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NCT02246621 · FLOW

Participant flow

A Study of Nonsteroidal Aromatase Inhibitors Plus Abemaciclib (LY2835219) in Postmenopausal Women With Breast Cancer · Source last updated 2026-02-03

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

groups
  1. description
    150 milligrams (mg) Abemaciclib orally every 12 hours plus either 1 mg anastrozole or 2.5 mg letrozole orally once daily for 28 days (28 day cycles).
    id
    FG000
    title
    Abemaciclib + NSAI (Nonsteroidal Aromatase Inhibitors)
  2. description
    Placebo orally every 12 hours plus either 1 mg anastrozole or 2.5 mg letrozole orally once daily for 28 days (28 day cycles).
    id
    FG001
    title
    Placebo + NSAI
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        28
      2. group Id
        FG001
        num Subjects
        16
      type
      Withdrawal by Subject
    2. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      type
      Lost to Follow-up
    3. reasons
      1. group Id
        FG000
        num Subjects
        236
      2. group Id
        FG001
        num Subjects
        119
      type
      On Study Treatment/ Follow Up
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        328
      2. group Id
        FG001
        num Subjects
        165
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        327
      2. group Id
        FG001
        num Subjects
        161
      type
      Received At Least One Dose of Study Drug
    3. achievements
      1. group Id
        FG000
        num Subjects
        63
      2. group Id
        FG001
        num Subjects
        30
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        265
      2. group Id
        FG001
        num Subjects
        135
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
Completers are participants who died.
Complete source fields
groups
  1. description
    150 milligrams (mg) Abemaciclib orally every 12 hours plus either 1 mg anastrozole or 2.5 mg letrozole orally once daily for 28 days (28 day cycles).
    id
    FG000
    title
    Abemaciclib + NSAI (Nonsteroidal Aromatase Inhibitors)
  2. description
    Placebo orally every 12 hours plus either 1 mg anastrozole or 2.5 mg letrozole orally once daily for 28 days (28 day cycles).
    id
    FG001
    title
    Placebo + NSAI
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        28
      2. group Id
        FG001
        num Subjects
        16
      type
      Withdrawal by Subject
    2. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      type
      Lost to Follow-up
    3. reasons
      1. group Id
        FG000
        num Subjects
        236
      2. group Id
        FG001
        num Subjects
        119
      type
      On Study Treatment/ Follow Up
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        328
      2. group Id
        FG001
        num Subjects
        165
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        327
      2. group Id
        FG001
        num Subjects
        161
      type
      Received At Least One Dose of Study Drug
    3. achievements
      1. group Id
        FG000
        num Subjects
        63
      2. group Id
        FG001
        num Subjects
        30
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        265
      2. group Id
        FG001
        num Subjects
        135
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
Completers are participants who died.

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Preserved source evidence · Not medical advice