Skip to content
← Full study record

NCT02064387 · OUTCOME

Area Under the Concentration-time Curve From Zero to Time of Last Quantifiable Concentration (AUC[0-tlast]) 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*nanogram per milliliter
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/kg1
Part 1: GSK2857916 0.06 mg/kg1
Part 1: GSK2857916 0.12 mg/kg4
Part 1: GSK2857916 0.24 mg/kg4
Part 1: GSK2857916 0.48 mg/kg3
Part 1: GSK2857916 0.96 mg/kg3
Part 1: GSK2857916 1.92 mg/kg3
Part 1: GSK2857916 3.40 mg/kg3
Part 1: GSK2857916 4.60 mg/kg6

Reported measurements

Source class 1
Values in Hours*nanogram per milliliter · Interval/dispersion: Geometric Coefficient of Variation
GroupValueSpreadLowerUpperComment
Part 1: GSK2857916 0.03 mg/kg44260.79NANot reportedNot reportedNA indicates that geometric coefficient of variation could not be calculated for a single participant.
Part 1: GSK2857916 0.06 mg/kg178485.20NANot reportedNot reportedNA indicates that geometric coefficient of variation could not be calculated for a single participant.
Part 1: GSK2857916 0.12 mg/kg637783.4835.67Not reportedNot reportedNot reported
Part 1: GSK2857916 0.24 mg/kg694825.13107.50Not reportedNot reportedNot reported
Part 1: GSK2857916 0.48 mg/kg2170746.9659.81Not reportedNot reportedNot reported
Part 1: GSK2857916 0.96 mg/kg4492292.6582.00Not reportedNot reportedNot reported
Part 1: GSK2857916 1.92 mg/kg10093784.7254.20Not reportedNot reportedNot reported
Part 1: GSK2857916 3.40 mg/kg19239850.6153.15Not reportedNot reportedNot reported
Part 1: GSK2857916 4.60 mg/kg10131666.8647.32Not 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
        OG000
        spread
        NA
        value
        44260.79
      2. comment
        NA indicates that geometric coefficient of variation could not be calculated for a single participant.
        group Id
        OG001
        spread
        NA
        value
        178485.20
      3. group Id
        OG002
        spread
        35.67
        value
        637783.48
      4. group Id
        OG003
        spread
        107.50
        value
        694825.13
      5. group Id
        OG004
        spread
        59.81
        value
        2170746.96
      6. group Id
        OG005
        spread
        82.00
        value
        4492292.65
      7. group Id
        OG006
        spread
        54.20
        value
        10093784.72
      8. group Id
        OG007
        spread
        53.15
        value
        19239850.61
      9. group Id
        OG008
        spread
        47.32
        value
        10131666.86
denoms
  1. counts
    1. group Id
      OG000
      value
      1
    2. group Id
      OG001
      value
      1
    3. group Id
      OG002
      value
      4
    4. group Id
      OG003
      value
      4
    5. group Id
      OG004
      value
      3
    6. group Id
      OG005
      value
      3
    7. group Id
      OG006
      value
      3
    8. group Id
      OG007
      value
      3
    9. group Id
      OG008
      value
      6
    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
Area Under the Concentration-time Curve From Zero to Time of Last Quantifiable Concentration (AUC[0-tlast]) of GSK2857916 Following IV Dose in Participants With Relapsed/Refractory MM- Part 1
type
SECONDARY
unit Of Measure
Hours*nanogram per milliliter

Download exact source JSON → · Snapshot ctgov-results-25a395029948b04d52b1253f

Preserved source evidence · Not medical advice