NCT01830816 · OUTCOME

Tmax: Time to Reach the Maximum Plasma Concentration (Cmax) for Ixazomib

Pharmacokinetics Study of Oral Ixazomib (MLN9708) in Relapsed/Refractory Multiple Myeloma and Advanced Solid Tumors Participants With Normal Renal Function or Severe Renal Impairment · Source last updated 2019-06-10

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: Part A, Day 1: Predose and at multiple timepoints (up to 336 hours) post-dose

Analysis population: PK evaluable population was defined as participants who received protocol-specified single dose in Part A; did not receive any excluded concomitant medications through the completion of PK sampling; and had sufficient concentration-time data to permit reliable estimation of PK parameters by non-compartmental analysis methods.

Groups in this outcome

Normal Renal Function: Ixazomib

Ixazomib 3.0 mg, capsule, orally on Day 1 of Part A (15-day PK cycle) and on Days 1, 8, and 15 of each 28-day cycle in Part B (4.0, 3.0, or 2.3 mg per protocol) until disease progression or unacceptable toxicity.

Severe Renal Impairment: Ixazomib

End-stage Renal Disease: Ixazomib

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

Analysis denominator · Participants

Group	Source count
Normal Renal Function: Ixazomib	18
Severe Renal Impairment: Ixazomib	14
End-stage Renal Disease: Ixazomib	6

Reported measurements

Source class 1

Values in hours · Interval/dispersion: Full Range
Group	Value	Spread	Lower	Upper	Comment
Normal Renal Function: Ixazomib	1.0400	Not reported	0.467	4.000	Not reported
Severe Renal Impairment: Ixazomib	1.0000	Not reported	0.450	1.500	Not reported
End-stage Renal Disease: Ixazomib	1.2500	Not reported	0.983	7.000	Not reported

Complete source fields

classes

categories
measurements
group Id
OG000
lower Limit
0.467
upper Limit
4.000
value
1.0400
group Id
OG001
lower Limit
0.450
upper Limit
1.500
value
1.0000
group Id
OG002
lower Limit
0.983
upper Limit
7.000
value
1.2500

denoms

counts
group Id
OG000
value
18
group Id
OG001
value
14
group Id
OG002
value
6
units
Participants

dispersion Type

Full Range

groups

description
Ixazomib 3.0 mg, capsule, orally on Day 1 of Part A (15-day PK cycle) and on Days 1, 8, and 15 of each 28-day cycle in Part B (4.0, 3.0, or 2.3 mg per protocol) until disease progression or unacceptable toxicity.
id
OG000
title
Normal Renal Function: Ixazomib
description
Ixazomib 3.0 mg, capsule, orally on Day 1 of Part A (15-day PK cycle) and on Days 1, 8, and 15 of each 28-day cycle in Part B (4.0, 3.0, or 2.3 mg per protocol) until disease progression or unacceptable toxicity.
id
OG001
title
Severe Renal Impairment: Ixazomib
description
Ixazomib 3.0 mg, capsule, orally on Day 1 of Part A (15-day PK cycle) and on Days 1, 8, and 15 of each 28-day cycle in Part B (4.0, 3.0, or 2.3 mg per protocol) until disease progression or unacceptable toxicity.
id
OG002
title
End-stage Renal Disease: Ixazomib

param Type

MEDIAN

population Description

PK evaluable population was defined as participants who received protocol-specified single dose in Part A; did not receive any excluded concomitant medications through the completion of PK sampling; and had sufficient concentration-time data to permit reliable estimation of PK parameters by non-compartmental analysis methods.

reporting Status

POSTED

time Frame

Part A, Day 1: Predose and at multiple timepoints (up to 336 hours) post-dose

title

Tmax: Time to Reach the Maximum Plasma Concentration (Cmax) for Ixazomib

type

PRIMARY

unit Of Measure

hours

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

Preserved source evidence · Not medical advice