Ignite Creation Date:
2025-12-24 @ 11:59 AM
Ignite Modification Date:
2025-12-30 @ 6:39 PM
Study NCT ID:
NCT00243061
Status:
COMPLETED
Last Update Posted:
2018-08-27
First Post:
2005-10-20
Is Gene Therapy:
True
Has Adverse Events:
True
Brief Title:
AZD2171 in Treating Patients With Recurrent or Stage IV Melanoma
Sponsor:
Organization:
Raw JSON
{'hasResults': True, 'derivedSection': {'miscInfoModule': {'versionHolder': '2025-12-24', 'removedCountries': ['United States']}, 'conditionBrowseModule': {'meshes': [{'id': 'D000098943', 'term': 'Uveal Melanoma'}, {'id': 'D008545', 'term': 'Melanoma'}], 'ancestors': [{'id': 'D018358', 'term': 'Neuroendocrine Tumors'}, {'id': 'D017599', 'term': 'Neuroectodermal Tumors'}, {'id': 'D009373', 'term': 'Neoplasms, Germ Cell and Embryonal'}, {'id': 'D009370', 'term': 'Neoplasms by Histologic Type'}, {'id': 'D009369', 'term': 'Neoplasms'}, {'id': 'D009380', 'term': 'Neoplasms, Nerve Tissue'}, {'id': 'D018326', 'term': 'Nevi and Melanomas'}, {'id': 'D014604', 'term': 'Uveal Neoplasms'}, {'id': 'D005134', 'term': 'Eye Neoplasms'}, {'id': 'D009371', 'term': 'Neoplasms by Site'}, {'id': 'D005128', 'term': 'Eye Diseases'}, {'id': 'D014603', 'term': 'Uveal Diseases'}, {'id': 'D012878', 'term': 'Skin Neoplasms'}, {'id': 'D012871', 'term': 'Skin Diseases'}, {'id': 'D017437', 'term': 'Skin and Connective Tissue Diseases'}]}, 'interventionBrowseModule': {'meshes': [{'id': 'C500926', 'term': 'cediranib'}]}}, 'resultsSection': {'moreInfoModule': {'pointOfContact': {'email': 'elaine.mcwhirter@hrcc.on.ca', 'phone': '905-387-9495', 'title': 'Dr. Elaine McWhirter', 'phoneExt': '67559', 'organization': 'Juravinski Cancer Centre'}, 'certainAgreement': {'restrictionType': 'LTE60', 'piSponsorEmployee': False, 'restrictiveAgreement': True}}, 'adverseEventsModule': {'eventGroups': [{'id': 'EG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally\n\nlaboratory biomarker analysis: Correlative studies\n\ndynamic contrast-enhanced magnetic resonance imaging: Correlative studies', 'otherNumAtRisk': 24, 'otherNumAffected': 24, 'seriousNumAtRisk': 24, 'seriousNumAffected': 9}], 'otherEvents': [{'term': 'Fatigue', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 19}], 'organSystem': 'General disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Diarrhea', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 18}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Hypertension', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 17}], 'organSystem': 'Vascular disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Hyperglycemia', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 15}], 'organSystem': 'Metabolism and nutrition disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}], 'seriousEvents': [{'term': 'Hypertension', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 3}], 'organSystem': 'Vascular disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Non-cardiac chest pain', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'General disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Abdominal pain', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Dehydration', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 3}], 'organSystem': 'Metabolism and nutrition disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Generalized muscle weakness', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'Musculoskeletal and connective tissue disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Anorexia', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Aspartate aminotransferase increased', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'Investigations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Dizziness', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'Nervous system disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Infections and infestations - Other, specify', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'Infections and infestations', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Nausea', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Vomiting', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Diarrhea', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'Gastrointestinal disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Fatigue', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'General disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Dysphasia', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'Nervous system disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}, {'term': 'Blurred vision', 'stats': [{'groupId': 'EG000', 'numAtRisk': 24, 