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NCT03088540 · FLOW

Participant flow

Study of REGN 2810 Compared to Platinum-Based Chemotherapies in Participants With Metastatic Non-Small Cell Lung Cancer (NSCLC) · Source last updated 2026-06-25

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

groups
  1. description
    Participants received cemiplimab monotherapy
    id
    FG000
    title
    Cemiplimab
  2. description
    Participants received platinum-based doublet chemotherapy
    id
    FG001
    title
    Chemotherapy
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        157
      2. group Id
        FG001
        num Subjects
        184
      type
      Death
    3. reasons
      1. group Id
        FG000
        num Subjects
        10
      2. group Id
        FG001
        num Subjects
        6
      type
      Lost to Follow-up
    4. reasons
      1. group Id
        FG000
        num Subjects
        33
      2. group Id
        FG001
        num Subjects
        24
      type
      Subject Decision
    5. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        1
      type
      Sponsor Decision
    6. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        6
      type
      Physician Decision
    7. reasons
      1. group Id
        FG000
        num Subjects
        35
      2. group Id
        FG001
        num Subjects
        35
      type
      Disease Progression
    8. reasons
      1. group Id
        FG000
        num Subjects
        39
      2. group Id
        FG001
        num Subjects
        56
      type
      Withdrawal by Subject
    9. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        8
      type
      Other Than Specified
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        357
      2. group Id
        FG001
        num Subjects
        355
      comment
      Randomized
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        356
      2. group Id
        FG001
        num Subjects
        343
      type
      Randomized and Treated
    3. achievements
      1. group Id
        FG000
        num Subjects
        73
      2. group Id
        FG001
        num Subjects
        161
      type
      Completed Treatment
    4. achievements
      1. group Id
        FG000
        num Subjects
        75
      2. group Id
        FG001
        num Subjects
        35
      comment
      Completed Study
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        282
      2. group Id
        FG001
        num Subjects
        320
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Participants received cemiplimab monotherapy
    id
    FG000
    title
    Cemiplimab
  2. description
    Participants received platinum-based doublet chemotherapy
    id
    FG001
    title
    Chemotherapy
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        0
      type
      Adverse Event
    2. reasons
      1. group Id
        FG000
        num Subjects
        157
      2. group Id
        FG001
        num Subjects
        184
      type
      Death
    3. reasons
      1. group Id
        FG000
        num Subjects
        10
      2. group Id
        FG001
        num Subjects
        6
      type
      Lost to Follow-up
    4. reasons
      1. group Id
        FG000
        num Subjects
        33
      2. group Id
        FG001
        num Subjects
        24
      type
      Subject Decision
    5. reasons
      1. group Id
        FG000
        num Subjects
        1
      2. group Id
        FG001
        num Subjects
        1
      type
      Sponsor Decision
    6. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        6
      type
      Physician Decision
    7. reasons
      1. group Id
        FG000
        num Subjects
        35
      2. group Id
        FG001
        num Subjects
        35
      type
      Disease Progression
    8. reasons
      1. group Id
        FG000
        num Subjects
        39
      2. group Id
        FG001
        num Subjects
        56
      type
      Withdrawal by Subject
    9. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        8
      type
      Other Than Specified
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        357
      2. group Id
        FG001
        num Subjects
        355
      comment
      Randomized
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        356
      2. group Id
        FG001
        num Subjects
        343
      type
      Randomized and Treated
    3. achievements
      1. group Id
        FG000
        num Subjects
        73
      2. group Id
        FG001
        num Subjects
        161
      type
      Completed Treatment
    4. achievements
      1. group Id
        FG000
        num Subjects
        75
      2. group Id
        FG001
        num Subjects
        35
      comment
      Completed Study
      type
      COMPLETED
    5. achievements
      1. group Id
        FG000
        num Subjects
        282
      2. group Id
        FG001
        num Subjects
        320
      type
      NOT COMPLETED
    title
    Overall Study

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

Preserved source evidence · Not medical advice