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NCT01943851 · OUTCOME

Part 1: Changes in Cardiac QT Duration Corrected for Heart Rate by Fridericia's Formula (QTcF) and Other Safety Parameters in Relation to GSK525762 PK Concentrations

A Dose Escalation Study to Investigate the Safety, Pharmacokinetics (PK), Pharmacodynamics (PD) and Clinical Activity of GSK525762 in Subjects With Relapsed, Refractory Hematologic Malignancies · Source last updated 2024-10-01

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

Measure
Not reported
Unit
Not reported
Interval / dispersion
Not reported
Time frame
Up to 86.9 weeks

What was measured

Changes in QTcF and other safety parameters in relation to GSK525762 PK concentrations was planned to be analyzed.

Analysis population: All Treated Population. This was an other pre-specified outcome measure. Data was not analyzed and reported.

Groups in this outcome

Part 1: GSK525762 5 mg QD

Participants were administered once daily oral dose of 5 milligrams (mg) GSK525762.

Part 1: GSK525762 10 mg QD

Participants were administered once daily oral dose of 10 mg GSK525762.

Part 1: GSK525762 20 mg QD

Participants were administered once daily oral dose of 20 mg GSK525762.

Part 1: GSK525762 30 mg QD MM

Participants with multiple myeloma (MM) were administered once daily oral dose of 30 mg GSK525762.

Part 1: GSK525762 40 mg QD

Participants were administered once daily oral dose of 40 mg GSK525762.

Part 1: GSK525762 40 mg QD MM

Participants with multiple myeloma were administered once daily oral dose of 40 mg GSK525762.

Part 1: GSK525762 60 mg QD AML

Participants with Acute Myeloid Leukemia (AML) were administered once daily oral dose of 60 mg GSK525762.

Part 1: GSK525762 60 mg QD NHL

Participants with Non-Hodgkin's Lymphoma (NHL) were administered once daily oral dose of 60 mg GSK525762.

Part 1: GSK525762 60 mg QD MM

Participants with MM were administered once daily oral dose of 60 mg GSK525762.

Part 1: GSK525762 75 mg QD AML

Participants with AML were administered once daily oral dose of 75 mg GSK525762.

Part 1: GSK525762 80 mg QD

Participants were administered once daily oral dose of 80 mg GSK525762.

Part 1: GSK525762 80 mg QD AML

Participants with AML were administered once daily oral dose of 80 mg GSK525762.

Part 1: GSK525762 80 mg QD NHL

Participants with NHL were administered once daily oral dose of 80 mg GSK525762.

Part 1: GSK525762 100 mg QD AML

Participants with AML were administered once daily oral dose of 100 mg GSK525762.

Part 1: GSK525762 120 mg QD AML

Participants with AML were administered once daily oral dose of 120 mg GSK525762.

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: GSK525762 5 mg QD0
Part 1: GSK525762 10 mg QD0
Part 1: GSK525762 20 mg QD0
Part 1: GSK525762 30 mg QD MM0
Part 1: GSK525762 40 mg QD0
Part 1: GSK525762 40 mg QD MM0
Part 1: GSK525762 60 mg QD AML0
Part 1: GSK525762 60 mg QD NHL0
Part 1: GSK525762 60 mg QD MM0
Part 1: GSK525762 75 mg QD AML0
Part 1: GSK525762 80 mg QD0
Part 1: GSK525762 80 mg QD AML0
Part 1: GSK525762 80 mg QD NHL0
Part 1: GSK525762 100 mg QD AML0
Part 1: GSK525762 120 mg QD AML0

Reported measurements

No numerical measurement classes were posted for this outcome. Missing is not zero.

Complete source fields
denoms
  1. counts
    1. group Id
      OG000
      value
      0
    2. group Id
      OG001
      value
      0
    3. group Id
      OG002
      value
      0
    4. group Id
      OG003
      value
      0
    5. group Id
      OG004
      value
      0
    6. group Id
      OG005
      value
      0
    7. group Id
      OG006
      value
      0
    8. group Id
      OG007
      value
      0
    9. group Id
      OG008
      value
      0
    10. group Id
      OG009
      value
      0
    11. group Id
      OG010
      value
      0
    12. group Id
      OG011
      value
      0
    units
    Participants
description
Changes in QTcF and other safety parameters in relation to GSK525762 PK concentrations was planned to be analyzed.
groups
  1. description
    Participants were administered once daily oral dose of 5 milligrams (mg) GSK525762.
    id
    OG000
    title
    Part 1: GSK525762 5 mg QD
  2. description
    Participants were administered once daily oral dose of 10 mg GSK525762.
    id
    OG001
    title
    Part 1: GSK525762 10 mg QD
  3. description
    Participants were administered once daily oral dose of 20 mg GSK525762.
    id
    OG002
    title
    Part 1: GSK525762 20 mg QD
  4. description
    Participants with multiple myeloma (MM) were administered once daily oral dose of 30 mg GSK525762.
    id
    OG003
    title
    Part 1: GSK525762 30 mg QD MM
  5. description
    Participants were administered once daily oral dose of 40 mg GSK525762.
    id
    OG004
    title
    Part 1: GSK525762 40 mg QD
  6. description
    Participants with multiple myeloma were administered once daily oral dose of 40 mg GSK525762.
    id
    OG005
    title
    Part 1: GSK525762 40 mg QD MM
  7. description
    Participants with Acute Myeloid Leukemia (AML) were administered once daily oral dose of 60 mg GSK525762.
    id
    OG006
    title
    Part 1: GSK525762 60 mg QD AML
  8. description
    Participants with Non-Hodgkin's Lymphoma (NHL) were administered once daily oral dose of 60 mg GSK525762.
    id
    OG007
    title
    Part 1: GSK525762 60 mg QD NHL
  9. description
    Participants with MM were administered once daily oral dose of 60 mg GSK525762.
    id
    OG008
    title
    Part 1: GSK525762 60 mg QD MM
  10. description
    Participants with AML were administered once daily oral dose of 75 mg GSK525762.
    id
    OG009
    title
    Part 1: GSK525762 75 mg QD AML
  11. description
    Participants were administered once daily oral dose of 80 mg GSK525762.
    id
    OG010
    title
    Part 1: GSK525762 80 mg QD
  12. description
    Participants with AML were administered once daily oral dose of 80 mg GSK525762.
    id
    OG011
    title
    Part 1: GSK525762 80 mg QD AML
population Description
All Treated Population. This was an other pre-specified outcome measure. Data was not analyzed and reported.
reporting Status
POSTED
time Frame
Up to 86.9 weeks
title
Part 1: Changes in Cardiac QT Duration Corrected for Heart Rate by Fridericia's Formula (QTcF) and Other Safety Parameters in Relation to GSK525762 PK Concentrations
type
OTHER_PRE_SPECIFIED

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

Preserved source evidence · Not medical advice