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NCT02064387 · OUTCOME

Terminal Half-life (t1/2) of GSK2857916 Following IV Dose in Participants With Relapsed/Refractory MM - Part 1

Dose Escalation Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics, Immunogenicity and Clinical Activity of GSK2857916 · Source last updated 2020-08-11

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

Measure
GEOMETRIC_MEAN
Unit
Hours
Interval / dispersion
Geometric Coefficient of Variation
Time frame
Pre-dose, 30 minutes post-SOI, at EOI, 1, 3, 8 and 24 hours post-EOI of Day 1 (Cycle 1)

What was measured

Blood samples were collected at designated timepoints. PK parameters of GSK2857916 were calculated using non-compartmental methods. NA indicates that geometric coefficient of variation could not be calculated for a single participant.

Analysis population: PK Part 1 Population. Only those participants with data available at the specified data points were analyzed.

Groups in this outcome

Part 1: GSK2857916 0.03 mg/kg

Participants were administered a dose of 0.03 milligrams per kilogram (mg/kg) GSK2857916 as intravenous (IV) infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).

Part 1: GSK2857916 0.06 mg/kg

Participants were administered a dose of 0.06 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).

Part 1: GSK2857916 0.12 mg/kg

Participants were administered a dose of 0.12 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).

Part 1: GSK2857916 0.24 mg/kg

Participants were administered a dose of 0.24 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).

Part 1: GSK2857916 0.48 mg/kg

Participants were administered a dose of 0.48 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).

Part 1: GSK2857916 0.96 mg/kg

Participants were administered a dose of 0.96 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).

Part 1: GSK2857916 1.92 mg/kg

Participants were administered a dose of 1.92 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).

Part 1: GSK2857916 3.40 mg/kg

Participants were administered a dose of 3.40 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).

Part 1: GSK2857916 4.60 mg/kg

Participants were administered a dose of 4.60 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).

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: GSK2857916 0.03 mg/kg0
Part 1: GSK2857916 0.06 mg/kg1
Part 1: GSK2857916 0.12 mg/kg4
Part 1: GSK2857916 0.24 mg/kg3
Part 1: GSK2857916 0.48 mg/kg3
Part 1: GSK2857916 0.96 mg/kg2
Part 1: GSK2857916 1.92 mg/kg1
Part 1: GSK2857916 3.40 mg/kg0
Part 1: GSK2857916 4.60 mg/kg4

Reported measurements

Source class 1
Values in Hours · Interval/dispersion: Geometric Coefficient of Variation
GroupValueSpreadLowerUpperComment
Part 1: GSK2857916 0.06 mg/kg126.18NANot reportedNot reportedNA indicates that geometric coefficient of variation could not be calculated for a single participant.
Part 1: GSK2857916 0.12 mg/kg188.2037.41Not reportedNot reportedNot reported
Part 1: GSK2857916 0.24 mg/kg117.8276.00Not reportedNot reportedNot reported
Part 1: GSK2857916 0.48 mg/kg198.4850.42Not reportedNot reportedNot reported
Part 1: GSK2857916 0.96 mg/kg264.9346.73Not reportedNot reportedNot reported
Part 1: GSK2857916 1.92 mg/kg308.39NANot reportedNot reportedNA indicates that geometric coefficient of variation could not be calculated for a single participant.
Part 1: GSK2857916 4.60 mg/kg103.7417.29Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. comment
        NA indicates that geometric coefficient of variation could not be calculated for a single participant.
        group Id
        OG001
        spread
        NA
        value
        126.18
      2. group Id
        OG002
        spread
        37.41
        value
        188.20
      3. group Id
        OG003
        spread
        76.00
        value
        117.82
      4. group Id
        OG004
        spread
        50.42
        value
        198.48
      5. group Id
        OG005
        spread
        46.73
        value
        264.93
      6. comment
        NA indicates that geometric coefficient of variation could not be calculated for a single participant.
        group Id
        OG006
        spread
        NA
        value
        308.39
      7. group Id
        OG008
        spread
        17.29
        value
        103.74
denoms
  1. counts
    1. group Id
      OG000
      value
      0
    2. group Id
      OG001
      value
      1
    3. group Id
      OG002
      value
      4
    4. group Id
      OG003
      value
      3
    5. group Id
      OG004
      value
      3
    6. group Id
      OG005
      value
      2
    7. group Id
      OG006
      value
      1
    8. group Id
      OG007
      value
      0
    9. group Id
      OG008
      value
      4
    units
    Participants
description
Blood samples were collected at designated timepoints. PK parameters of GSK2857916 were calculated using non-compartmental methods. NA indicates that geometric coefficient of variation could not be calculated for a single participant.
dispersion Type
Geometric Coefficient of Variation
groups
  1. description
    Participants were administered a dose of 0.03 milligrams per kilogram (mg/kg) GSK2857916 as intravenous (IV) infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).
    id
    OG000
    title
    Part 1: GSK2857916 0.03 mg/kg
  2. description
    Participants were administered a dose of 0.06 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).
    id
    OG001
    title
    Part 1: GSK2857916 0.06 mg/kg
  3. description
    Participants were administered a dose of 0.12 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).
    id
    OG002
    title
    Part 1: GSK2857916 0.12 mg/kg
  4. description
    Participants were administered a dose of 0.24 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).
    id
    OG003
    title
    Part 1: GSK2857916 0.24 mg/kg
  5. description
    Participants were administered a dose of 0.48 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).
    id
    OG004
    title
    Part 1: GSK2857916 0.48 mg/kg
  6. description
    Participants were administered a dose of 0.96 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).
    id
    OG005
    title
    Part 1: GSK2857916 0.96 mg/kg
  7. description
    Participants were administered a dose of 1.92 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).
    id
    OG006
    title
    Part 1: GSK2857916 1.92 mg/kg
  8. description
    Participants were administered a dose of 3.40 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).
    id
    OG007
    title
    Part 1: GSK2857916 3.40 mg/kg
  9. description
    Participants were administered a dose of 4.60 mg/kg GSK2857916 as IV infusion once every three weeks for a maximum of 16 cycles (1 cycle= 21 days).
    id
    OG008
    title
    Part 1: GSK2857916 4.60 mg/kg
param Type
GEOMETRIC_MEAN
population Description
PK Part 1 Population. Only those participants with data available at the specified data points were analyzed.
reporting Status
POSTED
time Frame
Pre-dose, 30 minutes post-SOI, at EOI, 1, 3, 8 and 24 hours post-EOI of Day 1 (Cycle 1)
title
Terminal Half-life (t1/2) of GSK2857916 Following IV Dose in Participants With Relapsed/Refractory MM - Part 1
type
SECONDARY
unit Of Measure
Hours

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Preserved source evidence · Not medical advice