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NCT02064387 · OUTCOME

AUC(0-tlast) of Cys Monomethyl Auristatin F (Cys-mcMMAF) Following IV Dose of GSK2857916 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*picogram 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 Cys-mcMMAF 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/kg0
Part 1: GSK2857916 0.12 mg/kg1
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*picogram per milliliter · Interval/dispersion: Geometric Coefficient of Variation
GroupValueSpreadLowerUpperComment
Part 1: GSK2857916 0.12 mg/kg1157.46NANot reportedNot reportedNA indicates that geometric coefficient of variation could not be calculated for a single participant.
Part 1: GSK2857916 0.24 mg/kg1623.8741.43Not reportedNot reportedNot reported
Part 1: GSK2857916 0.48 mg/kg14681.6291.88Not reportedNot reportedNot reported
Part 1: GSK2857916 0.96 mg/kg20787.48209.27Not reportedNot reportedNot reported
Part 1: GSK2857916 1.92 mg/kg72608.0017.60Not reportedNot reportedNot reported
Part 1: GSK2857916 3.40 mg/kg119177.3035.77Not reportedNot reportedNot reported
Part 1: GSK2857916 4.60 mg/kg181147.6194.32Not 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
        OG002
        spread
        NA
        value
        1157.46
      2. group Id
        OG003
        spread
        41.43
        value
        1623.87
      3. group Id
        OG004
        spread
        91.88
        value
        14681.62
      4. group Id
        OG005
        spread
        209.27
        value
        20787.48
      5. group Id
        OG006
        spread
        17.60
        value
        72608.00
      6. group Id
        OG007
        spread
        35.77
        value
        119177.30
      7. group Id
        OG008
        spread
        94.32
        value
        181147.61
denoms
  1. counts
    1. group Id
      OG000
      value
      0
    2. group Id
      OG001
      value
      0
    3. group Id
      OG002
      value
      1
    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 Cys-mcMMAF 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
AUC(0-tlast) of Cys Monomethyl Auristatin F (Cys-mcMMAF) Following IV Dose of GSK2857916 in Participants With Relapsed/Refractory MM- Part 1
type
SECONDARY
unit Of Measure
Hours*picogram per milliliter

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Preserved source evidence · Not medical advice