ID
50
Description
Evaluation of Bay 59-8862 in Patients With Advanced Renal Cell Carcinoma Inclusion Criteria: - measurable disease as defined by the presence of at least one measurable lesion - prior immunotherapy (up to 2 regimens) or prior radiotherapy is permitted but at least 4 weeks must have elapsed prior to enter study - life expectancy of at least 12 weeks - adequate bone marrow, liver and kidney function Exclusion Criteria: - excluded medical conditions like: pre-existing neuropathy, active heart diseases or ischemia, serious infections, HIV infection, chronic hepatitis B or C, brain metastasis, seizures, hypersensitivity to taxanes, organ transplants, some previous cancers - excluded therapies and medications, previous and concomitant such as: anticancer chemotherapy or immunotherapy during the study or within 4 weeks prior to study entry; more than two prior anticancer chemotherapy regimens; radiotherapy during study or within 4 weeks prior to study entry; bone marrow transplant - others: pregnant or breast-feeding patients; both men and women enrolled in this trial must use adequate barrier birth control measures during the course of the trial; substance abuse, medical, psychological or social conditions that may interfere with the patient's participation
Keywords
Versions (4)
- 11/11/11 11/11/11 -
- 11/11/11 11/11/11 -
- 3/21/14 3/21/14 - Martin Dugas
- 9/17/21 9/17/21 -
Uploaded on
November 11, 2011
DOI
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License
Creative Commons BY-NC 3.0 Legacy
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Eligibility Criteria NCT00044564
Eligibility
- StudyEvent: Eligibility
Description
Exclusion criteria
Description
excluded medical conditions
Data type
boolean
Description
excluded therapies and medications
Data type
boolean
Description
other exclusion criteria
Data type
boolean
Description
Medical concepts
Description
Diagnosis
Data type
string
Alias
- UMLS CUI
- C0011900
- SNOMED CT 2010_0731
- 439401001
Description
Immunotherapy
Data type
string
Alias
- UMLS CUI
- C0021083
- SNOMED CT 2010_0731
- 146638005
Description
Radiotherapy
Data type
string
Alias
- UMLS CUI
- C1522449
- SNOMED CT 2010_0731
- 302505005
Description
Life expectancy
Data type
string
Alias
- UMLS CUI
- C0023671
- LOINC Version 232
- LP75025-4
Description
WBC
Data type
string
Alias
- SNOMED CT 2010_0731
- 767002
- LOINC
- 6690-2
Description
Platelet count
Data type
string
Alias
- SNOMED CT 2010_0731
- 365632008
- UMLS CUI
- C1287267
- LOINC
- 777-3
Description
Hemoglobin
Data type
string
Alias
- SNOMED CT 2010_0731
- 38082009
- UMLS CUI
- C0019046
- MedDRA 13.1
- 10019481
- LOINC
- LP14449-0
Description
INR
Data type
string
Alias
- UMLS CUI
- C0525032
- SNOMED CT 2010_0731
- 165581004
- MedDRA 13.1
- 10022400
- LOINC
- LP20762-8
Description
Bilirubin
Data type
string
Alias
- SNOMED CT 2010_0731
- 79706000
- UMLS CUI
- C0011221
- MedDRA Version 13.1
- 10004683
- LOINC
- 1975-2
Description
Creatinine
Data type
string
Alias
- UMLS CUI
- C0010294
- SNOMED CT 2010_0731
- 15373003
- LOINC
