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NCT02654990 · FLOW

Participant flow

Panobinostat/Bortezomib/Dexamethasone in Relapsed or Relapsed-and-refractory Multiple Myeloma · Source last updated 2024-07-12

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

groups
  1. description
    Participants received 20 milligrams (mg) panobinostat thrice a week (TIW), 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
    id
    FG000
    title
    Arm A - Panobinostat (20 mg, TIW)
  2. description
    Participants received 20 mg panobinostat twice a week (BIW), 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
    id
    FG001
    title
    Arm B - Panobinostat (20 mg, BIW)
  3. description
    Participants received 10 mg panobinostat TIW, 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
    id
    FG002
    title
    Arm C - Panobinostat (10 mg, TIW)
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        82
      2. group Id
        FG001
        num Subjects
        83
      3. group Id
        FG002
        num Subjects
        83
      comment
      Full analysis set (FAS): all participants to whom study treatment was assigned by randomization.
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        79
      2. group Id
        FG001
        num Subjects
        82
      3. group Id
        FG002
        num Subjects
        80
      comment
      Safety Set: all participants who received any study treatment.
      type
      Received at Least 1 Dose of Study Drug
    3. achievements
      1. group Id
        FG000
        num Subjects
        82
      2. group Id
        FG001
        num Subjects
        83
      3. group Id
        FG002
        num Subjects
        83
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Participants received 20 milligrams (mg) panobinostat thrice a week (TIW), 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
    id
    FG000
    title
    Arm A - Panobinostat (20 mg, TIW)
  2. description
    Participants received 20 mg panobinostat twice a week (BIW), 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
    id
    FG001
    title
    Arm B - Panobinostat (20 mg, BIW)
  3. description
    Participants received 10 mg panobinostat TIW, 2 weeks on/1 week off in combination with subcutaneous bortezomib and oral dexamethasone.
    id
    FG002
    title
    Arm C - Panobinostat (10 mg, TIW)
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        82
      2. group Id
        FG001
        num Subjects
        83
      3. group Id
        FG002
        num Subjects
        83
      comment
      Full analysis set (FAS): all participants to whom study treatment was assigned by randomization.
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        79
      2. group Id
        FG001
        num Subjects
        82
      3. group Id
        FG002
        num Subjects
        80
      comment
      Safety Set: all participants who received any study treatment.
      type
      Received at Least 1 Dose of Study Drug
    3. achievements
      1. group Id
        FG000
        num Subjects
        82
      2. group Id
        FG001
        num Subjects
        83
      3. group Id
        FG002
        num Subjects
        83
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice