ID

34421

Beskrivning

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

Länk

https://clinicaltrials.gov/show/NCT01360554

Nyckelord

  1. 2019-01-17 2019-01-17 -
Rättsinnehavare

see on clinicaltrials.gov

Uppladdad den

17 januari 2019

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Non-Small Cell Lung Cancer (NSCLC) NCT01360554

Eligibility Non-Small Cell Lung Cancer (NSCLC) NCT01360554

Inclusion Criteria
Beskrivning

Inclusion Criteria

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

ID.1

Datatyp

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).
Beskrivning

ID.2

Datatyp

boolean

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

ID.3

Datatyp

boolean

adequate renal, hematologic, liver function.
Beskrivning

ID.4

Datatyp

boolean

ecog ps of 0-2.
Beskrivning

ID.5

Datatyp

boolean

radiologically measurable disease.
Beskrivning

ID.6

Datatyp

boolean

Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
small cell histology.
Beskrivning

ID.7

Datatyp

boolean

symptomatic brain mets or known leptomeningeal mets.
Beskrivning

ID.8

Datatyp

boolean

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

ID.9

Datatyp

boolean

uncontrolled medical disorders.
Beskrivning

ID.10

Datatyp

boolean

Similar models

Eligibility Non-Small Cell Lung Cancer (NSCLC) NCT01360554

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
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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