Post Marketing Surveillance Study To Observe Safety And Efficacy Of Sutene

NCT00444795 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 520

Last updated 2017-02-01

Study results available
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Summary

To monitor use in real practice including adverse events and efficacy on Sutent capsules (Sunitinib malate)

Conditions

Interventions

DRUG

Sunitinib malate

Sunitinib : dosing not pre-determined

DRUG

Sunitinib malate

Sunitinib : dosing not pre-determined

DRUG

sunitinib malate

Sunitinib : dosing not pre-determined

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-05-31
Primary Completion
2015-03-31
Completion
2015-03-31

Countries

  • South Korea

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00444795 on ClinicalTrials.gov