ID

34421

Description

ARCHER 1009 : A Study Of Dacomitinib (PF-00299804) Vs. Erlotinib In The Treatment Of Advanced Non-Small Cell Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01360554

Lien

https://clinicaltrials.gov/show/NCT01360554

Mots-clés

  1. 17/01/2019 17/01/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

17 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0

Modèle Commentaires :

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Eligibility Non-Small Cell Lung Cancer (NSCLC) NCT01360554

Eligibility Non-Small Cell Lung Cancer (NSCLC) NCT01360554

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
evidence of pathologically confirmed, advanced nsclc (with known histology).
Description

ID.1

Type de données

boolean

prior treatment with at least one and no more than two systemic therapy regimens (at least one must be standard chemotherapy for advanced nsclc).
Description

ID.2

Type de données

boolean

adequate tissue sample must be submitted prior to randomization for tumor biomarker analyses.
Description

ID.3

Type de données

boolean

adequate renal, hematologic, liver function.
Description

ID.4

Type de données

boolean

ecog ps of 0-2.
Description

ID.5

Type de données

boolean

radiologically measurable disease.
Description

ID.6

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
small cell histology.
Description

ID.7

Type de données

boolean

symptomatic brain mets or known leptomeningeal mets.
Description

ID.8

Type de données

boolean

prior therapy with agent known or proposed to be active by action on egfr tyrosine kinase or other her family proteins.
Description

ID.9

Type de données

boolean

uncontrolled medical disorders.
Description

ID.10

Type de données

boolean

Similar models

Eligibility Non-Small Cell Lung Cancer (NSCLC) NCT01360554

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
evidence of pathologically confirmed, advanced nsclc (with known histology).
boolean
ID.2
Item
prior treatment with at least one and no more than two systemic therapy regimens (at least one must be standard chemotherapy for advanced nsclc).
boolean
ID.3
Item
adequate tissue sample must be submitted prior to randomization for tumor biomarker analyses.
boolean
ID.4
Item
adequate renal, hematologic, liver function.
boolean
ID.5
Item
ecog ps of 0-2.
boolean
ID.6
Item
radiologically measurable disease.
boolean
Item Group
C0680251 (UMLS CUI)
ID.7
Item
small cell histology.
boolean
ID.8
Item
symptomatic brain mets or known leptomeningeal mets.
boolean
ID.9
Item
prior therapy with agent known or proposed to be active by action on egfr tyrosine kinase or other her family proteins.
boolean
ID.10
Item
uncontrolled medical disorders.
boolean

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