ID

41172

Descrizione

Study ID: 111582 Clinical Study ID: 111582 Study Title: An Open Label Study to Examine the Effects of Low-fat and High-fat Meals on the Pharmacokinetics of Orally Administered Lapatinib in Metastatic ErbB2 Positive Breast Cancer Patients. Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00821054 https://clinicaltrials.gov/ct2/show/NCT00821054 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: Lapatinib Trade Name: N/A Study Indication: Neoplasms, Breast The study consists of a screening, four study visits at day-1, week 1, 2 and 3 and a follow-up visit. This document contains the Lapatinib diary. This form is for dosing and meal data from the diary only. Go to visits Week 1 to Week 3 for Lapatinib and Meal data from clinic visits. This form has to be filled in for each week and each study day of the trial.

collegamento

https://clinicaltrials.gov/ct2/show/NCT00821054

Keywords

  1. 04/07/20 04/07/20 - Christian Arras
Titolare del copyright

GlaxoSmithKline

Caricato su

4 luglio 2020

DOI

Per favore, per richiedere un accesso.

Licenza

Creative Commons BY-NC 4.0

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Effects of Low-fat and high-fat meals on the Pharmacokinetics of Lapatinib in ErB2+ Breast Cancer patients, NCT00821054

Lapatinib diary

  1. StudyEvent: ODM
    1. Lapatinib diary
Administrative Data
Descrizione

Administrative Data

Alias
UMLS CUI-1
C1320722
Visit Date
Descrizione

Date of Visit

Tipo di dati

date

Alias
UMLS CUI [1]
C1320303
Subject number
Descrizione

Subject number

Tipo di dati

integer

Alias
UMLS CUI [1]
C2348585
Week number and study day
Descrizione

Week number and study day

Alias
UMLS CUI-1
C0439230
UMLS CUI-2
C0449788
UMLS CUI-3
C2826182
Week Number
Descrizione

Week number

Tipo di dati

integer

Alias
UMLS CUI [1,1]
C0439230
UMLS CUI [1,2]
C0449788
Study Day
Descrizione

Study day

Tipo di dati

text

Alias
UMLS CUI [1]
C2826182
Predose Overnight Fast
Descrizione

Predose Overnight Fast

Alias
UMLS CUI-1
C0439565
UMLS CUI-2
C0015663
UMLS CUI-3
C0439583
Date and Time of Last Meal
Descrizione

Date and Time of Last Meal

Tipo di dati

datetime

Alias
UMLS CUI [1,1]
C0578574
UMLS CUI [1,2]
C0011008
Study Medication - 1250 mg of lapatinib
Descrizione

Study Medication - 1250 mg of lapatinib

Alias
UMLS CUI-1
C1506770
UMLS CUI-2
C0178602
UMLS CUI-3
C0449788
Date and Time of Dose
Descrizione

Date and Time of Dose

Tipo di dati

datetime

Alias
UMLS CUI [1,1]
C0304229
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C1264639
Number of Tablets taken
Descrizione

Tablet dosage form, taken, count of entities

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0039225
UMLS CUI [1,2]
C1883727
UMLS CUI [1,3]
C0449788
Postdose Fast
Descrizione

Postdose Fast

Alias
UMLS CUI-1
C0439568
UMLS CUI-2
C0015663
Date and Time of next Meal
Descrizione

Start Date and Time of next Meal

Tipo di dati

datetime

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C1998602
UMLS CUI [1,3]
C0439568
UMLS CUI [2,1]
C1301880
UMLS CUI [2,2]
C1998602
UMLS CUI [2,3]
C0439568
Postdose Vomiting
Descrizione

Postdose Vomiting

Alias
UMLS CUI-1
C0042963
UMLS CUI-2
C0439568
Did you vomit within the four hours after you took the study drug?
Descrizione

Post-dose vomiting

Tipo di dati

text

Alias
UMLS CUI [1,1]
C0042963
UMLS CUI [1,2]
C0439568
Treatment Confirmation
Descrizione