- 38483-4
- MedDRA 13.1
- 10011358
Description
Neuropathy
Data type
string
Alias
- UMLS CUI
- C0442874
- SNOMED CT 2010_0731
- 386033004
- MedDRA 13.1
- 10029328
Description
Cardiac disease
Data type
string
Alias
- UMLS CUI
- C0018799
- SNOMED CT 2010_0731
- 56265001
- MedDRA 13.1
- 10061024
Description
Infection
Data type
string
Alias
- UMLS CUI
- C0021311
- SNOMED CT 2010_0731
- 257551009
- MedDRA Version 13.1
- 10021789
Description
HIV negative
Data type
string
Alias
- UMLS CUI
- C0481430
- SNOMED CT 2010_0731
- 143223008
- MedDRA 13.1
- 10020179
Description
Hepatitis
Data type
string
Alias
- SNOMED CT 2010_0731
- 29001004
- UMLS CUI
- C0019158
- MedDRA Version 13.1
- 10019717
- LOINC
- LP20771-9
Description
Metastasis
Data type
string
Alias
- UMLS CUI
- C0027627
- SNOMED CT 2010_0731
- 128462008
- MedDRA 13.1
- 10027449
- LOINC Version 232
- LP35033-7
Description
Allergic reaction, due to correct medicinal substance properly administered
Data type
string
Alias
- UMLS CUI
- C0274302
- SNOMED CT 2010_0731
- 57302007
Description
Organ transplant
Data type
string
Alias
- UMLS CUI
- C0029216
- MedDRA 13.1
- 10061890
- LOINC Version 232
- MTHU000173
Description
Pharmaceutical Preparations
Data type
string
Alias
- UMLS CUI
- C0013227
Description
Chemotherapy
Data type
string
Alias
- UMLS CUI
- C0392920
- SNOMED CT 2010_0731
- 150415003
Description
Immunomodulatory or immunosuppressive therapy
Data type
string
Alias
- SNOMED CT 2010_0731
- 86553008
- UMLS CUI
- C1963758
- MedDRA Version 13.1
- 10067473
Description
Radiotherapy
Data type
string
Alias
- UMLS CUI
- C1522449
- SNOMED CT 2010_0731
- 302505005
Description
pregnant
Data type
string
Alias
- UMLS CUI
- C0549206
- MedDRA 13.1
- 10036586
Description
Lactation
Data type
string
Alias
- UMLS CUI
- C0006147
- MedDRA 13.1
- 10006247
Description
Contraception
Data type
string
Alias
- UMLS CUI
- C0700589
- SNOMED CT 2010_0731
- 146680009
- MedDRA 13.1
- 10010808
Description
Drug abuse
Data type
string
Alias
- UMLS CUI
- C0013146
- SNOMED CT 2010_0731
- 26416006
- MedDRA 13.1
- 10013654
- LOINC
- LP36310-8
- ICD-9-CM Version 2011
- 305.90
Description
Compliance
Data type
string
Alias
- UMLS CUI
- C1321605
- SNOMED CT 2010_0731
- 405078008
Similar models
Eligibility
- StudyEvent: Eligibility
439401001 (SNOMED CT 2010_0731)
146638005 (SNOMED CT 2010_0731)
302505005 (SNOMED CT 2010_0731)
386033004 (SNOMED CT 2010_0731)
10029328 (MedDRA 13.1)
56265001 (SNOMED CT 2010_0731)
10061024 (MedDRA 13.1)
257551009 (SNOMED CT 2010_0731)
10021789 (MedDRA Version 13.1)
143223008 (SNOMED CT 2010_0731)
10020179 (MedDRA 13.1)
128462008 (SNOMED CT 2010_0731)
10027449 (MedDRA 13.1)
LP35033-7 (LOINC Version 232)
57302007 (SNOMED CT 2010_0731)
150415003 (SNOMED CT 2010_0731)
C1963758 (UMLS CUI)
10067473 (MedDRA Version 13.1)
302505005 (SNOMED CT 2010_0731)
10036586 (MedDRA 13.1)
10006247 (MedDRA 13.1)
146680009 (SNOMED CT 2010_0731)
10010808 (MedDRA 13.1)
26416006 (SNOMED CT 2010_0731)
10013654 (MedDRA 13.1)
LP36310-8 (LOINC)
305.90 (ICD-9-CM Version 2011)
405078008 (SNOMED CT 2010_0731)