Skip to content
← Full study record

NCT01776723 · FLOW

Participant flow

A Sequential Two-Stage Dose Escalation Study to Evaluate the Safety and Efficacy of Ruxolitinib · Source last updated 2022-09-22

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

groups
  1. description
    Phase 1, Level 1: Ruxolitinib 5 mg twice daily
    id
    FG000
    title
    Phase 1, Level 1: Ruxolitinib 10 mg
  2. description
    Phase 1 Level 2: Ruxolitinib 10 mg twice daily
    id
    FG001
    title
    Phase 1 Level 2: Ruxolitinib 20 mg
  3. description
    Phase 1 Level 3: Ruxolitinib 15 mg twice daily
    id
    FG002
    title
    Phase 1 Level 3: Ruxolitinib 30 mg
  4. description
    Phase 1 Level 4: 20 mg Ruxolitinib twice daily
    id
    FG003
    title
    Phase 1 Level 4: 40 mg Ruxolitinib
  5. description
    Phase II: Treatment at Maximum Tolerated Dose (MTD).
    id
    FG004
    title
    Phase 2: Maximum Tolerated Dose - Ruxolitinib
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        6
      2. group Id
        FG001
        num Subjects
        4
      3. group Id
        FG002
        num Subjects
        5
      4. group Id
        FG003
        num Subjects
        5
      5. group Id
        FG004
        num Subjects
        30
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        6
      2. group Id
        FG001
        num Subjects
        4
      3. group Id
        FG002
        num Subjects
        5
      4. group Id
        FG003
        num Subjects
        5
      5. group Id
        FG004
        num Subjects
        30
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      5. group Id
        FG004
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Phase 1, Level 1: Ruxolitinib 5 mg twice daily
    id
    FG000
    title
    Phase 1, Level 1: Ruxolitinib 10 mg
  2. description
    Phase 1 Level 2: Ruxolitinib 10 mg twice daily
    id
    FG001
    title
    Phase 1 Level 2: Ruxolitinib 20 mg
  3. description
    Phase 1 Level 3: Ruxolitinib 15 mg twice daily
    id
    FG002
    title
    Phase 1 Level 3: Ruxolitinib 30 mg
  4. description
    Phase 1 Level 4: 20 mg Ruxolitinib twice daily
    id
    FG003
    title
    Phase 1 Level 4: 40 mg Ruxolitinib
  5. description
    Phase II: Treatment at Maximum Tolerated Dose (MTD).
    id
    FG004
    title
    Phase 2: Maximum Tolerated Dose - Ruxolitinib
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        6
      2. group Id
        FG001
        num Subjects
        4
      3. group Id
        FG002
        num Subjects
        5
      4. group Id
        FG003
        num Subjects
        5
      5. group Id
        FG004
        num Subjects
        30
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        6
      2. group Id
        FG001
        num Subjects
        4
      3. group Id
        FG002
        num Subjects
        5
      4. group Id
        FG003
        num Subjects
        5
      5. group Id
        FG004
        num Subjects
        30
      type
      COMPLETED
    3. achievements
      1. group Id
        FG000
        num Subjects
        0
      2. group Id
        FG001
        num Subjects
        0
      3. group Id
        FG002
        num Subjects
        0
      4. group Id
        FG003
        num Subjects
        0
      5. group Id
        FG004
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study

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

Preserved source evidence · Not medical advice