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NCT03529422 · FLOW

Participant flow

Durvalumab With Radiotherapy for Adjuvant Treatment of Intermediate Risk SCCHN · Source last updated 2026-06-23

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

groups
  1. description
    Durvalumab in combination with intensity modulated radiotherapy (IMRT) treatments Durvalumab: Durvalumab 1500mg IV every 3 weeks for 6 cycles Intensity Modulated Radiotherapy Treatments: Total dose will be 60 Gray (Gy) at 2Gy per fractions for 30 fractions delivered Monday through Friday for 6 weeks
    id
    FG000
    title
    Open-label, Single-arm
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal by Subject
    2. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Protocol Violation
    3. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Disease progression
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        18
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        14
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        4
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
Participants were enrolled in the study between 10/07/2019 and 05/04/2021 at three cancer centers in the United States.
Complete source fields
groups
  1. description
    Durvalumab in combination with intensity modulated radiotherapy (IMRT) treatments Durvalumab: Durvalumab 1500mg IV every 3 weeks for 6 cycles Intensity Modulated Radiotherapy Treatments: Total dose will be 60 Gray (Gy) at 2Gy per fractions for 30 fractions delivered Monday through Friday for 6 weeks
    id
    FG000
    title
    Open-label, Single-arm
periods
  1. drop Withdraws
    1. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Withdrawal by Subject
    2. reasons
      1. group Id
        FG000
        num Subjects
        1
      type
      Protocol Violation
    3. reasons
      1. group Id
        FG000
        num Subjects
        2
      type
      Disease progression
    milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        18
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        14
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        4
      type
      NOT COMPLETED
    title
    Overall Study
recruitment Details
Participants were enrolled in the study between 10/07/2019 and 05/04/2021 at three cancer centers in the United States.

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice