Rollover Protocol for Prior SU011248 Protocols
A Treatment Protocol For Patients Continuing From A Prior SU011248 Protocol
1 other identifier
interventional
314
11 countries
59
Brief Summary
The objective of this protocol is to provide SU011248 treatment for patients who have participated in a SU011248 protocol and are eligible to enter this protocol
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2004
Longer than P75 for not_applicable
59 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
March 1, 2004
CompletedFirst Submitted
Initial submission to the registry
November 25, 2008
CompletedFirst Posted
Study publicly available on registry
November 26, 2008
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2011
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2011
CompletedResults Posted
Study results publicly available
January 21, 2013
CompletedJanuary 21, 2013
December 1, 2012
7.8 years
November 25, 2008
December 13, 2012
December 13, 2012
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Duration of Treatment
Baseline up to Day 28 after last dose of study treatment
Study Arms (1)
Sunitinib
EXPERIMENTALInterventions
Sunitinib dose varies according to the doses allowed in previous protocol. It is given once a day, orally with various schedules depending on the parent protocol
Eligibility Criteria
You may qualify if:
- Prior SU011248 Protocol.
- Eligible to continue SU011248 treatment.
You may not qualify if:
- Uncontrolled CNS metastasis.
- Unfit to receive SU011248.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Pfizerlead
Study Sites (59)
Pfizer Investigational Site
Birmingham, Alabama, 35233-2115, United States
Pfizer Investigational Site
Birmingham, Alabama, 35233, United States
Pfizer Investigational Site
Birmingham, Alabama, 35294, United States
Pfizer Investigational Site
Los Angeles, California, 90033, United States
Pfizer Investigational Site
Los Angeles, California, 90095, United States
Pfizer Investigational Site
San Francisco, California, 94115-1705, United States
Pfizer Investigational Site
San Francisco, California, 94115, United States
Pfizer Investigational Site
Santa Monica, California, 90404, United States
Pfizer Investigational Site
Aurora, Colorado, 80045, United States
Pfizer Investigational Site
Indianapolis, Indiana, 46202, United States
Pfizer Investigational Site
Boston, Massachusetts, 02114, United States
Pfizer Investigational Site
Boston, Massachusetts, 02115, United States
Pfizer Investigational Site
Boston, Massachusetts, 02215, United States
Pfizer Investigational Site
Ann Arbor, Michigan, 48109-0843, United States
Pfizer Investigational Site
Detroit, Michigan, 48201, United States
Pfizer Investigational Site
Farmington Hills, Michigan, 48334, United States
Pfizer Investigational Site
Minneapolis, Minnesota, 55455-0392, United States
Pfizer Investigational Site
St Louis, Missouri, 63110, United States
Pfizer Investigational Site
Albuquerque, New Mexico, 87131-0001, United States
Pfizer Investigational Site
Albuqurque, New Mexico, 87106, United States
Pfizer Investigational Site
New York, New York, 10021, United States
Pfizer Investigational Site
New York, New York, 10022, United States
Pfizer Investigational Site
New York, New York, 10032, United States
Pfizer Investigational Site
Durham, North Carolina, 27710, United States
Pfizer Investigational Site
Cleveland, Ohio, 44195, United States
Pfizer Investigational Site
Philadelphia, Pennsylvania, 19111, United States
Pfizer Investigational Site
Myrtle Beach, South Carolina, 29572, United States
Pfizer Investigational Site
Franklin, Tennessee, 37067, United States
Pfizer Investigational Site
Gallatin, Tennessee, 37066, United States
Pfizer Investigational Site
Hermitage, Tennessee, 37076, United States
Pfizer Investigational Site
Lebanon, Tennessee, 37087, United States
Pfizer Investigational Site
Murfreesboro, Tennessee, 37130, United States
Pfizer Investigational Site
Nashville, Tennessee, 37203, United States
Pfizer Investigational Site
Nashville, Tennessee, 37205, United States
Pfizer Investigational Site
Nashville, Tennessee, 37207, United States
Pfizer Investigational Site
Nashville, Tennessee, 37211, United States
Pfizer Investigational Site
Nashville, Tennessee, 37212, United States
Pfizer Investigational Site
Nashville, Tennessee, 37232, United States
Pfizer Investigational Site
Smyrna, Tennessee, 37167, United States
Pfizer Investigational Site
Dallas, Texas, 75246, United States
Pfizer Investigational Site
Houston, Texas, 77030-4009, United States
Pfizer Investigational Site
Madison, Wisconsin, 53792, United States
Pfizer Investigational Site
Randwick, New South Wales, 2031, Australia
Pfizer Investigational Site
East Melbourne, Victoria, 3002, Australia
Pfizer Investigational Site
Heidelberg, Victoria, 3084, Australia
Pfizer Investigational Site
Montreal, Quebec, H2L 4M1, Canada
Pfizer Investigational Site
Villejuif, 94805, France
Pfizer Investigational Site
Thessaloniki, 564 03, Greece
Pfizer Investigational Site
Milan, 20133, Italy
Pfizer Investigational Site
Milan, 20141, Italy
Pfizer Investigational Site
Nijmegen, Gelderland, 6525 GA, Netherlands
Pfizer Investigational Site
Singapore, Singapore, 308433, Singapore
Pfizer Investigational Site
Lund, Sweden
Pfizer Investigational Site
Stockholm, Sweden
Pfizer Investigational Site
Sankt Gallen, CH-9007, Switzerland
Pfizer Investigational Site
Leeds, LS9 7TF, United Kingdom
Pfizer Investigational Site
London, NW1 2PG, United Kingdom
Pfizer Investigational Site
London, SW3 6JJ, United Kingdom
Pfizer Investigational Site
Newcastle upon Tyne, NE4 6BE, United Kingdom
Related Links
MeSH Terms
Interventions
Intervention Hierarchy (Ancestors)
Results Point of Contact
- Title
- Pfizer ClinicalTrials.gov Call Center
- Organization
- Pfizer, Inc.
Study Officials
- STUDY DIRECTOR
Pfizer CT.gov Call Center
Pfizer
Publication Agreements
- PI is Sponsor Employee
- No
- Restriction Type
- OTHER
- Restrictive Agreement
- Yes
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- INDUSTRY
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
November 25, 2008
First Posted
November 26, 2008
Study Start
March 1, 2004
Primary Completion
December 1, 2011
Study Completion
December 1, 2011
Last Updated
January 21, 2013
Results First Posted
January 21, 2013
Record last verified: 2012-12