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NCT00585195 · OUTCOME

Rifampin Cohort: Ctrough of Crizotinib Alone and When Taken With Rifampin

A Study Of Oral PF-02341066, A C-Met/Hepatocyte Growth Factor Tyrosine Kinase Inhibitor, In Patients With Advanced Cancer · Source last updated 2023-02-08

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

Measure
GEOMETRIC_MEAN
Unit
nanogram per milliliter
Interval / dispersion
Geometric Coefficient of Variation
Time frame
pre-dose on Cycle 1 Day 15 (Crizotinib alone arm) and Cycle 2 Day 1 (Crizotinib with Rifampin arm)

What was measured

Ctrough refers to plasma concentration of Crizotinib observed just before treatment administration.

Analysis population: PK parameter population was defined as all participants in the Rifampin interaction cohort safety population who satisfied following criteria for Cycle 1 Day 15 or Cycle 2 Day 1: a) had at least 1 of the primary PK parameters of Crizotinib (AUCtau and Cmax). b) Received adequate dosing prior to PK sampling. Here, "Overall number of participants analyzed" signifies number of participants evaluable for this outcome measure.

Groups in this outcome

RP2D Cohort: Rifampin Interaction: Crizotinib 250 mg Alone

Participants received Crizotinib 250 mg (2 capsules/tablet of 100 mg each + 1 capsule/tablet of 50 mg) capsule/tablet twice daily (BID) with or without food from Cycle 1 Day 1 up to 13 cycles (each cycle 28 days).

RP2D Cohort: Rifampin Interaction: Crizotinib 250 mg With Rifampin

Participants received Crizotinib 250 mg (2 capsules/tablet of 100 mg each + 1 capsule/tablet of 50 mg) capsule/tablet twice daily (BID) form Cycle 1Day 1 up to 13 cycles (each cycle 28 days). Participants also received commercially available Rifampin 650 mg QD from Cycle 1 Day 16 to Cycle 2 Day 1 (14 days) either one hour before or 2 hours after a meal.

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

Analysis denominator · Participants

GroupSource count
RP2D Cohort: Rifampin Interaction: Crizotinib 250 mg Alone9
RP2D Cohort: Rifampin Interaction: Crizotinib 250 mg With Rifampin7

Reported measurements

Source class 1
Values in nanogram per milliliter · Interval/dispersion: Geometric Coefficient of Variation
GroupValueSpreadLowerUpperComment
RP2D Cohort: Rifampin Interaction: Crizotinib 250 mg Alone251.746Not reportedNot reportedNot reported
RP2D Cohort: Rifampin Interaction: Crizotinib 250 mg With Rifampin26.6750Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        spread
        46
        value
        251.7
      2. group Id
        OG001
        spread
        50
        value
        26.67
denoms
  1. counts
    1. group Id
      OG000
      value
      9
    2. group Id
      OG001
      value
      7
    units
    Participants
description
Ctrough refers to plasma concentration of Crizotinib observed just before treatment administration.
dispersion Type
Geometric Coefficient of Variation
groups
  1. description
    Participants received Crizotinib 250 mg (2 capsules/tablet of 100 mg each + 1 capsule/tablet of 50 mg) capsule/tablet twice daily (BID) with or without food from Cycle 1 Day 1 up to 13 cycles (each cycle 28 days).
    id
    OG000
    title
    RP2D Cohort: Rifampin Interaction: Crizotinib 250 mg Alone
  2. description
    Participants received Crizotinib 250 mg (2 capsules/tablet of 100 mg each + 1 capsule/tablet of 50 mg) capsule/tablet twice daily (BID) form Cycle 1Day 1 up to 13 cycles (each cycle 28 days). Participants also received commercially available Rifampin 650 mg QD from Cycle 1 Day 16 to Cycle 2 Day 1 (14 days) either one hour before or 2 hours after a meal.
    id
    OG001
    title
    RP2D Cohort: Rifampin Interaction: Crizotinib 250 mg With Rifampin
param Type
GEOMETRIC_MEAN
population Description
PK parameter population was defined as all participants in the Rifampin interaction cohort safety population who satisfied following criteria for Cycle 1 Day 15 or Cycle 2 Day 1: a) had at least 1 of the primary PK parameters of Crizotinib (AUCtau and Cmax). b) Received adequate dosing prior to PK sampling. Here, "Overall number of participants analyzed" signifies number of participants evaluable for this outcome measure.
reporting Status
POSTED
time Frame
pre-dose on Cycle 1 Day 15 (Crizotinib alone arm) and Cycle 2 Day 1 (Crizotinib with Rifampin arm)
title
Rifampin Cohort: Ctrough of Crizotinib Alone and When Taken With Rifampin
type
PRIMARY
unit Of Measure
nanogram per milliliter

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Preserved source evidence · Not medical advice