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NCT01034553 · FLOW

Participant flow

Aurora A Kinase Inhibitor MLN8237 and Bortezomib in Treating Patients With Relapsed or Refractory Multiple Myeloma · Source last updated 2016-05-25

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

groups
  1. description
    Patients receive 25mg aurora A kinase inhibitor MLN8237 once daily on days 1-14 and 1.3mg Bortezomib on days 1, 4,8, and 11. Aurora A kinase inhibitor MLN8237: Given orally bortezomib: Given IV
    id
    FG000
    title
    Phase I, Dose 0**
  2. description
    Patients receive 20mg aurora A kinase inhibitor MLN8237 twice daily on days 1-7 and 1.5mg Bortezomib on days 1, 8,15, and 22. Aurora A kinase inhibitor MLN8237: Given orally bortezomib: Given IV
    id
    FG001
    title
    Phase I, Dose 0
  3. description
    Patients receive 30mg aurora A kinase inhibitor MLN8237 twice daily on days 1-7 and 1.5mg Bortezomib on days 1, 8,15, and 22. Aurora A kinase inhibitor MLN8237: Given orally bortezomib: Given IV
    id
    FG002
    title
    Phase I, Dose 1
  4. description
    Patients receive 40mg aurora A kinase inhibitor MLN8237 twice daily on days 1-7 and 1.5mg Bortezomib on days 1, 8,15, and 22. Aurora A kinase inhibitor MLN8237: Given orally bortezomib: Given IV
    id
    FG003
    title
    Phase I, Dose 2
  5. description
    Patients receive 50mg aurora A kinase inhibitor MLN8237 twice daily on days 1-7 and 1.5mg Bortezomib on days 1, 8,15, and 22. Aurora A kinase inhibitor MLN8237: Given orally bortezomib: Given IV
    id
    FG004
    title
    Phase I, Dose 3
  6. description
    Patients receive 50mg aurora A kinase inhibitor MLN8237 twice daily on days 1-7 and 1.5mg Bortezomib on days 1, 8,15, and 22. \> \> Aurora A kinase inhibitor MLN8237: Given orally \> \> bortezomib: Given IV
    id
    FG005
    title
    Phase II, Dose 3
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        4
      3. group Id
        FG002
        num Subjects
        3
      4. group Id
        FG003
        num Subjects
        3
      5. group Id
        FG004
        num Subjects
        6
      6. group Id
        FG005
        num Subjects
        7
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        4
      3. group Id
        FG002
        num Subjects
        3
      4. group Id
        FG003
        num Subjects
        3
      5. group Id
        FG004
        num Subjects
        6
      6. group Id
        FG005
        num Subjects
        7
      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
      6. group Id
        FG005
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study
Complete source fields
groups
  1. description
    Patients receive 25mg aurora A kinase inhibitor MLN8237 once daily on days 1-14 and 1.3mg Bortezomib on days 1, 4,8, and 11. Aurora A kinase inhibitor MLN8237: Given orally bortezomib: Given IV
    id
    FG000
    title
    Phase I, Dose 0**
  2. description
    Patients receive 20mg aurora A kinase inhibitor MLN8237 twice daily on days 1-7 and 1.5mg Bortezomib on days 1, 8,15, and 22. Aurora A kinase inhibitor MLN8237: Given orally bortezomib: Given IV
    id
    FG001
    title
    Phase I, Dose 0
  3. description
    Patients receive 30mg aurora A kinase inhibitor MLN8237 twice daily on days 1-7 and 1.5mg Bortezomib on days 1, 8,15, and 22. Aurora A kinase inhibitor MLN8237: Given orally bortezomib: Given IV
    id
    FG002
    title
    Phase I, Dose 1
  4. description
    Patients receive 40mg aurora A kinase inhibitor MLN8237 twice daily on days 1-7 and 1.5mg Bortezomib on days 1, 8,15, and 22. Aurora A kinase inhibitor MLN8237: Given orally bortezomib: Given IV
    id
    FG003
    title
    Phase I, Dose 2
  5. description
    Patients receive 50mg aurora A kinase inhibitor MLN8237 twice daily on days 1-7 and 1.5mg Bortezomib on days 1, 8,15, and 22. Aurora A kinase inhibitor MLN8237: Given orally bortezomib: Given IV
    id
    FG004
    title
    Phase I, Dose 3
  6. description
    Patients receive 50mg aurora A kinase inhibitor MLN8237 twice daily on days 1-7 and 1.5mg Bortezomib on days 1, 8,15, and 22. \> \> Aurora A kinase inhibitor MLN8237: Given orally \> \> bortezomib: Given IV
    id
    FG005
    title
    Phase II, Dose 3
periods
  1. milestones
    1. achievements
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        4
      3. group Id
        FG002
        num Subjects
        3
      4. group Id
        FG003
        num Subjects
        3
      5. group Id
        FG004
        num Subjects
        6
      6. group Id
        FG005
        num Subjects
        7
      type
      STARTED
    2. achievements
      1. group Id
        FG000
        num Subjects
        3
      2. group Id
        FG001
        num Subjects
        4
      3. group Id
        FG002
        num Subjects
        3
      4. group Id
        FG003
        num Subjects
        3
      5. group Id
        FG004
        num Subjects
        6
      6. group Id
        FG005
        num Subjects
        7
      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
      6. group Id
        FG005
        num Subjects
        0
      type
      NOT COMPLETED
    title
    Overall Study

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Preserved source evidence · Not medical advice