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NCT03568461 · FLOW

Participant flow

Efficacy and Safety of Tisagenlecleucel in Adult Patients With Refractory or Relapsed Follicular Lymphoma · Source last updated 2026-07-09

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

groups
  1. description
    All participants who were enrolled in the study
    id
    FG000
    title
    CTL019
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        7
      type
      Physician Decision
    3. reasons
      1. group Id
        FG000
        num Subjects
        7
      type
      Patient decision
    4. reasons
      1. group Id
        FG000
        num Subjects
        3
      type
      Lost to Follow-up
    5. reasons
      1. group Id
        FG000
        num Subjects
        22
      type
      Death
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        98
      comment
      Started = enrolled and entered pre-treatment phase
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        97
      comment
      Treated = infused with tisagenlecleucel
      type
      Treated
    3. achievements
      1. group Id
        FG000
        num Subjects
        1
      type
      Discontinued prior to infusion with tisagenlecleucel
    4. achievements
      1. group Id
        FG000
        num Subjects
        58
      comment
      Completed = Ongoing/in follow-up
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        40
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
During the Screening phase and prior to enrolment into the study, participants' white blood cells were collected via leukapheresis.
recruitment Details
90 participants were planned, 98 patients were enrolled and 97 participants were infused with tisagenlecleucel.
Complete source fields
groups
  1. description
    All participants who were enrolled in the study
    id
    FG000
    title
    CTL019
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        7
      type
      Physician Decision
    3. reasons
      1. group Id
        FG000
        num Subjects
        7
      type
      Patient decision
    4. reasons
      1. group Id
        FG000
        num Subjects
        3
      type
      Lost to Follow-up
    5. reasons
      1. group Id
        FG000
        num Subjects
        22
      type
      Death
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        98
      comment
      Started = enrolled and entered pre-treatment phase
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        97
      comment
      Treated = infused with tisagenlecleucel
      type
      Treated
    3. achievements
      1. group Id
        FG000
        num Subjects
        1
      type
      Discontinued prior to infusion with tisagenlecleucel
    4. achievements
      1. group Id
        FG000
        num Subjects
        58
      comment
      Completed = Ongoing/in follow-up
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        40
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
During the Screening phase and prior to enrolment into the study, participants' white blood cells were collected via leukapheresis.
recruitment Details
90 participants were planned, 98 patients were enrolled and 97 participants were infused with tisagenlecleucel.

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Preserved source evidence · Not medical advice