'numAffected': 1}], 'organSystem': 'Eye disorders', 'assessmentType': 'SYSTEMATIC_ASSESSMENT'}], 'frequencyThreshold': '5'}, 'outcomeMeasuresModule': {'outcomeMeasures': [{'type': 'PRIMARY', 'title': 'Objective Tumor Response (Partial or Complete Response) According to RECIST', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally\n\nlaboratory biomarker analysis: Correlative studies\n\ndynamic contrast-enhanced magnetic resonance imaging: Correlative studies'}], 'classes': [{'categories': [{'measurements': [{'value': '0', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Up to 6 years', 'description': 'Response and progression will be evaluated in this study using the new international criteria proposed by the Response Evaluation Criteria in Solid Tumors (RECIST) Committee \\[J Nat Cancer Inst 92(3):205-216, 2000\\]. Changes in only the largest diameter (unidimensional measurement) of the tumor lesions, assessed by CT or MRI; Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), \\>=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR."', 'unitOfMeasure': 'participants', 'reportingStatus': 'POSTED', 'populationDescription': 'Out of 24 patients analyzed, 0 patients had objective response of PR or CR as defined by RECIST'}, {'type': 'PRIMARY', 'title': 'Prolonged Stable Disease According to RECIST', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally'}], 'classes': [{'categories': [{'measurements': [{'value': '9', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Up to 6 months', 'unitOfMeasure': 'participants', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Median Survival Time', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally'}], 'classes': [{'categories': [{'measurements': [{'value': '9.9', 'groupId': 'OG000', 'lowerLimit': '6.8', 'upperLimit': '20.6'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to 6 years', 'unitOfMeasure': 'months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Survival Rate', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally'}], 'classes': [{'categories': [{'measurements': [{'value': '41', 'groupId': 'OG000', 'lowerLimit': '24', 'upperLimit': '64'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'At 1 year', 'unitOfMeasure': 'percentage of participants', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Response Duration', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally'}], 'classes': [{'categories': [{'measurements': [{'value': '0', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'From the time measurement criteria are met for CR or PR (whichever is first recorded) until the first date that recurrent or progressive disease is objectively documented, assessed up to 6 years', 'unitOfMeasure': 'months', 'reportingStatus': 'POSTED', 'populationDescription': 'None of the patients had Partial or complete response'}, {'type': 'SECONDARY', 'title': 'Stable Disease Duration', 'denoms': [{'units': 'Participants', 'counts': [{'value': '17', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally\n\nlaboratory biomarker analysis: Correlative studies\n\ndynamic contrast-enhanced magnetic resonance imaging: Correlative studies'}], 'classes': [{'categories': [{'measurements': [{'value': '4.6', 'groupId': 'OG000', 'lowerLimit': '3.1', 'upperLimit': '9.1'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'From the start of the treatment until the criteria for progression are met, assessed up to 6 years', 'unitOfMeasure': 'months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': 'Only 17 of the 24 accrued patients were evaluable for response'}, {'type': 'SECONDARY', 'title': 'Highest Toxicity Grade Assessed by NCI CTCAE Version 3.0', 'denoms': [{'units': 'Participants', 'counts': [{'value': '23', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally\n\nlaboratory biomarker analysis: Correlative studies\n\ndynamic contrast-enhanced magnetic resonance imaging: Correlative studies'}], 'classes': [{'categories': [{'measurements': [{'value': '4', 'groupId': 'OG000'}]}]}], 'paramType': 'NUMBER', 'timeFrame': 'Up to 6 years after completion of treatment', 'unitOfMeasure': 'highest grade', 'reportingStatus': 'POSTED'}, {'type': 'SECONDARY', 'title': 'Time to Disease Progression', 'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally'}], 'classes': [{'categories': [{'measurements': [{'value': '4.1', 'groupId': 'OG000', 'lowerLimit': '1.8', 'upperLimit': '7.4'}]}]}], 'paramType': 'MEDIAN', 'timeFrame': 'Up to 6 years', 'unitOfMeasure': 'months', 'dispersionType': '95% Confidence Interval', 'reportingStatus': 'POSTED', 'populationDescription': '9 patients developed progressive