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NCT01946204 · FLOW

Participant flow

A Study of Apalutamide (ARN-509) in Men With Non-Metastatic Castration-Resistant Prostate Cancer · Source last updated 2026-08-31

Results reported by the registry submitting party. Population, time horizon, units and missing values must be read together.

groups
  1. 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
  2. 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
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        38
      2. group Id
        FG001
        num Subjects
        59
      type
      Death
    2. reasons
      1. group Id
        FG000
        num Subjects
        37
      2. group Id
        FG001
        num Subjects
        50
      type
      Withdrawal by Subject
    3. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        7
      type
      Lost to Follow-up
    4. reasons
      1. group Id
        FG000
        num Subjects
        316
      2. group Id
        FG001
        num Subjects
        687
      type
      Ongoing
    5. reasons
      1. group Id
        FG000
        num Subjects
        7
      2. group Id
        FG001
        num Subjects
        3
      type
      Other
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        401
      2. group Id
        FG001
        num Subjects
        806
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        398
      2. group Id
        FG001
        num Subjects
        803
      type
      Treated
    3. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        401
      2. group Id
        FG001
        num Subjects
        806
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. 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
  2. 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
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        38
      2. group Id
        FG001
        num Subjects
        59
      type
      Death
    2. reasons
      1. group Id
        FG000
        num Subjects
        37
      2. group Id
        FG001
        num Subjects
        50
      type
      Withdrawal by Subject
    3. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        7
      type
      Lost to Follow-up
    4. reasons
      1. group Id
        FG000
        num Subjects
        316
      2. group Id
        FG001
        num Subjects
        687
      type
      Ongoing
    5. reasons
      1. group Id
        FG000
        num Subjects
        7
      2. group Id
        FG001
        num Subjects
        3
      type
      Other
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        401
      2. group Id
        FG001
        num Subjects
        806
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        398
      2. group Id
        FG001
        num Subjects
        803
      type
      Treated
    3. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        401
      2. 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