NCT01946204 · FLOW
Participant flow
Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.
- groups
- description
- Participants received apalutamide matched placebo tablets orally on a continuous once daily dosing regimen along with androgen deprivation therapy (ADT) until disease progression, withdrawal of consent or unacceptable toxicity or death.
- id
- FG000
- title
- Placebo
- description
- Participants received apalutamide orally at a starting dose of 240 milligram (mg) (8 x 30 mg capsules then 4 x 60 mg tablets) in a continuous treatment cycles (each treatment cycle is of 28 days) once daily dosing regimen along with androgen deprivation therapy (ADT) until disease progression, withdrawal of consent or unacceptable toxicity or death.
- id
- FG001
- title
- Apalutamide
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 38
- group Id
- FG001
- num Subjects
- 59
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 37
- group Id
- FG001
- num Subjects
- 50
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 7
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 316
- group Id
- FG001
- num Subjects
- 687
- type
- Ongoing
- reasons
- group Id
- FG000
- num Subjects
- 7
- group Id
- FG001
- num Subjects
- 3
- type
- Other
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 401
- group Id
- FG001
- num Subjects
- 806
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 398
- group Id
- FG001
- num Subjects
- 803
- type
- Treated
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 401
- group Id
- FG001
- num Subjects
- 806
- type
- NOT COMPLETED
- title
- Overall Study
Complete source fields
- groups
- description
- Participants received apalutamide matched placebo tablets orally on a continuous once daily dosing regimen along with androgen deprivation therapy (ADT) until disease progression, withdrawal of consent or unacceptable toxicity or death.
- id
- FG000
- title
- Placebo
- description
- Participants received apalutamide orally at a starting dose of 240 milligram (mg) (8 x 30 mg capsules then 4 x 60 mg tablets) in a continuous treatment cycles (each treatment cycle is of 28 days) once daily dosing regimen along with androgen deprivation therapy (ADT) until disease progression, withdrawal of consent or unacceptable toxicity or death.
- id
- FG001
- title
- Apalutamide
- periods
- drop Withdraws
- reasons
- group Id
- FG000
- num Subjects
- 38
- group Id
- FG001
- num Subjects
- 59
- type
- Death
- reasons
- group Id
- FG000
- num Subjects
- 37
- group Id
- FG001
- num Subjects
- 50
- type
- Withdrawal by Subject
- reasons
- group Id
- FG000
- num Subjects
- 3
- group Id
- FG001
- num Subjects
- 7
- type
- Lost to Follow-up
- reasons
- group Id
- FG000
- num Subjects
- 316
- group Id
- FG001
- num Subjects
- 687
- type
- Ongoing
- reasons
- group Id
- FG000
- num Subjects
- 7
- group Id
- FG001
- num Subjects
- 3
- type
- Other
- milestones
- achievements
- group Id
- FG000
- num Subjects
- 401
- group Id
- FG001
- num Subjects
- 806
- type
- STARTED
- achievements
- group Id
- FG000
- num Subjects
- 398
- group Id
- FG001
- num Subjects
- 803
- type
- Treated
- achievements
- group Id
- FG000
- num Subjects
- 0
- group Id
- FG001
- num Subjects
- 0
- type
- COMPLETED
- achievements
- group Id
- FG000
- num Subjects
- 401
- group Id
- FG001
- num Subjects
- 806
- type
- NOT COMPLETED
- title
- Overall Study
Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0
Preserved source evidence · Not medical advice
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