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NCT02082977 · OUTCOME

Part 1: Maximum Observed Plasma Concentration (Cmax) Following Single and Repeat Dose Administration of GSK2816126

A Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics and Clinical Activity of GSK2816126 in Subjects With Relapsed/Refractory Diffuse Large B Cell Lymphoma, Transformed Follicular Lymphoma, Other Non-Hodgkin's Lymphomas, Solid Tumors and Multiple Myeloma · Source last updated 2020-02-25

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

Measure
GEOMETRIC_MEAN
Unit
Microgram per milliliter
Interval / dispersion
Geometric Coefficient of Variation
Time frame
Pre-dose, 0.5, 1, 2, (12, 18 on Day 1 only), 24, and 96 hours post-dose from start of infusion; 0.5, 1, 2, 4, 6 hours from end of infusion on Cycle 1 of Day 1 and Day 15 (Each cycle was of 28 days)

What was measured

Blood samples were collected from participants for pharmacokinetic analysis including Cmax following single (Day 1) and repeat dose (Day 15) administration of GSK2816126. Pharmacokinetic analysis of GSK2816126 in Part 1 was conducted by non-compartmental methods. NA indicates data was not available since geometric coefficient of variation could not be calculated for single participant. Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles).

Analysis population: Pharmacokinetic Population

Groups in this outcome

Part 1:GSK2816126 50 mg Twice-weekly

Eligible participants received GSK2816126 with a starting dose of 50 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).

Part 1:GSK2816126 100 mg Twice-weekly

Eligible participants received GSK2816126 with a dose of 100 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).

Part 1:GSK2816126 200 mg Twice-weekly

Eligible participants received GSK2816126 with a dose of 200 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).

Part 1:GSK2816126 400 mg Twice-weekly

Eligible participants received GSK2816126 with a dose of 400 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).

Part 1:GSK2816126 800 mg Twice-weekly

Eligible participants received GSK2816126 with a dose of 800 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).

Part 1:GSK2816126 1200 mg Twice-weekly

Eligible participants received GSK2816126 with a dose of 1200 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).

Part 1:GSK2816126 1800 mg Twice-weekly

Eligible participants received GSK2816126 with a dose of 1800 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).

Part 1:GSK2816126 2400 mg Twice-weekly

Eligible participants received GSK2816126 with a dose of 2400 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).

Part 1:GSK2816126 3000 mg Twice-weekly

Eligible participants received GSK2816126 with a dose of 3000 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).

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

Analysis denominator · Participants

GroupSource count
Part 1:GSK2816126 50 mg Twice-weekly2
Part 1:GSK2816126 100 mg Twice-weekly1
Part 1:GSK2816126 200 mg Twice-weekly1
Part 1:GSK2816126 400 mg Twice-weekly1
Part 1:GSK2816126 800 mg Twice-weekly3
Part 1:GSK2816126 1200 mg Twice-weekly4
Part 1:GSK2816126 1800 mg Twice-weekly10
Part 1:GSK2816126 2400 mg Twice-weekly12
Part 1:GSK2816126 3000 mg Twice-weekly7

Reported measurements

Day 1; n=2,1,1,1,3,4,10,12,7

Analysis denominator · Participants

GroupSource count
Part 1:GSK2816126 50 mg Twice-weekly2
Part 1:GSK2816126 100 mg Twice-weekly1
Part 1:GSK2816126 200 mg Twice-weekly1
Part 1:GSK2816126 400 mg Twice-weekly1
Part 1:GSK2816126 800 mg Twice-weekly3
Part 1:GSK2816126 1200 mg Twice-weekly4
Part 1:GSK2816126 1800 mg Twice-weekly10
Part 1:GSK2816126 2400 mg Twice-weekly12
Part 1:GSK2816126 3000 mg Twice-weekly7
Values in Microgram per milliliter · Interval/dispersion: Geometric Coefficient of Variation
GroupValueSpreadLowerUpperComment
Part 1:GSK2816126 50 mg Twice-weekly0.4252Not reportedNot reportedNot reported
Part 1:GSK2816126 100 mg Twice-weekly1.10NANot reportedNot reportedNA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
Part 1:GSK2816126 200 mg Twice-weekly1.40NANot reportedNot reportedNA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
Part 1:GSK2816126 400 mg Twice-weekly4.00NANot reportedNot reportedNA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
Part 1:GSK2816126 800 mg Twice-weekly7.3116Not reportedNot reportedNot reported
Part 1:GSK2816126 1200 mg Twice-weekly10.9110Not reportedNot reportedNot reported
Part 1:GSK2816126 1800 mg Twice-weekly13.0427Not reportedNot reportedNot reported
Part 1:GSK2816126 2400 mg Twice-weekly22.2635Not reportedNot reportedNot reported
Part 1:GSK2816126 3000 mg Twice-weekly23.8321Not reportedNot reportedNot reported
Day 15; n=1,1,1,1,3,4,9,11,4

