Skip to content
← Full study record

NCT02335983 · OUTCOME

Area Under the Curve From Time Zero to Time of Last Quantifiable Concentration of Carfilzomib on Day 8 of Cycle 1 by Dose Group

Phase 1b Study of Weekly Carfilzomib in Combination With Lenalidomide and Dexamethasone in Subjects With Multiple Myeloma · Source last updated 2020-11-06

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

Measure
MEAN
Unit
hr*ng/mL
Interval / dispersion
Standard Deviation
Time frame
Day 8 of Cycle 1 at predose, 15 minutes after the start of infusion, at the end of infusion, and 15 and 60 minutes after the end of infusion

Analysis population: Participants who received at least 1 dose of study drug who had sufficient carfilzomib exposure and plasma concentration versus time data for the estimation of pharmacokinetic parameters by a non-compartmental analysis on day 8 of cycle 1.

Groups in this outcome

Carfilzomib 56 mg/m²

Participants who received carfilzomib 56 mg/m² on Cycle 1 day 8.

Carfilzomib 70 mg/m²

Participants who received carfilzomib 70 mg/m² on Cycle 1 day 8.

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

Analysis denominator · Participants

GroupSource count
Carfilzomib 56 mg/m²46
Carfilzomib 70 mg/m²40

Reported measurements

Source class 1
Values in hr*ng/mL · Interval/dispersion: Standard Deviation
GroupValueSpreadLowerUpperComment
Carfilzomib 56 mg/m²415017500Not reportedNot reportedNot reported
Carfilzomib 70 mg/m²913032800Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        spread
        17500
        value
        4150
      2. group Id
        OG001
        spread
        32800
        value
        9130
denoms
  1. counts
    1. group Id
      OG000
      value
      46
    2. group Id
      OG001
      value
      40
    units
    Participants
dispersion Type
Standard Deviation
groups
  1. description
    Participants who received carfilzomib 56 mg/m² on Cycle 1 day 8.
    id
    OG000
    title
    Carfilzomib 56 mg/m²
  2. description
    Participants who received carfilzomib 70 mg/m² on Cycle 1 day 8.
    id
    OG001
    title
    Carfilzomib 70 mg/m²
param Type
MEAN
population Description
Participants who received at least 1 dose of study drug who had sufficient carfilzomib exposure and plasma concentration versus time data for the estimation of pharmacokinetic parameters by a non-compartmental analysis on day 8 of cycle 1.
reporting Status
POSTED
time Frame
Day 8 of Cycle 1 at predose, 15 minutes after the start of infusion, at the end of infusion, and 15 and 60 minutes after the end of infusion
title
Area Under the Curve From Time Zero to Time of Last Quantifiable Concentration of Carfilzomib on Day 8 of Cycle 1 by Dose Group
type
SECONDARY
unit Of Measure
hr*ng/mL

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

Preserved source evidence · Not medical advice