NCT00753688 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Matching placebo tablets administered orally once daily for a duration until participants experienced disease progression, death, unacceptable toxicity, or participants withdrew consent
- id
- FG000
- title
- Placebo
- description
- Pazopanib 200 milligrams (mg) and 400 mg film-coated tablets (containing pazopanib monohydrochloride) administered orally at a dose of 800 mg once daily for a duration until participants experienced disease progression, death, unacceptable toxicity, or participants withdrew consent
- id
- FG001
- title
- Pazopanib
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 102
- group Id
- FG001
- num Subjects
- 203
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 9
- type
- Missing
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 2
- type
- Participant Withdrew Consent
- reasons
- group Id
- FG000
- num Subjects
- 15
- group Id
- FG001
- num Subjects
- 31
- type
- Ongoing - in Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 1
- type
- Adverse Event
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 123
- group Id
- FG001
- num Subjects
- 246
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 15
- group Id
- FG001
- num Subjects
- 31
- type
- Ongoing - in Follow-up
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 123
- group Id
- FG001
- num Subjects
- 246
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Matching placebo tablets administered orally once daily for a duration until participants experienced disease progression, death, unacceptable toxicity, or participants withdrew consent
- id
- FG000
- title
- Placebo
- description
- Pazopanib 200 milligrams (mg) and 400 mg film-coated tablets (containing pazopanib monohydrochloride) administered orally at a dose of 800 mg once daily for a duration until participants experienced disease progression, death, unacceptable toxicity, or participants withdrew consent
- id
- FG001
- title
- Pazopanib
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 102
- group Id
- FG001
- num Subjects
- 203
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 4
- group Id
- FG001
- num Subjects
- 9
- type
- Missing
- reasons
- group Id
- FG000
- num Subjects
- 2
- group Id
- FG001
- num Subjects
- 2
- type
- Participant Withdrew Consent
- reasons
- group Id
- FG000
- num Subjects
- 15
- group Id
- FG001
- num Subjects
- 31
- type
- Ongoing - in Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 1
- type
- Adverse Event
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 123
- group Id
- FG001
- num Subjects
- 246
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 15
- group Id
- FG001
- num Subjects
- 31
- type
- Ongoing - in Follow-up
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 123
- group Id
- FG001
- num Subjects
- 246
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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