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NCT03433001 · FLOW

Participant flow

A Study in Relapsed and/or Refractory Multiple Myeloma Patients Treated With Ixazomib Plus Lenalidomide and Dexamethasone · Source last updated 2023-12-07

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

groups
  1. description
    Participants took ixazomib, lenalidomide, and dexamethasone under conditions of standard medical care in this study. The dosage and administration of ixazomib, lenalidomide, and dexamethasone were not defined by the protocol but according to the package insert of each drug.
    id
    FG000
    title
    Ixazomib + Lenalidomide + Dexamethasone
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        109
      type
      Lack of Efficacy
    2. reasons
      1. group Id
        FG000
        num Subjects
        69
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        10
      type
      Withdrawal by Subject
    4. reasons
      1. group Id
        FG000
        num Subjects
        12
      type
      Death
    5. reasons
      1. group Id
        FG000
        num Subjects
        4
      type
      Lost to Follow-up
    6. reasons
      1. group Id
        FG000
        num Subjects
        25
      type
      Other
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        295
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        66
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        229
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
A total of 295 participants were enrolled and received the study treatment in this study.
recruitment Details
Participant s took part in the survey at 101 investigative sites in Japan, from 2 April 2018 to 11 June 2021.
Complete source fields
groups
  1. description
    Participants took ixazomib, lenalidomide, and dexamethasone under conditions of standard medical care in this study. The dosage and administration of ixazomib, lenalidomide, and dexamethasone were not defined by the protocol but according to the package insert of each drug.
    id
    FG000
    title
    Ixazomib + Lenalidomide + Dexamethasone
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        109
      type
      Lack of Efficacy
    2. reasons
      1. group Id
        FG000
        num Subjects
        69
      type
      Adverse Event
    3. reasons
      1. group Id
        FG000
        num Subjects
        10
      type
      Withdrawal by Subject
    4. reasons
      1. group Id
        FG000
        num Subjects
        12
      type
      Death
    5. reasons
      1. group Id
        FG000
        num Subjects
        4
      type
      Lost to Follow-up
    6. reasons
      1. group Id
        FG000
        num Subjects
        25
      type
      Other
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        295
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        66
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        229
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
A total of 295 participants were enrolled and received the study treatment in this study.
recruitment Details
Participant s took part in the survey at 101 investigative sites in Japan, from 2 April 2018 to 11 June 2021.

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Preserved source evidence · Not medical advice