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Note: This record shows only the 20 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 17 October 2012
Main ID:  NCT00130897
Date of registration: 14/08/2005
Primary sponsor: Pfizer
Public title: Treatment Use Study With Sunitinib (SU011248) For Patients With Cytokine-Refractory Metastatic Renal Cell Carcinoma
Scientific title: A SU011248 Expanded Access Protocol For Systemic Therapy Of Patients With Metastatic Renal Cell Carcinoma Who Are Ineligible For Participation In Other SU011248 Protocols But May Derive Benefit From Treatment With SU011248
Date of first enrolment: July 2005
Target sample size:
Recruitment status: Approved for marketing
URL:  http://clinicaltrials.gov/show/NCT00130897
Study type:  Expanded Access
Study design:  N/A  
Countries of recruitment
Argentina Australia Austria Belgium Bosnia and Herzegovina Brazil Bulgaria Canada
Chile China Colombia Croatia Czech Republic Ecuador Egypt Finland
Former Serbia and Montenegro France Germany Greece Hong Kong Hungary India Ireland
Israel Italy Korea, Republic of Lebanon Malaysia Mexico Netherlands Norway
Panama Peru Philippines Poland Portugal Romania Russian Federation Serbia
Singapore Slovakia Slovenia Spain Sweden Switzerland Taiwan Thailand
Turkey United Kingdom United States Venezuela
Contacts
Name:   Pfizer CT.gov Call Center
Address: 
Telephone:
Email:
Affiliation:  Pfizer
Key inclusion & exclusion criteria

Inclusion Criteria:

- renal cell carcinoma that is not amendable to standard therapy with curative intent

Exclusion Criteria:

- current treatment in another therapeutic clinical trial



Age minimum: 18 Years
Age maximum: N/A
Gender: Both
Health Condition(s) or Problem(s) studied
Carcinoma, Renal Cell
Intervention(s)
Drug: Sutent
Primary Outcome(s)
Secondary Outcome(s)
Secondary ID(s)
A6181037
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
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