 'Zurich', 'country': 'Switzerland', 'facility': 'Universitäts-Kinderspital; Abteilung für Onkologie', 'geoPoint': {'lat': 47.36667, 'lon': 8.55}}, {'zip': 'B4 6NH', 'city': 'Birmingham', 'country': 'United Kingdom', 'facility': "Birmingham Children's Hospital", 'geoPoint': {'lat': 52.48142, 'lon': -1.89983}}, {'zip': 'BS2 8BJ', 'city': 'Bristol', 'country': 'United Kingdom', 'facility': 'Bristol Royal Hospital For Children', 'geoPoint': {'lat': 51.45523, 'lon': -2.59665}}, {'zip': 'LS1 3EX', 'city': 'Leeds', 'country': 'United Kingdom', 'facility': 'Leeds General Infirmary; Paediatric Oncology & Haematology', 'geoPoint': {'lat': 53.79648, 'lon': -1.54785}}, {'zip': 'NE1 4LP', 'city': 'Newcastle upon Tyne', 'country': 'United Kingdom', 'facility': 'The Royal Victoria Infirmary; Paediatric and Adolescent Oncology Unit', 'geoPoint': {'lat': 54.97328, 'lon': -1.61396}}, {'zip': 'SM2 5PT', 'city': 'Surrey', 'country': 'United Kingdom', 'facility': 'Royal Marsden Hospital; Pediatric Unit'}], 'overallOfficials': [{'name': 'Clinical Trials', 'role': 'STUDY_DIRECTOR', 'affiliation': 'Hoffmann-La Roche'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'Hoffmann-La Roche', 'class': 'INDUSTRY'}, 'responsibleParty': {'type': 'SPONSOR'}}}}