ID

42996

Description

Phase II Study of AZD4877 (a Novel Anti-mitotic Agent) See http://clinicaltrials.gov/ct2/show/record/NCT00661609

Link

http://clinicaltrials.gov/ct2/show/record/NCT00661609

Keywords

Versions (3)
  1. 11/18/11 11/18/11 -
  2. 3/26/14 3/26/14 - Martin Dugas
  3. 9/17/21 9/17/21 -
Uploaded on

September 17, 2021

DOI

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License

Creative Commons BY 4.0
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Eligibility DRKS00004052 NCT00661609 Bladder Cancer

English

Eligibility Advanced Bladder Cancer NCT00661609

1 forms  
Inclusion criteria
Description

Inclusion criteria

Alias
UMLS CUI-1
C1512693
Confirmed urothelial cancer (cancer of the bladder, renal pelvis, ureter, or urethra)
Description

Urothelial Neoplasm

Data type

boolean

Alias
UMLS CUI-1
C1519840
Tumor, Node, Metastasis (TNM) Stage IV urothelial cancer that can not be helped by curative surgery and/or curative radiotherapy
Description

Stage IV

Data type

boolean

Alias
UMLS CUI-1
C0441772
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
Description

Prior chemotherapy

Data type

boolean

Alias
UMLS CUI-1
C1514457
Ambulatory and capable of all selfcare more than 50% of waking hours
Description

General status

Data type

boolean

Alias
UMLS CUI-1
C0947124
Exclusion criteria
Description

Exclusion criteria

Alias
UMLS CUI-1
C0680251
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.
Description

Prior treatment

Data type

boolean

Alias
UMLS CUI-1
C1514463
Inadequate bone marrow reserve
Description

Inadequate bone marrow reserve

Data type

boolean

Alias
UMLS CUI-1
CL406855
Inadequate liver function in the presence of liver metastases
Description

Liver Dysfunction

Data type

boolean

Alias
UMLS CUI-1
C0086565
Impaired renal function
Description

Impaired renal function

Data type

boolean

Alias
UMLS CUI-1
C1565489
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Similar models

Eligibility Advanced Bladder Cancer NCT00661609

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Inclusion criteria
C1512693 (UMLS CUI-1)
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)
Item Group
Exclusion criteria
C0680251 (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
C1565489 (UMLS CUI-1)
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