ID

24621

Beskrivning

Open Label Trial of INCB07839 to Determine Effect and Safety of INCB007839 Plus Trastuzumab in HER2 Positive Metastatic Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00864175

Länk

https://clinicaltrials.gov/show/NCT00864175

Nyckelord

  1. 2017-08-09 2017-08-09 -
  2. 2021-09-17 2021-09-17 -
Uppladdad den

9 augusti 2017

DOI

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Licens

Creative Commons BY 4.0

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Eligibility Metastatic Breast Cancer NCT00864175

Eligibility Metastatic Breast Cancer NCT00864175

Inclusion Criteria
Beskrivning

Inclusion Criteria

Alias
UMLS CUI
C1512693
histologically or cytologically confirmed metastatic breast carcinoma that is her2 positive
Beskrivning

Secondary malignant neoplasm of female breast HER2/Neu Positive

Datatyp

boolean

Alias
UMLS CUI [1,1]
C0346993
UMLS CUI [1,2]
C2348909
measurable disease as defined by the recist criteria
Beskrivning

Measurable Disease

Datatyp

boolean

Alias
UMLS CUI [1]
C1513041
life expectancy greater than or equal to 6 months
Beskrivning

Life Expectancy

Datatyp

boolean

Alias
UMLS CUI [1]
C0023671
eastern cooperative oncology group (ecog) performance status of 0 or 1
Beskrivning

ECOG performance status

Datatyp

boolean

Alias
UMLS CUI [1]
C1520224
Exclusion Criteria
Beskrivning

Exclusion Criteria

Alias
UMLS CUI
C0680251
received any anticancer medications in the 28 days prior to enrollment into this study
Beskrivning

Antineoplastic Agents

Datatyp

boolean

Alias
UMLS CUI [1]
C0003392
received any anticancer medications for cancers other than breast cancer within 6 months prior to enrollment in this study.
Beskrivning

Antineoplastic Agents | Breast Carcinoma Excluded

Datatyp

boolean

Alias
UMLS CUI [1]
C0003392
UMLS CUI [2,1]
C0678222
UMLS CUI [2,2]
C2828389
history of deep venous thrombosis within the last year
Beskrivning

Deep Vein Thrombosis

Datatyp

boolean

Alias
UMLS CUI [1]
C0149871
contraindication to low dose warfarin therapy
Beskrivning

Medical contraindication Warfarin Low dose

Datatyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0043031
UMLS CUI [1,3]
C0445550
clinically significant cardiomyopathy
Beskrivning

Cardiomyopathy

Datatyp

boolean

Alias
UMLS CUI [1]
C0878544
prior treatment with incb007839 or trastuzumab or lapatinib
Beskrivning

INCB007839 | trastuzumab | lapatinib

Datatyp

boolean

Alias
UMLS CUI [1]
C2830216
UMLS CUI [2]
C0728747
UMLS CUI [3]
C1506770

Similar models

Eligibility Metastatic Breast Cancer NCT00864175

Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Item Group
C1512693 (UMLS CUI)
Secondary malignant neoplasm of female breast HER2/Neu Positive
Item
histologically or cytologically confirmed metastatic breast carcinoma that is her2 positive
boolean
C0346993 (UMLS CUI [1,1])
C2348909 (UMLS CUI [1,2])
Measurable Disease
Item
measurable disease as defined by the recist criteria
boolean
C1513041 (UMLS CUI [1])
Life Expectancy
Item
life expectancy greater than or equal to 6 months
boolean
C0023671 (UMLS CUI [1])
ECOG performance status
Item
eastern cooperative oncology group (ecog) performance status of 0 or 1
boolean
C1520224 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Antineoplastic Agents
Item
received any anticancer medications in the 28 days prior to enrollment into this study
boolean
C0003392 (UMLS CUI [1])
Antineoplastic Agents | Breast Carcinoma Excluded
Item
received any anticancer medications for cancers other than breast cancer within 6 months prior to enrollment in this study.
boolean
C0003392 (UMLS CUI [1])
C0678222 (UMLS CUI [2,1])
C2828389 (UMLS CUI [2,2])
Deep Vein Thrombosis
Item
history of deep venous thrombosis within the last year
boolean
C0149871 (UMLS CUI [1])
Medical contraindication Warfarin Low dose
Item
contraindication to low dose warfarin therapy
boolean
C1301624 (UMLS CUI [1,1])
C0043031 (UMLS CUI [1,2])
C0445550 (UMLS CUI [1,3])
Cardiomyopathy
Item
clinically significant cardiomyopathy
boolean
C0878544 (UMLS CUI [1])
INCB007839 | trastuzumab | lapatinib
Item
prior treatment with incb007839 or trastuzumab or lapatinib
boolean
C2830216 (UMLS CUI [1])
C0728747 (UMLS CUI [2])
C1506770 (UMLS CUI [3])

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