Skip to content
← Full study record

NCT01121393 · OUTCOME

Pharmacokinetics of Afatinib at Day 22

BIBW 2992 (Afatinib) vs Gemcitabine-cisplatin in 1st Line Non-small Cell Lung Cancer (NSCLC) · Source last updated 2018-12-14

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

Measure
GEOMETRIC_MEAN
Unit
nanogram/millilitre (ng/mL)
Interval / dispersion
Geometric Coefficient of Variation
Time frame
Day 22 (course 2, visit 1)

What was measured

Outcome data are the trough plasma concentrations of afatinib at day 22 after multiple daily dosing of 40mg afatinib and after dose escalation to 50mg or dose reduction to 30mg afatinib (no patient dose reduced to 20mg during the Pharmacokinetics (PK) assessment period).

Analysis population: All patients who had at least 1 afatinib dose and who had at least 1 valid afatinib plasma concentration available.

Groups in this outcome

Afatinib 30mg q.d.

Patients receiving Afatinib 30mg once daily (q.d.) orally after a dose reduction.

Afatinib 40mg q.d.

Patients receiving Afatinib 40mg once daily (q.d.) orally

Afatinib 50mg q.d.

Patients receiving Afatinib 50mg once daily (q.d.) orally after a dose escalation.

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

Analysis denominator · Participants

GroupSource count
Afatinib 30mg q.d.3
Afatinib 40mg q.d.210
Afatinib 50mg q.d.0

Reported measurements

Source class 1
Values in nanogram/millilitre (ng/mL) · Interval/dispersion: Geometric Coefficient of Variation
GroupValueSpreadLowerUpperComment
Afatinib 30mg q.d.17.7109Not reportedNot reportedNot reported
Afatinib 40mg q.d.23.165.1Not reportedNot reportedNot reported
Complete source fields
classes
  1. categories
    1. measurements
      1. group Id
        OG000
        spread
        109
        value
        17.7
      2. group Id
        OG001
        spread
        65.1
        value
        23.1
denoms
  1. counts
    1. group Id
      OG000
      value
      3
    2. group Id
      OG001
      value
      210
    3. group Id
      OG002
      value
      0
    units
    Participants
description
Outcome data are the trough plasma concentrations of afatinib at day 22 after multiple daily dosing of 40mg afatinib and after dose escalation to 50mg or dose reduction to 30mg afatinib (no patient dose reduced to 20mg during the Pharmacokinetics (PK) assessment period).
dispersion Type
Geometric Coefficient of Variation
groups
  1. description
    Patients receiving Afatinib 30mg once daily (q.d.) orally after a dose reduction.
    id
    OG000
    title
    Afatinib 30mg q.d.
  2. description
    Patients receiving Afatinib 40mg once daily (q.d.) orally
    id
    OG001
    title
    Afatinib 40mg q.d.
  3. description
    Patients receiving Afatinib 50mg once daily (q.d.) orally after a dose escalation.
    id
    OG002
    title
    Afatinib 50mg q.d.
param Type
GEOMETRIC_MEAN
population Description
All patients who had at least 1 afatinib dose and who had at least 1 valid afatinib plasma concentration available.
reporting Status
POSTED
time Frame
Day 22 (course 2, visit 1)
title
Pharmacokinetics of Afatinib at Day 22
type
SECONDARY
unit Of Measure
nanogram/millilitre (ng/mL)

Download exact source JSON → · Snapshot ctgov-results-191f4516d4760045304b24a0

Preserved source evidence · Not medical advice