Analysis denominator · Participants

GroupSource count
Part 1:GSK2816126 50 mg Twice-weekly1
Part 1:GSK2816126 100 mg Twice-weekly1
Part 1:GSK2816126 200 mg Twice-weekly1
Part 1:GSK2816126 400 mg Twice-weekly1
Part 1:GSK2816126 800 mg Twice-weekly3
Part 1:GSK2816126 1200 mg Twice-weekly4
Part 1:GSK2816126 1800 mg Twice-weekly9
Part 1:GSK2816126 2400 mg Twice-weekly11
Part 1:GSK2816126 3000 mg Twice-weekly4
Values in Microgram per milliliter · Interval/dispersion: Geometric Coefficient of Variation
GroupValueSpreadLowerUpperComment
Part 1:GSK2816126 50 mg Twice-weekly0.50NANot reportedNot reportedNA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
Part 1:GSK2816126 100 mg Twice-weekly1.00NANot reportedNot reportedNA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
Part 1:GSK2816126 200 mg Twice-weekly1.50NANot reportedNot reportedNA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
Part 1:GSK2816126 400 mg Twice-weekly3.50NANot reportedNot reportedNA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
Part 1:GSK2816126 800 mg Twice-weekly7.4613Not reportedNot reportedNot reported
Part 1:GSK2816126 1200 mg Twice-weekly11.6227Not reportedNot reportedNot reported
Part 1:GSK2816126 1800 mg Twice-weekly14.2127Not reportedNot reportedNot reported
Part 1:GSK2816126 2400 mg Twice-weekly21.6227Not reportedNot reportedNot reported
Part 1:GSK2816126 3000 mg Twice-weekly30.4814Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        spread
        52
        value
        0.42
      2. comment
        NA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
        group Id
        OG001
        spread
        NA
        value
        1.10
      3. comment
        NA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
        group Id
        OG002
        spread
        NA
        value
        1.40
      4. comment
        NA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
        group Id
        OG003
        spread
        NA
        value
        4.00
      5. group Id
        OG004
        spread
        16
        value
        7.31
      6. group Id
        OG005
        spread
        10
        value
        10.91
      7. group Id
        OG006
        spread
        27
        value
        13.04
      8. group Id
        OG007
        spread
        35
        value
        22.26
      9. group Id
        OG008
        spread
        21
        value
        23.83
    denoms
    1. counts
      1. group Id
        OG000
        value
        2
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        1
      4. group Id
        OG003
        value
        1
      5. group Id
        OG004
        value
        3
      6. group Id
        OG005
        value
        4
      7. group Id
        OG006
        value
        10
      8. group Id
        OG007
        value
        12
      9. group Id
        OG008
        value
        7
      units
      Participants
    title
    Day 1; n=2,1,1,1,3,4,10,12,7
  2. categories
    1. measurements
      1. comment
        NA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
        group Id
        OG000
        spread
        NA
        value
        0.50
      2. comment
        NA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
        group Id
        OG001
        spread
        NA
        value
        1.00
      3. comment
        NA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
        group Id
        OG002
        spread
        NA
        value
        1.50
      4. comment
        NA indicates data was not available since geometric coefficient of variation could not be calculated for single participant.
        group Id
        OG003
        spread
        NA
        value
        3.50
      5. group Id
        OG004
        spread
        13
        value
        7.46
      6. group Id
        OG005
        spread
        27
        value
        11.62
      7. group Id
        OG006
        spread
        27
        value
        14.21
      8. group Id
        OG007
        spread
        27
        value
        21.62
      9. group Id
        OG008
        spread
        14
        value