Treatment Confirmation

Alias
UMLS CUI-1
C0750484
UMLS CUI-2
C0087111
If entire dose was missed, or less than 5 tablets were taken, enter reason:
Descrizione

missed dose, tablet dosage form, reason

Tipo di dati

text

Alias
UMLS CUI [1,1]
C1709043
UMLS CUI [1,2]
C0566251
UMLS CUI [2,1]
C0039225
UMLS CUI [2,2]
C0449788
UMLS CUI [2,3]
C1709043
UMLS CUI [2,4]
C0566251

Similar models

Lapatinib diary

  1. StudyEvent: ODM
    1. Lapatinib diary
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Date of Visit
Item
Visit Date
date
C1320303 (UMLS CUI [1])
Subject number
Item
Subject number
integer
C2348585 (UMLS CUI [1])
Item Group
Week number and study day
C0439230 (UMLS CUI-1)
C0449788 (UMLS CUI-2)
C2826182 (UMLS CUI-3)
Item
Week Number
integer
C0439230 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
Code List
Week Number
CL Item
Week 1 (1)
CL Item
Week 2 (2)
CL Item
Week 3 (3)
Item
Study Day
text
C2826182 (UMLS CUI [1])
Code List
Study Day
CL Item
Day1 (DAY 1 DOSE)
CL Item
Day2 (DAY 2 DOSE)
CL Item
Day3 (DAY 3 DOSE)
CL Item
Day4 (DAY 4 DOSE)
CL Item
Day5 (DAY 5 DOSE)
CL Item
Day6 (DAY 6 DOSE)
CL Item
Day7 (DAY 7 DOSE)
CL Item
Day8 (DAY 8 DOSE)
Item Group
Predose Overnight Fast
C0439565 (UMLS CUI-1)
C0015663 (UMLS CUI-2)
C0439583 (UMLS CUI-3)
Date and Time of Last Meal
Item
Date and Time of Last Meal
datetime
C0578574 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Study Medication - 1250 mg of lapatinib
C1506770 (UMLS CUI-1)
C0178602 (UMLS CUI-2)
C0449788 (UMLS CUI-3)
Date and Time of Dose
Item
Date and Time of Dose
datetime
C0304229 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
Tablet dosage form, taken, count of entities
Item
Number of Tablets taken
text
C0039225 (UMLS CUI [1,1])
C1883727 (UMLS CUI [1,2])
C0449788 (UMLS CUI [1,3])
Item Group
Postdose Fast
C0439568 (UMLS CUI-1)
C0015663 (UMLS CUI-2)
Start Date and Time of next Meal
Item
Date and Time of next Meal
datetime
C0808070 (UMLS CUI [1,1])
C1998602 (UMLS CUI [1,2])
C0439568 (UMLS CUI [1,3])
C1301880 (UMLS CUI [2,1])
C1998602 (UMLS CUI [2,2])
C0439568 (UMLS CUI [2,3])
Item Group
Postdose Vomiting
C0042963 (UMLS CUI-1)
C0439568 (UMLS CUI-2)
Item
Did you vomit within the four hours after you took the study drug?
text
C0042963 (UMLS CUI [1,1])
C0439568 (UMLS CUI [1,2])
Code List
Did you vomit within the four hours after you took the study drug?
CL Item
Yes (Y)
CL Item
No (N)
Item Group
Treatment Confirmation
C0750484 (UMLS CUI-1)
C0087111 (UMLS CUI-2)
missed dose, tablet dosage form, reason
Item
If entire dose was missed, or less than 5 tablets were taken, enter reason:
text
C1709043 (UMLS CUI [1,1])
C0566251 (UMLS CUI [1,2])
C0039225 (UMLS CUI [2,1])
C0449788 (UMLS CUI [2,2])
C1709043 (UMLS CUI [2,3])
C0566251 (UMLS CUI [2,4])

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