ID

34205

Description

A Study of RO5083945 in Combination With FOLFIRI Versus FOLFIRI Plus Cetuximab or FOLFIRI Alone as Second Line Treatment in Patients With Metastatic Colorectal Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01326000

Lien

https://clinicaltrials.gov/show/NCT01326000

Mots-clés

  1. 15/01/2019 15/01/2019 -
  2. 14/05/2019 14/05/2019 -
Détendeur de droits

see on clinicaltrials.gov

Téléchargé le

15 janvier 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY-NC 3.0

Modèle Commentaires :

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Eligibility Colorectal Cancer NCT01326000

Eligibility Colorectal Cancer NCT01326000

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
adult patients, >/= 18 years of age
Description

ID.1

Type de données

boolean

carcinoma of the colon and/or rectum
Description

ID.2

Type de données

boolean

disease progression during or within 6 months of last dose of oxaliplatin containing first-line combination therapy for metastatic disease
Description

ID.3

Type de données

boolean

ecog performance status 0-1
Description

ID.4

Type de données

boolean

adequate hematological, renal and liver function
Description

ID.5

Type de données

boolean

Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
prior treatment with monoclonal antibody/small molecule against epidermal growth factor receptor (egfr)
Description

ID.6

Type de données

boolean

prior treatment with irinotecan
Description

ID.7

Type de données

boolean

radiotherapy within the last 4 weeks before first dose of study drug (except for limited field palliative radiotherapy for bone pain relief)
Description

ID.8

Type de données

boolean

cns metastasis
Description

ID.9

Type de données

boolean

history of or active autoimmune disorders/conditions
Description

ID.10

Type de données

boolean

Similar models

Eligibility Colorectal Cancer NCT01326000

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
ID.1
Item
adult patients, >/= 18 years of age
boolean
ID.2
Item
carcinoma of the colon and/or rectum
boolean
ID.3
Item
disease progression during or within 6 months of last dose of oxaliplatin containing first-line combination therapy for metastatic disease
boolean
ID.4
Item
ecog performance status 0-1
boolean
ID.5
Item
adequate hematological, renal and liver function
boolean
Item Group
C0680251 (UMLS CUI)
ID.6
Item
prior treatment with monoclonal antibody/small molecule against epidermal growth factor receptor (egfr)
boolean
ID.7
Item
prior treatment with irinotecan
boolean
ID.8
Item
radiotherapy within the last 4 weeks before first dose of study drug (except for limited field palliative radiotherapy for bone pain relief)
boolean
ID.9
Item
cns metastasis
boolean
ID.10
Item
history of or active autoimmune disorders/conditions
boolean

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