NCT02314169 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Patients receive nivolumab IV over 60 minutes once every two weeks. Treatment continues in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, MRI and blood sample collection throughout the study. Biospecimen Collection: Undergo blood sample collection Computed Tomography: Undergo CT scan Magnetic Resonance Imaging: Undergo MRI Nivolumab: Given IV
- id
- FG000
- title
- Part A (Nivolumab)
- description
- Patients receive nivolumab IV over 30 minutes once every 4 weeks. Treatment continues in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, MRI and blood sample collection throughout the study. Biospecimen Collection: Undergo blood sample collection Computed Tomography: Undergo CT scan Magnetic Resonance Imaging: Undergo MRI Nivolumab: Given IV
- id
- FG001
- title
- Part B Arm I (Nivolumab)
- description
- Patients receive nivolumab as in Arm I. Patients also receive ipilimumab IV over 30 minutes once every 8 weeks. Treatment continues in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, MRI and blood sample collection throughout the study. Biospecimen Collection: Undergo blood sample collection Computed Tomography: Undergo CT scan Ipilimumab: Given IV Magnetic Resonance Imaging: Undergo MRI Nivolumab: Given IV
- id
- FG002
- title
- Part B Arm II (Nivolumab, Ipilimumab)
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 3
- group Id
- FG002
- num Subjects
- 1
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 3
- type
- Protocol Violation
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- type
- Did not meet an eligibility criterion and not treated
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 39
- group Id
- FG001
- num Subjects
- 53
- group Id
- FG002
- num Subjects
- 51
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 37
- group Id
- FG001
- num Subjects
- 49
- group Id
- FG002
- num Subjects
- 47
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 4
- group Id
- FG002
- num Subjects
- 4
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Patients receive nivolumab IV over 60 minutes once every two weeks. Treatment continues in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, MRI and blood sample collection throughout the study. Biospecimen Collection: Undergo blood sample collection Computed Tomography: Undergo CT scan Magnetic Resonance Imaging: Undergo MRI Nivolumab: Given IV
- id
- FG000
- title
- Part A (Nivolumab)
- description
- Patients receive nivolumab IV over 30 minutes once every 4 weeks. Treatment continues in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, MRI and blood sample collection throughout the study. Biospecimen Collection: Undergo blood sample collection Computed Tomography: Undergo CT scan Magnetic Resonance Imaging: Undergo MRI Nivolumab: Given IV
- id
- FG001
- title
- Part B Arm I (Nivolumab)
- description
- Patients receive nivolumab as in Arm I. Patients also receive ipilimumab IV over 30 minutes once every 8 weeks. Treatment continues in the absence of disease progression or unacceptable toxicity. Patients undergo CT scan, MRI and blood sample collection throughout the study. Biospecimen Collection: Undergo blood sample collection Computed Tomography: Undergo CT scan Ipilimumab: Given IV Magnetic Resonance Imaging: Undergo MRI Nivolumab: Given IV
- id
- FG002
- title
- Part B Arm II (Nivolumab, Ipilimumab)
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 3
- group Id
- FG002
- num Subjects
- 1
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 1
- group Id
- FG002
- num Subjects
- 3
- type
- Protocol Violation
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 0
- group Id
- FG002
- num Subjects
- 0
- type
- Did not meet an eligibility criterion and not treated
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 39
- group Id
- FG001
- num Subjects
- 53
- group Id
- FG002
- num Subjects
- 51
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 37
- group Id
- FG001
- num Subjects
- 49
- group Id
- FG002
- num Subjects
- 47
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 4
- group Id
- FG002
- num Subjects
- 4
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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