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NCT01587703 · OUTCOME

Number of Participants With Prostate Specific Antigen (PSA)50 Response-Part 1 QD

A Study to Investigate the Safety, Pharmacokinetics, Pharmacodynamics, and Clinical Activity of GSK525762 in Subjects With NUT Midline Carcinoma (NMC) and Other Cancers · Source last updated 2020-03-16

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

Measure
NUMBER
Unit
Participants
Interval / dispersion
95% Confidence Interval
Time frame
Median of 1.38 months of drug exposure

What was measured

PSA 50 response rate is defined as the response rate that a PSA reduction from Baseline \>=50% is observed at 12 weeks and beyond (must be confirmed by a second value). The number of participants with PSA \>=50% reduction is presented along with 95% confidence intervals.

Analysis population: All Treated Population

Groups in this outcome

Part 1: GSK525762 2 mg QD

Participants were administered once daily (QD) oral dose of 2 milligrams (mg) GSK525762.

Part 1: GSK525762 4 mg QD

Participants were administered once daily oral dose of 4 mg GSK525762.

Part 1: GSK525762 8 mg QD

Participants were administered once daily oral dose of 8 mg GSK525762.

Part 1: GSK525762 16 mg QD

Participants were administered once daily oral dose of 16 mg GSK525762.

Part 1: GSK525762 30 mg QD

Participants were administered once daily oral dose of 30 mg GSK525762.

Part 1: GSK525762 60 mg QD

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

Part 1: GSK525762 80 mg QD

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

Part 1: GSK525762 100 mg QD

Participants were administered once daily oral dose of 100 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 2 mg QD3
Part 1: GSK525762 4 mg QD4
Part 1: GSK525762 8 mg QD1
Part 1: GSK525762 16 mg QD3
Part 1: GSK525762 30 mg QD4
Part 1: GSK525762 60 mg QD9
Part 1: GSK525762 80 mg QD32
Part 1: GSK525762 100 mg QD9

Reported measurements

Source class 1
Values in Participants · Interval/dispersion: 95% Confidence Interval
GroupValueSpreadLowerUpperComment
Part 1: GSK525762 2 mg QD0Not reportedNANAConfidence interval could not be calculated as there were no responders
Part 1: GSK525762 4 mg QD0Not reportedNANAConfidence interval could not be calculated as there were no responders
Part 1: GSK525762 8 mg QD0Not reportedNANAConfidence interval could not be calculated as there were no responders
Part 1: GSK525762 16 mg QD0Not reportedNANAConfidence interval could not be calculated as there were no responders
Part 1: GSK525762 30 mg QD0Not reportedNANAConfidence interval could not be calculated as there were no responders
Part 1: GSK525762 60 mg QD0Not reportedNANAConfidence interval could not be calculated as there were no responders
Part 1: GSK525762 80 mg QD2Not reportedNANAConfidence interval could not be calculated as there were no responders
Part 1: GSK525762 100 mg QD1Not reportedNANAConfidence interval could not be calculated as there were no responders
Complete source fields
classes
  1. categories
    1. measurements
      1. comment
        Confidence interval could not be calculated as there were no responders
        group Id
        OG000
        lower Limit
        NA
        upper Limit
        NA
        value
        0
      2. comment
        Confidence interval could not be calculated as there were no responders
        group Id
        OG001
        lower Limit
        NA
        upper Limit
        NA
        value
        0
      3. comment
        Confidence interval could not be calculated as there were no responders
        group Id
        OG002
        lower Limit
        NA
        upper Limit
        NA
        value
        0
      4. comment
        Confidence interval could not be calculated as there were no responders
        group Id
        OG003
        lower Limit
        NA
        upper Limit
        NA
        value
        0
      5. comment
        Confidence interval could not be calculated as there were no responders
        group Id
        OG004
        lower Limit
        NA
        upper Limit
        NA
        value
        0
      6. comment
        Confidence interval could not be calculated as there were no responders
        group Id
        OG005
        lower Limit
        NA
        upper Limit
        NA
        value
        0
      7. comment
        Confidence interval could not be calculated as there were no responders
        group Id
        OG006
        lower Limit
        NA
        upper Limit
        NA
        value
        2
      8. comment
        Confidence interval could not be calculated as there were no responders
        group Id
        OG007
        lower Limit
        NA
        upper Limit
        NA
        value
        1
denoms
  1. counts
    1. group Id
      OG000
      value
      3
    2. group Id
      OG001
      value
      4
    3. group Id
      OG002
      value
      1
    4. group Id
      OG003
      value
      3
    5. group Id
      OG004
      value
      4
    6. group Id
      OG005
      value
      9
    7. group Id
      OG006
      value
      32
    8. group Id
      OG007
      value
      9
    units
    Participants
description
PSA 50 response rate is defined as the response rate that a PSA reduction from Baseline \>=50% is observed at 12 weeks and beyond (must be confirmed by a second value). The number of participants with PSA \>=50% reduction is presented along with 95% confidence intervals.
dispersion Type
95% Confidence Interval
groups
  1. description
    Participants were administered once daily (QD) oral dose of 2 milligrams (mg) GSK525762.
    id
    OG000
    title
    Part 1: GSK525762 2 mg QD
  2. description
    Participants were administered once daily oral dose of 4 mg GSK525762.
    id
    OG001
    title
    Part 1: GSK525762 4 mg QD
  3. description
    Participants were administered once daily oral dose of 8 mg GSK525762.
    id
    OG002
    title
    Part 1: GSK525762 8 mg QD
  4. description
    Participants were administered once daily oral dose of 16 mg GSK525762.
    id
    OG003
    title
    Part 1: GSK525762 16 mg QD
  5. description
    Participants were administered once daily oral dose of 30 mg GSK525762.
    id
    OG004
    title
    Part 1: GSK525762 30 mg QD
  6. description
    Participants were administered once daily oral dose of 60 mg GSK525762.
    id
    OG005
    title
    Part 1: GSK525762 60 mg QD
  7. description
    Participants were administered once daily oral dose of 80 mg GSK525762.
    id
    OG006
    title
    Part 1: GSK525762 80 mg QD
  8. description
    Participants were administered once daily oral dose of 100 mg GSK525762.
    id
    OG007
    title
    Part 1: GSK525762 100 mg QD
param Type
NUMBER
population Description
All Treated Population
reporting Status
POSTED
time Frame
Median of 1.38 months of drug exposure
title
Number of Participants With Prostate Specific Antigen (PSA)50 Response-Part 1 QD
type
PRIMARY
unit Of Measure
Participants

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Preserved source evidence · Not medical advice