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NCT02418000 · OUTCOME

Pharmacokinetic Profile of E6201 in Plasma: Cmax

A Study of E6201 for the Treatment of Advanced Hematologic Malignancies With FLT3 and/or Ras Mutations · Source last updated 2019-03-20

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

Measure
MEAN
Unit
ng/mL
Interval / dispersion
Standard Deviation
Time frame
Assessed at Cycle 1 Days 1 and 15, Cycle 2 Day 1, pre-dose, 5 minutes following the end of the 2-hour infusion, 2, 4, 8 and 24 hours post-infusion. Summary PK parameters for Cycle 1 Day 1 reported.

What was measured

Cmax: Maximum measured plasma concentration over the collection period

Analysis population: All subjects in the FAS who completed at least 1 pharmacokinetic (PK) assessment.

Groups in this outcome

E6201 240 mg/m^2 Weekly

E6201 240 mg/m\^2 IV over 2 hours once weekly, on Days 1, 8, 15, and 22, repeated every 28 days (= 1 cycle) until progression of disease, toxicity or other reason for discontinuation of study drug, and followed for up to 6 months after the last dose.

E6201 320 mg/m^2 Weekly

E6201 320 mg/m\^2 IV over 2 hours once weekly, on Days 1, 8, 15, and 22, repeated every 28 days (= 1 cycle) until progression of disease, toxicity or other reason for discontinuation of study drug, and followed for up to 6 months after the last dose.

E6201 160 mg/m^2 Twice Weekly

E6201 160 mg/m\^2 IV over 2 hours twice weekly, on Days 1, 4, 8, 11, 15, 18, 22 and 25, repeated every 28 days (= 1 cycle) until progression of disease, toxicity or other reason for discontinuation of study drug, and followed for up to 6 months after the last dose.

E6201 240 mg/m^2 Twice Weekly

E6201 240 mg/m\^2 IV over 2 hours twice weekly, on Days 1, 4, 8, 11, 15, 18, 22 and 25, repeated every 28 days (= 1 cycle) until progression of disease, toxicity or other reason for discontinuation of study drug, and followed for up to 6 months after the last dose.

E6201 320 mg/m^2 Twice Weekly

E6201 320 mg/m\^2 IV over 2 hours twice weekly, on Days 1, 4, 8, 11, 15, 18, 22 and 25, repeated every 28 days (= 1 cycle) until progression of disease, toxicity or other reason for discontinuation of study drug, and followed for up to 6 months after the last dose.

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
E6201 240 mg/m^2 Weekly7
E6201 320 mg/m^2 Weekly10
E6201 160 mg/m^2 Twice Weekly3
E6201 240 mg/m^2 Twice Weekly3
E6201 320 mg/m^2 Twice Weekly4

Reported measurements

Source class 1
Values in ng/mL · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
E6201 240 mg/m^2 Weekly1195.0410.6Not reportedNot reportedNot reported
E6201 320 mg/m^2 Weekly1430.3976.2Not reportedNot reportedNot reported
E6201 160 mg/m^2 Twice Weekly736.8750.7Not reportedNot reportedNot reported
E6201 240 mg/m^2 Twice Weekly941.6647.7Not reportedNot reportedNot reported
E6201 320 mg/m^2 Twice Weekly1681.125.6Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        spread
        10.6
        value
        1195.04
      2. group Id
        OG001
        spread
        76.2
        value
        1430.39
      3. group Id
        OG002
        spread
        50.7
        value
        736.87
      4. group Id
        OG003
        spread
        47.7
        value
        941.66
      5. group Id
        OG004
        spread
        5.6
        value
        1681.12
denoms
  1. counts
    1. group Id
      OG000
      value
      7
    2. group Id
      OG001
      value
      10
    3. group Id
      OG002
      value
      3
    4. group Id
      OG003
      value
      3
    5. group Id
      OG004
      value
      4
    units
    Participants
description
Cmax: Maximum measured plasma concentration over the collection period
dispersion Type
Standard Deviation
groups
  1. description
    E6201 240 mg/m\^2 IV over 2 hours once weekly, on Days 1, 8, 15, and 22, repeated every 28 days (= 1 cycle) until progression of disease, toxicity or other reason for discontinuation of study drug, and followed for up to 6 months after the last dose.
    id
    OG000
    title
    E6201 240 mg/m^2 Weekly
  2. description
    E6201 320 mg/m\^2 IV over 2 hours once weekly, on Days 1, 8, 15, and 22, repeated every 28 days (= 1 cycle) until progression of disease, toxicity or other reason for discontinuation of study drug, and followed for up to 6 months after the last dose.
    id
    OG001
    title
    E6201 320 mg/m^2 Weekly
  3. description
    E6201 160 mg/m\^2 IV over 2 hours twice weekly, on Days 1, 4, 8, 11, 15, 18, 22 and 25, repeated every 28 days (= 1 cycle) until progression of disease, toxicity or other reason for discontinuation of study drug, and followed for up to 6 months after the last dose.
    id
    OG002
    title
    E6201 160 mg/m^2 Twice Weekly
  4. description
    E6201 240 mg/m\^2 IV over 2 hours twice weekly, on Days 1, 4, 8, 11, 15, 18, 22 and 25, repeated every 28 days (= 1 cycle) until progression of disease, toxicity or other reason for discontinuation of study drug, and followed for up to 6 months after the last dose.
    id
    OG003
    title
    E6201 240 mg/m^2 Twice Weekly
  5. description
    E6201 320 mg/m\^2 IV over 2 hours twice weekly, on Days 1, 4, 8, 11, 15, 18, 22 and 25, repeated every 28 days (= 1 cycle) until progression of disease, toxicity or other reason for discontinuation of study drug, and followed for up to 6 months after the last dose.
    id
    OG004
    title
    E6201 320 mg/m^2 Twice Weekly
param Type
MEAN
population Description
All subjects in the FAS who completed at least 1 pharmacokinetic (PK) assessment.
reporting Status
POSTED
time Frame
Assessed at Cycle 1 Days 1 and 15, Cycle 2 Day 1, pre-dose, 5 minutes following the end of the 2-hour infusion, 2, 4, 8 and 24 hours post-infusion. Summary PK parameters for Cycle 1 Day 1 reported.
title
Pharmacokinetic Profile of E6201 in Plasma: Cmax
type
SECONDARY
unit Of Measure
ng/mL

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Preserved source evidence · Not medical advice