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NCT04194944 · FLOW

Participant flow

A Study of Selpercatinib (LY3527723) in Participants With Advanced or Metastatic RET Fusion-Positive Non-Small Cell Lung Cancer · Source last updated 2025-10-21

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

groups
  1. description
    160 milligram (mg) Selpercatinib administered orally, twice daily (BID) continuously in 21-day cycles.
    id
    FG000
    title
    Selpercatinib (TRT A)
  2. description
    Pemetrexed 500 milligrams per meter squared (mg/m2) administered intravenously (IV) on Day 1, every 3 weeks (Q3W), plus investigator's choice of carboplatin area under the concentration versus time curve 5 (AUC 5 \[maximum dose 750 mg\]) IV, or cisplatin 75mg/m2 IV on Day 1 Q3W for 4 cycles, plus investigator's choice with or without 200 mg pembrolizumab IV on Day 1 Q3W up to 35 cycles.
    id
    FG001
    title
    Pemetrexed and Platinum With or Without Pembrolizumab (TRT B)
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      type
      Lost to Follow-up
    2. reasons
      1. group Id
        FG000
        num Subjects
        2
      2. group Id
        FG001
        num Subjects
        2
      type
      Withdrawal by Subject
    3. reasons
      1. group Id
        FG000
        num Subjects
        93
      2. group Id
        FG001
        num Subjects
        30
      type
      On Treatment
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        159
      2. group Id
        FG001
        num Subjects
        102
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        158
      2. group Id
        FG001
        num Subjects
        98
      type
      Received at Least One Dose of Study Drug
    3. achievements
      1. group Id
        FG000
        num Subjects
        61
      2. group Id
        FG001
        num Subjects
        70
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        98
      2. group Id
        FG001
        num Subjects
        32
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
If a participant has a recorded death on study, or is alive and being followed but off treatment, then the participant can be considered to be study completer.
Complete source fields
groups
  1. description
    160 milligram (mg) Selpercatinib administered orally, twice daily (BID) continuously in 21-day cycles.
    id
    FG000
    title
    Selpercatinib (TRT A)
  2. description
    Pemetrexed 500 milligrams per meter squared (mg/m2) administered intravenously (IV) on Day 1, every 3 weeks (Q3W), plus investigator's choice of carboplatin area under the concentration versus time curve 5 (AUC 5 \[maximum dose 750 mg\]) IV, or cisplatin 75mg/m2 IV on Day 1 Q3W for 4 cycles, plus investigator's choice with or without 200 mg pembrolizumab IV on Day 1 Q3W up to 35 cycles.
    id
    FG001
    title
    Pemetrexed and Platinum With or Without Pembrolizumab (TRT B)
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        0
      type
      Lost to Follow-up
    2. reasons
      1. group Id
        FG000
        num Subjects
        2
      2. group Id
        FG001
        num Subjects
        2
      type
      Withdrawal by Subject
    3. reasons
      1. group Id
        FG000
        num Subjects
        93
      2. group Id
        FG001
        num Subjects
        30
      type
      On Treatment
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        159
      2. group Id
        FG001
        num Subjects
        102
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        158
      2. group Id
        FG001
        num Subjects
        98
      type
      Received at Least One Dose of Study Drug
    3. achievements
      1. group Id
        FG000
        num Subjects
        61
      2. group Id
        FG001
        num Subjects
        70
      type
      COMPLETED
    4. achievements
      1. group Id
        FG000
        num Subjects
        98
      2. group Id
        FG001
        num Subjects
        32
      type
      NOT COMPLETED
    title
    Overall Study
pre Assignment Details
If a participant has a recorded death on study, or is alive and being followed but off treatment, then the participant can be considered to be study completer.

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Preserved source evidence · Not medical advice