ID

44718

Descrição

The purpose of this Phase II study is to determine if AZD4877, an experimental drug that is a novel anti-mitotic agent (Eg5 or Kinesin Spindle Protein inhibitor that interferes with tumor cell division leading to tumor growth), can reduce tumor sizes in patients with bladder cancer see http://clinicaltrials.gov/ct2/show/study/NCT00661609

Link

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

Palavras-chave

  1. 21/11/2011 21/11/2011 -
  2. 27/03/2014 27/03/2014 - Martin Dugas
  3. 17/09/2021 17/09/2021 -
  4. 27/09/2021 27/09/2021 - Sarah Riepenhausen
Titular dos direitos

AstraZeneca

Transferido a

27 de setembro de 2021

DOI

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Licença

Creative Commons BY 4.0

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A Phase II Study of AZD4877 (a Novel Anti-mitotic DRKS00004052

Eligibility Bladder Cancer NCT00661609

Inclusion criteria
Descrição

Inclusion criteria

Alias
UMLS CUI [1]
C1512693
Confirmed urothelial cancer (cancer of the bladder, renal pelvis, ureter, or urethra).
Descrição

Urothelial cancer

Tipo de dados

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
Descrição

Stage IV

Tipo de dados

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.
Descrição

Prior chemotherapy

Tipo de dados

boolean

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

Selfcare

Tipo de dados

boolean

Alias
UMLS CUI-1
C0036592
Exclusion criteria
Descrição

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.
Descrição

Prior treatment

Tipo de dados

boolean

Alias
UMLS CUI-1
C1514463
Inadequate bone marrow reserve
Descrição

Bone marrow

Tipo de dados

boolean

Alias
UMLS CUI-1
C0005953
Inadequate liver function in the presence of liver metastases
Descrição

Liver function

Tipo de dados

boolean

Alias
UMLS CUI
C0232744
Impaired renal function
Descrição

Renal function

Tipo de dados

boolean

Alias
UMLS CUI
C1565489

Similar models

Eligibility Bladder Cancer NCT00661609

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
Inclusion criteria
C1512693 (UMLS CUI [1])
Urothelial cancer
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)
Selfcare
Item
Ambulatory and capable of all selfcare more than 50% of waking hours
boolean
C0036592 (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)
Bone marrow
Item
Inadequate bone marrow reserve
boolean
C0005953 (UMLS CUI-1)
Liver function
Item
Inadequate liver function in the presence of liver metastases
boolean
C0232744 (UMLS CUI)
Renal function
Item
Impaired renal function
boolean
C1565489 (UMLS CUI)

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