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
Mots-clés
Versions (4)
- 11/11/2011 11/11/2011 -
- 11/11/2011 11/11/2011 -
- 21/03/2014 21/03/2014 - Martin Dugas
- 17/09/2021 17/09/2021 -
Téléchargé le
11 novembre 2011
DOI
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Licence
Creative Commons BY-NC 3.0 Legacy
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Eligibility Criteria NCT00044564
Eligibility
- StudyEvent: Eligibility
Description
Exclusion criteria
Description
Medical concepts
Description
Diagnosis
Type de données
string
Alias
- UMLS CUI
- C0011900
- SNOMED CT 2010_0731
- 439401001
Description
Immunotherapy
Type de données
string
Alias
- UMLS CUI
- C0021083
- SNOMED CT 2010_0731
- 146638005
Description
Radiotherapy
Type de données
string
Alias
- UMLS CUI
- C1522449
- SNOMED CT 2010_0731
- 302505005
Description
Life expectancy
Type de données
string
Alias
- UMLS CUI
- C0023671
- LOINC Version 232
- LP75025-4
Description
WBC
Type de données
string
Alias
- SNOMED CT 2010_0731
- 767002
- LOINC
- 6690-2
Description
Platelet count
Type de données
string
Alias
- SNOMED CT 2010_0731
- 365632008
- UMLS CUI
- C1287267
- LOINC
- 777-3
Description
Hemoglobin
Type de données
string
Alias
- SNOMED CT 2010_0731
- 38082009
- UMLS CUI
- C0019046
- MedDRA 13.1
- 10019481
- LOINC
- LP14449-0
Description
INR
Type de données
string
Alias
- UMLS CUI
- C0525032
- SNOMED CT 2010_0731
- 165581004
- MedDRA 13.1
- 10022400
- LOINC
- LP20762-8
Description
Bilirubin
Type de données
string
Alias
- SNOMED CT 2010_0731
- 79706000
- UMLS CUI
- C0011221
- MedDRA Version 13.1
- 10004683
- LOINC
- 1975-2
Description
Creatinine
Type de données
string
Alias
- UMLS CUI
- C0010294
- SNOMED CT 2010_0731
- 15373003
- LOINC
- 38483-4
- MedDRA 13.1
- 10011358
Description
Neuropathy
Type de données
string
Alias
- UMLS CUI
- C0442874
- SNOMED CT 2010_0731
- 386033004
- MedDRA 13.1
- 10029328
Description
Cardiac disease
Type de données
string
Alias
- UMLS CUI
- C0018799
- SNOMED CT 2010_0731
- 56265001
- MedDRA 13.1
- 10061024
Description
Infection
Type de données
string
Alias
- UMLS CUI
- C0021311
- SNOMED CT 2010_0731
- 257551009
- MedDRA Version 13.1
- 10021789
Description
HIV negative
Type de données
string
Alias
- UMLS CUI
- C0481430
- SNOMED CT 2010_0731
- 143223008
- MedDRA 13.1
- 10020179
Description
Hepatitis
Type de données
string
Alias
- SNOMED CT 2010_0731
- 29001004
- UMLS CUI
- C0019158
- MedDRA Version 13.1
- 10019717
- LOINC
- LP20771-9
Description
Metastasis
Type de données
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
Type de données
string
Alias
- UMLS CUI
- C0274302
- SNOMED CT 2010_0731
- 57302007
Description
Organ transplant
Type de données
string
Alias
- UMLS CUI
- C0029216
- MedDRA 13.1
- 10061890
- LOINC Version 232
- MTHU000173
Description
Pharmaceutical Preparations
Type de données
string
Alias
- UMLS CUI
- C0013227
Description
Chemotherapy
Type de données
string
Alias
- UMLS CUI
- C0392920
- SNOMED CT 2010_0731
- 150415003
Description
Immunomodulatory or immunosuppressive therapy
Type de données
string
Alias
- SNOMED CT 2010_0731
- 86553008
- UMLS CUI
- C1963758
- MedDRA Version 13.1
- 10067473
Description
Radiotherapy
Type de données
string
Alias
- UMLS CUI
- C1522449
- SNOMED CT 2010_0731
- 302505005
Description
pregnant
Type de données
string
Alias
- UMLS CUI
- C0549206
- MedDRA 13.1
- 10036586
Description
Lactation
Type de données
string
Alias
- UMLS CUI
- C0006147
- MedDRA 13.1
- 10006247
Description
Contraception
Type de données
string
Alias
- UMLS CUI
- C0700589
- SNOMED CT 2010_0731
- 146680009
- MedDRA 13.1
- 10010808
Description
Drug abuse
Type de données
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
Type de données
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)