Skip to content
Triangle logo TriangleGet started
← Full study record

NCT01999335 · OUTCOME

Time to Maximum Plasma Concentration (Tmax) of Oprozomib

A Study of Oprozomib, Pomalidomide, and Dexamethasone in Adults With Primary Refractory or Relapsed and Refractory Multiple Myeloma · Source last updated 2021-04-27

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

Measure
MEDIAN
Unit
hours
Interval / dispersion
Full Range
Time frame
Cycle 1 day 1 at predose and 0.25, 0.5, 1, 2, 3, 4, 6, and 24 hours postdose. Cycle 2 day 1 at predose and 0.25, 0.5, 1, 2, 3, 4, and 6 hours postdose.

What was measured

Oprozomib plasma concentrations were determined using liquid chromatography with tandem mass spectrometry.

Analysis population: Participants with adequate oprozomib plasma concentration-versus-time data to allow estimation of pharmacokinetic (PK) parameters. Treatment groups receiving the same dose of oprozomib were combined for PK analyses.

Groups in this outcome

Oprozomib 150 mg 5/14 + Pomalidomide + Dexamethasone

Participants received oprozomib 150 mg once daily on days 1 to 5 and days 15 to 19 (5/14 schedule) of each 28-day treatment cycle, in combination with pomalidomide 2 or 4 mg/day on days 1 to 21 and dexamethasone 20 mg on days 1, 2, 8, 9, 15, 16, 22, and 23 of each 28-day cycle.

Oprozomib 210 mg 2/7 + Pomalidomide + Dexamethasone

Participants received oprozomib 210 mg once daily on days 1, 2, 8, 9, 15, 16, 22, and 23 (2/7 schedule) of each 28-day treatment cycle, in combination with pomalidomide 4 mg on days 1 through 21 and dexamethasone 20 mg/day on days 1, 2, 8, 9, 15, 16, 22, and 23 of each 28-day cycle.

Oprozomib 240 mg 2/7 + Pomalidomide 4 mg + Dexamethasone

Participants received oprozomib 240 mg once daily on days 1, 2, 8, 9, 15, 16, 22, and 23 (2/7 schedule) of each 28-day treatment cycle, in combination with pomalidomide 4 mg on days 1 through 21 and dexamethasone 20 mg/day on days 1, 2, 8, 9, 15, 16, 22, and 23 of each 28-day cycle until disease progression or unacceptable toxicity.

Group identifiers and denominators belong to this outcome only. They may differ in another outcome or in safety reporting.

Analysis denominator · Participants

GroupSource count
Oprozomib 150 mg 5/14 + Pomalidomide + Dexamethasone3
Oprozomib 210 mg 2/7 + Pomalidomide + Dexamethasone16
Oprozomib 240 mg 2/7 + Pomalidomide 4 mg + Dexamethasone9

Reported measurements

Cycle 1 day 1

Analysis denominator · Participants

GroupSource count
Oprozomib 150 mg 5/14 + Pomalidomide + Dexamethasone3
Oprozomib 210 mg 2/7 + Pomalidomide + Dexamethasone16
Oprozomib 240 mg 2/7 + Pomalidomide 4 mg + Dexamethasone9
Values in hours · Interval/dispersion: Full Range
GroupValueSpreadLowerUpperComment
Oprozomib 150 mg 5/14 + Pomalidomide + Dexamethasone1.0Not reported1.06.1Not reported
Oprozomib 210 mg 2/7 + Pomalidomide + Dexamethasone1.6Not reported0.56.1Not reported
Oprozomib 240 mg 2/7 + Pomalidomide 4 mg + Dexamethasone2.2Not reported1.13.8Not reported
Cycle 2 day 1

