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NCT04101331 · FLOW

Participant flow

Phase II Study to Assess AFM13 in Patients With R/R CD30-positive T-cell Lymphoma or Transformed Mycosis Fungoides · Source last updated 2024-11-05

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

groups
  1. description
    Subjects with Relapsed or Refractory CD30 positive Peripheral T-cell Lymphoma (PTCL).
    id
    FG000
    title
    Cohort A
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        9
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        82
      type
      Disease progression
    3. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal by Subject
    4. reasons
      1. group Id
        FG000
        num Subjects
        6
      type
      Investigator decision
    5. reasons
      1. group Id
        FG000
        num Subjects
        6
      type
      Death
    6. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Allogenic transplant
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        108
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        3
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        105
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
All the subjects were screened for CD30 expression. Investigators assessed the subjects, and they were enrolled in the study if they met all inclusion criteria and none of the exclusion criteria.
recruitment Details
This study was a Phase II open-label multicenter study to assess the efficacy and safety of AFM13 in subjects with relapsed or refractory CD30-positive peripheral T-cell lymphoma.
Complete source fields
groups
  1. description
    Subjects with Relapsed or Refractory CD30 positive Peripheral T-cell Lymphoma (PTCL).
    id
    FG000
    title
    Cohort A
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        9
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        82
      type
      Disease progression
    3. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal by Subject
    4. reasons
      1. group Id
        FG000
        num Subjects
        6
      type
      Investigator decision
    5. reasons
      1. group Id
        FG000
        num Subjects
        6
      type
      Death
    6. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Allogenic transplant
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        108
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        3
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        105
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
All the subjects were screened for CD30 expression. Investigators assessed the subjects, and they were enrolled in the study if they met all inclusion criteria and none of the exclusion criteria.
recruitment Details
This study was a Phase II open-label multicenter study to assess the efficacy and safety of AFM13 in subjects with relapsed or refractory CD30-positive peripheral T-cell lymphoma.

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Preserved source evidence · Not medical advice