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NCT03595657 · FLOW

Participant flow

A Study of CS1001 in Subjects With Relapsed or Refractory Extranodal Natural Killer/ T Cell Lymphoma(ENKTL) · Source last updated 2024-06-18

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

groups
  1. description
    Participants received sugemalimab (CS1001) 1200 mg intravenously every 3 weeks (Q3W)
    id
    FG000
    title
    R/R ENKTL
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        14
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Death
    3. reasons
      1. group Id
        FG000
        num Subjects
        40
      type
      Lack of Efficacy
    4. reasons
      1. group Id
        FG000
        num Subjects
        10
      type
      Withdrawal by Subject
    5. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Dosing delayed over 9 weeks
    6. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Achieved CR and completed 2 years of treatment
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        80
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        13
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        67
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Participants received sugemalimab (CS1001) 1200 mg intravenously every 3 weeks (Q3W)
    id
    FG000
    title
    R/R ENKTL
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        14
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Death
    3. reasons
      1. group Id
        FG000
        num Subjects
        40
      type
      Lack of Efficacy
    4. reasons
      1. group Id
        FG000
        num Subjects
        10
      type
      Withdrawal by Subject
    5. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Dosing delayed over 9 weeks
    6. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Achieved CR and completed 2 years of treatment
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        80
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        13
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        67
      type
      NOT COMPLETED
    title
    Overall Study

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Independent clinical review pending · Not medical advice