NCT00798889

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

98
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
314

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Mar 2004

Longer than P75 for not_applicable

Geographic Reach
11 countries

59 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2004

Completed
4.7 years until next milestone

First Submitted

Initial submission to the registry

November 25, 2008

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 26, 2008

Completed
3 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 1, 2011

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 1, 2011

Completed
1.1 years until next milestone

Results Posted

Study results publicly available

January 21, 2013

Completed
Last Updated

January 21, 2013

Status Verified

December 1, 2012

Enrollment Period

7.8 years

First QC Date

November 25, 2008

Results QC Date

December 13, 2012

Last Update Submit

December 13, 2012

Conditions

Keywords

Solid tumors

Outcome Measures

Primary Outcomes (1)

  • Duration of Treatment

    Baseline up to Day 28 after last dose of study treatment

Study Arms (1)

Sunitinib

EXPERIMENTAL
Drug: Sunitinib

Interventions

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

Sunitinib

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (59)

Pfizer Investigational Site

Birmingham, Alabama, 35233-2115, United States

Location

Pfizer Investigational Site

Birmingham, Alabama, 35233, United States

Location

Pfizer Investigational Site

Birmingham, Alabama, 35294, United States

Location

Pfizer Investigational Site

Los Angeles, California, 90033, United States

Location

Pfizer Investigational Site

Los Angeles, California, 90095, United States

Location

Pfizer Investigational Site

San Francisco, California, 94115-1705, United States

Location

Pfizer Investigational Site

San Francisco, California, 94115, United States

Location

Pfizer Investigational Site

Santa Monica, California, 90404, United States

Location

Pfizer Investigational Site

Aurora, Colorado, 80045, United States

Location

Pfizer Investigational Site

Indianapolis, Indiana, 46202, United States

Location

Pfizer Investigational Site

Boston, Massachusetts, 02114, United States

Location

Pfizer Investigational Site

Boston, Massachusetts, 02115, United States

Location

Pfizer Investigational Site

Boston, Massachusetts, 02215, United States

Location

Pfizer Investigational Site

Ann Arbor, Michigan, 48109-0843, United States

Location

Pfizer Investigational Site

Detroit, Michigan, 48201, United States

Location

Pfizer Investigational Site

Farmington Hills, Michigan, 48334, United States

Location

Pfizer Investigational Site

Minneapolis, Minnesota, 55455-0392, United States

Location

Pfizer Investigational Site

St Louis, Missouri, 63110, United States

Location

Pfizer Investigational Site

Albuquerque, New Mexico, 87131-0001, United States

Location

Pfizer Investigational Site

Albuqurque, New Mexico, 87106, United States

Location

Pfizer Investigational Site

New York, New York, 10021, United States

Location

Pfizer Investigational Site

New York, New York, 10022, United States

Location

Pfizer Investigational Site

New York, New York, 10032, United States

Location

Pfizer Investigational Site

Durham, North Carolina, 27710, United States

Location

Pfizer Investigational Site

Cleveland, Ohio, 44195, United States

Location

Pfizer Investigational Site

Philadelphia, Pennsylvania, 19111, United States

Location

Pfizer Investigational Site

Myrtle Beach, South Carolina, 29572, United States

Location

Pfizer Investigational Site

Franklin, Tennessee, 37067, United States

Location

Pfizer Investigational Site

Gallatin, Tennessee, 37066, United States

Location

Pfizer Investigational Site

Hermitage, Tennessee, 37076, United States

Location

Pfizer Investigational Site

Lebanon, Tennessee, 37087, United States

Location

Pfizer Investigational Site

Murfreesboro, Tennessee, 37130, United States

Location

Pfizer Investigational Site

Nashville, Tennessee, 37203, United States

Location

Pfizer Investigational Site

Nashville, Tennessee, 37205, United States

Location

Pfizer Investigational Site

Nashville, Tennessee, 37207, United States

Location

Pfizer Investigational Site

Nashville, Tennessee, 37211, United States

Location

Pfizer Investigational Site

Nashville, Tennessee, 37212, United States

Location

Pfizer Investigational Site

Nashville, Tennessee, 37232, United States

Location

Pfizer Investigational Site

Smyrna, Tennessee, 37167, United States

Location

Pfizer Investigational Site

Dallas, Texas, 75246, United States

Location

Pfizer Investigational Site

Houston, Texas, 77030-4009, United States

Location

Pfizer Investigational Site

Madison, Wisconsin, 53792, United States

Location

Pfizer Investigational Site

Randwick, New South Wales, 2031, Australia

Location

Pfizer Investigational Site

East Melbourne, Victoria, 3002, Australia

Location

Pfizer Investigational Site

Heidelberg, Victoria, 3084, Australia

Location

Pfizer Investigational Site

Montreal, Quebec, H2L 4M1, Canada

Location

Pfizer Investigational Site

Villejuif, 94805, France

Location

Pfizer Investigational Site

Thessaloniki, 564 03, Greece

Location

Pfizer Investigational Site

Milan, 20133, Italy

Location

Pfizer Investigational Site

Milan, 20141, Italy

Location

Pfizer Investigational Site

Nijmegen, Gelderland, 6525 GA, Netherlands

Location

Pfizer Investigational Site

Singapore, Singapore, 308433, Singapore

Location

Pfizer Investigational Site

Lund, Sweden

Location

Pfizer Investigational Site

Stockholm, Sweden

Location

Pfizer Investigational Site

Sankt Gallen, CH-9007, Switzerland

Location

Pfizer Investigational Site

Leeds, LS9 7TF, United Kingdom

Location

Pfizer Investigational Site

London, NW1 2PG, United Kingdom

Location

Pfizer Investigational Site

London, SW3 6JJ, United Kingdom

Location

Pfizer Investigational Site

Newcastle upon Tyne, NE4 6BE, United Kingdom

Location

Related Links

MeSH Terms

Interventions

Sunitinib

Intervention Hierarchy (Ancestors)

PyrrolesAzolesHeterocyclic Compounds, 1-RingHeterocyclic CompoundsIndolesHeterocyclic Compounds, 2-RingHeterocyclic Compounds, Fused-Ring

Results Point of Contact

Title
Pfizer ClinicalTrials.gov Call Center
Organization
Pfizer, Inc.

Study Officials

  • Pfizer CT.gov Call Center

    Pfizer

    STUDY DIRECTOR

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

Locations