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NCT00445068 · FLOW

Participant flow

Efficacy and Safety of LBH589B in Adult Patients With Multiple Myeloma · Source last updated 2021-07-14

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

groups
  1. description
    Participants received panobinostat 20 milligrams (mg) orally once daily (OD), three times a week on days: 1, 3 and 5, then 8, 10 and 12, then 15, 17 and 19 of each cycle, as part of a 3-week (21 days) treatment cycle. Participants could continue treatment until disease progression or unacceptable toxicity.
    id
    FG000
    title
    Panobinostat
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        26
      type
      Disease progression
    2. reasons
      1. group Id
        FG000
        num Subjects
        5
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Abnormal laboratory value
    4. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Withdrawal by Subject
    5. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Death
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        38
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        2
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        36
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
A total 38 participants were enrolled in the study, of which 38 discontinued the study.
recruitment Details
The study was conducted at 27 centers in 6 countries
Complete source fields
groups
  1. description
    Participants received panobinostat 20 milligrams (mg) orally once daily (OD), three times a week on days: 1, 3 and 5, then 8, 10 and 12, then 15, 17 and 19 of each cycle, as part of a 3-week (21 days) treatment cycle. Participants could continue treatment until disease progression or unacceptable toxicity.
    id
    FG000
    title
    Panobinostat
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        26
      type
      Disease progression
    2. reasons
      1. group Id
        FG000
        num Subjects
        5
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Abnormal laboratory value
    4. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Withdrawal by Subject
    5. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Death
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        38
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        2
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        36
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
A total 38 participants were enrolled in the study, of which 38 discontinued the study.
recruitment Details
The study was conducted at 27 centers in 6 countries

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Preserved source evidence · Not medical advice