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NCT02108652 · FLOW

Participant flow

A Study of Atezolizumab in Participants With Locally Advanced or Metastatic Urothelial Bladder Cancer (Cohort 2) · Source last updated 2024-03-28

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

groups
  1. description
    Participants who had disease progression during or following treatment with at least one platinum-containing chemotherapy regimen in the metastatic setting received atezolizumab 1200 milligrams (mg) via intravenous (IV) infusion on Day 1 of 21-day cycles until loss of clinical benefit or unmanageable toxicity.
    id
    FG000
    title
    Cohort 2: Participants With Second-line or Beyond Treatments
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        253
      type
      Death
    2. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Lost to Follow-up
    3. reasons
      1. group Id
        FG000
        num Subjects
        16
      type
      Withdrawal by Subject
    4. reasons
      1. group Id
        FG000
        num Subjects
        31
      type
      Study Terminated By Sponsor
    5. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Non-Compliance
    6. reasons
      1. group Id
        FG000
        num Subjects
        6
      type
      Physician Decision
    7. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Progression Of Disease
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        310
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        0
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        310
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
The analysis included data up to cutoff date 28 February 2023.
recruitment Details
The study is considered "Completed" because the planned study activities and analyses have been performed.
Complete source fields
groups
  1. description
    Participants who had disease progression during or following treatment with at least one platinum-containing chemotherapy regimen in the metastatic setting received atezolizumab 1200 milligrams (mg) via intravenous (IV) infusion on Day 1 of 21-day cycles until loss of clinical benefit or unmanageable toxicity.
    id
    FG000
    title
    Cohort 2: Participants With Second-line or Beyond Treatments
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        253
      type
      Death
    2. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Lost to Follow-up
    3. reasons
      1. group Id
        FG000
        num Subjects
        16
      type
      Withdrawal by Subject
    4. reasons
      1. group Id
        FG000
        num Subjects
        31
      type
      Study Terminated By Sponsor
    5. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Non-Compliance
    6. reasons
      1. group Id
        FG000
        num Subjects
        6
      type
      Physician Decision
    7. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Progression Of Disease
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        310
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        0
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        310
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
The analysis included data up to cutoff date 28 February 2023.
recruitment Details
The study is considered "Completed" because the planned study activities and analyses have been performed.

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Preserved source evidence · Not medical advice