Analysis denominator · Participants

GroupSource count
Oprozomib 150 mg 5/14 + Pomalidomide + Dexamethasone3
Oprozomib 210 mg 2/7 + Pomalidomide + Dexamethasone14
Oprozomib 240 mg 2/7 + Pomalidomide 4 mg + Dexamethasone7
Values in hours · Interval/dispersion: Full Range
GroupValueSpreadLowerUpperComment
Oprozomib 150 mg 5/14 + Pomalidomide + Dexamethasone4.0Not reported1.04.1Not reported
Oprozomib 210 mg 2/7 + Pomalidomide + Dexamethasone1.1Not reported0.424.0Not reported
Oprozomib 240 mg 2/7 + Pomalidomide 4 mg + Dexamethasone1.1Not reported0.634.0Not reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        1.0
        upper Limit
        6.1
        value
        1.0
      2. group Id
        OG001
        lower Limit
        0.5
        upper Limit
        6.1
        value
        1.6
      3. group Id
        OG002
        lower Limit
        1.1
        upper Limit
        3.8
        value
        2.2
    denoms
    1. counts
      1. group Id
        OG000
        value
        3
      2. group Id
        OG001
        value
        16
      3. group Id
        OG002
        value
        9
      units
      Participants
    title
    Cycle 1 day 1
  2. categories
    1. measurements
      1. group Id
        OG000
        lower Limit
        1.0
        upper Limit
        4.1
        value
        4.0
      2. group Id
        OG001
        lower Limit
        0.42
        upper Limit
        4.0
        value
        1.1
      3. group Id
        OG002
        lower Limit
        0.63
        upper Limit
        4.0
        value
        1.1
    denoms
    1. counts
      1. group Id
        OG000
        value
        3
      2. group Id
        OG001
        value
        14
      3. group Id
        OG002
        value
        7
      units
      Participants
    title
    Cycle 2 day 1
denoms
  1. counts
    1. group Id
      OG000
      value
      3
    2. group Id
      OG001
      value
      16
    3. group Id
      OG002
      value
      9
    units
    Participants
description
Oprozomib plasma concentrations were determined using liquid chromatography with tandem mass spectrometry.
dispersion Type
Full Range
groups
  1. description
    Participants received oprozomib 150 mg once daily on days 1 to 5 and days 15 to 19 (5/14 schedule) of each 28-day treatment cycle, in combination with pomalidomide 2 or 4 mg/day on days 1 to 21 and dexamethasone 20 mg on days 1, 2, 8, 9, 15, 16, 22, and 23 of each 28-day cycle.
    id
    OG000
    title
    Oprozomib 150 mg 5/14 + Pomalidomide + Dexamethasone
  2. description
    Participants received oprozomib 210 mg once daily on days 1, 2, 8, 9, 15, 16, 22, and 23 (2/7 schedule) of each 28-day treatment cycle, in combination with pomalidomide 4 mg on days 1 through 21 and dexamethasone 20 mg/day on days 1, 2, 8, 9, 15, 16, 22, and 23 of each 28-day cycle.
    id
    OG001
    title
    Oprozomib 210 mg 2/7 + Pomalidomide + Dexamethasone
  3. description
    Participants received oprozomib 240 mg once daily on days 1, 2, 8, 9, 15, 16, 22, and 23 (2/7 schedule) of each 28-day treatment cycle, in combination with pomalidomide 4 mg on days 1 through 21 and dexamethasone 20 mg/day on days 1, 2, 8, 9, 15, 16, 22, and 23 of each 28-day cycle until disease progression or unacceptable toxicity.
    id
    OG002
    title
    Oprozomib 240 mg 2/7 + Pomalidomide 4 mg + Dexamethasone
param Type
MEDIAN
population Description
Participants with adequate oprozomib plasma concentration-versus-time data to allow estimation of pharmacokinetic (PK) parameters. Treatment groups receiving the same dose of oprozomib were combined for PK analyses.
reporting Status
POSTED
time Frame
Cycle 1 day 1 at predose and 0.25, 0.5, 1, 2, 3, 4, 6, and 24 hours postdose. Cycle 2 day 1 at predose and 0.25, 0.5, 1, 2, 3, 4, and 6 hours postdose.
title
Time to Maximum Plasma Concentration (Tmax) of Oprozomib
type
SECONDARY
unit Of Measure
hours

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

Preserved source evidence · Not medical advice