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NCT01536145 · OUTCOME

Single Dose End-of-infusion Concentration (Cinf) for CP-751,871

CP-751,871 Treatment For Patients With Multiple Myeloma · Source last updated 2013-03-15

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

Measure
MEAN
Unit
milligram/liter (mg/L)
Interval / dispersion
Standard Deviation
Time frame
1 hour postdose in Cycle 1

Analysis population: All participants treated who had at least 1 concentration.

Groups in this outcome

CP-751,871 0.025 mg/kg

CP-751,871 0.025 milligram/kilogram (mg/kg) administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)

CP-751,871 0.05 mg/kg

CP-751,871 0.05 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)

CP-751,871 0.1 mg/kg

CP-751,871 0.1 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)

CP-751,871 0.2 mg/kg

CP-751,871 0.2 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)

CP-751,871 0.4 mg/kg

CP-751,871 0.4 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)

CP-751,871 0.8 mg/kg

CP-751,871 0.8 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)

CP-751,871 1.5 mg/kg

CP-751,871 1.5 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)

CP-751,871 3 mg/kg

CP-751,871 3 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent Cycles, starting from Cycle 2 (4 weeks)

CP-751,871 6 mg/kg

CP-751,871 6 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)

CP-751,871 10 mg/kg

CP-751,871 10 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks) and subsequent cycles, starting from Cycle 2 (4 weeks)

CP-751,871 20 mg/kg

CP-751,871 20 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks) and subsequent cycles, starting from Cycle 2 (4 weeks)

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

Analysis denominator · Participants

GroupSource count
CP-751,871 0.025 mg/kg2
CP-751,871 0.05 mg/kg4
CP-751,871 0.1 mg/kg3
CP-751,871 0.2 mg/kg3
CP-751,871 0.4 mg/kg4
CP-751,871 0.8 mg/kg2
CP-751,871 1.5 mg/kg3
CP-751,871 3 mg/kg4
CP-751,871 6 mg/kg3
CP-751,871 10 mg/kg7
CP-751,871 20 mg/kg9

Reported measurements

Source class 1
Values in milligram/liter (mg/L) · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
CP-751,871 0.025 mg/kg0NANot reportedNot reportedNumber of participants analyzed was less than 3, thus standard deviation was not calculated.
CP-751,871 0.05 mg/kg0.3810.448Not reportedNot reportedNot reported
CP-751,871 0.1 mg/kg5.326.85Not reportedNot reportedNot reported
CP-751,871 0.2 mg/kg5.361.52Not reportedNot reportedNot reported
CP-751,871 0.4 mg/kg6.662.84Not reportedNot reportedNot reported
CP-751,871 0.8 mg/kg14.6NANot reportedNot reportedNumber of participants analyzed was less than 3, thus standard deviation was not calculated.
CP-751,871 1.5 mg/kg26.09.03Not reportedNot reportedNot reported
CP-751,871 3 mg/kg62.713.5Not reportedNot reportedNot reported
CP-751,871 6 mg/kg15957.2Not reportedNot reportedNot reported
CP-751,871 10 mg/kg16557.3Not reportedNot reportedNot reported
CP-751,871 20 mg/kg238215Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. comment
        Number of participants analyzed was less than 3, thus standard deviation was not calculated.
        group Id
        OG000
        spread
        NA
        value
        0
      2. group Id
        OG001
        spread
        0.448
        value
        0.381
      3. group Id
        OG002
        spread
        6.85
        value
        5.32
      4. group Id
        OG003
        spread
        1.52
        value
        5.36
      5. group Id
        OG004
        spread
        2.84
        value
        6.66
      6. comment
        Number of participants analyzed was less than 3, thus standard deviation was not calculated.
        group Id
        OG005
        spread
        NA
        value
        14.6
      7. group Id
        OG006
        spread
        9.03
        value
        26.0
      8. group Id
        OG007
        spread
        13.5
        value
        62.7
      9. group Id
        OG008
        spread
        57.2
        value
        159
      10. group Id
        OG009
        spread
        57.3
        value
        165
      11. group Id
        OG010
        spread
        215
        value
        238
denoms
  1. counts
    1. group Id
      OG000
      value
      2
    2. group Id
      OG001
      value
      4
    3. group Id
      OG002
      value
      3
    4. group Id
      OG003
      value
      3
    5. group Id
      OG004
      value
      4
    6. group Id
      OG005
      value
      2
    7. group Id
      OG006
      value
      3
    8. group Id
      OG007
      value
      4
    9. group Id
      OG008
      value
      3
    10. group Id
      OG009
      value
      7
    11. group Id
      OG010
      value
      9
    units
    Participants
dispersion Type
Standard Deviation
groups
  1. description
    CP-751,871 0.025 milligram/kilogram (mg/kg) administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)
    id
    OG000
    title
    CP-751,871 0.025 mg/kg
  2. description
    CP-751,871 0.05 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)
    id
    OG001
    title
    CP-751,871 0.05 mg/kg
  3. description
    CP-751,871 0.1 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)
    id
    OG002
    title
    CP-751,871 0.1 mg/kg
  4. description
    CP-751,871 0.2 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)
    id
    OG003
    title
    CP-751,871 0.2 mg/kg
  5. description
    CP-751,871 0.4 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)
    id
    OG004
    title
    CP-751,871 0.4 mg/kg
  6. description
    CP-751,871 0.8 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)
    id
    OG005
    title
    CP-751,871 0.8 mg/kg
  7. description
    CP-751,871 1.5 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)
    id
    OG006
    title
    CP-751,871 1.5 mg/kg
  8. description
    CP-751,871 3 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent Cycles, starting from Cycle 2 (4 weeks)
    id
    OG007
    title
    CP-751,871 3 mg/kg
  9. description
    CP-751,871 6 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks), and dose of 50% from the Cycle 1 dose administered on Day 1 of subsequent cycles, starting from Cycle 2 (4 weeks)
    id
    OG008
    title
    CP-751,871 6 mg/kg
  10. description
    CP-751,871 10 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks) and subsequent cycles, starting from Cycle 2 (4 weeks)
    id
    OG009
    title
    CP-751,871 10 mg/kg
  11. description
    CP-751,871 20 mg/kg administered intravenously on Day 1 of Cycle 1 (4 weeks or 8 weeks) and subsequent cycles, starting from Cycle 2 (4 weeks)
    id
    OG010
    title
    CP-751,871 20 mg/kg
param Type
MEAN
population Description
All participants treated who had at least 1 concentration.
reporting Status
POSTED
time Frame
1 hour postdose in Cycle 1
title
Single Dose End-of-infusion Concentration (Cinf) for CP-751,871
type
SECONDARY
unit Of Measure
milligram/liter (mg/L)

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Preserved source evidence · Not medical advice