disease'}, {'type': 'SECONDARY', 'title': 'Clinical Benefit Response', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally\n\nlaboratory biomarker analysis: Correlative studies\n\ndynamic contrast-enhanced magnetic resonance imaging: Correlative studies'}], 'timeFrame': 'Up to 6 years', 'reportingStatus': 'POSTED', 'populationDescription': 'data were not collected'}, {'type': 'SECONDARY', 'title': 'Changes in Levels of Soluble Angiogenic Factors', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally\n\nlaboratory biomarker analysis: Correlative studies\n\ndynamic contrast-enhanced magnetic resonance imaging: Correlative studies'}], 'timeFrame': 'From baseline to up to 6 years', 'reportingStatus': 'POSTED', 'populationDescription': 'data were not collected'}, {'type': 'SECONDARY', 'title': 'Change in Vessel Permeability and Blood Flow by DCE-MRI', 'denoms': [{'units': 'Participants', 'counts': [{'value': '0', 'groupId': 'OG000'}]}], 'groups': [{'id': 'OG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally\n\nlaboratory biomarker analysis: Correlative studies\n\ndynamic contrast-enhanced magnetic resonance imaging: Correlative studies'}], 'timeFrame': 'From baseline to up to 28 days after starting daily oral dosing', 'reportingStatus': 'POSTED', 'populationDescription': 'data were not collected'}]}, 'participantFlowModule': {'groups': [{'id': 'FG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally\n\nlaboratory biomarker analysis: Correlative studies\n\ndynamic contrast-enhanced magnetic resonance imaging: Correlative studies'}], 'periods': [{'title': 'Overall Study', 'milestones': [{'type': 'STARTED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '24'}]}, {'type': 'COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '24'}]}, {'type': 'NOT COMPLETED', 'achievements': [{'groupId': 'FG000', 'numSubjects': '0'}]}]}]}, 'baselineCharacteristicsModule': {'denoms': [{'units': 'Participants', 'counts': [{'value': '24', 'groupId': 'BG000'}]}], 'groups': [{'id': 'BG000', 'title': 'Treatment (Cediranib Maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\ncediranib maleate: Given orally\n\nlaboratory biomarker analysis: Correlative studies\n\ndynamic contrast-enhanced magnetic resonance imaging: Correlative studies'}], 'measures': [{'title': 'Age, Continuous', 'classes': [{'categories': [{'measurements': [{'value': '67', 'groupId': 'BG000', 'lowerLimit': '28', 'upperLimit': '82'}]}]}], 'paramType': 'MEDIAN', 'unitOfMeasure': 'years', 'dispersionType': 'FULL_RANGE'}, {'title': 'Age, Categorical', 'classes': [{'categories': [{'title': '<=18 years', 'measurements': [{'value': '0', 'groupId': 'BG000'}]}, {'title': 'Between 18 and 65 years', 'measurements': [{'value': '11', 'groupId': 'BG000'}]}, {'title': '>=65 years', 'measurements': [{'value': '13', 'groupId': 'BG000'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Sex: Female, Male', 'classes': [{'categories': [{'title': 'Female', 'measurements': [{'value': '7', 'groupId': 'BG000'}]}, {'title': 'Male', 'measurements': [{'value': '17', 'groupId': 'BG000'}]}]}], 'paramType': 'COUNT_OF_PARTICIPANTS', 'unitOfMeasure': 'Participants'}, {'title': 'Region of Enrollment', 'classes': [{'title': 'Canada', 'categories': [{'measurements': [{'value': '10', 'groupId': 'BG000'}]}]}, {'title': 'United States', 'categories': [{'measurements': [{'value': '14', 'groupId': 'BG000'}]}]}], 'paramType': 'NUMBER', 'unitOfMeasure': 'participants'}]}}, 'protocolSection': {'designModule': {'phases': ['PHASE2'], 'studyType': 'INTERVENTIONAL', 'designInfo': {'allocation': 'NA', 'maskingInfo': {'masking': 'NONE'}, 'primaryPurpose': 'TREATMENT', 'interventionModel': 'SINGLE_GROUP'}, 'enrollmentInfo': {'type': 'ACTUAL', 'count': 24}}, 'statusModule': {'overallStatus': 'COMPLETED', 'startDateStruct': {'date': '2006-01'}, 'expandedAccessInfo': {'hasExpandedAccess': False}, 'statusVerifiedDate': '2018-07', 'completionDateStruct': {'date': '2012-03', 'type': 'ACTUAL'}, 'lastUpdateSubmitDate': '2018-07-27', 'studyFirstSubmitDate': '2005-10-20', 'resultsFirstSubmitDate': '2014-07-09', 'studyFirstSubmitQcDate': '2005-10-20', 'lastUpdatePostDateStruct': {'date': '2018-08-27', 'type': 'ACTUAL'}, 'resultsFirstSubmitQcDate': '2015-06-01', 'studyFirstPostDateStruct': {'date': '2005-10-21', 'type': 'ESTIMATED'}, 'resultsFirstPostDateStruct': {'date': '2015-06-23', 'type': 'ESTIMATED'}, 'primaryCompletionDateStruct': {'date': '2012-03', 'type': 'ACTUAL'}}, 'outcomesModule': {'primaryOutcomes': [{'measure': 'Objective Tumor Response (Partial or Complete Response) According to RECIST', 'timeFrame': 'Up to 6 years', 'description': 'Response and progression will be evaluated in this study using the new international criteria proposed by the Response Evaluation Criteria in Solid Tumors (RECIST) Committee \\[J Nat Cancer Inst 92(3):205-216, 2000\\]. Changes in only the largest diameter (unidimensional measurement) of the tumor lesions, assessed by CT or MRI; Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), \\>=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR."'