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Information:
Fel:
ID
4755
Beskrivning
Phase II Study of AZD4877 (a Novel Anti-mitotic Agent) See http://clinicaltrials.gov/ct2/show/record/NCT00661609
Länk
http://clinicaltrials.gov/ct2/show/record/NCT00661609
Nyckelord
Versioner (3)
- 2011-11-18 2011-11-18 -
- 2014-03-26 2014-03-26 - Martin Dugas
- 2021-09-17 2021-09-17 -
Uppladdad den
26 mars 2014
DOI
För en begäran logga in.
Licens
Creative Commons BY 4.0
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Eligibility DRKS00004052 NCT00661609 Bladder Cancer
Eligibility Advanced Bladder Cancer NCT00661609
- StudyEvent: Eligibility
Similar models
Eligibility Advanced Bladder Cancer NCT00661609
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Urothelial Neoplasm
Item
Confirmed urothelial cancer (cancer of the bladder, renal pelvis, ureter, or urethra)
boolean
C1519840 (UMLS CUI-1)
Stage IV
Item
Tumor, Node, Metastasis (TNM) Stage IV urothelial cancer that can not be helped by curative surgery and/or curative radiotherapy
boolean
C0441772 (UMLS CUI-1)
Prior chemotherapy
Item
Must have had a maximum of 2 prior chemotherapeutic regimens, one for unremovable and/or metastasized disease, and the other in the adjuvant or neo-adjuvant setting
boolean
C1514457 (UMLS CUI-1)
General status
Item
Ambulatory and capable of all selfcare more than 50% of waking hours
boolean
C0947124 (UMLS CUI-1)
Prior treatment
Item
Prior treatment with investigational or standard anti-cancer agents, including radiotherapy, within 4 weeks prior to first dose of study medication, 6 weeks if prior systemic mitomycin, nitrosourea, or suramin.
boolean
C1514463 (UMLS CUI-1)
Inadequate bone marrow reserve
Item
Inadequate bone marrow reserve
boolean
CL406855 (UMLS CUI-1)
Liver Dysfunction
Item
Inadequate liver function in the presence of liver metastases
boolean
C0086565 (UMLS CUI-1)
Impaired renal function
Item
Impaired renal function
boolean
C0341697 (UMLS CUI-1)