A Retrospective Real World Analysis Of Sutent In Patients With Metastatic Renal Cell Carcinoma In Community And Academic Centers To Assess The Impact Of Dose Variation On Duration Of Response And Overall Survival
NCT ID: NCT01917214
Last Updated: 2015-03-26
Study Results
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View full resultsBasic Information
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COMPLETED
212 participants
OBSERVATIONAL
2013-08-31
2014-03-31
Brief Summary
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The factors which will be analysed include patient characteristics, dosage and adverse event management and tries to correlate these factors with survival.
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Study Groups
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Non-Interventional Study
Sutent: Observational Study
Sutent oral therapy
Interventions
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Sutent: Observational Study
Sutent oral therapy
Eligibility Criteria
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Inclusion Criteria
* Male or female
* Metastatic renal cell cancer
* First presentation with metastatic disease prior to 1st Jan 2012 since 2006, i.e. between 1st Jan 2006 to 31st Dec 2011
Exclusion Criteria
* No record available in electronic database
18 Years
ALL
No
Sponsors
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Pfizer
INDUSTRY
Responsible Party
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Principal Investigators
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Pfizer CT.gov Call Center
Role: STUDY_DIRECTOR
Pfizer
Related Links
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To obtain contact information for a study center near you, click here.
Other Identifiers
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A6181210
Identifier Type: -
Identifier Source: org_study_id
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