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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT00428220
Registration number
NCT00428220
Ethics application status
Date submitted
26/01/2007
Date registered
29/01/2007
Date last updated
27/06/2019
Titles & IDs
Public title
A Continuation Study Using Sunitinib Malate For Patients Leaving Treatment On A Previous Sunitinib Study.
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Scientific title
An Open-label Sunitinib Malate (su011248) Continuation Protocol For Patients Who Have Completed A Prior Sunitinib Study And Are Judged By The Investigator To Have The Potential To Benefit From Sunitinib Treatment
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Secondary ID [1]
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2006-006538-16
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Secondary ID [2]
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A6181114
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Metastatic Breast Cancer
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Advanced Breast Cancer
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Metastatic Castration Resistant Prostate Cancer
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Metastatic Renal Cell Cancer
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0
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Non-Small Cell Lung Cancer
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Thyroid Cancer
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Advanced/Metastatic Non-Small Cell Lung Cancer
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Advanced Gastric Cancer
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Gastrointestinal Stromal Tumor
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Hepatocellular Carcinoma
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Pancreatic Islet Cell Carcinoma
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Pancreatic Neuroendocrine Tumor
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Condition category
Condition code
Cancer
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0
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Non melanoma skin cancer
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Cancer
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Kidney
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Cancer
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Breast
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Cancer
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Lung - Mesothelioma
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Cancer
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Lung - Non small cell
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Cancer
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Lung - Small cell
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Cancer
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Neuroendocrine tumour (NET)
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Cancer
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Stomach
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Cancer
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Bowel - Small bowel (duodenum and ileum)
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Cancer
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0
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Bowel - Back passage (rectum) or large bowel (colon)
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Cancer
0
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Pancreatic
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Treatment: Drugs - sunitinib
Experimental: A - Sunitinib will be administered in a continuous daily dose (oral, once per day). Starting dose will be 37.5 mg daily unless the patient was on a different dose (25 mg or 50 mg daily) on the previous trial. In that case, they will begin treatment on this study at the same dose used at the end of the previous study.
The protocol now allows for patients on dosing regimens other than only continuous dosing (e.g. 4/2, etc.) to be enrolled if eligible.
Treatment: Drugs: sunitinib
sunitinib
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Intervention code [1]
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Treatment: Drugs
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Number of Participants With Treatment-emergent Adverse Events (AEs) (All Causalities)
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Assessment method [1]
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Assessment of AEs included type, incidence, severity (graded by the National Cancer Institute \[NCI\] Common Terminology Criteria for Adverse Events \[CTCAE\], Version 3.0, timing, seriousness, and relatedness; and laboratory abnormalities.
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Timepoint [1]
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From first day of treatment on the current study up to 28 days post the last dose of study treatment
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Primary outcome [2]
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Number of Participants With Treatment-emergent AEs (Treatment-Related)
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Assessment method [2]
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Assessment of AEs included type, incidence, severity (graded by the National Cancer Institute \[NCI\] Common Terminology Criteria for Adverse Events \[CTCAE\], Version 3.0, timing, seriousness, and relatedness; and laboratory abnormalities.
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Timepoint [2]
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From first day of treatment on the current study up to 28 days post the last dose of study treatment
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Eligibility
Key inclusion criteria
* Must have ended treatment from one of the following sunitinib studies: A6181030, A6181064, A6181078, A6181087, A6181094, A6181107, A6181108, A6181110, A6181111, A6181112, A6181113, A6181120, A6181126 and A6181170. Other Pfizer sponsored sunitinib studies may be included in the future.
