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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00798889
Other study ID # A6181030
Secondary ID
Status Completed
Phase N/A
First received November 25, 2008
Last updated December 13, 2012
Start date March 2004
Est. completion date December 2011

Study information

Verified date December 2012
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial 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


Other known NCT identifiers
  • NCT00569725

Recruitment information / eligibility

Status Completed
Enrollment 314
Est. completion date December 2011
Est. primary completion date December 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Prior SU011248 Protocol.

- Eligible to continue SU011248 treatment.

Exclusion Criteria:

- Uncontrolled CNS metastasis.

- Unfit to receive SU011248.

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Sunitinib
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

Locations

Country Name City State
Australia Pfizer Investigational Site East Melbourne Victoria
Australia Pfizer Investigational Site Heidelberg Victoria
Australia Pfizer Investigational Site Randwick New South Wales
Canada Pfizer Investigational Site Montreal Quebec
France Pfizer Investigational Site Villejuif Cedex
Greece Pfizer Investigational Site Thessaloniki
Italy Pfizer Investigational Site Milano
Italy Pfizer Investigational Site Milano
Netherlands Pfizer Investigational Site Nijmegen Gld
Singapore Pfizer Investigational Site Singapore
Sweden Pfizer Investigational Site Lund
Sweden Pfizer Investigational Site Stockholm
Switzerland Pfizer Investigational Site St. Gallen
United Kingdom Pfizer Investigational Site Leeds
United Kingdom Pfizer Investigational Site London
United Kingdom Pfizer Investigational Site London
United Kingdom Pfizer Investigational Site Newcastle-Upon-Tyne
United States Pfizer Investigational Site Albuquerque New Mexico
United States Pfizer Investigational Site Albuqurque New Mexico
United States Pfizer Investigational Site Ann Arbor Michigan
United States Pfizer Investigational Site Aurora Colorado
United States Pfizer Investigational Site Birmingham Alabama
United States Pfizer Investigational Site Birmingham Alabama
United States Pfizer Investigational Site Birmingham Alabama
United States Pfizer Investigational Site Boston Massachusetts
United States Pfizer Investigational Site Boston Massachusetts
United States Pfizer Investigational Site Boston Massachusetts
United States Pfizer Investigational Site Cleveland Ohio
United States Pfizer Investigational Site Dallas Texas
United States Pfizer Investigational Site Detroit Michigan
United States Pfizer Investigational Site Durham North Carolina
United States Pfizer Investigational Site Farmington Hills Michigan
United States Pfizer Investigational Site Franklin Tennessee
United States Pfizer Investigational Site Gallatin Tennessee
United States Pfizer Investigational Site Hermitage Tennessee
United States Pfizer Investigational Site Houston Texas
United States Pfizer Investigational Site Indianapolis Indiana
United States Pfizer Investigational Site Lebanon Tennessee
United States Pfizer Investigational Site Los Angeles California
United States Pfizer Investigational Site Los Angeles California
United States Pfizer Investigational Site Madison Wisconsin
United States Pfizer Investigational Site Minneapolis Minnesota
United States Pfizer Investigational Site Murfreesboro Tennessee
United States Pfizer Investigational Site Myrtle Beach South Carolina
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site Nashville Tennessee
United States Pfizer Investigational Site New York New York
United States Pfizer Investigational Site New York New York
United States Pfizer Investigational Site New York New York
United States Pfizer Investigational Site Philadelphia Pennsylvania
United States Pfizer Investigational Site San Francisco California
United States Pfizer Investigational Site San Francisco California
United States Pfizer Investigational Site Santa Monica, California
United States Pfizer Investigational Site Smyrna Tennessee
United States Pfizer Investigational Site St. Louis Missouri

Sponsors (1)

Lead Sponsor Collaborator
Pfizer

Countries where clinical trial is conducted

United States,  Australia,  Canada,  France,  Greece,  Italy,  Netherlands,  Singapore,  Sweden,  Switzerland,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Duration of Treatment Baseline up to Day 28 after last dose of study treatment Yes
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