A Treatment Protocol For Patients Continuing From A Prior SU011248 Protocol.

NCT ID: NCT00443534

Last Updated: 2013-05-24

Study Results

Results available

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Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

123 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-05-31

Study Completion Date

2011-12-31

Brief Summary

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This protocol allows subjects who have participated in a previous SU011248 protocol the ability to continue to receive SU011248 after their study has ended.

Detailed Description

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Conditions

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Neoplasms

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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1

Group Type EXPERIMENTAL

SU011248

Intervention Type DRUG

Administered orally in doses ranging from 25 to 50 mg once daily; dosing schedule and dosage depends on the patients dosing from the prior protocol

Interventions

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SU011248

Administered orally in doses ranging from 25 to 50 mg once daily; dosing schedule and dosage depends on the patients dosing from the prior protocol

Intervention Type DRUG

Other Intervention Names

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Sutent/Sunitinib

Eligibility Criteria

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Inclusion Criteria

* Participation in a previous SU011248 protocol and are judged by the investigator to have the potential to derive clinical benefit by remaining on SU011248 after the prior protocol ends.

Exclusion Criteria

* Severe acute or chronic medical or psychiatric condition, or laboratory abnormality that may increase the risk associated with study participation or study drug administration, or may interfere with the interpretation of study results, and in the judgment of the investigator would make the patient inappropriate for entry into this study.
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

Aurora, Colorado, United States

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Littleton, Colorado, United States

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Orlando, Florida, United States

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Atlanta, Georgia, United States

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Harvey, Illinois, United States

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Harvey, Illinois, United States

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Maywood, Illinois, United States

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Tinley Park, Illinois, United States

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Zion, Illinois, United States

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Munster, Indiana, United States

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Baltimore, Maryland, United States

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Grand Rapids, Michigan, United States

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City of Saint Peters, Missouri, United States

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Creve Coeur, Missouri, United States

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St Louis, Missouri, United States

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Las Vegas, Nevada, United States

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Hackensack, New Jersey, United States

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Chapel Hill, North Carolina, United States

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Clinton, North Carolina, United States

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Goldsboro, North Carolina, United States

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Hickory, North Carolina, United States

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Wilson, North Carolina, United States

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Oklahoma City, Oklahoma, United States

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Tulsa, Oklahoma, United States

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Tulsa, Oklahoma, United States

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Tulsa, Oklahoma, United States

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Hershey, Pennsylvania, United States

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Greenville, South Carolina, United States

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Greer, South Carolina, United States

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Spartanburg, South Carolina, United States

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Bedford, Texas, United States

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Dallas, Texas, United States

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Fort Worth, Texas, United States

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Houston, Texas, United States

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San Antonio, Texas, United States

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San Antonio, Texas, United States

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San Antonio, Texas, United States

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San Antonio, Texas, United States

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Edmonton, Alberta, Canada

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Ottawa, Ontario, Canada

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Montreal, Quebec, Canada

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Montreal, Quebec, Canada

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Montreal, Quebec, Canada

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Lyon, , France

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Marseille, , France

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Villejuif, , France

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Berlin, , Germany

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Großhansdorf, , Germany

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Hamburg, , Germany

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Wiesbaden, , Germany

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Bologna, , Italy

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Cremona, , Italy

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Genova, , Italy

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Milan, , Italy

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Orbassano (TO), , Italy

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Rozzano (MI), , Italy

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Elche, Alicante, Spain

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Barcelona, Barcelona, Spain

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Córdoba, Cordoba, Spain

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Sutton, Surrey, United Kingdom

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London, , United Kingdom

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Manchester, , United Kingdom

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Countries

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United States Canada France Germany Italy Spain United Kingdom

Related Links

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Other Identifiers

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A6181078

Identifier Type: -

Identifier Source: org_study_id

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