ID

22314

Description

XELODA and Lapatinib Advanced or Metastatic Breast Cancer Study ID: 100151 Clinical Study ID: EGF100151 Study Title: A Phase III, Randomized, Open-label, Multicenter Study Comparing GW572016 and Capecitabine (XELODA) versus Capecitabine in Women with Refractory Advanced or Metastatic Breast Cancer Clinicaltrials.gov Identifier: NCT00078572 https://clinicaltrials.gov/ct2/show/NCT00078572 Procedure: Concomitant Medications Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: lapatinib Trade Name: Tyverb,Tykerb,Tycerb Study Indication: Breast Cancer; Neoplasms, Breast

Lien

https://clinicaltrials.gov/ct2/show/NCT00078572

Mots-clés

  1. 29/05/2017 29/05/2017 -
Téléchargé le

29 mai 2017

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

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XELODA and Lapatinib Advanced or Metastatic Breast Cancer Concomitant Medications NCT00078572

XELODA and Lapatinib Advanced or Metastatic Breast Cancer Concomitant Medications NCT00078572

Concomitant Medications
Description

Concomitant Medications

Alias
UMLS CUI-1
C2347852
Drug, Trade name preferred
Description

Drug

Type de données

text

Alias
UMLS CUI [1,1]
C2347852
UMLS CUI [1,2]
C2360065
Date started
Description

Date started

Type de données

date

Alias
UMLS CUI [1,1]
C0808070
UMLS CUI [1,2]
C2347852
Check if started Pre-study
Description

started Pre-study

Type de données

text

Alias
UMLS CUI [1]
C2347852
Date stopped
Description

Date stopped

Type de données

date

Alias
UMLS CUI [1,1]
C0806020
UMLS CUI [1,2]
C2347852
Check if continued Post- study
Description

continued Post- study

Type de données

text

Alias
UMLS CUI [1]
C2347852
Conditions treated/ indication
Description

Conditions treated or indication

Type de données

text

Alias
UMLS CUI [1,1]
C3146298
UMLS CUI [1,2]
C2347852

Similar models

XELODA and Lapatinib Advanced or Metastatic Breast Cancer Concomitant Medications NCT00078572

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Concomitant Medications
C2347852 (UMLS CUI-1)
Drug
Item
Drug, Trade name preferred
text
C2347852 (UMLS CUI [1,1])
C2360065 (UMLS CUI [1,2])
Date started
Item
Date started
date
C0808070 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Item
Check if started Pre-study
text
C2347852 (UMLS CUI [1])
Code List
Check if started Pre-study
CL Item
Yes (Y)
CL Item
No (N)
Date stopped
Item
Date stopped
date
C0806020 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])
Item
Check if continued Post- study
text
C2347852 (UMLS CUI [1])
Code List
Check if continued Post- study
CL Item
Yes (Y)
CL Item
No (N)
Conditions treated or indication
Item
Conditions treated/ indication
text
C3146298 (UMLS CUI [1,1])
C2347852 (UMLS CUI [1,2])

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