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
* See inclusion criteria
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Study design
Purpose of the study
Treatment
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Allocation to intervention
NA
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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Other design features
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Phase
NA
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Type of endpoint/s
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
1/07/2007
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
1/09/2014
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Sample size
Target
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Accrual to date
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Final
223
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Recruitment in Australia
Recruitment state(s)
QLD,SA,VIC,WA
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Recruitment hospital [1]
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Royal Brisbane & Women's Hospital - Herston
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Recruitment hospital [2]
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Royal Adelaide Hospital, Department of Medical Oncology - Adelaide
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Recruitment hospital [3]
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Austin Health - Heidelberg
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Recruitment hospital [4]
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Royal Melbourne Hospital - Parkville
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Recruitment hospital [5]
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Mount Medical Centre - Perth
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Recruitment postcode(s) [1]
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4029 - Herston
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Recruitment postcode(s) [2]
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5000 - Adelaide
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Recruitment postcode(s) [3]
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3084 - Heidelberg
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Recruitment postcode(s) [4]
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3050 - Parkville
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Recruitment postcode(s) [5]
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6000 - Perth
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Recruitment outside Australia
Country [1]
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United States of America
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Georgia
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United States of America
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Illinois
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United States of America
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Iowa
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United States of America
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Missouri
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Nevada
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United States of America
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Oregon
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United States of America
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Texas
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United States of America
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Virginia
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Argentina
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Rio Negro
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Argentina
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Santa Fé
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Argentina
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State/province [11]
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Nueva Cordoba
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Country [12]
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Argentina
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San Miguel de Tucuman
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Belgium
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Bruxelles
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Belgium
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Leuven
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Belgium
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Liege
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Belgium
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Sint-Niklaas
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Belgium
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Wilrijk
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Brazil
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RS
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Brazil
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SP
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Canada
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British Columbia
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Canada
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Nova Scotia
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Canada
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Ontario
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Canada
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Quebec
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Colombia
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Anquioquia
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Colombia
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Antioquia
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France
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Cedex 02
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France
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Cedex
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France
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Besancon
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France
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Bordeaux Cedex
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France
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Clermont Ferrand
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France
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Lille
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France
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Lyon Cedex 03
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France
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Lyon
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France
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Marseille Cedex 5
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France
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Neuilly Sur Seine
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France
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Paris
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France
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Rennes Cedex
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Germany
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Bad Berka
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Germany
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Berlin
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Germany
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Jena
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Germany
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Kiel
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Germany
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Luebeck
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Germany
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Marburg
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Germany
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Meiningen
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Germany
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Muenchen
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Hong Kong
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New Territories
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Hong Kong
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Hong Kong
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Hong Kong
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Kowloon
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Hong Kong
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State/province [49]
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Tuen Mun, New Territories
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Hong Kong
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State/province [50]
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Wan Chai,
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Korea, Republic of
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Gyeonggi-do
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Korea, Republic of
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Republic Of Korea
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Korea, Republic of
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Daegu
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Korea, Republic of
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Seoul
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Mexico
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Nuevo Leon
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Mexico
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State/province [56]
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Chihuahua
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Philippines
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State/province [57]
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Quezon City, Metro Manila
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Singapore
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State/province [58]
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Singapore
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Spain
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Barcelona
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Spain
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Madrid
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Spain
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La Coruña
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Taiwan
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Taoyuan
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Taiwan
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Changhua
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Taiwan
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State/province [64]
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Kaohsiung
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0
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Taiwan
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State/province [65]
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Liouying Township, Tainan,
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Country [66]
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Taiwan
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State/province [66]
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Taichung
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Taiwan
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Taipei
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Country [68]
0
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Taiwan
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State/province [68]
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YungKang City, Tainan
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Country [69]
0
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United Kingdom
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State/province [69]
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Merseyside
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Country [70]
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United Kingdom
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State/province [70]
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Glasgow
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0
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United Kingdom
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State/province [71]
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Leeds
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Country [72]
0
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United Kingdom
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London
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Country [73]
0
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United Kingdom
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State/province [73]
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Manchester
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Country [74]
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United Kingdom
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State/province [74]
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Nottingham
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Funding & Sponsors
Primary sponsor type
Commercial sector/industry
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Name
Pfizer
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Address
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Country
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Ethics approval
Ethics application status
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Summary
Brief summary
This is a study using sunitinib for patients ending treatment on a previous sunitinib malate protocol to continue to receive sunitinib. The patient must have been enrolled in one of the following studies: A6181030, A6181064, A6181078, A6181087, A6181094, A6181107, A6181108, A6181110, A6181111, A6181112, A6181113, A6181120, A6181126 and A6181170. Other Pfizer sponsored sunitinib studies may be included in the future.
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Trial website
https://clinicaltrials.gov/study/NCT00428220
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Pfizer CT.gov Call Center
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Address
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Pfizer
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Address
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Phone
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Fax
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Email
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results are available at
https://clinicaltrials.gov/study/NCT00428220
Download to PDF