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Trial · NCT01753713

Results by group28

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Arm 1: Progression Free Survival (PFS)Anti-angiogenic Therapy Naive Patients0Participants
Arm 1: Progression Free Survival (PFS)Anti-angiogenic Therapy Patients0Participants
Arm 2: Determine Median Time to ProgressionAnti-angiogenic Therapy Naive Patients1.895% Confidence Interval 1.3 to 2.8Months
Arm 2: Determine Median Time to ProgressionAnti-angiogenic Therapy Patients1.895% Confidence Interval 0.7 to 1.8Months
Toxicity Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0Anti-angiogenic Therapy Naive PatientsGrade 1217Events
Toxicity Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0Anti-angiogenic Therapy PatientsGrade 1119Events
Toxicity Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0Anti-angiogenic Therapy Naive PatientsGrade 2109Events
Toxicity Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0Anti-angiogenic Therapy PatientsGrade 285Events
Toxicity Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0Anti-angiogenic Therapy Naive PatientsGrade 355Events
Toxicity Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0Anti-angiogenic Therapy PatientsGrade 340Events
Toxicity Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0Anti-angiogenic Therapy Naive PatientsGrade 42Events
Toxicity Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0Anti-angiogenic Therapy PatientsGrade 45Events
Toxicity Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0Anti-angiogenic Therapy Naive PatientsGrade 51Events
Toxicity Assessed Using Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0Anti-angiogenic Therapy PatientsGrade 52Events
Objective Response Rate Using Modified Revised Assessment in Neuro-Oncology (RANO) CriteriaAnti-angiogenic Therapy Naive PatientsComplete Response0Participants
Objective Response Rate Using Modified Revised Assessment in Neuro-Oncology (RANO) CriteriaAnti-angiogenic Therapy PatientsComplete Response0Participants
Objective Response Rate Using Modified Revised Assessment in Neuro-Oncology (RANO) CriteriaAnti-angiogenic Therapy Naive PatientsProgressive Disease8Participants
Objective Response Rate Using Modified Revised Assessment in Neuro-Oncology (RANO) CriteriaAnti-angiogenic Therapy PatientsProgressive Disease8Participants
Objective Response Rate Using Modified Revised Assessment in Neuro-Oncology (RANO) CriteriaAnti-angiogenic Therapy Naive PatientsStable Disease3Participants
Objective Response Rate Using Modified Revised Assessment in Neuro-Oncology (RANO) CriteriaAnti-angiogenic Therapy PatientsStable Disease2Participants

Source ClinicalTrials.govtrials-2026-11-12-0.5.0

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

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