}, {'measure': 'Prolonged Stable Disease According to RECIST', 'timeFrame': 'Up to 6 months'}], 'secondaryOutcomes': [{'measure': 'Median Survival Time', 'timeFrame': 'Up to 6 years'}, {'measure': 'Survival Rate', 'timeFrame': 'At 1 year'}, {'measure': 'Response Duration', 'timeFrame': 'From the time measurement criteria are met for CR or PR (whichever is first recorded) until the first date that recurrent or progressive disease is objectively documented, assessed up to 6 years'}, {'measure': 'Stable Disease Duration', 'timeFrame': 'From the start of the treatment until the criteria for progression are met, assessed up to 6 years'}, {'measure': 'Highest Toxicity Grade Assessed by NCI CTCAE Version 3.0', 'timeFrame': 'Up to 6 years after completion of treatment'}, {'measure': 'Time to Disease Progression', 'timeFrame': 'Up to 6 years'}, {'measure': 'Clinical Benefit Response', 'timeFrame': 'Up to 6 years'}, {'measure': 'Changes in Levels of Soluble Angiogenic Factors', 'timeFrame': 'From baseline to up to 6 years'}, {'measure': 'Change in Vessel Permeability and Blood Flow by DCE-MRI', 'timeFrame': 'From baseline to up to 28 days after starting daily oral dosing'}]}, 'oversightModule': {'oversightHasDmc': True}, 'conditionsModule': {'conditions': ['Acral Lentiginous Malignant Melanoma', 'Ciliary Body and Choroid Melanoma, Medium/Large Size', 'Ciliary Body and Choroid Melanoma, Small Size', 'Extraocular Extension Melanoma', 'Intraocular Melanoma', 'Iris Melanoma', 'Lentigo Maligna Malignant Melanoma', 'Recurrent Melanoma', 'Stage, Intraocular Melanoma', 'Stage IV Melanoma', 'Superficial Spreading Malignant Melanoma']}, 'descriptionModule': {'briefSummary': 'This phase II trial is studying how well AZD2171 works in treating patients with recurrent or stage IV melanoma. AZD2171 may stop the growth of tumor cells by blocking blood flow to the tumor and by blocking some of the enzymes needed for cell growth.', 'detailedDescription': "PRIMARY OBJECTIVES:\n\nI. To assess the objective tumor response rate of AZD2171 administered to patients with recurrent or metastatic malignant melanoma.\n\nII. To assess the toxicity, median survival time, 1-year survival rate, response or stable disease duration, time to disease progression and clinical benefit response of AZD2171 administered to patients with recurrent or metastatic malignant melanoma.\n\nIII. To measure baseline and post-treatment levels of angiogenic growth factors and receptors, as well as circulating endothelial cells, and to explore the relationship between these potential correlative endpoints and clinical outcome.\n\nIV. To assess changes in blood flow and vessel permeability using dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) pre- and post-treatment, and to explore the relationship between these potential imaging endpoints and clinical outcome.\n\nV. To look for polymorphisms of kdr/flk-1, and other genes in this pathway, by performing pharmacogenetic analysis of pbmc's, and correlate genotype with VEGF levels and response to therapy.\n\nOUTLINE: This is an open-label, multicenter study.\n\nPatients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.\n\nAfter completion of study treatment, patients are followed for survival."}, 'eligibilityModule': {'sex': 'ALL', 'stdAges': ['ADULT', 'OLDER_ADULT'], 'minimumAge': '18 Years', 'healthyVolunteers': False, 'eligibilityCriteria': "Inclusion Criteria:\n\n* Histologically/cytologically confirmed recurrent/metastatic malignant melanoma (stage IV acral lentiginous, lentigo maligna, superficial spreading or ocular malignant melanoma)\n* Measurable disease- at least 1 lesion accurately measured in at least 1 dimension (longest diameter) as \\>=20mm with conventional techniques or \\>=10mm with spiral CT scan\n\n * Previously irradiated lesions not considered measurable unless they demonstrated progression prior to study entry\n* No prior chemotherapy (including regional therapy); prior adjuvant immunotherapy permitted if completed \\>3 months prior to study entry; patients may have received prior radiation therapy if completed \\>=4 weeks prior to study entry\n\n * Previous surgery permissible