ID

34430

Beschrijving

A Safety and Efficacy Study of INC280 Alone, and in Combination With Erlotinib, Compared to Chemotherapy, in Advanced/Metastatic Non-small Cell Lung Cancer Patients With EGFR Mutation and cMET Amplification; ODM derived from: https://clinicaltrials.gov/show/NCT02468661

Link

https://clinicaltrials.gov/show/NCT02468661

Trefwoorden

  1. 17-01-19 17-01-19 -
  2. 20-04-20 20-04-20 -
  3. 25-04-20 25-04-20 -
Houder van rechten

see on clinicaltrials.gov

Geüploaded op

17 januari 2019

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Non-Small Cell Lung Cancer NCT02468661

Eligibility Non-Small Cell Lung Cancer NCT02468661

Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
locally advanced or metastatic nsclc
Beschrijving

ID.1

Datatype

boolean

egfr mutation (l858r and /or ex19del)
Beschrijving

ID.2

Datatype

boolean

cmet amplification by fish (gcn ≥ 6),
Beschrijving

ID.3

Datatype

boolean

acquired resistance to egfr tki (1st or 2nd génération)
Beschrijving

ID.4

Datatype

boolean

ecog performance status (ps) ≤ 1.
Beschrijving

ID.5

Datatype

boolean

Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior treatment with 3rd generation tki
Beschrijving

ID.6

Datatype

boolean

phaseii : prior treatment with any of the following agents:
Beschrijving

ID.7

Datatype

boolean

crizotinib, or any other cmet inhibitor or hgf-targeting inhibitor.
Beschrijving

ID.8

Datatype

boolean

concomitant egfr tki and platinum based chemotherapy as first line regimen.
Beschrijving

ID.9

Datatype

boolean

platinum-based chemotherapy as first line treatment
Beschrijving

ID.10

Datatype

boolean

Similar models

Eligibility Non-Small Cell Lung Cancer NCT02468661

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
locally advanced or metastatic nsclc
boolean
ID.2
Item
egfr mutation (l858r and /or ex19del)
boolean
ID.3
Item
cmet amplification by fish (gcn ≥ 6),
boolean
ID.4
Item
acquired resistance to egfr tki (1st or 2nd génération)
boolean
ID.5
Item
ecog performance status (ps) ≤ 1.
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
prior treatment with 3rd generation tki
boolean
ID.7
Item
phaseii : prior treatment with any of the following agents:
boolean
ID.8
Item
crizotinib, or any other cmet inhibitor or hgf-targeting inhibitor.
boolean
ID.9
Item
concomitant egfr tki and platinum based chemotherapy as first line regimen.
boolean
ID.10
Item
platinum-based chemotherapy as first line treatment
boolean

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