Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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ClinicalTrials.gov |
Last refreshed on:
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19 October 2017 |
Main ID: |
NCT00443534 |
Date of registration:
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02/03/2007 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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A Treatment Protocol For Patients Continuing From A Prior SU011248 Protocol.
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Scientific title:
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A Treatment Protocol For Patients Continuing From A Prior SU011248 Protocol. |
Date of first enrolment:
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May 2006 |
Target sample size:
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123 |
Recruitment status: |
Completed |
URL:
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https://clinicaltrials.gov/show/NCT00443534 |
Study type:
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Interventional |
Study design:
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Phase:
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N/A
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Countries of recruitment
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Canada
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France
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Germany
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Italy
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Spain
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United Kingdom
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United States
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Contacts
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Name:
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Pfizer CT.gov Call Center |
Address:
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Telephone:
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Email:
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Affiliation:
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Pfizer |
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Key inclusion & exclusion 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.
Age minimum:
18 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Neoplasms
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Intervention(s)
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Drug: SU011248
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Primary Outcome(s)
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Number of Participants With Adverse Events (AEs) and Serious Adverse Events (SAEs)
[Time Frame: Baseline up to Day 28 after last dose of study treatment]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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