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Clinical Trial Summary

The objective of this surveillance is to collect information about 1) adverse drug reaction not expected from the LPD (unknown adverse drug reaction), 2) the incidence of adverse drug reactions in this surveillance, and 3)factors considered to affect the safety and/or efficacy of this drug.


Clinical Trial Description

All the patients whom an investigator prescribes the first SUNITINIB MALATE(Sutent) should be registered. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT00716820
Study type Observational
Source Pfizer
Contact
Status Completed
Phase
Start date April 2008
Completion date September 2016

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