        30.48
    denoms
    1. counts
      1. group Id
        OG000
        value
        1
      2. group Id
        OG001
        value
        1
      3. group Id
        OG002
        value
        1
      4. group Id
        OG003
        value
        1
      5. group Id
        OG004
        value
        3
      6. group Id
        OG005
        value
        4
      7. group Id
        OG006
        value
        9
      8. group Id
        OG007
        value
        11
      9. group Id
        OG008
        value
        4
      units
      Participants
    title
    Day 15; n=1,1,1,1,3,4,9,11,4
denoms
  1. counts
    1. group Id
      OG000
      value
      2
    2. group Id
      OG001
      value
      1
    3. group Id
      OG002
      value
      1
    4. group Id
      OG003
      value
      1
    5. group Id
      OG004
      value
      3
    6. group Id
      OG005
      value
      4
    7. group Id
      OG006
      value
      10
    8. group Id
      OG007
      value
      12
    9. group Id
      OG008
      value
      7
    units
    Participants
description
Blood samples were collected from participants for pharmacokinetic analysis including Cmax following single (Day 1) and repeat dose (Day 15) administration of GSK2816126. Pharmacokinetic analysis of GSK2816126 in Part 1 was conducted by non-compartmental methods. NA indicates data was not available since geometric coefficient of variation could not be calculated for single participant. Only those participants with data available at the specified data points were analyzed (represented by n= X in the category titles).
dispersion Type
Geometric Coefficient of Variation
groups
  1. description
    Eligible participants received GSK2816126 with a starting dose of 50 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).
    id
    OG000
    title
    Part 1:GSK2816126 50 mg Twice-weekly
  2. description
    Eligible participants received GSK2816126 with a dose of 100 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).
    id
    OG001
    title
    Part 1:GSK2816126 100 mg Twice-weekly
  3. description
    Eligible participants received GSK2816126 with a dose of 200 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).
    id
    OG002
    title
    Part 1:GSK2816126 200 mg Twice-weekly
  4. description
    Eligible participants received GSK2816126 with a dose of 400 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).
    id
    OG003
    title
    Part 1:GSK2816126 400 mg Twice-weekly
  5. description
    Eligible participants received GSK2816126 with a dose of 800 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).
    id
    OG004
    title
    Part 1:GSK2816126 800 mg Twice-weekly
  6. description
    Eligible participants received GSK2816126 with a dose of 1200 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).
    id
    OG005
    title
    Part 1:GSK2816126 1200 mg Twice-weekly
  7. description
    Eligible participants received GSK2816126 with a dose of 1800 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).
    id
    OG006
    title
    Part 1:GSK2816126 1800 mg Twice-weekly
  8. description
    Eligible participants received GSK2816126 with a dose of 2400 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).
    id
    OG007
    title
    Part 1:GSK2816126 2400 mg Twice-weekly
  9. description
    Eligible participants received GSK2816126 with a dose of 3000 mg twice-weekly, as an intravenous solution for 28 days (3 weeks on/1 week off).
    id
    OG008
    title
    Part 1:GSK2816126 3000 mg Twice-weekly
param Type
GEOMETRIC_MEAN
population Description
Pharmacokinetic Population
reporting Status
POSTED
time Frame
Pre-dose, 0.5, 1, 2, (12, 18 on Day 1 only), 24, and 96 hours post-dose from start of infusion; 0.5, 1, 2, 4, 6 hours from end of infusion on Cycle 1 of Day 1 and Day 15 (Each cycle was of 28 days)
title
Part 1: Maximum Observed Plasma Concentration (Cmax) Following Single and Repeat Dose Administration of GSK2816126
type
SECONDARY
unit Of Measure
Microgram per milliliter

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Preserved source evidence · Not medical advice