if performed \\>=4 weeks prior to study entry\n* Life expectancy \\>12 weeks\n* ECOG performance status=\\< 2 (Karnofsky\\>=60%)\n* Leukocytes\\>=3,000/mcL\n* Absolute neutrophil count\\>=1,500/mcL\n* Platelets\\>=100,000/mcL\n* Hemoglobin\\>=8g/dL\n* Total bilirubin\\<1.5x institutional ULN (IULN)\n* AST/ALT=\\<3 x IULN (5xULN if liver metastases)\n* Creatinine within IULN\n* Creatinine within IULN OR\n* Creatinine clearance\\>=60mL/min/m\\^2 if creatinine levels above IULN\n* Baseline blood pressure \\<140/90mmHg; may be taking antihypertensive medications\n* AZD2171 has shown to terminate fetal development in rat as expected for process dependent on VEGF signaling; women of childbearing potential must have negative pregnancy test prior to study entry; women of childbearing potential/men must agree to use adequate contraception (hormonal/barrier method of birth control; abstinence) prior to study entry and for duration of study\n* Ability to understand/willingness to sign written informed consent\n\nExclusion Criteria:\n\n* Any previous chemotherapy or immunotherapy for recurrent/metastatic disease; patients who have had radiotherapy or major surgery within 4 weeks prior to entering study or those who have not recovered from AEs due to treatment received more than 4 weeks earlier\n* May not be concurrently receiving other investigational agents nor have participated in an investigational trial of bio-, chemo- or immunotherapy agents\n* Known brain metastases because of their poor prognosis and because patients often develop progressive neurologic dysfunction that would confound evaluation of neurologic and other AEs\n* History of allergic reactions attributed to compounds of similar chemical/biologic composition to AZD2171\n* Mean QTc\\>470msec (Bazett's correction) in screening electrocardiogram or history of familial long QT syndrome\n* \\>+1 proteinuria on 2 consecutive dipsticks taken no less than 1 week apart\n* Uncontrolled intercurrent illness including but not limited to hypertension, ongoing/active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness/social situations that would limit compliance with study requirements\n* Pregnant women excluded from study because AZD2171 is a VEGF inhibitor with known abortifacient effects; breastfeeding should be discontinued if mother is treated with AZD2171\n* HIV-positive patients on combination antiretroviral therapy are ineligible because of potential for PK interactions with AZD2171; appropriate studies will be undertaken in patients receiving combination antiretroviral therapy when indicated\n* Any significant abnormality noted in ECG within 14 days of treatment\n* A NYHA classification of III or IV (NOTE: Patients classified as class II controlled with treatment may continue with increase monitoring)\n* Conditions requiring concurrent use of drugs/biologics with proarrhythmic potential; these drugs are prohibited during studies with AZD2171"}, 'identificationModule': {'nctId': 'NCT00243061', 'briefTitle': 'AZD2171 in Treating Patients With Recurrent or Stage IV Melanoma', 'organization': {'class': 'NIH', 'fullName': 'National Cancer Institute (NCI)'}, 'officialTitle': 'A Phase II Study of AZD2171 in Previously Untreated Patients With Metastatic or Recurrent Malignant Melanoma', 'orgStudyIdInfo': {'id': 'NCI-2012-03026'}, 'secondaryIdInfos': [{'id': 'PHL-038', 'type': 'OTHER_GRANT', 'domain': 'N01CM62203'}, {'id': 'N01CM62203', 'link': 'https://reporter.nih.gov/quickSearch/N01CM62203', 'type': 'NIH'}, {'id': 'N01CM62201', 'link': 'https://reporter.nih.gov/quickSearch/N01CM62201', 'type': 'NIH'}]}, 'armsInterventionsModule': {'armGroups': [{'type': 'EXPERIMENTAL', 'label': 'Treatment (cediranib maleate)', 'description': 'Patients receive oral AZD2171 once daily on days 1-28. Courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.', 'interventionNames': ['Drug: cediranib maleate']}], 'interventions': [{'name': 'cediranib maleate', 'type': 'DRUG', 'otherNames': ['AZD2171'], 'description': 'Given orally', 'armGroupLabels': ['Treatment (cediranib maleate)']}]}, 'contactsLocationsModule': {'locations': [{'zip': 'M5G 2M9', 'city': 'Toronto', 'state': 'Ontario', 'country': 'Canada', 'facility': 'Princess Margaret Hospital Phase 2 Consortium', 'geoPoint': {'lat': 43.70643, 'lon': -79.39864}}], 'overallOfficials': [{'name': 'Elaine McWhirter', 'role': 'PRINCIPAL_INVESTIGATOR', 'affiliation': 'Princess Margaret Hospital Phase 2 Consortium'}]}, 'sponsorCollaboratorsModule': {'leadSponsor': {'name': 'National Cancer Institute (NCI)', 'class': 'NIH'}, 'responsibleParty': {'type': 'SPONSOR'}}}}