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NCT00099437 · FLOW

Participant flow

Comparison of Fulvestrant (FASLODEX™) 250 mg and 500 mg in Postmenopausal Women With Oestrogen Receptor Positive Advanced Breast Cancer Progressing or Relapsing After Previous Endocrine Therapy. · Source last updated 2026-06-11

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

groups
  1. description
    Fulvestrant 250 mg Intramuscular Injection every 28 days
    id
    FG000
    title
    Fulvestrant 250 mg
  2. description
    Fulvestrant 500 mg Intramuscular Injection every 28 days plus 500 mg on day 14
    id
    FG001
    title
    Fulvestrant 500 mg
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        30
      2. group Id
        FG001
        num Subjects
        33
      type
      Lost to Follow-up
    2. reasons
      1. group Id
        FG000
        num Subjects
        293
      2. group Id
        FG001
        num Subjects
        261
      type
      Death
    3. reasons
      1. group Id
        FG000
        num Subjects
        6
      2. group Id
        FG001
        num Subjects
        10
      type
      Withdrawal by Subject
    4. reasons
      1. group Id
        FG000
        num Subjects
        37
      2. group Id
        FG001
        num Subjects
        45
      type
      Ongoing in FU but not on treatment
    milestones
    1. achievements
      1. comment
        randomised patients
        group Id
        FG000
        num Subjects
        374
      2. comment
        randomised patients
        group Id
        FG001
        num Subjects
        362
      type
      STARTED
    2. achievements
      1. comment
        ongoing study treatment at survival follow-up data cut-off
        group Id
        FG000
        num Subjects
        8
      2. comment
        ongoing study treatment at survival follow-up data cut-off
        group Id
        FG001
        num Subjects
        13
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        366
      2. group Id
        FG001
        num Subjects
        349
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Fulvestrant 250 mg Intramuscular Injection every 28 days
    id
    FG000
    title
    Fulvestrant 250 mg
  2. description
    Fulvestrant 500 mg Intramuscular Injection every 28 days plus 500 mg on day 14
    id
    FG001
    title
    Fulvestrant 500 mg
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        30
      2. group Id
        FG001
        num Subjects
        33
      type
      Lost to Follow-up
    2. reasons
      1. group Id
        FG000
        num Subjects
        293
      2. group Id
        FG001
        num Subjects
        261
      type
      Death
    3. reasons
      1. group Id
        FG000
        num Subjects
        6
      2. group Id
        FG001
        num Subjects
        10
      type
      Withdrawal by Subject
    4. reasons
      1. group Id
        FG000
        num Subjects
        37
      2. group Id
        FG001
        num Subjects
        45
      type
      Ongoing in FU but not on treatment
    milestones
    1. achievements
      1. comment
        randomised patients
        group Id
        FG000
        num Subjects
        374
      2. comment
        randomised patients
        group Id
        FG001
        num Subjects
        362
      type
      STARTED
    2. achievements
      1. comment
        ongoing study treatment at survival follow-up data cut-off
        group Id
        FG000
        num Subjects
        8
      2. comment
        ongoing study treatment at survival follow-up data cut-off
        group Id
        FG001
        num Subjects
        13
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        366
      2. group Id
        FG001
        num Subjects
        349
      type
      NOT COMPLETED
    title
    Overall Study

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Not medical advice