ID

22435

Descrizione

Study of Pemetrexed + Carboplatin + Bevacizumab + Enzastaurin Versus Pemetrexed + Carboplatin + Bevacizumab + Placebo in Patients With Non-Small Cell Lung Cancer Who Have Not Been Previously Treated With Chemotherapy; ODM derived from: https://clinicaltrials.gov/show/NCT00533429

collegamento

https://clinicaltrials.gov/show/NCT00533429

Keywords

versioni (1)
  1. 04/06/17 04/06/17 -
Caricato su

4 giugno 2017

DOI

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Licenza

Creative Commons BY 4.0
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Eligibility Non-small Cell Lung Cancer NCT00533429

Inglese

Eligibility Non-small Cell Lung Cancer NCT00533429

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
they or their legal representative must have signed an informed consent document for clinical research
Descrizione

informed consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0021430
have laboratory confirmed diagnosis of advanced, nonsquamous cell nsclc (stage iiib or iv disease) which is not curable
Descrizione

nonsquamous cell nsclc, tumor stage, incurable

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C2585890
UMLS CUI [1,2]
C1300072
UMLS CUI [1,3]
C0175969
have not received any prior systemic chemotherapy, immunotherapy, targeted therapy, or biological therapy for advanced nsclc, prior radiation therapy is allowed to less than 25% of the bone marrow
Descrizione

prior therapy, chemotherapy, immunotherapy, targeted therapy, or biological therapy, prior radiation therapy, advanced nsclc

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C0392920
UMLS CUI [1,3]
C0021083
UMLS CUI [1,4]
C2985566
UMLS CUI [1,5]
C0005527
UMLS CUI [1,6]
C0205179
UMLS CUI [1,7]
C0007131
UMLS CUI [2,1]
C0279134
UMLS CUI [2,2]
C0205179
UMLS CUI [2,3]
C0007131
have measurable disease
Descrizione

measurable disease

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1513041
have adequate organ function and estimated life expectancy of 12 weeks
Descrizione

organ function, life expectancy

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0678852
UMLS CUI [2]
C0023671
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
have known cns disease; major surgery within 28 days; minor surgery within 7 days; serious concommitant systemic disorder; serious cardiac condition; have a serious, nonhealing wound, ulcer, or bone fracture
Descrizione

cns disease, major surgery; minor surgery; serious systemic disorder; serious cardiac condition; nonhealing wound, ulcer, or bone fracture

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0007682
UMLS CUI [2]
C0679637
UMLS CUI [3]
C0038904
UMLS CUI [4]
C0442893
UMLS CUI [5]
C0018799
UMLS CUI [6,1]
C0043250
UMLS CUI [6,2]
C3845448
UMLS CUI [7,1]
C0041582
UMLS CUI [7,2]
C3845448
UMLS CUI [8,1]
C0016658
UMLS CUI [8,2]
C3845448
have received treatment within the last 30 days with any drug that has not received regulatory approval for any indication at the time of study entry
Descrizione

prior therapy, drugs, regulatory approval

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C0013227
UMLS CUI [1,3]
C3899556
have previously received treatment with enzastaurin, pemetrexed, or bevacizumab
Descrizione

prior therapy enzastaurin, pemetrexed, or bevacizumab

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C1327830
UMLS CUI [2,1]
C1514463
UMLS CUI [2,2]
C0210657
UMLS CUI [3,1]
C1514463
UMLS CUI [3,2]
C0796392
are pregnant or breast-feeding
Descrizione

pregnancy, breast feeding

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147
are unable to swallow tablets
Descrizione

are unable to swallow tablets

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0566355
UMLS CUI [1,2]
C0039225
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Similar models

Eligibility Non-small Cell Lung Cancer NCT00533429

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
informed consent
Item
they or their legal representative must have signed an informed consent document for clinical research
boolean
C0021430 (UMLS CUI [1])
nonsquamous cell nsclc, tumor stage, incurable
Item
have laboratory confirmed diagnosis of advanced, nonsquamous cell nsclc (stage iiib or iv disease) which is not curable
boolean
C2585890 (UMLS CUI [1,1])
C1300072 (UMLS CUI [1,2])
C0175969 (UMLS CUI [1,3])
prior therapy, chemotherapy, immunotherapy, targeted therapy, or biological therapy, prior radiation therapy, advanced nsclc
Item
have not received any prior systemic chemotherapy, immunotherapy, targeted therapy, or biological therapy for advanced nsclc, prior radiation therapy is allowed to less than 25% of the bone marrow
boolean
C1514463 (UMLS CUI [1,1])
C0392920 (UMLS CUI [1,2])
C0021083 (UMLS CUI [1,3])
C2985566 (UMLS CUI [1,4])
C0005527 (UMLS CUI [1,5])
C0205179 (UMLS CUI [1,6])
C0007131 (UMLS CUI [1,7])
C0279134 (UMLS CUI [2,1])
C0205179 (UMLS CUI [2,2])
C0007131 (UMLS CUI [2,3])
measurable disease
Item
have measurable disease
boolean
C1513041 (UMLS CUI [1])
organ function, life expectancy
Item
have adequate organ function and estimated life expectancy of 12 weeks
boolean
C0678852 (UMLS CUI [1])
C0023671 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
cns disease, major surgery; minor surgery; serious systemic disorder; serious cardiac condition; nonhealing wound, ulcer, or bone fracture
Item
have known cns disease; major surgery within 28 days; minor surgery within 7 days; serious concommitant systemic disorder; serious cardiac condition; have a serious, nonhealing wound, ulcer, or bone fracture
boolean
C0007682 (UMLS CUI [1])
C0679637 (UMLS CUI [2])
C0038904 (UMLS CUI [3])
C0442893 (UMLS CUI [4])
C0018799 (UMLS CUI [5])
C0043250 (UMLS CUI [6,1])
C3845448 (UMLS CUI [6,2])
C0041582 (UMLS CUI [7,1])
C3845448 (UMLS CUI [7,2])
C0016658 (UMLS CUI [8,1])
C3845448 (UMLS CUI [8,2])
prior therapy, drugs, regulatory approval
Item
have received treatment within the last 30 days with any drug that has not received regulatory approval for any indication at the time of study entry
boolean
C1514463 (UMLS CUI [1,1])
C0013227 (UMLS CUI [1,2])
C3899556 (UMLS CUI [1,3])
prior therapy enzastaurin, pemetrexed, or bevacizumab
Item
have previously received treatment with enzastaurin, pemetrexed, or bevacizumab
boolean
C1514463 (UMLS CUI [1,1])
C1327830 (UMLS CUI [1,2])
C1514463 (UMLS CUI [2,1])
C0210657 (UMLS CUI [2,2])
C1514463 (UMLS CUI [3,1])
C0796392 (UMLS CUI [3,2])
pregnancy, breast feeding
Item
are pregnant or breast-feeding
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])
are unable to swallow tablets
Item
are unable to swallow tablets
boolean
C0566355 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
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