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NCT00153920 · FLOW

Participant flow

Bortezomib (Velcade) in Patients With Untreated Multiple Myeloma · Source last updated 2019-06-11

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

groups
  1. description
    Participants received intravenous bortezomib on a 3-week dosing cycle: 1.3 mg/m2 on days 1, 4, 8 and 11 followed by 10 day rest period for up to 8 cycles or for 2 cycles beyond complete response. Participants with progressive disease or unacceptable toxicity discontinued treatment.
    id
    FG000
    title
    Bortezomib
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        9
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        9
      type
      Progressive Disease
    3. reasons
      1. group Id
        FG000
        num Subjects
        3
      type
      Physician Decision
    4. reasons
      1. group Id
        FG000
        num Subjects
        3
      type
      Lack of Response
    5. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Death
    6. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal by Subject
    7. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Non-Protocol Therapy
    8. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal of Consent before Trt
    9. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Progressive Disease before Trt
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        66
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        64
      type
      Eligible and Treated
    3. achievements
      1. group Id
        FG000
        num Subjects
        36
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        30
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
66 participants were enrolled between December 2003 and September 2005.
Complete source fields
groups
  1. description
    Participants received intravenous bortezomib on a 3-week dosing cycle: 1.3 mg/m2 on days 1, 4, 8 and 11 followed by 10 day rest period for up to 8 cycles or for 2 cycles beyond complete response. Participants with progressive disease or unacceptable toxicity discontinued treatment.
    id
    FG000
    title
    Bortezomib
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        9
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        9
      type
      Progressive Disease
    3. reasons
      1. group Id
        FG000
        num Subjects
        3
      type
      Physician Decision
    4. reasons
      1. group Id
        FG000
        num Subjects
        3
      type
      Lack of Response
    5. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Death
    6. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal by Subject
    7. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Non-Protocol Therapy
    8. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal of Consent before Trt
    9. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Progressive Disease before Trt
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        66
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        64
      type
      Eligible and Treated
    3. achievements
      1. group Id
        FG000
        num Subjects
        36
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        30
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
66 participants were enrolled between December 2003 and September 2005.

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Preserved source evidence · Not medical advice