Rollover Protocol for Prior SU011248 Protocols

NCT ID: NCT00798889

Last Updated: 2013-01-21

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

314 participants

Study Classification

INTERVENTIONAL

Study Start Date

2004-03-31

Study Completion Date

2011-12-31

Brief Summary

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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

Detailed Description

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Conditions

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Solid Tumors

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Sunitinib

Group Type EXPERIMENTAL

Sunitinib

Intervention Type DRUG

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

Interventions

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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

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Prior SU011248 Protocol.
* Eligible to continue SU011248 treatment.

Exclusion Criteria

* Uncontrolled CNS metastasis.
* Unfit to receive SU011248.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Pfizer CT.gov Call Center

Role: STUDY_DIRECTOR

Pfizer

Locations

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Pfizer Investigational Site

Birmingham, Alabama, United States

Site Status

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Birmingham, Alabama, United States

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Birmingham, Alabama, United States

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Los Angeles, California, United States

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Los Angeles, California, United States

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San Francisco, California, United States

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San Francisco, California, United States

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Santa Monica, California, United States

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Aurora, Colorado, United States

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Indianapolis, Indiana, United States

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Boston, Massachusetts, United States

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Boston, Massachusetts, United States

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Boston, Massachusetts, United States

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Ann Arbor, Michigan, United States

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Detroit, Michigan, United States

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Farmington Hills, Michigan, United States

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Minneapolis, Minnesota, United States

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St Louis, Missouri, United States

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Albuquerque, New Mexico, United States

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Albuqurque, New Mexico, United States

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New York, New York, United States

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New York, New York, United States

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New York, New York, United States

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Durham, North Carolina, United States

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Cleveland, Ohio, United States

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Philadelphia, Pennsylvania, United States

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Myrtle Beach, South Carolina, United States

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Franklin, Tennessee, United States

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Gallatin, Tennessee, United States

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Hermitage, Tennessee, United States

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Lebanon, Tennessee, United States

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Murfreesboro, Tennessee, United States

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Nashville, Tennessee, United States

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Nashville, Tennessee, United States

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Nashville, Tennessee, United States

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Nashville, Tennessee, United States

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Nashville, Tennessee, United States

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Nashville, Tennessee, United States

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Smyrna, Tennessee, United States

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Dallas, Texas, United States

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Houston, Texas, United States

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Madison, Wisconsin, United States

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Randwick, New South Wales, Australia

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East Melbourne, Victoria, Australia

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Heidelberg, Victoria, Australia

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Montreal, Quebec, Canada

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Villejuif, , France

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Thessaloniki, , Greece

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Milan, , Italy

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Milan, , Italy

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Nijmegen, Gelderland, Netherlands

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Singapore, Singapore, Singapore

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Lund, , Sweden

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Stockholm, , Sweden

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Sankt Gallen, , Switzerland

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Leeds, , United Kingdom

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London, , United Kingdom

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London, , United Kingdom

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Newcastle upon Tyne, , United Kingdom

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Countries

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

Related Links

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Other Identifiers

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A6181030

Identifier Type: -

Identifier Source: org_study_id

NCT00569725

Identifier Type: -

Identifier Source: nct_alias

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